{"title":"Single-Use","description":null,"products":[{"product_id":"portable-filter-integrity-tester","title":"Portable Filter Integrity Tester it-02 – Bubble Point, Diffusion \u0026 WFT","description":"\u003csection class=\"fi-integrity-detail\" aria-labelledby=\"fi-it02-heading\"\u003e\n\n\u003cstyle\u003e\n.fi-integrity-detail{\n  --fi-dark:#10242d;\n  --fi-accent:#2b7d77;\n  --fi-text:#172126;\n  --fi-muted:#5d6a70;\n  --fi-soft:#f4f8f7;\n  --fi-border:#dce7e5;\n  color:var(--fi-text);\n}\n.fi-integrity-detail *,\n.fi-integrity-detail *:before,\n.fi-integrity-detail *:after{box-sizing:border-box;}\n.fi-integrity-detail h2,\n.fi-integrity-detail h3{color:var(--fi-text);line-height:1.2;}\n.fi-integrity-detail h2{\n  margin:42px 0 16px;\n  font-size:clamp(25px,3vw,34px);\n}\n.fi-integrity-detail h2:first-of-type{margin-top:0;}\n.fi-integrity-detail h3{margin:25px 0 10px;font-size:20px;}\n.fi-integrity-detail p,\n.fi-integrity-detail li{\n  color:var(--fi-muted);\n  font-size:16px;\n  line-height:1.7;\n}\n.fi-integrity-detail strong{color:var(--fi-text);}\n.fi-lead{font-size:18px!important;line-height:1.65!important;}\n\n.fi-highlight{\n  margin:26px 0 34px;\n  padding:24px;\n  background:var(--fi-soft);\n  border:1px solid var(--fi-border);\n  border-radius:12px;\n}\n.fi-highlight-grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n}\n.fi-stat{\n  padding:15px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n.fi-stat span{\n  display:block;\n  margin-bottom:5px;\n  color:var(--fi-muted);\n  font-size:12px;\n}\n.fi-stat strong{display:block;font-size:16px;}\n\n.fi-table-wrap{\n  overflow-x:auto;\n  margin:22px 0 30px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n.fi-table{\n  width:100%;\n  min-width:680px;\n  border-collapse:collapse;\n}\n.fi-table th,\n.fi-table td{\n  padding:13px 15px;\n  border-bottom:1px solid var(--fi-border);\n  text-align:left;\n  vertical-align:top;\n  font-size:14px;\n}\n.fi-table th{\n  width:34%;\n  background:var(--fi-soft);\n  color:var(--fi-text);\n  font-weight:700;\n}\n.fi-table tr:last-child th,\n.fi-table tr:last-child td{border-bottom:0;}\n\n.fi-note{\n  margin:22px 0;\n  padding:18px 20px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n\n.fi-grid{\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:16px;\n  margin:22px 0 34px;\n}\n.fi-card{\n  padding:21px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n  background:#fff;\n}\n.fi-card h3{margin-top:0;}\n\n.fi-regulatory{\n  margin:36px 0;\n  padding:28px;\n  background:var(--fi-dark);\n  border-radius:13px;\n}\n.fi-regulatory h2,\n.fi-regulatory h3{color:#fff;}\n.fi-regulatory p,\n.fi-regulatory li{color:rgba(255,255,255,.78);}\n.fi-regulatory strong{color:#fff;}\n\n.fi-regulatory-grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n  margin-top:21px;\n}\n.fi-regulatory-item{\n  padding:17px;\n  background:rgba(255,255,255,.07);\n  border:1px solid rgba(255,255,255,.12);\n  border-radius:9px;\n  color:rgba(255,255,255,.78);\n  font-size:14px;\n  line-height:1.6;\n}\n.fi-regulatory-item strong{\n  display:block;\n  margin-bottom:5px;\n}\n\n.fi-links{\n  margin:35px 0;\n  padding:27px;\n  background:var(--fi-dark);\n  border-radius:12px;\n}\n.fi-links h2,\n.fi-links p{color:#fff;}\n.fi-links p{color:rgba(255,255,255,.78);}\n\n.fi-buttons{\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:20px;\n}\n.fi-button{\n  display:inline-flex;\n  min-height:46px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n.fi-button-primary{background:var(--fi-accent);color:#fff!important;}\n.fi-button-secondary{background:#fff;color:var(--fi-dark)!important;}\n\n.fi-faq details{\n  margin-bottom:10px;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n  background:#fff;\n}\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n.fi-faq details \u003e div{padding:0 19px 17px;}\n.fi-faq details p{margin:0;}\n\n@media(max-width:900px){\n  .fi-highlight-grid,\n  .fi-regulatory-grid{grid-template-columns:repeat(2,minmax(0,1fr));}\n  .fi-grid{grid-template-columns:1fr;}\n}\n@media(max-width:500px){\n  .fi-highlight-grid,\n  .fi-regulatory-grid{grid-template-columns:1fr;}\n  .fi-button{width:100%;}\n}\n\u003c\/style\u003e\n\n\n\u003ch2 id=\"fi-it02-heading\"\u003e\n  Compact Mobile Filter Integrity Tester it-02\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-lead\"\u003e\n  The \u003cstrong\u003eit-02 portable filter integrity tester\u003c\/strong\u003e is a compact,\n  hand-portable mobile system for integrity testing of hydrophilic and\n  hydrophobic membrane filters in pharmaceutical, biotechnology and other\n  regulated filtration environments.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  With a stainless-steel IP65 enclosure, rechargeable-battery capability,\n  7-inch touchscreen and integrated test reporting, the it-02 can be carried\n  directly to filtration points throughout laboratories, cleanrooms and\n  production facilities.\n\u003c\/p\u003e\n\n\n\u003cdiv class=\"fi-highlight\"\u003e\n\u003cdiv class=\"fi-highlight-grid\"\u003e\n\n\u003cdiv class=\"fi-stat\"\u003e\n\u003cspan\u003ePressure measurement\u003c\/span\u003e\n\u003cstrong\u003e0–6 bar\u003c\/strong\u003e\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-stat\"\u003e\n\u003cspan\u003ePrimary test methods\u003c\/span\u003e\n\u003cstrong\u003eDiffusion · BP · WFT\u003c\/strong\u003e\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-stat\"\u003e\n\u003cspan\u003eStored test results\u003c\/span\u003e\n\u003cstrong\u003e\u0026gt;12,000\u003c\/strong\u003e\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-stat\"\u003e\n\u003cspan\u003eWeight\u003c\/span\u003e\n\u003cstrong\u003eApprox. 11.5 kg\u003c\/strong\u003e\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\u003c\/div\u003e\n\n\n\u003ch2\u003ePortable integrity testing at the filter location\u003c\/h2\u003e\n\n\u003cp\u003e\n  The it-02 is designed for applications where the integrity tester must be\n  moved easily between different filter systems and test locations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Unlike a trolley-mounted test station, the compact instrument can be carried\n  directly to the test point and transported in its protective mobile case.\n  Battery operation further supports flexible use where mains power is not\n  immediately available.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The instrument can be used with membrane cartridges, capsule filters,\n  mini-cartridges, disposable filters and other compatible membrane-filter\n  formats.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eFilter integrity test methods\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003eDiffusion \/ Forward Flow Test\u003c\/h3\u003e\n\u003cp\u003e\nMeasures gas diffusion through a wetted membrane at a defined pressure.\nThis method is widely used for integrity testing of suitable hydrophilic\nliquid membrane filters.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003eBubble Point Test\u003c\/h3\u003e\n\u003cp\u003e\nEvaluates the pressure at which wetting liquid is displaced from the largest\nmembrane pores. A combined Diffusion + Bubble Point programme is also\navailable.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003eWater Flow Test – WFT \/ WIT\u003c\/h3\u003e\n\u003cp\u003e\nThe Water Flow Test, historically also referred to as Water Intrusion Test,\nis available for suitable hydrophobic membrane-filter applications.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003ePressure Drop Test\u003c\/h3\u003e\n\u003cp\u003e\nMeasures pressure change during a defined test sequence and provides another\nnon-destructive method for appropriate filter or system integrity\napplications.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003eUpstream Volume Measurement\u003c\/h3\u003e\n\u003cp\u003e\nThe instrument can measure the upstream volume of a connected filter system\nto support automated integrity-test calculations and setup.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003carticle class=\"fi-card\"\u003e\n\u003ch3\u003eCombined Test Programmes\u003c\/h3\u003e\n\u003cp\u003e\nDiffusion and Bubble Point testing can be combined into one programmed test\nsequence to reduce operator handling between tests.\n\u003c\/p\u003e\n\u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\n\u003ch2\u003eit-02 technical specifications\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n\u003cth\u003eModel\u003c\/th\u003e\n\u003ctd\u003e\u003cstrong\u003eit-02\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eSystem type\u003c\/th\u003e\n\u003ctd\u003eCompact hand-portable mobile membrane filter integrity tester\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eCabinet material\u003c\/th\u003e\n\u003ctd\u003eStainless steel 1.4301, electropolished and splash protected\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eDimensions\u003c\/th\u003e\n\u003ctd\u003eApprox. 220 × 300 × 245 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eWeight\u003c\/th\u003e\n\u003ctd\u003eApprox. 11.5 kg\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eProtection class\u003c\/th\u003e\n\u003ctd\u003eIP65\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003ePower supply\u003c\/th\u003e\n\u003ctd\u003e20 V \/ 3.3 A low-voltage mains adapter or rechargeable battery\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eHMI\u003c\/th\u003e\n\u003ctd\u003e7-inch capacitive TFT touchscreen\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eDisplay\u003c\/th\u003e\n\u003ctd\u003e1280 × 720 pixels\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eOperating system\u003c\/th\u003e\n\u003ctd\u003eProtected Linux operating system\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eStored test programmes\u003c\/th\u003e\n\u003ctd\u003eMore than 500\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eStored test results\u003c\/th\u003e\n\u003ctd\u003eMore than 12,000\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eInternal pressure sensor\u003c\/th\u003e\n\u003ctd\u003e0–6 bar, class 0.2\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eExternal pressure sensor\u003c\/th\u003e\n\u003ctd\u003e0–6 bar relative, class 0.05\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eBarometric pressure sensor\u003c\/th\u003e\n\u003ctd\u003e800–1070 mbar relative, class 0.5\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eData transfer\u003c\/th\u003e\n\u003ctd\u003eUSB Type-C and Bluetooth\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eLanguages\u003c\/th\u003e\n\u003ctd\u003eEnglish and German\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eAmbient operating temperature\u003c\/th\u003e\n\u003ctd\u003e5–40 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003ch2\u003eMeasurement accuracy\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n\u003cth\u003ePressure Drop Test\u003c\/th\u003e\n\u003ctd\u003e±0.6 mbar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth\u003eWater Flow Test\u003c\/th\u003e\n\u003ctd\u003e≤3%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth\u003eDiffusion Test\u003c\/th\u003e\n\u003ctd\u003e≤4%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth\u003eBubble Point Test\u003c\/th\u003e\n\u003ctd\u003e±50 mbar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003cth\u003eVolume Measurement\u003c\/th\u003e\n\u003ctd\u003e≤2%\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eFilter-specific limits:\u003c\/strong\u003e test pressure, wetting medium,\n  stabilisation time, test duration and acceptance criteria must be selected\n  according to the validated specification of the membrane filter being\n  tested.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eDirect capsule filter integrity testing\u003c\/h2\u003e\n\n\u003cp\u003e\n  A dedicated filter holder on the rear of the it-02 allows small membrane\n  filters to be connected directly to the instrument.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Compatible formats can include \u003cstrong\u003ecapsule filters, approximately\n  50 mm disposable filters, mini-cartridges and syringe filters\u003c\/strong\u003e.\n  This makes the it-02 particularly useful for laboratory development,\n  pilot-scale filtration and pharmaceutical single-use filtration systems.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filtra also supplies\n  \u003ca href=\"\/collections\/capsule-and-lab-filters\"\u003e\u003cstrong\u003ePES, PTFE, PVDF,\n  Nylon and polypropylene capsule filters\u003c\/strong\u003e\u003c\/a\u003e\n  for laboratory, pilot and process filtration.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eHydrophilic and hydrophobic membrane testing\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003eMembrane application\u003c\/th\u003e\n\u003cth\u003eRelevant integrity-test approach\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n\u003ctd\u003e\n\u003cstrong\u003eHydrophilic liquid membranes\u003c\/strong\u003e\u003cbr\u003e\nPES, PVDF, Nylon and comparable wetted membranes\n\u003c\/td\u003e\n\u003ctd\u003e\nDiffusion \/ Forward Flow, Bubble Point, combined testing and applicable\npressure-based tests according to the validated filter specification\n\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003ctd\u003e\n\u003cstrong\u003eHydrophobic gas and vent membranes\u003c\/strong\u003e\u003cbr\u003e\nPTFE and comparable hydrophobic membranes\n\u003c\/td\u003e\n\u003ctd\u003e\nWater Flow \/ Water Intrusion-type testing and other validated methods\nspecified for the individual filter\n\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003ch2\u003eOptional automatic membrane wetting\u003c\/h2\u003e\n\n\u003cp\u003e\n  The it-02 can be configured with an automatic wetting system for compatible\n  membrane filters.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Pressure-assisted wetting helps prepare the membrane consistently before the\n  integrity test, reducing operator-dependent variation. Dedicated wetting\n  configurations are available for both cartridge filters and capsule filters.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The integrity test can then follow immediately after the controlled wetting\n  procedure.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eSingle-use bag assembly leak testing\u003c\/h2\u003e\n\n\u003cp\u003e\n  With the optional low-pressure test module, the it-02 platform can also be\n  extended to \u003cstrong\u003eleak testing of sterile single-use bag assemblies\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The documented low-pressure unit operates between\n  \u003cstrong\u003e50 and 500 mbar\u003c\/strong\u003e and can also be applied to selected small\n  storage tanks and fermenters. An integrated vacuum pump enables evacuation\n  of the connected bag before testing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This allows membrane-filter integrity testing and selected single-use\n  assembly leak testing to form part of the same broader quality-control\n  platform.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eTest reporting and data integrity\u003c\/h2\u003e\n\n\u003cp\u003e\n  The it-02 is designed for documented filter testing in regulated\n  pharmaceutical and biotechnology environments.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eMore than 12,000 test results can be stored internally\u003c\/li\u003e\n  \u003cli\u003eIntegrated front-mounted thermal printer\u003c\/li\u003e\n  \u003cli\u003eAutomatic or manual report printing\u003c\/li\u003e\n  \u003cli\u003eDesktop software for receiving, managing and archiving test reports\u003c\/li\u003e\n  \u003cli\u003ePDF report storage\u003c\/li\u003e\n  \u003cli\u003eMobile report management for compatible smartphones and tablets\u003c\/li\u003e\n  \u003cli\u003eSecure timestamps on electronic reports\u003c\/li\u003e\n  \u003cli\u003eOriginal test data remains stored on the instrument\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003cdiv class=\"fi-regulatory\"\u003e\n\n\u003ch2\u003eGMP, 21 CFR Part 11 \u0026amp; Qualification Support\u003c\/h2\u003e\n\n\u003cp\u003e\n  The it-02 combines membrane integrity testing with electronic documentation,\n  traceability and qualification support for regulated pharmaceutical and\n  biotechnology environments.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-regulatory-grid\"\u003e\n\n\u003cdiv class=\"fi-regulatory-item\"\u003e\n\u003cstrong\u003e21 CFR Part 11\u003c\/strong\u003e\nThe system is designed to support regulated electronic-record and data\nintegrity requirements.\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-regulatory-item\"\u003e\n\u003cstrong\u003eCybersecurity\u003c\/strong\u003e\nThe documented platform addresses requirements associated with the\nEU Cyber Resilience Act.\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-regulatory-item\"\u003e\n\u003cstrong\u003eIQ \/ OQ\u003c\/strong\u003e\nQualification documentation packages can be supplied for Installation and\nOperational Qualification.\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-regulatory-item\"\u003e\n\u003cstrong\u003ePQ support\u003c\/strong\u003e\nPerformance Qualification support can be provided for the installed filter\nsystem and test application.\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\u003c\/div\u003e\n\n\n\u003ch2\u003eCalibration, IQ, OQ and PQ\u003c\/h2\u003e\n\n\u003cp\u003e\n  Annual inspection and calibration of the pressure sensors and pressure\n  control system are recommended to maintain measurement accuracy.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Qualification support can include Installation Qualification, Operational\n  Qualification and support for Performance Qualification of the installed\n  filter system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Test programmes and parameters can be established according to the filter,\n  application and validated integrity limits.\n\u003c\/p\u003e\n\n\n\u003ch2\u003eStandard scope of delivery\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eit-02 portable filter integrity tester\u003c\/li\u003e\n  \u003cli\u003eReference vessel\u003c\/li\u003e\n  \u003cli\u003e67 W \/ 20 V power supply\u003c\/li\u003e\n  \u003cli\u003eOutlet tube\u003c\/li\u003e\n  \u003cli\u003eAir regulator with 8 µm filter and inlet tube\u003c\/li\u003e\n  \u003cli\u003eMobile transport case\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch2\u003eit-02 vs ita-02: two mobile integrity-testing systems\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003e\u003c\/th\u003e\n\u003cth\u003eit-02\u003c\/th\u003e\n\u003cth\u003eita-02\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n\u003cth\u003eMobility\u003c\/th\u003e\n\u003ctd\u003e\u003cstrong\u003eHand-portable mobile tester\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003e\u003cstrong\u003eWheeled mobile trolley system\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eFormat\u003c\/th\u003e\n\u003ctd\u003eCompact standalone instrument\u003c\/td\u003e\n\u003ctd\u003eComplete mobile production test station\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eWeight\u003c\/th\u003e\n\u003ctd\u003eApprox. 11.5 kg\u003c\/td\u003e\n\u003ctd\u003eApprox. 55 kg\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eMovement\u003c\/th\u003e\n\u003ctd\u003eCarried directly to the filter location\u003c\/td\u003e\n\u003ctd\u003eRolled between production stations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eBest suited to\u003c\/th\u003e\n\u003ctd\u003eFlexible laboratory, cleanroom and production testing\u003c\/td\u003e\n\u003ctd\u003eRoutine integrity testing across multiple production stations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eCapsule testing\u003c\/th\u003e\n\u003ctd\u003eDirect capsule and small-filter testing\u003c\/td\u003e\n\u003ctd\u003eDirect capsule and small-filter testing\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eBattery operation\u003c\/th\u003e\n\u003ctd\u003eAvailable\u003c\/td\u003e\n\u003ctd\u003eAvailable\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n\u003cth\u003eAutomatic wetting\u003c\/th\u003e\n\u003ctd\u003eOptional\u003c\/td\u003e\n\u003ctd\u003eOptional\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eConfigure your it-02 integrity-testing system\u003c\/h2\u003e\n\n\u003cp\u003e\n  Send us your membrane type, filter format, test method, production\n  environment and qualification requirements. We can configure the it-02 for\n  cartridge filters, capsule filters, hydrophilic or hydrophobic membranes and\n  selected single-use assembly testing.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n\u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\nRequest it-02 Configuration\n\u003c\/a\u003e\n\n\u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/filter-integrity-testers\"\u003e\nCompare Integrity Testers\n\u003c\/a\u003e\n\n\u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/mobile-filter-integrity-test-system\"\u003e\nView Mobile Trolley ita-02\n\u003c\/a\u003e\n\n\u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\nCapsule Filters\n\u003c\/a\u003e\n\n\u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/filter-integrity-testing-guide\"\u003e\nIntegrity Testing Guide\n\u003c\/a\u003e\n\n\u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\nPharmaceutical Filtration\n\u003c\/a\u003e\n\n\u003c\/div\u003e\n\u003c\/div\u003e\n\n\n\u003ch2\u003eit-02 Filter Integrity Tester FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs the it-02 a mobile filter integrity tester?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nYes. The it-02 is a compact hand-portable mobile integrity tester designed\nto be carried directly between filter locations. A protective transport case\nis included in the documented standard scope.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat tests can the it-02 perform?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nThe it-02 supports Diffusion \/ Forward Flow, Bubble Point, combined\nDiffusion + Bubble Point, Pressure Drop, Water Flow Test and upstream-volume\nmeasurement.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan the it-02 test capsule filters?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nYes. A dedicated holder allows compatible capsule filters, disposable filters,\nmini-cartridges and syringe filters to be connected directly to the tester.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan the it-02 test PTFE hydrophobic filters?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nYes. The platform supports Water Flow \/ Water Intrusion-type integrity\ntesting for suitable hydrophobic membrane-filter applications.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs automatic membrane wetting available?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nYes. Optional automatic wetting configurations are available for compatible\ncapsule and cartridge filters.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan the it-02 test single-use bags?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nWith the optional low-pressure module, the platform can perform leak testing\nof sterile single-use bag assemblies. Additional hardware is required.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eDoes the it-02 support 21 CFR Part 11 requirements?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nThe system includes electronic reporting, traceability and data-integrity\nfunctions designed to support regulated electronic-record requirements.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan the it-02 operate on battery power?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nYes. The compact tester can operate from a rechargeable battery or its\n20 V low-voltage mains supply.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre IQ, OQ and PQ services available?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nQualification documentation can be supplied for IQ and OQ, with PQ support\navailable for the installed filter and test application.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between the it-02 and ita-02?\u003c\/summary\u003e\n\u003cdiv\u003e\u003cp\u003e\nBoth systems are mobile. The it-02 is a compact hand-portable tester, whereas\nthe ita-02 is a complete wheeled trolley-based integrity-testing station for\nroutine production use.\n\u003c\/p\u003e\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is the it-02 a mobile filter integrity tester?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The it-02 is a compact hand-portable mobile integrity tester designed to be carried directly between filter locations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What tests can the it-02 perform?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The it-02 supports Diffusion or Forward Flow, Bubble Point, combined Diffusion and Bubble Point, Pressure Drop, Water Flow Test and upstream-volume measurement.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can the it-02 test capsule filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A dedicated holder allows compatible capsule filters, disposable filters, mini-cartridges and syringe filters to be connected directly to the tester.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can the it-02 test PTFE hydrophobic filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The platform supports Water Flow or Water Intrusion-type integrity testing for suitable hydrophobic membrane-filter applications.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is automatic membrane wetting available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. Optional automatic wetting configurations are available for compatible capsule and cartridge filters.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can the it-02 test single-use bags?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"With the optional low-pressure module, the platform can perform leak testing of sterile single-use bag assemblies. Additional hardware is required.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between the it-02 and ita-02?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Both systems are mobile. The it-02 is a compact hand-portable tester, whereas the ita-02 is a complete wheeled trolley-based integrity-testing station for routine production use.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e\n\n\u003c\/section\u003e\n","brand":"Filtra International","offers":[{"title":"Liquid Membrane Filters \/ Standard it-02 \/ Standard Documentation","offer_id":56102147522886,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Liquid Membrane Filters \/ Standard it-02 \/ IQ \/ OQ Documentation Package","offer_id":57329713676614,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Liquid Membrane Filters \/ Standard it-02 \/ IQ \/ OQ + PQ Support","offer_id":57329713709382,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Liquid Membrane Filters \/ it-02 + Automatic Wetting – Capsule Filters \/ Standard Documentation","offer_id":57329713742150,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Liquid Membrane 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0 30px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-table{\n  width:100%;\n  min-width:650px;\n  border-collapse:collapse;\n}\n\n.fi-table th,\n.fi-table td{\n  padding:13px 15px;\n  border-bottom:1px solid var(--fi-border);\n  text-align:left;\n  vertical-align:top;\n  font-size:14px;\n}\n\n.fi-table th{\n  width:34%;\n  background:var(--fi-soft);\n  color:var(--fi-text);\n  font-weight:700;\n}\n\n.fi-table tr:last-child th,\n.fi-table tr:last-child td{\n  border-bottom:0;\n}\n\n.fi-note{\n  margin:22px 0;\n  padding:17px 19px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n\n.fi-grid{\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:16px;\n  margin:22px 0 34px;\n}\n\n.fi-card{\n  padding:21px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-card h3{\n  margin-top:0;\n}\n\n.fi-quality{\n  margin:36px 0;\n  padding:27px;\n  background:var(--fi-dark);\n  border-radius:13px;\n}\n\n.fi-quality h2,\n.fi-quality h3{\n  color:#fff;\n}\n\n.fi-quality p,\n.fi-quality li{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-quality strong{\n  color:#fff;\n}\n\n.fi-quality-grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n  margin-top:20px;\n}\n\n.fi-quality-item{\n  padding:17px;\n  background:rgba(255,255,255,.07);\n  border:1px solid rgba(255,255,255,.12);\n  border-radius:9px;\n  color:rgba(255,255,255,.78);\n  font-size:14px;\n  line-height:1.6;\n}\n\n.fi-quality-item strong{\n  display:block;\n  margin-bottom:5px;\n}\n\n.fi-links{\n  margin:35px 0;\n  padding:26px;\n  background:var(--fi-dark);\n  border-radius:12px;\n}\n\n.fi-links h2,\n.fi-links p{\n  color:#fff;\n}\n\n.fi-links p{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-buttons{\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:19px;\n}\n\n.fi-button{\n  display:inline-flex;\n  min-height:46px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n\n.fi-button-primary{\n  background:var(--fi-accent);\n  color:#fff!important;\n}\n\n.fi-button-secondary{\n  background:#fff;\n  color:var(--fi-dark)!important;\n}\n\n.fi-faq details{\n  margin-bottom:10px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n\n.fi-faq details \u003e div{\n  padding:0 19px 17px;\n}\n\n.fi-faq details p{\n  margin:0;\n}\n\n@media(max-width:850px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n\n  .fi-grid{\n    grid-template-columns:1fr;\n  }\n}\n\n@media(max-width:480px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-button{\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\n\u003c!-- INTRO --\u003e\n\n\u003ch2 id=\"fi-pes-capsule-heading\"\u003e\n  PES Membrane Capsule Filter – Hydrophilic Filtration from 0.03 to 5.0 µm\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-capsule-lead\"\u003e\n  Filtra International supplies \u003cstrong\u003ehydrophilic PES membrane capsule filters\u003c\/strong\u003e\n  for precision filtration of aqueous liquids in laboratory, biotechnology,\n  pharmaceutical process development and industrial applications.\n  Available membrane ratings range from \u003cstrong\u003e0.03 to 5.0 µm\u003c\/strong\u003e,\n  including the widely specified \u003cstrong\u003e0.2 µm PES capsule filter\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Polyethersulfone (PES) combines strong hydrophilicity with\n  \u003cstrong\u003elow protein adsorption\u003c\/strong\u003e, making it particularly useful for\n  aqueous buffers, process solutions and applications where interaction between\n  the membrane and valuable dissolved components should be minimised.\n\u003c\/p\u003e\n\n\n\u003c!-- KEY SPECS --\u003e\n\n\u003cdiv class=\"fi-capsule-highlight\"\u003e\n  \u003cdiv class=\"fi-capsule-highlight__grid\"\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eMembrane\u003c\/span\u003e\n      \u003cstrong\u003eHydrophilic PES\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003ePore sizes\u003c\/span\u003e\n      \u003cstrong\u003e0.03–5.0 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eKey characteristic\u003c\/span\u003e\n      \u003cstrong\u003eLow protein adsorption\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eCompact filter area\u003c\/span\u003e\n      \u003cstrong\u003eApprox. 300 cm²*\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003e*Configuration note:\u003c\/strong\u003e approximately 300 cm² is documented\n  for the compact PES capsule configuration. Filtra also offers larger capsule\n  formats. Effective filtration area, flow capacity and operating limits\n  therefore depend on the selected capsule size and configuration.\n\u003c\/p\u003e\n\n\n\u003c!-- TECHNICAL --\u003e\n\n\u003ch2\u003ePES capsule filter technical overview\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter type\u003c\/th\u003e\n  \u003ctd\u003eDisposable hydrophilic PES membrane capsule filter\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter membrane\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003ePolyethersulfone (PES)\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane behaviour\u003c\/th\u003e\n  \u003ctd\u003eStrongly hydrophilic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eProtein interaction\u003c\/th\u003e\n  \u003ctd\u003eLow protein adsorption\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical service\u003c\/th\u003e\n  \u003ctd\u003eAqueous solutions and compatible process liquids\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMedia support\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCapsule hardware \/ housing\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eOptional filling bell\u003c\/th\u003e\n  \u003ctd\u003ePolycarbonate, configuration-dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAvailable pore sizes\u003c\/th\u003e\n  \u003ctd\u003e\n    \u003cstrong\u003e0.03, 0.04, 0.1, 0.2, 0.45, 0.65, 0.8, 1.2, 3.0 and 5.0 µm\u003c\/strong\u003e\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFiltra selectable capsule lengths\u003c\/th\u003e\n  \u003ctd\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration filter area\u003c\/th\u003e\n  \u003ctd\u003eApprox. 300 cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration working pressure\u003c\/th\u003e\n  \u003ctd\u003eUp to 5 bar at 20 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eDocumented maximum operating temperature\u003c\/th\u003e\n  \u003ctd\u003e80 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003e100% integrity tested for the documented compact capsule range\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eBiological safety\u003c\/th\u003e\n  \u003ctd\u003eDocumented components meet USP Class VI-121°C specifications for plastics\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHot-water sanitisation\u003c\/th\u003e\n  \u003ctd\u003e90 °C for 30 minutes, multiple cycles\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAutoclaving\u003c\/th\u003e\n  \u003ctd\u003e121 °C for 30 minutes, multiple cycles for the documented compact configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMaterial compliance\u003c\/th\u003e\n  \u003ctd\u003eDocumented FDA 21 CFR and EU 10\/2011 food-contact material compliance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- OPERATING PRINCIPLE --\u003e\n\n\u003ch2\u003eHow does a PES membrane capsule filter work?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Process liquid enters through the selected inlet connection and passes through\n  the hydrophilic PES membrane. The controlled membrane pore structure retains\n  particulate, colloidal and other contamination according to the selected\n  membrane rating, while filtered liquid exits through the outlet connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Because PES is hydrophilic, compatible aqueous liquids wet the membrane\n  readily. This provides straightforward start-up for water-based process\n  fluids without the pre-wetting typically required by hydrophobic membranes\n  such as PTFE.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The membrane and housing form one enclosed disposable capsule assembly,\n  eliminating the need for a separate cartridge-filter housing for the capsule\n  itself.\n\u003c\/p\u003e\n\n\n\u003c!-- WHY PES --\u003e\n\n\u003ch2\u003eWhy choose a hydrophilic PES membrane?\u003c\/h2\u003e\n\n\u003cp\u003e\n  PES is particularly suited to aqueous filtration because of its strong\n  hydrophilicity. Another important characteristic is\n  \u003cstrong\u003elow protein adsorption\u003c\/strong\u003e, which can help reduce unwanted\n  interaction between the membrane and proteins or other valuable dissolved\n  components.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This makes PES an important membrane to evaluate for buffers, purified water,\n  biotechnology process liquids, pharmaceutical process development and other\n  compatible aqueous solutions.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For protein-containing or high-value biological products, actual product\n  recovery should still be verified under representative process conditions.\n\u003c\/p\u003e\n\n\n\u003c!-- 0.2 MICRON --\u003e\n\n\u003ch2\u003e0.2 micron PES capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  The \u003cstrong\u003e0.2 µm PES capsule filter\u003c\/strong\u003e is one of the most relevant\n  configurations for fine filtration of aqueous pharmaceutical, biotechnology\n  and laboratory process fluids.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Its hydrophilic membrane is well suited to water-based solutions, buffers\n  and other compatible liquids where a fine membrane pore size is required.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eSterile-filtration note:\u003c\/strong\u003e a nominal 0.2 µm pore size and\n  manufacturing integrity test do not by themselves demonstrate that every\n  PES capsule configuration is a validated sterilizing-grade filter.\n  Where validated microbial retention is required, confirm the exact filter\n  grade, integrity-test specification and supporting validation documentation.\n\u003c\/p\u003e\n\n\n\u003c!-- PORE SIZES --\u003e\n\n\u003ch2\u003ePES capsule filters from 0.03 to 5.0 micron\u003c\/h2\u003e\n\n\u003cp\u003e\n  The broad PES pore-size range allows the membrane platform to be used for\n  different clarification, fine-filtration and process-development duties.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.03–0.1 µm PES filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Very fine membrane configurations for applications requiring particularly\n      small documented pore sizes and high particulate retention.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.2–0.45 µm PES filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Common fine-filtration ratings for aqueous process solutions,\n      pharmaceutical development, biotechnology and laboratory filtration.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.65–5.0 µm PES filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Larger-pore configurations for clarification, particle reduction and\n      upstream filtration where lower membrane resistance or greater solids\n      tolerance is required.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Available ratings are \u003cstrong\u003e0.03, 0.04, 0.1, 0.2, 0.45, 0.65,\n  0.8, 1.2, 3.0 and 5.0 µm\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\n\u003c!-- AQUEOUS --\u003e\n\n\u003ch2\u003ePES capsule filters for aqueous buffers and process solutions\u003c\/h2\u003e\n\n\u003cp\u003e\n  PES is primarily suited to filtration of compatible aqueous liquids.\n  Typical applications can include purified water, laboratory solutions,\n  aqueous buffers, process intermediates and biotechnology or pharmaceutical\n  process-development fluids.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Membrane selection should consider not only pore size, but also the complete\n  fluid composition, pH, temperature, additives, solids loading and required\n  downstream retention.\n\u003c\/p\u003e\n\n\n\u003c!-- PROTEIN --\u003e\n\n\u003ch2\u003eLow protein adsorption for biotech and pharmaceutical filtration\u003c\/h2\u003e\n\n\u003cp\u003e\n  Low protein adsorption is one of the useful characteristics of PES membrane\n  media. For protein-containing solutions, this can help reduce unnecessary\n  adsorption onto the filtration membrane.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Applications involving valuable proteins, biological products or sensitive\n  formulations should still be tested under representative conditions because\n  actual adsorption and product recovery depend on the formulation as well as\n  the membrane material.\n\u003c\/p\u003e\n\n\n\u003c!-- CONNECTIONS --\u003e\n\n\u003ch2\u003ePES capsule filter connection options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra offers multiple connection configurations for integration into\n  laboratory tubing, pilot systems and process installations.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNPT connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\" NPT male, 3\/8\" NPT male, 1\/2\" NPT male and\n    3\/8\" NPT female options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSwagelok connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\", 5\/16\", 3\/8\" and 1\/2\" selectable configurations\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCPC quick-connect\u003c\/th\u003e\n  \u003ctd\u003e1\/4\" CPC PLC male and female configurations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHose barb\u003c\/th\u003e\n  \u003ctd\u003e\n    3\/8\", 1\/2\" and 1\/4\"–3\/8\" stepped hose-barb options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSanitary connection\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003e1\" Tri-Clamp \/ Tri-Clover\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  Exact connection availability can depend on capsule format and selected\n  configuration. Confirm the required inlet and outlet arrangement when\n  requesting a quotation.\n\u003c\/p\u003e\n\n\n\u003c!-- LENGTH --\u003e\n\n\u003ch2\u003ePES capsule lengths from 1.5 to 20 inches\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra's selectable PES capsule configurations include\n  \u003cstrong\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/strong\u003e\n  formats.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Capsule size influences effective membrane area, flow capacity, pressure\n  drop, dirt-holding capacity and total throughput. The documented\n  \u003cstrong\u003e300 cm² filter area applies specifically to the compact capsule\n  configuration\u003c\/strong\u003e and should not be extrapolated to larger formats.\n\u003c\/p\u003e\n\n\n\u003c!-- APPLICATIONS --\u003e\n\n\u003ch2\u003eTypical PES capsule filter applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAqueous buffer filtration\u003c\/li\u003e\n  \u003cli\u003ePurified-water filtration\u003c\/li\u003e\n  \u003cli\u003eLaboratory sample preparation\u003c\/li\u003e\n  \u003cli\u003eBiotechnology process development\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical R\u0026amp;D and pilot filtration\u003c\/li\u003e\n  \u003cli\u003eCompatible biological-solution filtration\u003c\/li\u003e\n  \u003cli\u003eFine particle and colloid reduction\u003c\/li\u003e\n  \u003cli\u003eSmall-batch process filtration\u003c\/li\u003e\n  \u003cli\u003eProcess-solution clarification\u003c\/li\u003e\n  \u003cli\u003eFiltration before analytical or downstream process steps\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- COMPARISON --\u003e\n\n\u003ch2\u003ePES vs PVDF and PTFE capsule filters\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003ePES\u003c\/th\u003e\n  \u003cth\u003ePVDF\u003c\/th\u003e\n  \u003cth\u003ePTFE\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eWettability\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003eHydrophilic\u003c\/strong\u003e\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n  \u003ctd\u003eHydrophobic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eKey characteristic\u003c\/th\u003e\n  \u003ctd\u003eStrong hydrophilicity and low protein adsorption\u003c\/td\u003e\n  \u003ctd\u003eLow protein adsorption\u003c\/td\u003e\n  \u003ctd\u003eHydrophobicity and chemical resistance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical starting point\u003c\/th\u003e\n  \u003ctd\u003eAqueous buffers and process liquids\u003c\/td\u003e\n  \u003ctd\u003eProtein-sensitive and compatible biological\/process liquids\u003c\/td\u003e\n  \u003ctd\u003eGas, venting and compatible solvents\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFinal selection\u003c\/th\u003e\n  \u003ctd colspan=\"3\"\u003e\n    Compare chemical compatibility, protein recovery, pore size, flow,\n    operating conditions and required validation documentation.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- QUALITY --\u003e\n\n\u003cdiv class=\"fi-quality\"\u003e\n\n\u003ch2\u003eIntegrity Testing, Biological Safety \u0026amp; Material Compliance\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented compact PES capsule configuration includes several\n  quality and material-safety characteristics relevant to laboratory,\n  biotechnology and pharmaceutical process filtration.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-quality-grid\"\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003e100% integrity tested\u003c\/strong\u003e\n    The documented compact PES capsule range is individually integrity tested\n    during manufacturing.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n    Documented components meet biological-safety specifications for\n    USP Class VI-121°C plastics.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eAutoclave compatible\u003c\/strong\u003e\n    The documented compact configuration supports autoclaving at\n    121 °C for 30 minutes over multiple cycles.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eMaterial compliance\u003c\/strong\u003e\n    Documented construction materials have FDA 21 CFR and EU 10\/2011\n    food-contact material compliance.\n  \u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  The documented compact configuration also specifies hot-water sanitisation\n  at 90 °C for 30 minutes, a maximum working pressure of 5 bar at 20 °C\n  and a maximum operating temperature of 80 °C.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For regulated pharmaceutical applications, documentation should always be\n  confirmed against the exact membrane grade, pore size, capsule format and\n  selected configuration.\n\u003c\/p\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- PHARMA --\u003e\n\n\u003ch2\u003ePES capsule filters for pharmaceutical and biotechnology applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hydrophilic PES is an important membrane option for pharmaceutical and\n  biotechnology liquid filtration because it combines aqueous wettability\n  with low protein adsorption.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Potential applications include buffers, process solutions, purified water,\n  biological liquids, method development, pilot filtration and other compatible\n  aqueous process streams.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For regulated or sterile manufacturing processes, the product specification\n  should also consider microbial-retention validation, integrity-test limits,\n  sterilisation method, material compliance, extractables requirements,\n  traceability and any application-specific quality documentation.\n\u003c\/p\u003e\n\n\n\u003c!-- SELECTION --\u003e\n\n\u003ch2\u003eHow to select a PES capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  Correct PES capsule selection should consider the complete filtration duty,\n  not only the micron rating.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired pore size from 0.03 to 5.0 µm\u003c\/li\u003e\n  \u003cli\u003eProcess liquid and complete formulation\u003c\/li\u003e\n  \u003cli\u003eAqueous buffer or process-solution composition\u003c\/li\u003e\n  \u003cli\u003eProtein or biological-product recovery requirements\u003c\/li\u003e\n  \u003cli\u003eRequired particulate or microbial retention\u003c\/li\u003e\n  \u003cli\u003eFlow rate and total process volume\u003c\/li\u003e\n  \u003cli\u003eExpected solids and colloidal loading\u003c\/li\u003e\n  \u003cli\u003e1.5\", 2.5\", 5\", 10\" or 20\" capsule format\u003c\/li\u003e\n  \u003cli\u003eNPT, Swagelok, CPC, hose-barb or Tri-Clamp connection\u003c\/li\u003e\n  \u003cli\u003eOperating pressure and temperature\u003c\/li\u003e\n  \u003cli\u003eSanitisation or autoclaving requirements\u003c\/li\u003e\n  \u003cli\u003eIntegrity-testing and pharmaceutical validation requirements\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- LINKS --\u003e\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eNeed help selecting a PES capsule filter?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Send us your liquid composition, required pore size, process volume,\n  flow rate, connection type and documentation requirements. We can help\n  determine the appropriate PES configuration or compare PES with PVDF,\n  PTFE and polypropylene alternatives.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n  \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n    Request Technical Selection\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n    Compare Capsule Filters\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pvdf-membrane-capsule-filter\"\u003e\n    Compare PVDF Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/ptfe-membrane-capsule-filter\"\u003e\n    Compare PTFE Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\n    Pharmaceutical Filtration\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/sterile-filtration-of-injectable-drugs\"\u003e\n    Sterile Filtration Guide\n  \u003c\/a\u003e\n\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ --\u003e\n\n\u003ch2\u003ePES Membrane Capsule Filter FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is a PES membrane capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nA PES membrane capsule filter is a self-contained disposable filtration\ndevice containing a polyethersulfone membrane inside a polymer capsule.\nHydrophilic PES is primarily used for fine filtration of compatible aqueous\nlaboratory, biotechnology and process liquids.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs PES hydrophilic?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. PES membrane in this range is strongly hydrophilic, making it well\nsuited to filtration of compatible aqueous liquids without the pre-wetting\ntypically required by hydrophobic membranes.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eDoes PES have low protein adsorption?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. Low protein adsorption is a documented characteristic of this PES\nmembrane. This can be useful when filtering protein-containing or other\nvaluable process solutions, although actual product recovery should be\nverified for the specific formulation.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PES capsule filter pore sizes are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nAvailable pore sizes include 0.03, 0.04, 0.1, 0.2, 0.45, 0.65,\n0.8, 1.2, 3.0 and 5.0 µm.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a 0.2 micron PES capsule filter available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. A 0.2 µm hydrophilic PES configuration is available and is relevant\nto fine filtration of aqueous pharmaceutical, biotechnology and laboratory\nprocess liquids.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eDoes 0.2 micron mean the PES filter is sterilizing grade?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nNo. A nominal 0.2 µm pore size alone does not prove validated\nsterilizing-grade performance. The exact membrane grade, microbial-retention\nvalidation, integrity-test specification and supporting documentation must\nmeet the process requirement.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PES capsule lengths are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nFiltra offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch\nPES capsule configurations. Technical specifications such as effective\nfilter area vary by capsule format.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich connection types are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nFiltra connection configurations include NPT, Swagelok, CPC quick-connect,\nhose-barb and 1-inch Tri-Clamp \/ Tri-Clover options.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the filtration area of a PES capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PES capsule configuration provides approximately\n300 cm² of filtration area. Larger capsule formats can provide different\neffective filtration areas and should be specified separately.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PES capsule filters be autoclaved?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PES capsule configuration supports autoclaving at\n121 °C for 30 minutes over multiple cycles. Always confirm the applicable\nlimit for the exact capsule configuration selected.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre PES capsule filters integrity tested?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PES capsule range is 100% integrity tested during\nmanufacturing. For regulated filtration processes, confirm the applicable\ntest method and acceptance specification for the exact selected grade.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between PES and PTFE capsule filters?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nPES is hydrophilic and is commonly selected for aqueous buffers and process\nliquids. PTFE is hydrophobic and is commonly selected for air, gas, venting\nand compatible solvent filtration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between PES and PVDF capsule filters?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nBoth are hydrophilic membrane options with low protein adsorption\ncharacteristics. PES is commonly selected for a broad range of aqueous\nbuffers and process liquids, while PVDF can be evaluated for\nprotein-sensitive and other compatible biological applications. Final\nselection should be based on the actual formulation and required filtration\nperformance.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ JSON-LD --\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is a PES membrane capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"A PES membrane capsule filter is a self-contained disposable filtration device containing a polyethersulfone membrane inside a polymer capsule. Hydrophilic PES is primarily used for fine filtration of compatible aqueous laboratory, biotechnology and process liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is PES hydrophilic?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. PES membrane in this range is strongly hydrophilic and is well suited to filtration of compatible aqueous liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Does PES have low protein adsorption?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. Low protein adsorption is a documented characteristic of this PES membrane. Actual product recovery should be verified for the specific formulation.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PES capsule filter pore sizes are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Available pore sizes include 0.03, 0.04, 0.1, 0.2, 0.45, 0.65, 0.8, 1.2, 3.0 and 5.0 µm.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a 0.2 micron PES capsule filter available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A 0.2 µm hydrophilic PES configuration is available and is relevant to fine filtration of aqueous pharmaceutical, biotechnology and laboratory process liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Does 0.2 micron mean the PES filter is sterilizing grade?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"No. A nominal 0.2 µm pore size alone does not prove validated sterilizing-grade performance. The exact membrane grade, microbial-retention validation, integrity-test specification and supporting documentation must meet the process requirement.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PES capsule lengths are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Filtra offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch PES capsule configurations. Technical specifications such as effective filter area vary by capsule format.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which connection types are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Filtra connection configurations include NPT, Swagelok, CPC quick-connect, hose-barb and 1-inch Tri-Clamp or Tri-Clover options.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the filtration area of a PES capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PES capsule configuration provides approximately 300 cm² of filtration area. Larger capsule formats can have different effective filtration areas.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PES capsule filters be autoclaved?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PES capsule configuration supports autoclaving at 121 °C for 30 minutes over multiple cycles. Confirm the applicable limit for the exact selected capsule configuration.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Are PES capsule filters integrity tested?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PES capsule range is 100% integrity tested during manufacturing. For regulated processes, confirm the applicable test method and acceptance specification for the exact selected grade.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between PES and PTFE capsule filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"PES is hydrophilic and is commonly selected for aqueous buffers and process liquids. PTFE is hydrophobic and is commonly selected for air, gas, venting and compatible solvent filtration.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between PES and PVDF capsule filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Both are hydrophilic membrane options with low protein adsorption characteristics. PES is commonly selected for aqueous buffers and process liquids, while PVDF can be evaluated for protein-sensitive and other compatible biological applications.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e\n\n\u003c\/section\u003e","brand":"Filtra International","offers":[{"title":"0.03 µm \/ 1.5\" \/ 1\/4\" NPT Male (4N)","offer_id":56108555993414,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.03 µm \/ 1.5\" \/ 3\/8\" NPT Male (6N)","offer_id":56113215308102,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.03 µm \/ 1.5\" \/ 1\/2\" NPT Male (8N)","offer_id":56113215340870,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.03 µm \/ 1.5\" \/ 3\/8\" NPT Female (6NF)","offer_id":56113215373638,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.03 µm \/ 1.5\" \/ 1\/4\" Swagelok (4C)","offer_id":56113215406406,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.03 µm \/ 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align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n\n.fi-button-primary{\n  background:var(--fi-accent);\n  color:#fff!important;\n}\n\n.fi-button-secondary{\n  background:#fff;\n  color:var(--fi-dark)!important;\n}\n\n.fi-faq details{\n  margin-bottom:10px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n\n.fi-faq details \u003e div{\n  padding:0 19px 17px;\n}\n\n.fi-faq details p{\n  margin:0;\n}\n\n@media(max-width:850px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n\n  .fi-grid{\n    grid-template-columns:1fr;\n  }\n}\n\n@media(max-width:480px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-button{\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\n\u003c!-- INTRO --\u003e\n\n\u003ch2 id=\"fi-ptfe-capsule-heading\"\u003e\n  PTFE Capsule Filter – Hydrophobic Membrane for Gas, Vent \u0026amp; Solvent Filtration\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-capsule-lead\"\u003e\n  Filtra International supplies \u003cstrong\u003ehydrophobic PTFE capsule filters\u003c\/strong\u003e\n  for precision filtration of air, gases, organic solvents and compatible\n  chemical solutions. Available membrane ratings range from\n  \u003cstrong\u003e0.05 to 0.65 µm\u003c\/strong\u003e, including the widely specified\n  \u003cstrong\u003e0.2 µm PTFE capsule filter\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  PTFE combines strong hydrophobic behaviour with excellent chemical inertness,\n  making this membrane particularly useful for gas and vent filtration and for\n  liquid applications involving compatible organic solvents or chemically\n  demanding process fluids.\n\u003c\/p\u003e\n\n\n\u003c!-- KEY SPECS --\u003e\n\n\u003cdiv class=\"fi-capsule-highlight\"\u003e\n  \u003cdiv class=\"fi-capsule-highlight__grid\"\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eMembrane\u003c\/span\u003e\n      \u003cstrong\u003eHydrophobic PTFE\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003ePore sizes\u003c\/span\u003e\n      \u003cstrong\u003e0.05–0.65 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eTypical media\u003c\/span\u003e\n      \u003cstrong\u003eGas · Air · Solvents\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eCompact filter area\u003c\/span\u003e\n      \u003cstrong\u003eApprox. 300 cm²*\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003e*Configuration note:\u003c\/strong\u003e approximately 300 cm² is documented\n  for the compact PTFE capsule configuration. Filtra also offers larger capsule\n  formats. Effective filtration area, flow capacity and operating limits depend\n  on the exact capsule size and configuration.\n\u003c\/p\u003e\n\n\n\u003c!-- TECHNICAL --\u003e\n\n\u003ch2\u003ePTFE capsule filter technical overview\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter type\u003c\/th\u003e\n  \u003ctd\u003eDisposable hydrophobic PTFE membrane capsule filter\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter membrane\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003ePTFE – polytetrafluoroethylene\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane behaviour\u003c\/th\u003e\n  \u003ctd\u003eHydrophobic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical media\u003c\/th\u003e\n  \u003ctd\u003eAir, gases, organic solvents and compatible chemical liquids\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMedia support\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCapsule hardware \/ housing\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eOptional filling bell\u003c\/th\u003e\n  \u003ctd\u003ePolycarbonate, configuration-dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAvailable pore sizes\u003c\/th\u003e\n  \u003ctd\u003e\n    \u003cstrong\u003e0.05, 0.1, 0.2, 0.45 and 0.65 µm\u003c\/strong\u003e\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFiltra selectable capsule lengths\u003c\/th\u003e\n  \u003ctd\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration filter area\u003c\/th\u003e\n  \u003ctd\u003eApprox. 300 cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration working pressure\u003c\/th\u003e\n  \u003ctd\u003eUp to 5 bar at 20 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eDocumented maximum operating temperature\u003c\/th\u003e\n  \u003ctd\u003e80 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003e100% integrity tested for the documented compact capsule range\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eBiological safety\u003c\/th\u003e\n  \u003ctd\u003eDocumented components meet USP Class VI-121°C specifications for plastics\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHot-water sanitisation\u003c\/th\u003e\n  \u003ctd\u003e90 °C for 30 minutes, multiple cycles\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAutoclaving\u003c\/th\u003e\n  \u003ctd\u003e121 °C for 30 minutes, multiple cycles for the documented compact configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMaterial compliance\u003c\/th\u003e\n  \u003ctd\u003eDocumented FDA 21 CFR and EU 10\/2011 food-contact material compliance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- OPERATION --\u003e\n\n\u003ch2\u003eHow does a hydrophobic PTFE capsule filter work?\u003c\/h2\u003e\n\n\u003cp\u003e\n  The process gas or compatible liquid enters through the selected inlet\n  connection and passes through the PTFE membrane. The membrane pore structure\n  retains particulate contamination, aerosols and microorganisms according to\n  the selected membrane rating while the filtered stream exits through the\n  outlet.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  In gas and vent applications, the hydrophobic nature of PTFE is especially\n  important. The membrane permits gas flow while resisting penetration by\n  liquid water under suitable process conditions.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The membrane and housing are supplied as one enclosed capsule assembly,\n  allowing installation without a separate cartridge-filter housing.\n\u003c\/p\u003e\n\n\n\u003c!-- 0.2 MICRON --\u003e\n\n\u003ch2\u003e0.2 micron PTFE capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  The \u003cstrong\u003e0.2 µm PTFE capsule filter\u003c\/strong\u003e is an important configuration\n  for critical air, gas and vent filtration. Hydrophobic PTFE is particularly\n  suited to applications where gas must pass through the membrane while liquid\n  moisture penetration should be resisted.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Potential applications include process air, tank and vessel venting,\n  biotechnology gas filtration and pharmaceutical process development.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eSterile filtration note:\u003c\/strong\u003e a nominal 0.2 µm membrane rating\n  and manufacturing integrity test do not by themselves establish that every\n  PTFE capsule configuration is a validated sterilizing-grade filter.\n  Where validated sterile gas filtration is required, confirm the exact\n  membrane grade and supporting retention-validation documentation.\n\u003c\/p\u003e\n\n\n\u003c!-- PORE SIZE --\u003e\n\n\u003ch2\u003ePTFE capsule filters from 0.05 to 0.65 micron\u003c\/h2\u003e\n\n\u003cp\u003e\n  Five selectable membrane ratings allow the PTFE capsule range to address\n  different gas, vent and compatible liquid-filtration requirements.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.05–0.1 µm PTFE filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Very fine hydrophobic membrane configurations for applications requiring\n      a smaller pore-size option in gas, air or compatible process filtration.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.2 µm PTFE filters\u003c\/h3\u003e\n    \u003cp\u003e\n      A commonly specified fine membrane configuration for critical gas,\n      air and vent filtration applications.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.45–0.65 µm PTFE filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Larger-pore PTFE configurations for applications where the required\n      particle retention permits lower membrane resistance.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Available ratings are \u003cstrong\u003e0.05, 0.1, 0.2, 0.45 and 0.65 µm\u003c\/strong\u003e.\n  Final selection should consider retention requirements, flow, pressure drop,\n  gas or liquid composition and any validation requirements.\n\u003c\/p\u003e\n\n\n\u003c!-- GAS \u0026 VENT --\u003e\n\n\u003ch2\u003ePTFE capsule filters for air, gas and tank vent filtration\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hydrophobic PTFE is widely suited to gas and vent filtration because the\n  membrane provides a barrier to liquid-water penetration while allowing gas\n  transmission under appropriate process conditions.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This makes the PTFE capsule useful for applications such as\n  \u003cstrong\u003etank vent filtration, vessel venting, process air filtration,\n  compressed or process-gas filtration and laboratory gas filtration\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where steam-in-place sterilisation is required, use the dedicated\n  \u003ca href=\"\/products\/sip-ptfe-capsule-filter\"\u003e\u003cstrong\u003eSIP PTFE capsule filter\u003c\/strong\u003e\u003c\/a\u003e\n  rather than assuming the standard capsule has the same SIP capability.\n\u003c\/p\u003e\n\n\n\u003c!-- SOLVENT --\u003e\n\n\u003ch2\u003ePTFE capsule filters for solvents and chemical filtration\u003c\/h2\u003e\n\n\u003cp\u003e\n  PTFE is chemically inert and is documented for terminal filtration of\n  organic solvents and corrosive solutions. This gives the membrane a strong\n  role in laboratory, fine-chemical and industrial applications where standard\n  aqueous-focused membranes may not be suitable.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The complete capsule construction must still be considered. Compatibility\n  is determined not only by the PTFE membrane, but also by the polypropylene\n  support and housing components, seals or fittings where applicable, solvent\n  concentration, temperature and exposure time.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eChemical compatibility:\u003c\/strong\u003e always confirm the full capsule\n  configuration against the actual chemical or solvent before use. PTFE\n  membrane compatibility alone does not establish compatibility of every\n  component in the assembled capsule.\n\u003c\/p\u003e\n\n\n\u003c!-- CONNECTIONS --\u003e\n\n\u003ch2\u003ePTFE capsule filter connection options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra offers a broad range of inlet and outlet configurations, allowing\n  PTFE capsules to be integrated into laboratory tubing, pilot units and\n  industrial process systems.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNPT connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\" NPT male, 3\/8\" NPT male, 1\/2\" NPT male and\n    3\/8\" NPT female\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSwagelok connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\", 5\/16\", 3\/8\" and 1\/2\" selectable configurations\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCPC quick-connect\u003c\/th\u003e\n  \u003ctd\u003e1\/4\" CPC PLC male and female configurations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHose barb\u003c\/th\u003e\n  \u003ctd\u003e\n    3\/8\", 1\/2\" and 1\/4\"–3\/8\" stepped hose-barb options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSanitary connection\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003e1\" Tri-Clamp \/ Tri-Clover\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Exact fitting availability can depend on capsule size and configuration.\n  Confirm the inlet and outlet combination required for the installation.\n\u003c\/p\u003e\n\n\n\u003c!-- LENGTHS --\u003e\n\n\u003ch2\u003ePTFE capsule lengths from 1.5 to 20 inches\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra's current selectable PTFE capsule configurations include\n  \u003cstrong\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/strong\u003e\n  capsule lengths.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Capsule format influences available filtration area, gas or liquid flow,\n  pressure drop and total throughput. The documented 300 cm² filtration area\n  belongs to the compact configuration and should not be applied automatically\n  to larger capsule formats.\n\u003c\/p\u003e\n\n\n\u003c!-- APPLICATIONS --\u003e\n\n\u003ch2\u003eTypical PTFE capsule filter applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAir and gas filtration\u003c\/li\u003e\n  \u003cli\u003eTank and vessel vent filtration\u003c\/li\u003e\n  \u003cli\u003eProcess-gas filtration\u003c\/li\u003e\n  \u003cli\u003eLaboratory gas filtration\u003c\/li\u003e\n  \u003cli\u003eOrganic-solvent filtration\u003c\/li\u003e\n  \u003cli\u003eFine-chemical filtration\u003c\/li\u003e\n  \u003cli\u003eCompatible corrosive-solution filtration\u003c\/li\u003e\n  \u003cli\u003eAerosol and particulate removal from gas streams\u003c\/li\u003e\n  \u003cli\u003eProtection of analytical and process equipment\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical and biotechnology process development\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- PTFE VS PES --\u003e\n\n\u003ch2\u003ePTFE vs PES capsule filters\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003ePTFE\u003c\/th\u003e\n  \u003cth\u003ePES\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eWettability\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003eHydrophobic\u003c\/strong\u003e\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical starting point\u003c\/th\u003e\n  \u003ctd\u003eGas, venting and compatible solvents\u003c\/td\u003e\n  \u003ctd\u003eAqueous process liquids and buffers\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAqueous filtration\u003c\/th\u003e\n  \u003ctd\u003eHydrophobic PTFE generally requires appropriate wetting if used with aqueous liquids\u003c\/td\u003e\n  \u003ctd\u003eReadily wets with compatible aqueous liquids\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eChemical applications\u003c\/th\u003e\n  \u003ctd\u003eStrong choice where PTFE chemical resistance is required\u003c\/td\u003e\n  \u003ctd\u003eSelection depends on PES compatibility with the specific liquid\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFinal selection\u003c\/th\u003e\n  \u003ctd colspan=\"2\"\u003e\n    Compare membrane wettability, chemical compatibility, required retention,\n    pressure drop and process-validation requirements.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- STANDARD VS SIP --\u003e\n\n\u003ch2\u003eStandard PTFE capsule filter vs SIP PTFE capsule filter\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003eStandard PTFE Capsule\u003c\/th\u003e\n  \u003cth\u003eSIP PTFE Capsule\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003ePrimary use\u003c\/th\u003e\n  \u003ctd\u003eGas, vent, solvent and chemical filtration\u003c\/td\u003e\n  \u003ctd\u003eSystems requiring steam-in-place procedures\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane\u003c\/th\u003e\n  \u003ctd\u003eHydrophobic PTFE\u003c\/td\u003e\n  \u003ctd\u003eHydrophobic PTFE configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSIP design\u003c\/th\u003e\n  \u003ctd\u003eDo not assume SIP capability\u003c\/td\u003e\n  \u003ctd\u003ePurpose-designed for SIP applications\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSelection\u003c\/th\u003e\n  \u003ctd colspan=\"2\"\u003e\n    Choose according to sterilisation procedure, gas or liquid service,\n    pore size, connections and validation requirements.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- QUALITY --\u003e\n\n\u003cdiv class=\"fi-quality\"\u003e\n\n\u003ch2\u003eIntegrity Testing, Biological Safety \u0026amp; Material Compliance\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented compact PTFE capsule configuration includes quality and\n  material characteristics relevant to laboratory and process filtration.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-quality-grid\"\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003e100% integrity tested\u003c\/strong\u003e\n    The documented compact PTFE capsule range is individually integrity tested\n    during manufacturing.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n    Documented components meet biological-safety specifications for\n    USP Class VI-121°C plastics.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eAutoclave compatible\u003c\/strong\u003e\n    The documented compact configuration supports autoclaving at\n    121 °C for 30 minutes over multiple cycles.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eMaterial compliance\u003c\/strong\u003e\n    Documented construction materials have FDA 21 CFR and EU 10\/2011\n    food-contact material compliance.\n  \u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  For pharmaceutical, sterile or otherwise validated applications, request\n  the documentation applicable to the exact membrane grade, pore size,\n  capsule format and selected configuration.\n\u003c\/p\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- PHARMA --\u003e\n\n\u003ch2\u003ePTFE capsule filters for pharmaceutical and biotechnology processes\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hydrophobic PTFE capsule filters can be considered for pharmaceutical and\n  biotechnology applications involving process air, gas, vessel venting,\n  compatible solvents and other chemically compatible streams.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For critical pharmaceutical applications, the filter specification should\n  extend beyond membrane material and micron rating. Relevant requirements can\n  include integrity-test limits, microbial-retention validation, biological\n  safety, sterilisation method, extractables requirements and material\n  compliance.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filtra can assist with selecting between a standard PTFE capsule,\n  an SIP-compatible PTFE capsule or another membrane configuration according\n  to the process requirement.\n\u003c\/p\u003e\n\n\n\u003c!-- SELECTION --\u003e\n\n\u003ch2\u003eHow to select a PTFE capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  Correct PTFE capsule selection should consider the full gas or liquid\n  filtration duty.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired pore size: 0.05, 0.1, 0.2, 0.45 or 0.65 µm\u003c\/li\u003e\n  \u003cli\u003eAir, gas, vent, solvent or compatible chemical application\u003c\/li\u003e\n  \u003cli\u003eFull chemical composition and concentration\u003c\/li\u003e\n  \u003cli\u003eRequired particle or microbial retention\u003c\/li\u003e\n  \u003cli\u003eGas or liquid flow rate\u003c\/li\u003e\n  \u003cli\u003eTotal process volume where applicable\u003c\/li\u003e\n  \u003cli\u003e1.5\", 2.5\", 5\", 10\" or 20\" capsule size\u003c\/li\u003e\n  \u003cli\u003eNPT, Swagelok, CPC, hose-barb or Tri-Clamp connection\u003c\/li\u003e\n  \u003cli\u003eOperating pressure and temperature\u003c\/li\u003e\n  \u003cli\u003eMoisture \/ liquid-water exposure\u003c\/li\u003e\n  \u003cli\u003eAutoclaving or SIP requirements\u003c\/li\u003e\n  \u003cli\u003eIntegrity-testing and validation-documentation requirements\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- LINKS --\u003e\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eNeed help selecting a PTFE capsule filter?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Send us your gas or liquid, chemical composition, required pore size,\n  flow rate, operating conditions and connection requirements. We can help\n  determine the correct PTFE capsule configuration or compare PTFE with PES,\n  PVDF and SIP-capable alternatives.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n  \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n    Request Technical Selection\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n    Compare Capsule Filters\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/sip-ptfe-capsule-filter\"\u003e\n    View SIP PTFE Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pes-membrane-capsule-filter\"\u003e\n    Compare PES Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/ptfe-filters\"\u003e\n    PTFE Filter Guide\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\n    Pharmaceutical Filtration\n  \u003c\/a\u003e\n\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ --\u003e\n\n\u003ch2\u003ePTFE Capsule Filter FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is a PTFE capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nA PTFE capsule filter is a self-contained disposable filtration device\ncontaining a polytetrafluoroethylene membrane inside a polymer capsule.\nHydrophobic PTFE is particularly suited to air, gas, venting, organic-solvent\nand compatible chemical-filtration applications.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a PTFE membrane hydrophobic?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. The PTFE membrane used in this capsule range is hydrophobic. This makes\nit particularly useful for gas and vent applications where gas transmission\nis required while penetration by liquid water should be resisted.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PTFE capsule filter pore sizes are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nAvailable pore sizes include 0.05, 0.1, 0.2, 0.45 and 0.65 µm.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a 0.2 micron PTFE capsule filter available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. A 0.2 µm hydrophobic PTFE configuration is available and is relevant to\ncritical air, gas and vent filtration. Where validated sterilizing-grade\nperformance is required, confirm the supporting validation documentation for\nthe exact grade.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PTFE capsule filters be used for tank vent filtration?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. Hydrophobic PTFE is well suited to compatible tank and vessel vent\napplications because it allows gas flow while resisting liquid-water\npenetration under suitable operating conditions.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PTFE capsule filters filter organic solvents?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nPTFE membrane is documented for filtration of organic solvents and corrosive\nsolutions. Compatibility of the complete capsule construction must still be\nverified against the exact solvent, concentration and temperature.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PTFE capsule lengths are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nFiltra currently offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch and\n20-inch PTFE capsule configurations.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich connection types are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nCurrent Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb\nand 1-inch Tri-Clamp \/ Tri-Clover configurations.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the filtration area of a PTFE capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PTFE capsule configuration provides approximately\n300 cm² of filtration area. Larger capsule formats can have different\neffective filtration areas.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PTFE capsule filters be autoclaved?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PTFE capsule configuration supports autoclaving at\n121 °C for 30 minutes over multiple cycles. Confirm the applicable limit for\nthe exact configuration selected.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre PTFE capsule filters integrity tested?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PTFE capsule range is 100% integrity tested during\nmanufacturing. For regulated filtration processes, confirm the applicable\ntest method and acceptance limits for the exact membrane grade.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between PTFE and PES capsule filters?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nPTFE is hydrophobic and is commonly selected for gas, vent and compatible\nsolvent filtration. PES is hydrophilic and is commonly selected for aqueous\nprocess liquids and buffers. Final membrane selection depends on the actual\nprocess fluid and filtration requirement.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between standard PTFE and SIP PTFE capsules?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe standard PTFE capsule is intended for general gas, vent, solvent and\ncompatible chemical filtration. The dedicated SIP PTFE capsule is designed\nfor process installations requiring steam-in-place sterilisation.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ JSON-LD --\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is a PTFE capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"A PTFE capsule filter is a self-contained disposable filtration device containing a polytetrafluoroethylene membrane inside a polymer capsule. Hydrophobic PTFE is particularly suited to air, gas, venting, organic-solvent and compatible chemical-filtration applications.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a PTFE membrane hydrophobic?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The PTFE membrane used in this capsule range is hydrophobic, making it particularly useful for gas and vent applications.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PTFE capsule filter pore sizes are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Available pore sizes include 0.05, 0.1, 0.2, 0.45 and 0.65 µm.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a 0.2 micron PTFE capsule filter available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A 0.2 µm hydrophobic PTFE configuration is available and is relevant to critical air, gas and vent filtration. Where validated sterilizing-grade performance is required, supporting validation documentation should be confirmed for the exact grade.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PTFE capsule filters be used for tank vent filtration?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. Hydrophobic PTFE is well suited to compatible tank and vessel vent applications because it allows gas flow while resisting liquid-water penetration under suitable operating conditions.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PTFE capsule filters filter organic solvents?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"PTFE membrane is documented for filtration of organic solvents and corrosive solutions. Compatibility of the complete capsule construction must still be verified against the exact solvent, concentration and temperature.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PTFE capsule lengths are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Filtra currently offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch PTFE capsule configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which connection types are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Current Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb and 1-inch Tri-Clamp or Tri-Clover configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the filtration area of a PTFE capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PTFE capsule configuration provides approximately 300 cm² of filtration area. Larger capsule formats can have different effective filtration areas.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PTFE capsule filters be autoclaved?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PTFE capsule configuration supports autoclaving at 121 °C for 30 minutes over multiple cycles. Confirm the applicable limit for the exact configuration selected.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Are PTFE capsule filters integrity tested?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PTFE capsule range is 100% integrity tested during manufacturing. For regulated filtration processes, confirm the applicable test method and acceptance limits for the exact membrane grade.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between PTFE and PES capsule filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"PTFE is hydrophobic and is commonly selected for gas, vent and compatible solvent filtration. PES is hydrophilic and is commonly selected for aqueous process liquids and buffers.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between standard PTFE and SIP PTFE capsules?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The standard PTFE capsule is intended for general gas, vent, solvent and compatible chemical filtration. 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1.5\"","offer_id":56113209868614,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 3\/8\" Swagelok (6C) \/ 2.5\"","offer_id":56113209901382,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 3\/8\" Swagelok (6C) \/ 5\"","offer_id":56113209934150,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 3\/8\" Swagelok (6C) \/ 10\"","offer_id":56113209966918,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 3\/8\" Swagelok (6C) \/ 20\"","offer_id":56113209999686,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 1\/2\" Swagelok (8C) \/ 1.5\"","offer_id":56113210032454,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 1\/2\" Swagelok (8C) \/ 2.5\"","offer_id":56113210065222,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 1\/2\" Swagelok (8C) \/ 5\"","offer_id":56113210097990,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 1\/2\" Swagelok (8C) \/ 10\"","offer_id":56113210130758,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45 µm \/ 1\/2\" Swagelok (8C) \/ 20\"","offer_id":56113210163526,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/ptfe-membrane-capsule-filter..png?v=1772807960"},{"product_id":"pvdf-membrane-capsule-filter","title":"PVDF Membrane Capsule Filter – Low Protein Adsorption | 0.1–3.0 µm","description":"\u003csection class=\"fi-capsule-detail\" aria-labelledby=\"fi-pvdf-capsule-heading\"\u003e\n\n\u003cstyle\u003e\n.fi-capsule-detail{\n  --fi-dark:#10242d;\n  --fi-accent:#2b7d77;\n  --fi-text:#172126;\n  --fi-muted:#5d6a70;\n  --fi-soft:#f4f8f7;\n  --fi-border:#dce7e5;\n  color:var(--fi-text);\n}\n\n.fi-capsule-detail *,\n.fi-capsule-detail 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var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-capsule-stat span{\n  display:block;\n  margin-bottom:4px;\n  color:var(--fi-muted);\n  font-size:12px;\n}\n\n.fi-capsule-stat strong{\n  display:block;\n  font-size:16px;\n}\n\n.fi-table-wrap{\n  overflow-x:auto;\n  margin:22px 0 30px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-table{\n  width:100%;\n  min-width:650px;\n  border-collapse:collapse;\n}\n\n.fi-table th,\n.fi-table td{\n  padding:13px 15px;\n  border-bottom:1px solid var(--fi-border);\n  text-align:left;\n  vertical-align:top;\n  font-size:14px;\n}\n\n.fi-table th{\n  width:34%;\n  background:var(--fi-soft);\n  color:var(--fi-text);\n  font-weight:700;\n}\n\n.fi-table tr:last-child th,\n.fi-table tr:last-child td{\n  border-bottom:0;\n}\n\n.fi-note{\n  margin:22px 0;\n  padding:17px 19px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n\n.fi-grid{\n  display:grid;\n  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border-radius:12px;\n}\n\n.fi-links h2,\n.fi-links p{\n  color:#fff;\n}\n\n.fi-links p{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-buttons{\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:19px;\n}\n\n.fi-button{\n  display:inline-flex;\n  min-height:46px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n\n.fi-button-primary{\n  background:var(--fi-accent);\n  color:#fff!important;\n}\n\n.fi-button-secondary{\n  background:#fff;\n  color:var(--fi-dark)!important;\n}\n\n.fi-faq details{\n  margin-bottom:10px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n\n.fi-faq details \u003e div{\n  padding:0 19px 17px;\n}\n\n.fi-faq details p{\n  margin:0;\n}\n\n@media(max-width:850px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n\n  .fi-grid{\n    grid-template-columns:1fr;\n  }\n}\n\n@media(max-width:480px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-button{\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\n\u003c!-- INTRO --\u003e\n\n\u003ch2 id=\"fi-pvdf-capsule-heading\"\u003e\n  PVDF Membrane Capsule Filter – Low Protein Adsorption\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-capsule-lead\"\u003e\n  Filtra International supplies \u003cstrong\u003ehydrophilic PVDF membrane capsule filters\u003c\/strong\u003e\n  for precision filtration of aqueous solutions, biological process liquids\n  and other compatible fluids. PVDF combines hydrophilic membrane behaviour\n  with \u003cstrong\u003elow protein adsorption\u003c\/strong\u003e, making it particularly relevant\n  where product recovery and interaction between the process fluid and filter\n  membrane are important.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available pore sizes range from \u003cstrong\u003e0.1 to 3.0 µm\u003c\/strong\u003e, with multiple\n  capsule lengths and connection options for laboratory filtration, biotechnology\n  development, pharmaceutical R\u0026amp;D and pilot-scale process filtration.\n\u003c\/p\u003e\n\n\n\u003c!-- KEY SPECS --\u003e\n\n\u003cdiv class=\"fi-capsule-highlight\"\u003e\n  \u003cdiv class=\"fi-capsule-highlight__grid\"\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eMembrane\u003c\/span\u003e\n      \u003cstrong\u003eHydrophilic PVDF\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003ePore sizes\u003c\/span\u003e\n      \u003cstrong\u003e0.1–3.0 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eKey characteristic\u003c\/span\u003e\n      \u003cstrong\u003eLow protein adsorption\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eCompact filter area\u003c\/span\u003e\n      \u003cstrong\u003eApprox. 300 cm²*\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003e*Configuration note:\u003c\/strong\u003e approximately 300 cm² is documented\n  for the compact PVDF capsule configuration. Filtra also offers larger capsule\n  formats. Effective filtration area, flow capacity and other technical limits\n  depend on the exact capsule size and configuration.\n\u003c\/p\u003e\n\n\n\u003c!-- TECHNICAL --\u003e\n\n\u003ch2\u003ePVDF capsule filter technical overview\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter type\u003c\/th\u003e\n  \u003ctd\u003eDisposable hydrophilic PVDF membrane capsule filter\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter membrane\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003ePVDF – polyvinylidene fluoride\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane behaviour\u003c\/th\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eProtein interaction\u003c\/th\u003e\n  \u003ctd\u003eLow protein adsorption\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMedia support\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCapsule hardware \/ housing\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eOptional filling bell\u003c\/th\u003e\n  \u003ctd\u003ePolycarbonate, configuration-dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAvailable pore sizes\u003c\/th\u003e\n  \u003ctd\u003e\n    \u003cstrong\u003e0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm\u003c\/strong\u003e\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFiltra selectable capsule lengths\u003c\/th\u003e\n  \u003ctd\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration filter area\u003c\/th\u003e\n  \u003ctd\u003eApprox. 300 cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration working pressure\u003c\/th\u003e\n  \u003ctd\u003eUp to 5 bar at 20 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eDocumented maximum operating temperature\u003c\/th\u003e\n  \u003ctd\u003e80 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003e100% integrity tested for the documented compact capsule range\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eBiological safety\u003c\/th\u003e\n  \u003ctd\u003eDocumented components meet USP Class VI-121°C specifications for plastics\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHot-water sanitisation\u003c\/th\u003e\n  \u003ctd\u003e90 °C for 30 minutes, multiple cycles\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAutoclaving\u003c\/th\u003e\n  \u003ctd\u003e121 °C for 30 minutes, multiple cycles for the documented compact configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMaterial compliance\u003c\/th\u003e\n  \u003ctd\u003eDocumented FDA 21 CFR and EU 10\/2011 food-contact material compliance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- OPERATING PRINCIPLE --\u003e\n\n\u003ch2\u003eHow does a PVDF membrane capsule filter work?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Process liquid enters the capsule through the selected inlet connection and\n  passes through the PVDF membrane. The controlled membrane pore structure\n  retains particulate and colloidal contamination according to the selected\n  pore-size rating, while filtered liquid exits through the outlet connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Because the membrane and housing are supplied as one enclosed capsule,\n  the filtration device can be installed without a separate cartridge-filter\n  housing. This makes the format useful for laboratory equipment, pilot systems,\n  process development and other compact filtration installations.\n\u003c\/p\u003e\n\n\n\u003c!-- WHY PVDF --\u003e\n\n\u003ch2\u003eWhy use hydrophilic PVDF for low protein adsorption?\u003c\/h2\u003e\n\n\u003cp\u003e\n  One of the distinguishing characteristics of this PVDF membrane is its\n  \u003cstrong\u003elow protein adsorption\u003c\/strong\u003e. This can be important when filtering\n  valuable biological or protein-containing process liquids where unnecessary\n  adsorption onto the filter membrane may reduce product recovery.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The documented hydrophilic PVDF membrane also provides good wetting with\n  aqueous solutions and is described as having stable filtration flux,\n  resistance to clogging and anti-fouling characteristics.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Actual product recovery and membrane interaction depend on the specific\n  protein, formulation, concentration and process conditions. Compatibility\n  and recovery should therefore be evaluated for sensitive applications.\n\u003c\/p\u003e\n\n\n\u003c!-- PORE SIZE --\u003e\n\n\u003ch2\u003e0.1 to 3.0 micron PVDF capsule filters\u003c\/h2\u003e\n\n\u003cp\u003e\n  The PVDF capsule range includes six selectable pore sizes for different\n  fine-filtration and clarification requirements.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.1–0.2 µm PVDF filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Fine membrane configurations for applications requiring a high level\n      of particulate retention. A 0.2 µm configuration is also relevant to\n      pharmaceutical and biotechnology process development.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.45–0.65 µm PVDF filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Useful for fine clarification, laboratory filtration and compatible\n      biological or aqueous process solutions.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e1.0–3.0 µm PVDF filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Larger-pore options for particulate reduction and applications where\n      lower flow resistance or higher solids tolerance is required.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Available ratings are \u003cstrong\u003e0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm\u003c\/strong\u003e.\n  Final selection should consider required retention, fluid composition,\n  solids loading, product recovery and allowable pressure drop.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003ePharmaceutical note:\u003c\/strong\u003e a nominal 0.2 µm pore size does not\n  by itself establish validated sterilizing-grade performance. Where sterile\n  filtration or validated microbial retention is required, confirm the exact\n  filter grade and its supporting validation documentation.\n\u003c\/p\u003e\n\n\n\u003c!-- PROTEIN --\u003e\n\n\u003ch2\u003ePVDF capsule filters for protein and biological solutions\u003c\/h2\u003e\n\n\u003cp\u003e\n  Low protein adsorption makes PVDF an important membrane option to evaluate\n  for protein-sensitive filtration duties. Potential applications can include\n  biotechnology process development, compatible biological solutions,\n  pharmaceutical R\u0026amp;D and laboratory filtration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For valuable proteins, enzymes or other biological products, filter selection\n  should include recovery testing under representative process conditions.\n  The correct membrane cannot be selected from pore size alone.\n\u003c\/p\u003e\n\n\n\u003c!-- CHEMICAL COMPATIBILITY --\u003e\n\n\u003ch2\u003ePVDF filtration of aqueous solutions and compatible solvents\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented PVDF membrane is suitable for aqueous solutions and selected\n  organic-solvent applications. This can make PVDF useful where a combination\n  of hydrophilic behaviour, low protein adsorption and chemical compatibility\n  is required.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eChemical compatibility:\u003c\/strong\u003e suitability with an organic solvent\n  depends on the complete capsule construction, solvent concentration,\n  temperature and exposure time. Always confirm compatibility for the actual\n  process fluid rather than relying on membrane material alone.\n\u003c\/p\u003e\n\n\n\u003c!-- CONNECTIONS --\u003e\n\n\u003ch2\u003ePVDF capsule filter connection options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The current Filtra PVDF capsule range includes multiple inlet and outlet\n  configurations for laboratory, pilot and process integration.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNPT connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\" NPT male, 3\/8\" NPT male, 1\/2\" NPT male and\n    3\/8\" NPT female\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSwagelok connections\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\", 5\/16\", 3\/8\" and 1\/2\" selectable configurations\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCPC quick-connect\u003c\/th\u003e\n  \u003ctd\u003e1\/4\" CPC PLC male and female configurations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHose barb\u003c\/th\u003e\n  \u003ctd\u003e\n    3\/8\", 1\/2\" and 1\/4\"–3\/8\" stepped hose-barb options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSanitary connection\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003e1\" Tri-Clamp \/ Tri-Clover\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Exact fitting availability can depend on capsule size and configuration.\n  Confirm the required inlet and outlet combination when specifying the filter.\n\u003c\/p\u003e\n\n\n\u003c!-- LENGTH --\u003e\n\n\u003ch2\u003ePVDF capsule lengths from 1.5 to 20 inches\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra's current selectable PVDF capsule configurations include\n  \u003cstrong\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/strong\u003e\n  formats.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Capsule size influences available filtration area, flow capacity,\n  pressure drop and total process throughput. The documented 300 cm² filter\n  area applies to the compact configuration and should not be extrapolated\n  automatically to larger capsule formats.\n\u003c\/p\u003e\n\n\n\u003c!-- APPLICATIONS --\u003e\n\n\u003ch2\u003eTypical PVDF capsule filter applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eProtein-sensitive liquid filtration\u003c\/li\u003e\n  \u003cli\u003eBiotechnology process development\u003c\/li\u003e\n  \u003cli\u003eCompatible biological-fluid filtration\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical research and pilot filtration\u003c\/li\u003e\n  \u003cli\u003eAqueous process-solution filtration\u003c\/li\u003e\n  \u003cli\u003eLaboratory sample preparation\u003c\/li\u003e\n  \u003cli\u003eFine particle and colloid reduction\u003c\/li\u003e\n  \u003cli\u003ePure-water filtration\u003c\/li\u003e\n  \u003cli\u003eCompatible fine-chemical filtration\u003c\/li\u003e\n  \u003cli\u003eSelected compatible organic-solvent applications\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- COMPARISON --\u003e\n\n\u003ch2\u003ePVDF vs PES and Nylon capsule filters\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003ePVDF\u003c\/th\u003e\n  \u003cth\u003ePES\u003c\/th\u003e\n  \u003cth\u003eNylon\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eWettability\u003c\/th\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eKey selection characteristic\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003eLow protein adsorption\u003c\/strong\u003e\u003c\/td\u003e\n  \u003ctd\u003eStrong hydrophilicity and low protein adsorption\u003c\/td\u003e\n  \u003ctd\u003eAlcohol resistance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical starting point\u003c\/th\u003e\n  \u003ctd\u003eProtein-sensitive and compatible biological\/process liquids\u003c\/td\u003e\n  \u003ctd\u003eAqueous buffers and general aqueous-process filtration\u003c\/td\u003e\n  \u003ctd\u003eAqueous and compatible alcohol-containing liquids\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFinal selection\u003c\/th\u003e\n  \u003ctd colspan=\"3\"\u003e\n    Compare chemical compatibility, protein recovery, required retention,\n    process conditions and validation requirements.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- QUALITY --\u003e\n\n\u003cdiv class=\"fi-quality\"\u003e\n\n\u003ch2\u003eIntegrity Testing, Biological Safety \u0026amp; Material Compliance\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented compact PVDF capsule configuration includes quality and\n  material-safety characteristics relevant to laboratory, biotechnology and\n  process filtration.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-quality-grid\"\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003e100% integrity tested\u003c\/strong\u003e\n    The documented compact PVDF capsule range is individually integrity tested\n    during manufacturing.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n    Documented components meet biological-safety specifications for\n    USP Class VI-121°C plastics.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eAutoclave compatible\u003c\/strong\u003e\n    The documented compact configuration supports autoclaving at\n    121 °C for 30 minutes over multiple cycles.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eMaterial compliance\u003c\/strong\u003e\n    Documented construction materials have FDA 21 CFR and EU 10\/2011\n    food-contact material compliance.\n  \u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  For regulated pharmaceutical or biotechnology applications, documentation\n  should always be confirmed against the exact membrane grade, capsule size\n  and selected configuration.\n\u003c\/p\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- PHARMA --\u003e\n\n\u003ch2\u003ePVDF capsule filters for pharmaceutical and biotechnology applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hydrophilic PVDF can be considered for pharmaceutical development and\n  biotechnology filtration where low protein adsorption and compatible liquid\n  filtration are important.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For regulated production, filter selection should also consider microbial\n  retention requirements, integrity-test specifications, sterilisation method,\n  material compliance, extractables requirements and any application-specific\n  validation documentation.\n\u003c\/p\u003e\n\n\n\u003c!-- SELECTION --\u003e\n\n\u003ch2\u003eHow to select a PVDF capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  Correct PVDF filter selection should consider membrane interaction as well\n  as pore size and flow.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired pore size from 0.1 to 3.0 µm\u003c\/li\u003e\n  \u003cli\u003eProcess liquid and complete chemical composition\u003c\/li\u003e\n  \u003cli\u003eProtein, enzyme or biological-product recovery requirements\u003c\/li\u003e\n  \u003cli\u003eRequired particulate or microbial retention level\u003c\/li\u003e\n  \u003cli\u003eFlow rate and total process volume\u003c\/li\u003e\n  \u003cli\u003eExpected solids or colloidal loading\u003c\/li\u003e\n  \u003cli\u003e1.5\", 2.5\", 5\", 10\" or 20\" capsule size\u003c\/li\u003e\n  \u003cli\u003eNPT, Swagelok, CPC, hose-barb or Tri-Clamp connection\u003c\/li\u003e\n  \u003cli\u003eOperating pressure and temperature\u003c\/li\u003e\n  \u003cli\u003eSanitisation or autoclaving requirements\u003c\/li\u003e\n  \u003cli\u003eIntegrity-testing and pharmaceutical documentation requirements\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- INTERNAL LINKS --\u003e\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eCompare PVDF with other capsule filter membranes\u003c\/h2\u003e\n\n\u003cp\u003e\n  Unsure whether PVDF, PES, Nylon or PTFE is the correct membrane? Send us\n  the fluid composition, pore size, process volume, protein-recovery\n  requirements and connection details for technical selection support.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n  \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n    Request Technical Selection\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n    Compare Capsule Filters\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pes-membrane-capsule-filter\"\u003e\n    View PES Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/nylon-membrane-capsule-filter\"\u003e\n    View Nylon Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\n    Pharmaceutical Filtration\n  \u003c\/a\u003e\n\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ --\u003e\n\n\u003ch2\u003ePVDF Membrane Capsule Filter FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is a PVDF membrane capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nA PVDF membrane capsule filter is a self-contained disposable filtration\ndevice containing a polyvinylidene fluoride membrane inside a polymer\ncapsule housing. Hydrophilic PVDF is used for fine filtration of compatible\naqueous, biological and process liquids.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs this PVDF membrane hydrophilic?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. The documented PVDF membrane is hydrophilic, making it suitable for\nwetting and filtration with compatible aqueous solutions.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eDoes PVDF have low protein adsorption?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. Low protein adsorption is a documented characteristic of this hydrophilic\nPVDF membrane. This makes PVDF useful to evaluate for protein-sensitive\nfiltration, although actual product recovery should be confirmed under\nrepresentative process conditions.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PVDF capsule filter pore sizes are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nAvailable pore sizes include 0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a 0.2 micron PVDF capsule filter available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. A 0.2 µm hydrophilic PVDF configuration is available. A nominal\n0.2 µm rating alone should not be interpreted as proof of validated\nsterilizing-grade performance.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PVDF capsule filters be used for protein solutions?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nPVDF can be considered for compatible protein-containing and biological\nsolutions because the membrane has low protein adsorption. For valuable\nproducts, actual compatibility and recovery testing is recommended.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich PVDF capsule lengths are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nFiltra currently offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch\nand 20-inch PVDF capsule configurations.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich connection types are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nCurrent Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb\nand 1-inch Tri-Clamp \/ Tri-Clover configurations.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the filtration area of a PVDF capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PVDF capsule configuration provides approximately\n300 cm² of filtration area. Larger capsule formats can have different\neffective filtration areas.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan PVDF capsule filters be autoclaved?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact configuration supports autoclaving at 121 °C for\n30 minutes over multiple cycles. Confirm the applicable sterilisation limit\nfor the exact selected configuration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre PVDF capsule filters integrity tested?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact PVDF capsule range is 100% integrity tested during\nmanufacturing. For regulated processes, confirm the applicable integrity-test\nmethod and acceptance specification for the exact filter grade.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between PVDF and PES capsule filters?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nBoth are hydrophilic membrane options. PVDF is particularly useful to evaluate\nwhere low protein adsorption and product recovery are important, while PES is\ncommonly selected for a broad range of aqueous buffer and process-liquid\napplications. Final selection should be based on the actual process fluid and\nrequired filtration performance.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ JSON-LD --\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is a PVDF membrane capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"A PVDF membrane capsule filter is a self-contained disposable filtration device containing a polyvinylidene fluoride membrane inside a polymer capsule housing. Hydrophilic PVDF is used for fine filtration of compatible aqueous, biological and process liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is this PVDF membrane hydrophilic?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The documented PVDF membrane is hydrophilic, making it suitable for wetting and filtration with compatible aqueous solutions.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Does PVDF have low protein adsorption?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. Low protein adsorption is a documented characteristic of this hydrophilic PVDF membrane. Actual product recovery should be confirmed under representative process conditions.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PVDF capsule filter pore sizes are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Available pore sizes include 0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a 0.2 micron PVDF capsule filter available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A 0.2 µm hydrophilic PVDF configuration is available. A nominal 0.2 µm rating alone should not be interpreted as proof of validated sterilizing-grade performance.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PVDF capsule filters be used for protein solutions?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"PVDF can be considered for compatible protein-containing and biological solutions because the membrane has low protein adsorption. For valuable products, compatibility and recovery testing is recommended.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which PVDF capsule lengths are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Filtra currently offers selectable 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch PVDF capsule configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which connection types are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Current Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb and 1-inch Tri-Clamp or Tri-Clover configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the filtration area of a PVDF capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PVDF capsule configuration provides approximately 300 cm² of filtration area. Larger capsule formats can have different effective filtration areas.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can PVDF capsule filters be autoclaved?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact configuration supports autoclaving at 121 °C for 30 minutes over multiple cycles. Confirm the applicable sterilisation limit for the exact selected configuration.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Are PVDF capsule filters integrity tested?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact PVDF capsule range is 100% integrity tested during manufacturing. For regulated processes, confirm the applicable integrity-test method and acceptance specification for the exact filter grade.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between PVDF and PES capsule filters?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Both are hydrophilic membrane options. PVDF is particularly useful to evaluate where low protein adsorption and product recovery are important, while PES is commonly selected for a broad range of aqueous buffer and process-liquid applications.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e\n\n\u003c\/section\u003e","brand":"Filtra International","offers":[{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 1.5\"","offer_id":56113156129094,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 2.5\"","offer_id":56113156161862,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 5\"","offer_id":56113156194630,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 10\"","offer_id":56113156227398,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 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1.5\"","offer_id":56113195352390,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.65 µm \/ 1\/2\" Swagelok (8C) \/ 2.5\"","offer_id":56113195385158,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.65 µm \/ 1\/2\" Swagelok (8C) \/ 5\"","offer_id":56113195417926,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.65 µm \/ 1\/2\" Swagelok (8C) \/ 10\"","offer_id":56113195450694,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.65 µm \/ 1\/2\" Swagelok (8C) \/ 20\"","offer_id":56113195483462,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/pvdf-membrane-capsule-filter.png?v=1772807928"},{"product_id":"nylon-membrane-capsule-filter","title":"Nylon Membrane Capsule Filter – 0.1 to 3.0 µm | Aqueous \u0026 Alcohol Filtration","description":"\u003csection class=\"fi-capsule-detail\" aria-labelledby=\"fi-nylon-capsule-heading\"\u003e\n\n\u003cstyle\u003e\n.fi-capsule-detail{\n  --fi-dark:#10242d;\n  --fi-accent:#2b7d77;\n  --fi-text:#172126;\n  --fi-muted:#5d6a70;\n  --fi-soft:#f4f8f7;\n  --fi-border:#dce7e5;\n  color:var(--fi-text);\n}\n\n.fi-capsule-detail *,\n.fi-capsule-detail *:before,\n.fi-capsule-detail *:after{\n  box-sizing:border-box;\n}\n\n.fi-capsule-detail h2,\n.fi-capsule-detail h3{\n  color:var(--fi-text);\n  line-height:1.2;\n}\n\n.fi-capsule-detail h2{\n  margin:42px 0 16px;\n  font-size:clamp(25px,3vw,34px);\n}\n\n.fi-capsule-detail h2:first-of-type{\n  margin-top:0;\n}\n\n.fi-capsule-detail h3{\n  margin:26px 0 10px;\n  font-size:20px;\n}\n\n.fi-capsule-detail p,\n.fi-capsule-detail li{\n  color:var(--fi-muted);\n  font-size:16px;\n  line-height:1.7;\n}\n\n.fi-capsule-detail strong{\n  color:var(--fi-text);\n}\n\n.fi-capsule-lead{\n  font-size:18px!important;\n  line-height:1.65!important;\n}\n\n.fi-capsule-highlight{\n  margin:26px 0 34px;\n  padding:24px;\n  background:var(--fi-soft);\n  border:1px solid var(--fi-border);\n  border-radius:12px;\n}\n\n.fi-capsule-highlight__grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n}\n\n.fi-capsule-stat{\n  padding:14px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-capsule-stat span{\n  display:block;\n  margin-bottom:4px;\n  color:var(--fi-muted);\n  font-size:12px;\n}\n\n.fi-capsule-stat strong{\n  display:block;\n  font-size:16px;\n}\n\n.fi-table-wrap{\n  overflow-x:auto;\n  margin:22px 0 30px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-table{\n  width:100%;\n  min-width:650px;\n  border-collapse:collapse;\n}\n\n.fi-table th,\n.fi-table td{\n  padding:13px 15px;\n  border-bottom:1px solid var(--fi-border);\n  text-align:left;\n  vertical-align:top;\n  font-size:14px;\n}\n\n.fi-table th{\n  width:34%;\n  background:var(--fi-soft);\n  color:var(--fi-text);\n  font-weight:700;\n}\n\n.fi-table tr:last-child th,\n.fi-table tr:last-child td{\n  border-bottom:0;\n}\n\n.fi-note{\n  margin:22px 0;\n  padding:17px 19px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n\n.fi-grid{\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:16px;\n  margin:22px 0 34px;\n}\n\n.fi-card{\n  padding:21px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-card h3{\n  margin-top:0;\n}\n\n.fi-quality{\n  margin:36px 0;\n  padding:27px;\n  background:var(--fi-dark);\n  border-radius:13px;\n}\n\n.fi-quality h2,\n.fi-quality h3{\n  color:#fff;\n}\n\n.fi-quality p,\n.fi-quality li{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-quality strong{\n  color:#fff;\n}\n\n.fi-quality-grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n  margin-top:20px;\n}\n\n.fi-quality-item{\n  padding:17px;\n  background:rgba(255,255,255,.07);\n  border:1px solid rgba(255,255,255,.12);\n  border-radius:9px;\n  color:rgba(255,255,255,.78);\n  font-size:14px;\n  line-height:1.6;\n}\n\n.fi-quality-item strong{\n  display:block;\n  margin-bottom:5px;\n}\n\n.fi-links{\n  margin:35px 0;\n  padding:26px;\n  background:var(--fi-dark);\n  border-radius:12px;\n}\n\n.fi-links h2,\n.fi-links p{\n  color:#fff;\n}\n\n.fi-links p{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-buttons{\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:19px;\n}\n\n.fi-button{\n  display:inline-flex;\n  min-height:46px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n\n.fi-button-primary{\n  background:var(--fi-accent);\n  color:#fff!important;\n}\n\n.fi-button-secondary{\n  background:#fff;\n  color:var(--fi-dark)!important;\n}\n\n.fi-faq details{\n  margin-bottom:10px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n\n.fi-faq details \u003e div{\n  padding:0 19px 17px;\n}\n\n.fi-faq details p{\n  margin:0;\n}\n\n@media(max-width:850px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n\n  .fi-grid{\n    grid-template-columns:1fr;\n  }\n}\n\n@media(max-width:480px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-button{\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\n\u003c!-- INTRO --\u003e\n\n\u003ch2 id=\"fi-nylon-capsule-heading\"\u003e\n  Nylon Membrane Capsule Filter – 0.1 to 3.0 µm\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-capsule-lead\"\u003e\n  Filtra International supplies \u003cstrong\u003ehydrophilic Nylon membrane capsule filters\u003c\/strong\u003e\n  for precision filtration of aqueous solutions, alcohol-containing liquids\n  and compatible process fluids. Available pore sizes range from\n  \u003cstrong\u003e0.1 to 3.0 µm\u003c\/strong\u003e, with multiple capsule lengths and connection\n  configurations for laboratory, pilot and process filtration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Nylon combines natural hydrophilicity with documented alcohol resistance,\n  making it particularly useful where aqueous and alcohol-based liquids need\n  to be filtered using the same general membrane chemistry.\n\u003c\/p\u003e\n\n\n\u003c!-- KEY SPECS --\u003e\n\n\u003cdiv class=\"fi-capsule-highlight\"\u003e\n  \u003cdiv class=\"fi-capsule-highlight__grid\"\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eMembrane\u003c\/span\u003e\n      \u003cstrong\u003eHydrophilic Nylon\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003ePore sizes\u003c\/span\u003e\n      \u003cstrong\u003e0.1–3.0 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eLiquid type\u003c\/span\u003e\n      \u003cstrong\u003eAqueous \u0026amp; alcohol\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eCompact filter area\u003c\/span\u003e\n      \u003cstrong\u003eApprox. 300 cm²*\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003e*Configuration note:\u003c\/strong\u003e approximately 300 cm² is documented for\n  the compact Nylon capsule configuration. Filtra also offers larger selectable\n  capsule formats; filtration area and other technical properties vary with\n  the exact capsule size and configuration.\n\u003c\/p\u003e\n\n\n\u003c!-- TECHNICAL --\u003e\n\n\u003ch2\u003eNylon capsule filter technical overview\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter type\u003c\/th\u003e\n  \u003ctd\u003eDisposable Nylon membrane capsule filter for liquid filtration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter membrane\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003eHydrophilic Nylon\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane characteristics\u003c\/th\u003e\n  \u003ctd\u003eHydrophilic, alcohol resistant and low protein adsorption\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMedia support\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCapsule hardware \/ housing\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eOptional filling bell\u003c\/th\u003e\n  \u003ctd\u003ePolycarbonate, configuration-dependent\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAvailable pore sizes\u003c\/th\u003e\n  \u003ctd\u003e\n    \u003cstrong\u003e0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm\u003c\/strong\u003e\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFiltra selectable capsule lengths\u003c\/th\u003e\n  \u003ctd\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration filter area\u003c\/th\u003e\n  \u003ctd\u003eApprox. 300 cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCompact configuration maximum working pressure\u003c\/th\u003e\n  \u003ctd\u003e5 bar at 20 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eDocumented maximum operating temperature\u003c\/th\u003e\n  \u003ctd\u003e80 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003e100% integrity tested for the documented compact capsule range\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eBiological safety\u003c\/th\u003e\n  \u003ctd\u003eDocumented components meet USP Class VI-121°C specifications for plastics\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHot-water sanitisation\u003c\/th\u003e\n  \u003ctd\u003e90 °C for 30 minutes, multiple cycles\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eAutoclaving\u003c\/th\u003e\n  \u003ctd\u003e121 °C for 30 minutes, multiple cycles for the documented compact configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMaterial compliance\u003c\/th\u003e\n  \u003ctd\u003eDocumented FDA 21 CFR and EU 10\/2011 food-contact material compliance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- OPERATING PRINCIPLE --\u003e\n\n\u003ch2\u003eHow does a Nylon membrane capsule filter work?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Process liquid enters the capsule through the selected inlet connection and\n  passes through the Nylon membrane. The controlled membrane pore structure\n  retains particulate contamination according to the selected pore-size rating,\n  while filtered liquid exits through the outlet connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The membrane and housing form one enclosed disposable assembly, so no\n  separate reusable cartridge housing is required for the capsule itself.\n  This simplifies filter replacement in laboratory, pilot and small-process\n  filtration systems.\n\u003c\/p\u003e\n\n\n\u003c!-- WHY NYLON --\u003e\n\n\u003ch2\u003eWhy choose a hydrophilic Nylon membrane?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Nylon is naturally hydrophilic, allowing aqueous liquids to wet the membrane\n  readily. The documented membrane also combines this hydrophilic behaviour\n  with \u003cstrong\u003ealcohol resistance\u003c\/strong\u003e, which makes Nylon particularly\n  interesting for compatible aqueous and alcohol-containing process fluids.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The membrane is also documented as having low protein adsorption. However,\n  membrane selection for valuable proteins or biological products should still\n  be based on actual compatibility and recovery testing rather than membrane\n  material alone.\n\u003c\/p\u003e\n\n\n\u003c!-- PORE SIZES --\u003e\n\n\u003ch2\u003e0.1 to 3.0 micron Nylon capsule filters\u003c\/h2\u003e\n\n\u003cp\u003e\n  Six selectable pore sizes allow the Nylon capsule to cover different fine\n  filtration and clarification requirements.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.1–0.2 µm Nylon filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Fine-pore configurations for applications requiring a high level of\n      particulate retention. Where microbial or sterile performance is required,\n      the exact filter grade and validation documentation must be confirmed.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.45–0.65 µm Nylon filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Common fine-filtration ratings for clarification, laboratory filtration\n      and compatible aqueous or alcohol-containing solutions.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e1.0–3.0 µm Nylon filters\u003c\/h3\u003e\n    \u003cp\u003e\n      Larger-pore configurations for particulate reduction and clarification\n      where higher solids loading or lower flow resistance is required.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Available ratings are \u003cstrong\u003e0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm\u003c\/strong\u003e.\n  Selection should consider required retention, solids loading, liquid\n  compatibility and allowable pressure drop.\n\u003c\/p\u003e\n\n\n\u003c!-- AQUEOUS \/ ALCOHOL --\u003e\n\n\u003ch2\u003eNylon capsule filters for aqueous and alcohol-based liquids\u003c\/h2\u003e\n\n\u003cp\u003e\n  Nylon membrane capsules are especially relevant when the process includes\n  water-based liquids, alcohol-containing solutions or compatible solvent\n  mixtures.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Typical use can include laboratory analysis, sample preparation, process\n  development and fine filtration of compatible aqueous or alcohol-based\n  process fluids.\n\u003c\/p\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eChemical compatibility:\u003c\/strong\u003e “alcohol resistant” should not be\n  interpreted as universal compatibility with every organic solvent or chemical.\n  Confirm membrane and housing compatibility against the actual liquid,\n  concentration, temperature and exposure time.\n\u003c\/p\u003e\n\n\n\u003c!-- CONNECTIONS --\u003e\n\n\u003ch2\u003eNylon capsule filter connection options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The current Filtra Nylon capsule range includes multiple inlet and outlet\n  options for integration into laboratory tubing, pilot equipment and process\n  systems.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNPT\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\" NPT male, 3\/8\" NPT male, 1\/2\" NPT male and\n    3\/8\" NPT female options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSwagelok\u003c\/th\u003e\n  \u003ctd\u003e\n    1\/4\", 5\/16\", 3\/8\" and 1\/2\" selectable connection options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCPC quick-connect\u003c\/th\u003e\n  \u003ctd\u003e1\/4\" CPC PLC male and female configurations\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eHose barb\u003c\/th\u003e\n  \u003ctd\u003e\n    3\/8\", 1\/2\" and 1\/4\"–3\/8\" stepped hose-barb options\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eSanitary connection\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003e1\" Tri-Clamp \/ Tri-Clover\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Exact fitting availability can depend on capsule size and configuration.\n  Confirm the inlet and outlet combination required for the installation.\n\u003c\/p\u003e\n\n\n\u003c!-- LENGTH --\u003e\n\n\u003ch2\u003eNylon capsule lengths from 1.5 to 20 inches\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra's current selectable Nylon capsule configurations include\n  \u003cstrong\u003e1.5\", 2.5\", 5\", 10\" and 20\"\u003c\/strong\u003e\n  lengths.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Larger capsule formats can provide increased filtration area and throughput,\n  but the documented 300 cm² specification belongs to the compact capsule\n  configuration and should not be applied automatically to every larger size.\n\u003c\/p\u003e\n\n\n\u003c!-- APPLICATIONS --\u003e\n\n\u003ch2\u003eTypical Nylon capsule filter applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eLaboratory sample preparation\u003c\/li\u003e\n  \u003cli\u003eAqueous-solution filtration\u003c\/li\u003e\n  \u003cli\u003eAlcohol-containing liquid filtration\u003c\/li\u003e\n  \u003cli\u003eCompatible solvent filtration\u003c\/li\u003e\n  \u003cli\u003eFine particle removal\u003c\/li\u003e\n  \u003cli\u003eLiquid clarification\u003c\/li\u003e\n  \u003cli\u003eLaboratory analysis\u003c\/li\u003e\n  \u003cli\u003ePilot-scale filtration\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical research and process development\u003c\/li\u003e\n  \u003cli\u003eBiotechnology laboratory filtration\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- NYLON VS PES\/PVDF --\u003e\n\n\u003ch2\u003eNylon vs PES and PVDF capsule filters\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003eNylon\u003c\/th\u003e\n  \u003cth\u003ePES\u003c\/th\u003e\n  \u003cth\u003ePVDF\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eWettability\u003c\/th\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n  \u003ctd\u003eHydrophilic\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eKey selection feature\u003c\/th\u003e\n  \u003ctd\u003eAlcohol resistance\u003c\/td\u003e\n  \u003ctd\u003eStrong hydrophilicity and low protein adsorption\u003c\/td\u003e\n  \u003ctd\u003eLow protein adsorption\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical starting point\u003c\/th\u003e\n  \u003ctd\u003eAqueous and compatible alcohol-based liquids\u003c\/td\u003e\n  \u003ctd\u003eAqueous process liquids and buffers\u003c\/td\u003e\n  \u003ctd\u003eProtein-sensitive and compatible process liquids\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFinal selection\u003c\/th\u003e\n  \u003ctd colspan=\"3\"\u003e\n    Confirm chemical compatibility, retention requirement, product recovery\n    and process conditions for the actual liquid.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- QUALITY --\u003e\n\n\u003cdiv class=\"fi-quality\"\u003e\n\n\u003ch2\u003eIntegrity Testing, Biological Safety \u0026amp; Material Compliance\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented compact Nylon capsule range includes several quality and\n  material characteristics relevant to laboratory, biotechnology and process\n  filtration.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-quality-grid\"\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003e100% integrity tested\u003c\/strong\u003e\n    The documented compact Nylon capsule range is individually integrity tested\n    during manufacturing.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n    Documented components meet biological-safety specifications for\n    USP Class VI-121°C plastics.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eAutoclave compatible\u003c\/strong\u003e\n    The documented compact configuration supports autoclaving at\n    121 °C for 30 minutes over multiple cycles.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eMaterial compliance\u003c\/strong\u003e\n    Documented construction materials have FDA 21 CFR and EU 10\/2011\n    food-contact material compliance.\n  \u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  These specifications apply to the documented capsule configuration.\n  Requirements for regulated pharmaceutical processes should be confirmed\n  against the exact membrane grade, size and supporting documentation.\n\u003c\/p\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- PHARMA --\u003e\n\n\u003ch2\u003eNylon capsule filters for pharmaceutical and biotechnology development\u003c\/h2\u003e\n\n\u003cp\u003e\n  Nylon capsules can be useful in pharmaceutical R\u0026amp;D, biotechnology\n  laboratories and pilot-scale filtration where the process liquid is\n  chemically compatible with the membrane.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For regulated sterile or bioburden-reduction processes, a nominal\n  \u003cstrong\u003e0.2 µm Nylon membrane should not automatically be treated as\n  sterilizing grade\u003c\/strong\u003e. The applicable retention validation,\n  integrity-test limits and product documentation must be confirmed for the\n  exact filter grade.\n\u003c\/p\u003e\n\n\n\u003c!-- SELECTION --\u003e\n\n\u003ch2\u003eHow to select a Nylon capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  Correct selection should consider the complete liquid and process conditions.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired pore size from 0.1 to 3.0 µm\u003c\/li\u003e\n  \u003cli\u003eAqueous, alcohol-containing or other compatible process liquid\u003c\/li\u003e\n  \u003cli\u003eAlcohol concentration and chemical composition\u003c\/li\u003e\n  \u003cli\u003eRequired particle-retention level\u003c\/li\u003e\n  \u003cli\u003eRequired flow rate\u003c\/li\u003e\n  \u003cli\u003eTotal batch or process volume\u003c\/li\u003e\n  \u003cli\u003e1.5\", 2.5\", 5\", 10\" or 20\" capsule format\u003c\/li\u003e\n  \u003cli\u003eNPT, Swagelok, CPC, hose-barb or Tri-Clamp connection\u003c\/li\u003e\n  \u003cli\u003eOperating pressure and temperature\u003c\/li\u003e\n  \u003cli\u003eSanitisation or autoclaving requirements\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical documentation requirements where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- LINKS --\u003e\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eCompare Nylon with other capsule filter membranes\u003c\/h2\u003e\n\n\u003cp\u003e\n  Not sure whether Nylon, PES, PVDF or PTFE is the best membrane for your\n  liquid? Send us the fluid composition, pore size, process volume and\n  connection requirements for technical selection support.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n  \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n    Request Technical Selection\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n    Compare Capsule Filters\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pes-membrane-capsule-filter\"\u003e\n    View PES Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pvdf-membrane-capsule-filter\"\u003e\n    View PVDF Capsules\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\n    Pharmaceutical Filtration\n  \u003c\/a\u003e\n\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ --\u003e\n\n\u003ch2\u003eNylon Membrane Capsule Filter FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is a Nylon membrane capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nA Nylon membrane capsule filter is a self-contained disposable filter containing\na hydrophilic Nylon membrane inside a polymer capsule. It is used for fine\nfiltration and clarification of compatible aqueous, alcohol-containing and\nprocess liquids.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a Nylon membrane hydrophilic?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. The documented Nylon membrane is naturally hydrophilic and can therefore\nwet readily with compatible aqueous liquids without hydrophobic-membrane\npre-wetting.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan Nylon capsule filters be used with alcohol?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. The documented Nylon membrane combines hydrophilicity with alcohol\nresistance and is suitable for compatible aqueous and alcohol-based liquids.\nCompatibility should still be checked for the specific alcohol concentration,\ntemperature and process conditions.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich pore sizes are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nAvailable Nylon capsule pore sizes include 0.1, 0.2, 0.45, 0.65,\n1.0 and 3.0 µm.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a 0.2 micron Nylon capsule filter available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. A 0.2 µm Nylon configuration is available. A 0.2 µm pore size alone,\nhowever, should not be interpreted as proof of validated sterilizing-grade\nperformance.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich Nylon capsule lengths are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nFiltra currently offers 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch\nselectable Nylon capsule configurations.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat connection types are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nCurrent Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb\nand 1-inch Tri-Clamp \/ Tri-Clover connections.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the filtration area of a Nylon capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact Nylon capsule configuration provides approximately\n300 cm² of filtration area. Larger capsule configurations can have different\neffective filtration areas.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan Nylon capsule filters be autoclaved?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact Nylon capsule configuration supports autoclaving at\n121 °C for 30 minutes over multiple cycles. Confirm the limit for the exact\ncapsule configuration selected.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre Nylon capsule filters integrity tested?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented compact Nylon capsule range is 100% integrity tested during\nmanufacturing. For regulated applications, confirm the test method and\nacceptance specification for the exact selected configuration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ JSON-LD --\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is a Nylon membrane capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"A Nylon membrane capsule filter is a self-contained disposable filter containing a hydrophilic Nylon membrane inside a polymer capsule. It is used for fine filtration and clarification of compatible aqueous, alcohol-containing and process liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a Nylon membrane hydrophilic?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The documented Nylon membrane is naturally hydrophilic and can wet readily with compatible aqueous liquids.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can Nylon capsule filters be used with alcohol?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The documented Nylon membrane combines hydrophilicity with alcohol resistance and is suitable for compatible aqueous and alcohol-based liquids. Compatibility should be checked for the specific concentration, temperature and process conditions.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which pore sizes are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Available Nylon capsule pore sizes include 0.1, 0.2, 0.45, 0.65, 1.0 and 3.0 µm.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a 0.2 micron Nylon capsule filter available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A 0.2 µm Nylon configuration is available. A 0.2 µm pore size alone should not be interpreted as proof of validated sterilizing-grade performance.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which Nylon capsule lengths are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Filtra currently offers 1.5-inch, 2.5-inch, 5-inch, 10-inch and 20-inch selectable Nylon capsule configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What connection types are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Current Filtra options include NPT, Swagelok, CPC quick-connect, hose-barb and 1-inch Tri-Clamp or Tri-Clover connections.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the filtration area of a Nylon capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact Nylon capsule configuration provides approximately 300 cm² of filtration area. Larger capsule configurations can have different effective filtration areas.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can Nylon capsule filters be autoclaved?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact Nylon capsule configuration supports autoclaving at 121 °C for 30 minutes over multiple cycles. Confirm the limit for the exact capsule configuration selected.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Are Nylon capsule filters integrity tested?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented compact Nylon capsule range is 100% integrity tested during manufacturing. For regulated applications, confirm the test method and acceptance specification for the exact selected configuration.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e\n\n\u003c\/section\u003e","brand":"Filtra International","offers":[{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 1.5\"","offer_id":56113172709702,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 2.5\"","offer_id":56113172742470,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 5\"","offer_id":56113172775238,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 10\"","offer_id":56113172808006,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/4\" NPT Male (4N) \/ 20\"","offer_id":56113172840774,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 3\/8\" NPT Male (6N) \/ 1.5\"","offer_id":56113172873542,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 3\/8\" NPT Male (6N) \/ 2.5\"","offer_id":56113172906310,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 3\/8\" NPT Male (6N) \/ 5\"","offer_id":56113172939078,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 3\/8\" NPT Male (6N) \/ 10\"","offer_id":56113172971846,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 3\/8\" NPT Male (6N) \/ 20\"","offer_id":56113173004614,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/2\" NPT Male (8N) \/ 1.5\"","offer_id":56113173037382,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/2\" NPT Male (8N) \/ 2.5\"","offer_id":56113173070150,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 1\/2\" NPT Male (8N) \/ 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background:#fff;\n}\n.fi-pp-capsule .fi-stat span {\n  display:block;\n  margin-bottom:5px;\n  color:var(--fi-muted);\n  font-size:12px;\n}\n.fi-pp-capsule .fi-stat strong {\n  display:block;\n  font-size:16px;\n}\n.fi-pp-capsule .fi-table-wrap {\n  overflow-x:auto;\n  margin:21px 0 28px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n.fi-pp-capsule .fi-table {\n  border-collapse:collapse;\n  width:100%;\n  min-width:570px;\n}\n.fi-pp-capsule .fi-table th,\n.fi-pp-capsule .fi-table td {\n  padding:12px 15px;\n  border-bottom:1px solid var(--fi-border);\n  text-align:left;\n  vertical-align:top;\n  font-size:14px;\n  line-height:1.55;\n}\n.fi-pp-capsule .fi-table th {\n  width:36%;\n  color:var(--fi-text);\n  background:var(--fi-soft);\n}\n.fi-pp-capsule .fi-table tr:last-child th,\n.fi-pp-capsule .fi-table tr:last-child td {\n  border-bottom:0;\n}\n.fi-pp-capsule .fi-note {\n  margin:22px 0;\n  padding:17px 19px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n.fi-pp-capsule .fi-note p {\n  margin:0;\n}\n.fi-pp-capsule .fi-cards {\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:15px;\n  margin:23px 0 33px;\n}\n.fi-pp-capsule .fi-card {\n  padding:20px;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n  background:#fff;\n}\n.fi-pp-capsule .fi-card p {\n  margin:0;\n}\n.fi-pp-capsule .fi-quality {\n  padding:27px;\n  margin:35px 0;\n  border-radius:12px;\n  background:var(--fi-dark);\n}\n.fi-pp-capsule .fi-quality h2,\n.fi-pp-capsule .fi-quality strong {\n  color:#fff;\n}\n.fi-pp-capsule .fi-quality p {\n  color:rgba(255,255,255,.8);\n}\n.fi-pp-capsule .fi-quality-grid {\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:13px;\n  margin:20px 0;\n}\n.fi-pp-capsule .fi-quality-item {\n  padding:17px;\n  border:1px solid rgba(255,255,255,.14);\n  border-radius:9px;\n  background:rgba(255,255,255,.07);\n  color:rgba(255,255,255,.82);\n  font-size:14px;\n  line-height:1.6;\n}\n.fi-pp-capsule .fi-quality-item strong {\n  display:block;\n  margin-bottom:6px;\n}\n.fi-pp-capsule .fi-cta {\n  margin:35px 0;\n  padding:27px;\n  border-radius:12px;\n  background:var(--fi-dark);\n}\n.fi-pp-capsule .fi-cta h2 {\n  color:#fff;\n}\n.fi-pp-capsule .fi-cta p {\n  color:rgba(255,255,255,.8);\n}\n.fi-pp-capsule .fi-buttons {\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:19px;\n}\n.fi-pp-capsule .fi-button {\n  display:inline-flex;\n  min-height:45px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-weight:700;\n  font-size:14px;\n  text-decoration:none!important;\n}\n.fi-pp-capsule .fi-button-primary {\n  color:#fff!important;\n  background:var(--fi-accent);\n}\n.fi-pp-capsule .fi-button-secondary {\n  color:var(--fi-dark)!important;\n  background:#fff;\n}\n.fi-pp-capsule .fi-faq details {\n  margin:0 0 10px;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n  background:#fff;\n}\n.fi-pp-capsule .fi-faq summary {\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n.fi-pp-capsule .fi-faq details div {\n  padding:0 19px 17px;\n}\n.fi-pp-capsule .fi-faq details p {\n  margin:0;\n}\n@media(max-width:850px) {\n  .fi-pp-capsule .fi-stats {\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n  .fi-pp-capsule .fi-cards,\n  .fi-pp-capsule .fi-quality-grid {\n    grid-template-columns:1fr;\n  }\n}\n@media(max-width:480px) {\n  .fi-pp-capsule .fi-stats {\n    grid-template-columns:1fr;\n  }\n  .fi-pp-capsule .fi-button {\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\u003c!-- INTRODUCTION --\u003e\n\u003ch2 id=\"fi-pp-absolute-title\"\u003e\n  Polypropylene Capsule Filter – Absolute Rated | 0.3–50 µm\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-lead\"\u003e\n  Filtra International supplies\n  \u003cstrong\u003eabsolute-rated polypropylene capsule filters\u003c\/strong\u003e\n  for clarification, particle removal and prefiltration\n  of compatible process liquids. The filter uses\n  \u003cstrong\u003epleated polypropylene media with graded porosity\u003c\/strong\u003e\n  inside a self-contained disposable capsule.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The Filtra PP capsule range covers filtration ratings from\n  \u003cstrong\u003e0.3 to 50 µm\u003c\/strong\u003e, making it suitable for\n  a broad variety of fine- and coarse-particle filtration duties.\n  Standard selectable capsule lengths are\n  \u003cstrong\u003e2.5\", 5\" and 10\"\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The pleated filtration structure offers a large effective\n  filtration surface, while the graded media construction\n  is designed to capture particles through different regions\n  of the filter material. This can support contaminant-holding\n  capacity and efficient use of the available media.\n\u003c\/p\u003e\n\n\u003c!-- KEY SPECIFICATIONS --\u003e\n\u003cdiv class=\"fi-highlight\"\u003e\n  \u003cdiv class=\"fi-stats\"\u003e\n    \u003cdiv class=\"fi-stat\"\u003e\n      \u003cspan\u003eFilter media\u003c\/span\u003e\n      \u003cstrong\u003ePolypropylene (PP)\u003c\/strong\u003e\n    \u003c\/div\u003e\n    \u003cdiv class=\"fi-stat\"\u003e\n      \u003cspan\u003eFiltration classification\u003c\/span\u003e\n      \u003cstrong\u003eAbsolute Rated\u003c\/strong\u003e\n    \u003c\/div\u003e\n    \u003cdiv class=\"fi-stat\"\u003e\n      \u003cspan\u003eMicron ratings\u003c\/span\u003e\n      \u003cstrong\u003e0.3–50 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n    \u003cdiv class=\"fi-stat\"\u003e\n      \u003cspan\u003e10-inch reference area\u003c\/span\u003e\n      \u003cstrong\u003e5,000 cm²\u003c\/strong\u003e\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003c!-- PRODUCT SPECIFICATIONS --\u003e\n\u003ch2\u003ePP Capsule Filter – Technical Specifications\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eFilter type\u003c\/th\u003e\n    \u003ctd\u003eDisposable pleated polypropylene capsule filter\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eFiltra filtration classification\u003c\/th\u003e\n    \u003ctd\u003eAbsolute Rated\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eFilter medium\u003c\/th\u003e\n    \u003ctd\u003eGraded-porosity pleated polypropylene\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eAvailable filtration ratings\u003c\/th\u003e\n    \u003ctd\u003e\n      0.3, 0.6, 1.0, 3.0, 5.0,\n      10, 20, 30 and 50 µm\n    \u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eFiltra selectable capsule lengths\u003c\/th\u003e\n    \u003ctd\u003e2.5\", 5\" and 10\"\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eReference filtration area\u003c\/th\u003e\n    \u003ctd\u003e5,000 cm² (0.5 m²) for the 10\" configuration\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eFilter media support\u003c\/th\u003e\n    \u003ctd\u003ePolypropylene\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eEnd caps\u003c\/th\u003e\n    \u003ctd\u003ePolypropylene\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eInner core\u003c\/th\u003e\n    \u003ctd\u003ePolypropylene\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eOuter cage\u003c\/th\u003e\n    \u003ctd\u003ePolypropylene\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eProcess connections\u003c\/th\u003e\n    \u003ctd\u003e\n      1.5\" Tri-Clamp, 0.5\" Tri-Clamp,\n      1\/2\" Hose Barb, 3\/4\" Hose Barb\n      or 1\/2\" NPT Male\n    \u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eVent and drain options\u003c\/th\u003e\n    \u003ctd\u003eStäubli-type connection or Hose Barb\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eMinimum burst pressure\u003c\/th\u003e\n    \u003ctd\u003e8.5 barg (not the permissible operating pressure)\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eDocumented autoclaving\u003c\/th\u003e\n    \u003ctd\u003e\n      Up to 25 cycles at 125 °C for 30 minutes,\n      subject to the applicable procedure\n    \u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eSteam-in-place (SIP)\u003c\/th\u003e\n    \u003ctd\u003eNot permitted for this capsule construction\u003c\/td\u003e\n  \u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-note\"\u003e\n  \u003cp\u003e\n    \u003cstrong\u003eTechnical selection note:\u003c\/strong\u003e\n    the 5,000 cm² filtration area applies to the\n    documented 10\" capsule configuration.\n    The maximum operating pressure, temperature and\n    allowable differential pressure must be confirmed\n    for the exact filter and operating conditions.\n    Where quantified absolute particle retention is\n    required, request the corresponding efficiency\n    specification or retention-test documentation.\n  \u003c\/p\u003e\n\u003c\/div\u003e\n\n\u003c!-- OPERATING PRINCIPLE --\u003e\n\u003ch2\u003eHow Does a Pleated PP Capsule Filter Work?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Contaminated liquid enters the capsule through the\n  selected inlet connection and passes through the\n  pleated polypropylene filtration medium.\n  Suspended particles are retained as the liquid\n  travels through the graded filtration structure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The pleated configuration increases the available\n  filtration surface within the capsule, while the\n  graded porosity helps distribute particle loading\n  rather than concentrating all contamination at\n  one location.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filtered liquid exits through the outlet connection.\n  The complete filter is replaced as a disposable\n  enclosed capsule, removing the need to open a\n  separate cartridge-filter housing.\n\u003c\/p\u003e\n\n\u003c!-- KEY BENEFITS --\u003e\n\u003ch2\u003eAdvantages of Polypropylene Capsule Filtration\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-cards\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003eGraded-Porosity Media\u003c\/h3\u003e\n    \u003cp\u003e\n      The filtration medium combines more open and\n      finer regions to distribute particulate loading\n      through the filter material.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003ePleated Filter Construction\u003c\/h3\u003e\n    \u003cp\u003e\n      The pleated media provides a large filtration\n      surface in a compact, disposable capsule assembly.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003eBroad Micron Selection\u003c\/h3\u003e\n    \u003cp\u003e\n      Filtra offers ratings from 0.3 to 50 µm for\n      different clarification, particle-reduction\n      and upstream filtration requirements.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003c!-- MICRON RANGE --\u003e\n\u003ch2\u003eAbsolute-Rated PP Capsules from 0.3 to 50 Micron\u003c\/h2\u003e\n\n\u003cp\u003e\n  Different filtration ratings are selected according\n  to the size and quantity of suspended particles,\n  the required downstream cleanliness and the\n  acceptable pressure drop.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-cards\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.3–1.0 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Fine polypropylene filtration ratings for\n      applications where smaller suspended particles\n      must be reduced before subsequent process steps.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e3–10 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Intermediate filtration ratings for general\n      clarification, process-liquid filtration and\n      upstream protection of finer filtration stages.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e20–50 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Coarser filtration ratings for larger particles,\n      process-liquid clarification and the reduction\n      of particulate load before downstream equipment.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Available ratings:\n  \u003cstrong\u003e\n    0.3, 0.6, 1.0, 3.0, 5.0, 10, 20, 30 and 50 µm.\n  \u003c\/strong\u003e\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For applications specifying a particular absolute\n  removal efficiency, the relevant test standard,\n  particle size and efficiency requirement should\n  be confirmed for the selected grade.\n\u003c\/p\u003e\n\n\u003c!-- PREFILTRATION --\u003e\n\u003ch2\u003ePP Capsule Filters for Prefiltration\u003c\/h2\u003e\n\n\u003cp\u003e\n  Polypropylene capsule filters can be installed\n  upstream of finer membrane-filtration stages to\n  reduce suspended particulate loading before\n  the liquid reaches a more sensitive final filter.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the application, a PP prefilter can\n  be evaluated upstream of PES, PVDF, PTFE or other\n  fine membrane filters. The appropriate sequence\n  depends on the liquid composition, particle-size\n  distribution and required final retention.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Prefilter selection should consider both the\n  desired particle removal and the effect of\n  contamination loading on pressure drop and\n  total process throughput.\n\u003c\/p\u003e\n\n\u003c!-- APPLICATIONS --\u003e\n\u003ch2\u003eTypical Applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eIndustrial process-water filtration\u003c\/li\u003e\n  \u003cli\u003eClarification of compatible aqueous process liquids\u003c\/li\u003e\n  \u003cli\u003ePrefiltration before fine membrane filters\u003c\/li\u003e\n  \u003cli\u003eParticle removal in bulk chemical processing\u003c\/li\u003e\n  \u003cli\u003eFiltration of compatible pharmaceutical intermediates\u003c\/li\u003e\n  \u003cli\u003eCosmetic and personal-care manufacturing\u003c\/li\u003e\n  \u003cli\u003eParts-cleaning and suitable cleaning solutions\u003c\/li\u003e\n  \u003cli\u003eFiltration of compatible inks and process fluids\u003c\/li\u003e\n  \u003cli\u003eProtection of downstream filtration equipment\u003c\/li\u003e\n  \u003cli\u003eLaboratory, pilot-plant and small-batch filtration\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Chemical compatibility must be evaluated for the\n  complete polypropylene filter assembly. Suitability\n  for a particular solvent, chemical concentration\n  or process temperature must not be assumed solely\n  from the selected filtration rating.\n\u003c\/p\u003e\n\n\u003c!-- CONNECTIONS --\u003e\n\u003ch2\u003ePP Capsule Filter Connection Options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra offers the standard polypropylene capsule\n  range with several process-connection options\n  for integration into compatible liquid-filtration\n  systems.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eSanitary connections\u003c\/th\u003e\n    \u003ctd\u003e1.5\" Tri-Clamp and 0.5\" Tri-Clamp\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eHose-barb connections\u003c\/th\u003e\n    \u003ctd\u003e1\/2\" Hose Barb and 3\/4\" Hose Barb\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eThreaded connection\u003c\/th\u003e\n    \u003ctd\u003e1\/2\" NPT Male\u003c\/td\u003e\n  \u003c\/tr\u003e\n  \u003ctr\u003e\n    \u003cth scope=\"row\"\u003eVent and drain\u003c\/th\u003e\n    \u003ctd\u003eStäubli-type quick connection or Hose Barb\u003c\/td\u003e\n  \u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cdiv class=\"fi-note\"\u003e\n  \u003cp\u003e\n    \u003cstrong\u003eConnection availability:\u003c\/strong\u003e\n    fitting combinations and vent\/drain\n    configurations should be confirmed against\n    the selected capsule length and installation.\n  \u003c\/p\u003e\n\u003c\/div\u003e\n\n\u003c!-- SIZES --\u003e\n\u003ch2\u003eAvailable PP Capsule Lengths\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filtra International offers the following\n  standard capsule lengths for this PP range:\n  \u003cstrong\u003e2.5\", 5\" and 10\"\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Capsule length affects filtration area, flow\n  capacity, differential pressure and contaminant\n  capacity. The supplier's 5,000 cm² reference\n  area applies specifically to the 10\" capsule\n  and must not be assumed for the smaller sizes.\n\u003c\/p\u003e\n\n\u003c!-- PERFORMANCE --\u003e\n\u003ch2\u003eFlow Rate and Pressure Drop\u003c\/h2\u003e\n\n\u003cp\u003e\n  The technical literature provides reference\n  liquid-flow performance for the 10\" polypropylene\n  capsule format with a 1.5\" Tri-Clamp connection.\n  Flow and differential pressure depend on\n  the selected filtration rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Real operating performance also depends on\n  liquid viscosity, temperature, contamination\n  loading, capsule size and the selected fittings.\n  Reference curves should not be used without\n  considering these process conditions.\n\u003c\/p\u003e\n\n\u003c!-- SANITISATION --\u003e\n\u003ch2\u003eAutoclaving, Sanitisation and SIP Restrictions\u003c\/h2\u003e\n\n\u003cp\u003e\n  The supplier documents autoclaving capability\n  of up to \u003cstrong\u003e25 cycles at 125 °C for\n  30 minutes\u003c\/strong\u003e for the described PP\n  capsule construction.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The source also describes chemical sanitisation\n  and limited hot-water sanitisation at up to\n  90 °C, depending on exposure time and the\n  applicable procedure.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-note\"\u003e\n  \u003cp\u003e\n    \u003cstrong\u003eImportant:\u003c\/strong\u003e\n    the documented PP capsules\n    \u003cstrong\u003emust not be steam-sterilized in situ\u003c\/strong\u003e.\n    Autoclaving capability does not mean\n    steam-in-place compatibility. Sanitisation\n    methods and limits must be confirmed for\n    the actual selected configuration.\n  \u003c\/p\u003e\n\u003c\/div\u003e\n\n\u003c!-- MATERIAL AND QUALITY --\u003e\n\u003cdiv class=\"fi-quality\"\u003e\n  \u003ch2\u003eMaterials, Biological Safety and Quality\u003c\/h2\u003e\n\n  \u003cp\u003e\n    The source technical documentation reports\n    the following characteristics for its\n    polypropylene capsule construction.\n    Application-specific declarations should\n    be confirmed for the supplied filter.\n  \u003c\/p\u003e\n\n  \u003cdiv class=\"fi-quality-grid\"\u003e\n    \u003cdiv class=\"fi-quality-item\"\u003e\n      \u003cstrong\u003ePolypropylene Construction\u003c\/strong\u003e\n      PP filtration media, media support,\n      end caps, inner core and outer cage.\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-quality-item\"\u003e\n      \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n      The technical literature reports\n      biological-safety compliance of\n      materials to USP Class VI at 121 °C.\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-quality-item\"\u003e\n      \u003cstrong\u003eFood-Contact Materials\u003c\/strong\u003e\n      The supplier reports applicable\n      material compliance with FDA 21 CFR\n      and EU Regulation 10\/2011.\n    \u003c\/div\u003e\n  \u003c\/div\u003e\n\n  \u003cp\u003e\n    Where regulatory documentation or\n    a defined absolute filtration efficiency\n    is required, confirm the relevant\n    declarations and retention-test data\n    for the specific micron rating and\n    product configuration.\n  \u003c\/p\u003e\n\u003c\/div\u003e\n\n\u003c!-- HOW TO SELECT --\u003e\n\u003ch2\u003eHow to Select an Absolute-Rated PP Capsule Filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  For correct filter sizing and selection,\n  consider the complete filtration duty:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired filtration rating, from 0.3 to 50 µm\u003c\/li\u003e\n  \u003cli\u003eTarget particle-removal efficiency\u003c\/li\u003e\n  \u003cli\u003eLiquid composition and chemical compatibility\u003c\/li\u003e\n  \u003cli\u003eFlow rate and total batch volume\u003c\/li\u003e\n  \u003cli\u003eTemperature and maximum operating pressure\u003c\/li\u003e\n  \u003cli\u003eExpected suspended solids and contaminant loading\u003c\/li\u003e\n  \u003cli\u003eAllowable initial and final differential pressure\u003c\/li\u003e\n  \u003cli\u003eCapsule length: 2.5\", 5\" or 10\"\u003c\/li\u003e\n  \u003cli\u003eRequired process connections\u003c\/li\u003e\n  \u003cli\u003eVent, drain and sanitisation requirements\u003c\/li\u003e\n  \u003cli\u003eApplication-specific quality documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003c!-- CTA --\u003e\n\u003cdiv class=\"fi-cta\"\u003e\n  \u003ch2\u003eNeed Help Selecting a PP Capsule Filter?\u003c\/h2\u003e\n\n  \u003cp\u003e\n    Send Filtra International your micron rating,\n    process liquid, flow rate, batch volume,\n    required particle retention and connection\n    requirements. We can help determine an\n    appropriate capsule configuration for\n    the intended filtration duty.\n  \u003c\/p\u003e\n\n  \u003cdiv class=\"fi-buttons\"\u003e\n    \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n      Request Technical Quotation\n    \u003c\/a\u003e\n\n    \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n      Compare Capsule Filters\n    \u003c\/a\u003e\n\n    \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/pes-membrane-capsule-filter\"\u003e\n      Compare PES Membrane Capsules\n    \u003c\/a\u003e\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\u003c!-- FAQ --\u003e\n\u003ch2\u003ePolypropylene Absolute Capsule Filter – FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eWhat is a polypropylene capsule filter?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        A polypropylene capsule filter is a\n        self-contained disposable filtration\n        device containing PP filtration media\n        within a polymer capsule assembly.\n        It is used for particulate removal\n        and clarification of compatible liquids.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eWhich PP capsule filtration ratings are available?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        The Filtra range covers 0.3, 0.6, 1.0,\n        3.0, 5.0, 10, 20, 30 and 50 µm.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eAre these PP capsules absolute rated?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        Filtra International offers this\n        capsule range as absolute rated.\n        Where a project requires a specific\n        removal efficiency or beta ratio,\n        the corresponding retention\n        specification should be confirmed\n        for the selected filtration rating.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eCan PP capsules be used for prefiltration?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        Yes. They can be evaluated for\n        particle reduction upstream of\n        finer membrane filters and other\n        sensitive process equipment.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eWhat capsule lengths does Filtra offer?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        Standard selectable lengths are\n        2.5\", 5\" and 10\".\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eWhat is the filtration area of the 10-inch capsule?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        The documented 10\" configuration\n        has a reference filtration area of\n        5,000 cm² (0.5 m²). Other lengths\n        have different filtration areas.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eCan polypropylene capsule filters be autoclaved?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        The technical literature describes\n        autoclaving for up to 25 cycles\n        at 125 °C for 30 minutes for the\n        specified capsule construction.\n        Confirm the procedure for the\n        selected filter.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n  \u003cdetails\u003e\n    \u003csummary\u003eCan these PP capsules be sterilized by SIP?\u003c\/summary\u003e\n    \u003cdiv\u003e\n      \u003cp\u003e\n        No. The source technical\n        documentation explicitly excludes\n        in-situ steam sterilisation for\n        this capsule construction.\n      \u003c\/p\u003e\n    \u003c\/div\u003e\n  \u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\u003c\/section\u003e\n\n\n\n  \n{% if product and product.handle == 'polypropylene-capsule-filter' %}\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"ProductGroup\",\n  \"@id\": {{ canonical_url | append: '#pp-absolute-product-group' | json }},\n  \"url\": {{ canonical_url | json }},\n  \"name\": {{ product.title | json }},\n  \"description\": \"Absolute-rated polypropylene capsule filters for liquid clarification, particle reduction and prefiltration. 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20\"","offer_id":57657400590662,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" Hose Barb \/ 2.5\"","offer_id":57657400623430,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" Hose Barb \/ 5\"","offer_id":57657400656198,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" Hose Barb \/ 10\"","offer_id":57657400688966,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" Hose Barb \/ 20\"","offer_id":57657400721734,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 3\/4\" Hose Barb \/ 2.5\"","offer_id":57657400754502,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 3\/4\" Hose Barb \/ 5\"","offer_id":57657400787270,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 3\/4\" Hose Barb \/ 10\"","offer_id":57657400820038,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 3\/4\" Hose Barb \/ 20\"","offer_id":57657400852806,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" NPT Male \/ 2.5\"","offer_id":57657400885574,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" NPT Male \/ 5\"","offer_id":57657400918342,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" NPT Male \/ 10\"","offer_id":57657400951110,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 µm \/ 1\/2\" NPT Male \/ 20\"","offer_id":57657400983878,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/Polypropylene_filter_capsule.png?v=1772809180"},{"product_id":"sip-ptfe-capsule-filter","title":"SIP PTFE Capsule Filter for Sterile Air, Gas \u0026 Vent Filtration","description":"\u003csection class=\"fi-capsule-detail\" aria-labelledby=\"fi-sip-ptfe-heading\"\u003e\n\n\u003cstyle\u003e\n.fi-capsule-detail{\n  --fi-dark:#10242d;\n  --fi-accent:#2b7d77;\n  --fi-text:#172126;\n  --fi-muted:#5d6a70;\n  --fi-soft:#f4f8f7;\n  --fi-border:#dce7e5;\n  color:var(--fi-text);\n}\n\n.fi-capsule-detail *,\n.fi-capsule-detail *:before,\n.fi-capsule-detail *:after{\n  box-sizing:border-box;\n}\n\n.fi-capsule-detail h2,\n.fi-capsule-detail h3{\n  color:var(--fi-text);\n  line-height:1.2;\n}\n\n.fi-capsule-detail h2{\n  margin:42px 0 16px;\n  font-size:clamp(25px,3vw,34px);\n}\n\n.fi-capsule-detail h2:first-of-type{\n  margin-top:0;\n}\n\n.fi-capsule-detail h3{\n  margin:26px 0 10px;\n  font-size:20px;\n}\n\n.fi-capsule-detail p,\n.fi-capsule-detail li{\n  color:var(--fi-muted);\n  font-size:16px;\n  line-height:1.7;\n}\n\n.fi-capsule-detail strong{\n  color:var(--fi-text);\n}\n\n.fi-capsule-lead{\n  font-size:18px!important;\n  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width:34%;\n  background:var(--fi-soft);\n  color:var(--fi-text);\n  font-weight:700;\n}\n\n.fi-table tr:last-child th,\n.fi-table tr:last-child td{\n  border-bottom:0;\n}\n\n.fi-note{\n  margin:22px 0;\n  padding:17px 19px;\n  background:var(--fi-soft);\n  border-left:4px solid var(--fi-accent);\n  border-radius:4px 10px 10px 4px;\n}\n\n.fi-grid{\n  display:grid;\n  grid-template-columns:repeat(3,minmax(0,1fr));\n  gap:16px;\n  margin:22px 0 34px;\n}\n\n.fi-card{\n  padding:21px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:11px;\n}\n\n.fi-card h3{\n  margin-top:0;\n}\n\n.fi-quality{\n  margin:36px 0;\n  padding:27px;\n  background:var(--fi-dark);\n  border-radius:13px;\n}\n\n.fi-quality h2,\n.fi-quality h3{\n  color:#fff;\n}\n\n.fi-quality p,\n.fi-quality li{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-quality strong{\n  color:#fff;\n}\n\n.fi-quality-grid{\n  display:grid;\n  grid-template-columns:repeat(4,minmax(0,1fr));\n  gap:14px;\n  margin-top:20px;\n}\n\n.fi-quality-item{\n  padding:17px;\n  background:rgba(255,255,255,.07);\n  border:1px solid rgba(255,255,255,.12);\n  border-radius:9px;\n  color:rgba(255,255,255,.78);\n  font-size:14px;\n  line-height:1.6;\n}\n\n.fi-quality-item strong{\n  display:block;\n  margin-bottom:5px;\n}\n\n.fi-links{\n  margin:35px 0;\n  padding:26px;\n  background:var(--fi-dark);\n  border-radius:12px;\n}\n\n.fi-links h2,\n.fi-links p{\n  color:#fff;\n}\n\n.fi-links p{\n  color:rgba(255,255,255,.78);\n}\n\n.fi-buttons{\n  display:flex;\n  flex-wrap:wrap;\n  gap:12px;\n  margin-top:19px;\n}\n\n.fi-button{\n  display:inline-flex;\n  min-height:46px;\n  align-items:center;\n  justify-content:center;\n  padding:11px 18px;\n  border-radius:8px;\n  font-size:14px;\n  font-weight:700;\n  text-decoration:none!important;\n}\n\n.fi-button-primary{\n  color:#fff!important;\n  background:var(--fi-accent);\n}\n\n.fi-button-secondary{\n  color:var(--fi-dark)!important;\n  background:#fff;\n}\n\n.fi-faq details{\n  margin-bottom:10px;\n  background:#fff;\n  border:1px solid var(--fi-border);\n  border-radius:9px;\n}\n\n.fi-faq summary{\n  cursor:pointer;\n  padding:17px 19px;\n  color:var(--fi-text);\n  font-size:15px;\n  font-weight:700;\n}\n\n.fi-faq details \u003e div{\n  padding:0 19px 17px;\n}\n\n.fi-faq details p{\n  margin:0;\n}\n\n@media(max-width:850px){\n  .fi-capsule-highlight__grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n\n  .fi-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-quality-grid{\n    grid-template-columns:repeat(2,minmax(0,1fr));\n  }\n}\n\n@media(max-width:480px){\n  .fi-capsule-highlight__grid,\n  .fi-quality-grid{\n    grid-template-columns:1fr;\n  }\n\n  .fi-button{\n    width:100%;\n  }\n}\n\u003c\/style\u003e\n\n\n\u003c!-- INTRO --\u003e\n\n\u003ch2 id=\"fi-sip-ptfe-heading\"\u003e\n  SIP PTFE Capsule Filter for Sterile Air, Gas \u0026amp; Vent Filtration\n\u003c\/h2\u003e\n\n\u003cp class=\"fi-capsule-lead\"\u003e\n  The SIP PTFE capsule filter is a compact, self-contained membrane filtration\n  assembly designed for processes requiring \u003cstrong\u003esteam-in-place (SIP)\n  sterilisation\u003c\/strong\u003e. With a hydrophobic PTFE membrane configuration, it is\n  particularly suited to sterile air, process gas, tank vent and bioprocess\n  filtration applications in pharmaceutical and biotechnology environments.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The SIP-capable capsule format combines membrane filtration and housing in one\n  assembly and is designed to remain integrated into the process during steam\n  sterilisation procedures. This can simplify sterile gas and vent filtration\n  installations compared with separate cartridge-and-housing systems.\n\u003c\/p\u003e\n\n\n\u003c!-- KEY SPECS --\u003e\n\n\u003cdiv class=\"fi-capsule-highlight\"\u003e\n  \u003cdiv class=\"fi-capsule-highlight__grid\"\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eMembrane option\u003c\/span\u003e\n      \u003cstrong\u003eHydrophobic PTFE\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eDocumented pore sizes\u003c\/span\u003e\n      \u003cstrong\u003e0.04–0.45 µm\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003eCapsule formats\u003c\/span\u003e\n      \u003cstrong\u003e2.5\" \/ 5\"\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"fi-capsule-stat\"\u003e\n      \u003cspan\u003ePrimary use\u003c\/span\u003e\n      \u003cstrong\u003eSterile air \u0026amp; gas\u003c\/strong\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- TECHNICAL TABLE --\u003e\n\n\u003ch2\u003eSIP PTFE capsule filter technical overview\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eFilter type\u003c\/th\u003e\n  \u003ctd\u003eSteam-in-place compatible membrane capsule filter\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003ePTFE membrane configuration\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane behaviour\u003c\/th\u003e\n  \u003ctd\u003eHydrophobic, suitable for air, gas and vent filtration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMedia support\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eEnd caps\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eInner core\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eOuter cage\u003c\/th\u003e\n  \u003ctd\u003ePolypropylene\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eDocumented pore sizes\u003c\/th\u003e\n  \u003ctd\u003e\u003cstrong\u003e0.04, 0.1, 0.2 and 0.45 µm\u003c\/strong\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eCapsule length options\u003c\/th\u003e\n  \u003ctd\u003e2.5\" and 5\"\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNominal length – 2.5\"\u003c\/th\u003e\n  \u003ctd\u003eApprox. 84 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eNominal length – 5\"\u003c\/th\u003e\n  \u003ctd\u003eApprox. 159 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eVent options\u003c\/th\u003e\n  \u003ctd\u003eStaubli or hose-barb configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eProcess connection\u003c\/th\u003e\n  \u003ctd\u003eSanitary flange connection available depending on configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003eDesigned for connection to an automatic integrity-testing system\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eBiological safety\u003c\/th\u003e\n  \u003ctd\u003eSelected component materials meet USP Class VI-121°C requirements for plastics\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMaterial compliance\u003c\/th\u003e\n  \u003ctd\u003eDocumented FDA 21 CFR and EU 10\/2011 food-contact material compliance\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp class=\"fi-note\"\u003e\n  \u003cstrong\u003eConfiguration note:\u003c\/strong\u003e pore size, membrane grade, connection\n  arrangement and validation requirements should be confirmed for the exact\n  capsule configuration. A nominal pore size alone does not establish\n  sterilizing-grade performance for every configuration.\n\u003c\/p\u003e\n\n\n\u003c!-- WHAT IS SIP --\u003e\n\n\u003ch2\u003eWhat is a steam-in-place capsule filter?\u003c\/h2\u003e\n\n\u003cp\u003e\n  A \u003cstrong\u003esteam-in-place capsule filter\u003c\/strong\u003e is designed to remain connected\n  to the process system while the filtration assembly is exposed to a steam\n  sterilisation procedure. This is especially useful in pharmaceutical and\n  biotechnology systems where removing and reinstalling a filter between\n  sterilisation cycles is undesirable.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The SIP capsule construction provides a compact alternative to a separate\n  membrane cartridge installed inside a stainless-steel filter housing,\n  particularly for smaller process lines, pilot installations and critical\n  vent or gas filtration points.\n\u003c\/p\u003e\n\n\n\u003c!-- HYDROPHOBIC PTFE --\u003e\n\n\u003ch2\u003eWhy use hydrophobic PTFE for sterile gas filtration?\u003c\/h2\u003e\n\n\u003cp\u003e\n  PTFE membrane is naturally hydrophobic. For gas and vent applications this\n  helps maintain gas flow while resisting penetration by liquid water under\n  suitable operating conditions.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This behaviour makes PTFE particularly relevant for applications such as\n  sterile air supply, tank and vessel venting, fermentation gas filtration\n  and controlled gas exchange in pharmaceutical and biotechnology processes.\n\u003c\/p\u003e\n\n\n\u003c!-- PORE SIZES --\u003e\n\n\u003ch2\u003e0.04, 0.1, 0.2 and 0.45 micron SIP capsule filters\u003c\/h2\u003e\n\n\u003cp\u003e\n  The documented SIP capsule platform supports several membrane pore-size\n  configurations rather than only one fixed 0.2 µm option.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-grid\"\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.04 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Fine membrane configuration for applications requiring a smaller\n      documented pore-size option. Final suitability depends on required\n      retention performance and process validation.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.1 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Fine PTFE membrane option for critical air, gas and vent filtration\n      where a 0.1 µm configuration is specified.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n  \u003carticle class=\"fi-card\"\u003e\n    \u003ch3\u003e0.2 µm\u003c\/h3\u003e\n    \u003cp\u003e\n      Widely relevant to critical pharmaceutical gas and vent filtration.\n      Where sterilizing-grade performance is required, the exact grade and\n      supporting validation documentation must be confirmed.\n    \u003c\/p\u003e\n  \u003c\/article\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  A 0.45 µm configuration is also documented for the SIP capsule platform\n  and may be considered where the required retention level permits a larger\n  pore size.\n\u003c\/p\u003e\n\n\n\u003c!-- LENGTH --\u003e\n\n\u003ch2\u003e2.5-inch and 5-inch SIP capsule configurations\u003c\/h2\u003e\n\n\u003cp\u003e\n  Two compact capsule lengths are documented for this SIP platform:\n  \u003cstrong\u003e2.5 inches\u003c\/strong\u003e and \u003cstrong\u003e5 inches\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003e2.5\" capsule\u003c\/th\u003e\n  \u003ctd\u003e\n    Approx. 84 mm nominal length. Suitable where compact installation space\n    and lower process-scale requirements are important.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003e5\" capsule\u003c\/th\u003e\n  \u003ctd\u003e\n    Approx. 159 mm nominal length. Provides a larger capsule format for\n    applications requiring increased filtration capacity.\n  \u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Final capsule size should be selected from the required gas or liquid flow,\n  pressure drop, process conditions and validation requirements rather than\n  physical length alone.\n\u003c\/p\u003e\n\n\n\u003c!-- APPLICATIONS --\u003e\n\n\u003ch2\u003eTypical SIP PTFE capsule filter applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSterile air filtration\u003c\/li\u003e\n  \u003cli\u003eSterile process gas filtration\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical tank vent filtration\u003c\/li\u003e\n  \u003cli\u003eBioreactor and fermentation vent filtration\u003c\/li\u003e\n  \u003cli\u003eBiotechnology process gas filtration\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical and biological process filtration\u003c\/li\u003e\n  \u003cli\u003eSmall-scale sterile process installations\u003c\/li\u003e\n  \u003cli\u003ePilot-scale SIP filtration systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- QUALITY --\u003e\n\n\u003cdiv class=\"fi-quality\"\u003e\n\n\u003ch2\u003eQuality, Material Compliance \u0026amp; Integrity Testing\u003c\/h2\u003e\n\n\u003cp\u003e\n  For pharmaceutical and biotechnology filtration, membrane selection is only\n  part of the specification. The materials, sterilisation approach and ability\n  to verify filter integrity are also important.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-quality-grid\"\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003ePurpose-designed for SIP\u003c\/strong\u003e\n    The capsule platform is designed specifically for applications using\n    steam-in-place sterilisation.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eUSP Class VI\u003c\/strong\u003e\n    Documented component materials meet biological-safety requirements for\n    USP Class VI-121°C plastics.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eIntegrity-test connection\u003c\/strong\u003e\n    The design supports connection to an automatic filter integrity-testing\n    system.\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"fi-quality-item\"\u003e\n    \u003cstrong\u003eMaterial compliance\u003c\/strong\u003e\n    Selected construction materials have documented FDA 21 CFR and EU 10\/2011\n    food-contact compliance.\n  \u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\u003cp\u003e\n  Where a regulated pharmaceutical process requires validated sterile\n  filtration, request the documentation applicable to the exact membrane\n  grade, pore size and capsule configuration selected.\n\u003c\/p\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- INTEGRITY TESTING --\u003e\n\n\u003ch2\u003eSIP capsule filter integrity testing\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filter integrity verification is important in critical membrane filtration\n  processes because it provides a non-destructive way to check whether the\n  installed membrane assembly remains within its defined integrity limits.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The SIP capsule design includes configurations that can be connected to an\n  automatic integrity tester. The appropriate test method and acceptance\n  limits depend on the exact membrane grade and pore-size configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filtra International also supplies membrane\n  \u003ca href=\"\/collections\/filter-integrity-testers\"\u003e\u003cstrong\u003efilter integrity testing equipment\u003c\/strong\u003e\u003c\/a\u003e\n  for pharmaceutical and biotechnology filtration systems.\n\u003c\/p\u003e\n\n\n\u003c!-- STANDARD PTFE VS SIP --\u003e\n\n\u003ch2\u003eSIP PTFE capsule filter vs standard PTFE capsule filter\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-table-wrap\"\u003e\n\u003ctable class=\"fi-table\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n  \u003cth\u003e\u003c\/th\u003e\n  \u003cth\u003eSIP PTFE capsule\u003c\/th\u003e\n  \u003cth\u003eStandard PTFE capsule\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\n\u003ctr\u003e\n  \u003cth\u003ePrimary design objective\u003c\/th\u003e\n  \u003ctd\u003eIntegration into systems requiring steam-in-place procedures\u003c\/td\u003e\n  \u003ctd\u003eCompact gas, vent, solvent and laboratory filtration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eMembrane\u003c\/th\u003e\n  \u003ctd\u003eHydrophobic PTFE configuration\u003c\/td\u003e\n  \u003ctd\u003eHydrophobic PTFE\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eTypical use\u003c\/th\u003e\n  \u003ctd\u003eCritical sterile air, gas and process vent filtration\u003c\/td\u003e\n  \u003ctd\u003eGas, vent, solvent and general PTFE capsule filtration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003ctr\u003e\n  \u003cth\u003eIntegrity testing\u003c\/th\u003e\n  \u003ctd\u003eConfiguration supports connection to automatic integrity tester\u003c\/td\u003e\n  \u003ctd\u003eDepends on selected capsule configuration\u003c\/td\u003e\n\u003c\/tr\u003e\n\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\n\n\u003c!-- SELECTION --\u003e\n\n\u003ch2\u003eHow to select a SIP PTFE capsule filter\u003c\/h2\u003e\n\n\u003cp\u003e\n  Correct selection should start with the process conditions rather than the\n  pore size alone.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAir, gas, vent or compatible liquid application\u003c\/li\u003e\n  \u003cli\u003eRequired pore size: 0.04, 0.1, 0.2 or 0.45 µm\u003c\/li\u003e\n  \u003cli\u003e2.5\" or 5\" capsule configuration\u003c\/li\u003e\n  \u003cli\u003eRequired gas or liquid flow rate\u003c\/li\u003e\n  \u003cli\u003eAllowable pressure drop\u003c\/li\u003e\n  \u003cli\u003eSteam-in-place sterilisation procedure\u003c\/li\u003e\n  \u003cli\u003eProcess operating pressure and temperature\u003c\/li\u003e\n  \u003cli\u003eRequired sanitary connection arrangement\u003c\/li\u003e\n  \u003cli\u003eStaubli or hose-barb vent configuration\u003c\/li\u003e\n  \u003cli\u003eIntegrity-testing requirements\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical validation and documentation requirements\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003c!-- INTERNAL LINKS --\u003e\n\n\u003cdiv class=\"fi-links\"\u003e\n\n\u003ch2\u003eNeed help selecting the correct SIP capsule?\u003c\/h2\u003e\n\n\u003cp\u003e\n  Send us your process gas or liquid, required pore size, flow rate,\n  sterilisation procedure and connection requirements. We can help determine\n  whether an SIP PTFE capsule, standard PTFE capsule or another membrane\n  configuration is more appropriate.\n\u003c\/p\u003e\n\n\u003cdiv class=\"fi-buttons\"\u003e\n\n  \u003ca class=\"fi-button fi-button-primary\" href=\"\/pages\/quote-request\"\u003e\n    Request Technical Selection\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/collections\/capsule-and-lab-filters\"\u003e\n    Compare Capsule Filters\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/products\/ptfe-membrane-capsule-filter\"\u003e\n    Standard PTFE Capsule\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/ptfe-filters\"\u003e\n    PTFE Filter Guide\n  \u003c\/a\u003e\n\n  \u003ca class=\"fi-button fi-button-secondary\" href=\"\/pages\/pharmaceutical-filtration-solutions\"\u003e\n    Pharmaceutical Filtration\n  \u003c\/a\u003e\n\n\u003c\/div\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ --\u003e\n\n\u003ch2\u003eSIP PTFE Capsule Filter FAQ\u003c\/h2\u003e\n\n\u003cdiv class=\"fi-faq\"\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is a SIP PTFE capsule filter?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nA SIP PTFE capsule filter is a self-contained membrane filter designed for\nprocess systems using steam-in-place sterilisation. The PTFE configuration is\nparticularly suited to critical air, gas and vent filtration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich pore sizes are available for the SIP capsule platform?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nDocumented pore-size options include 0.04 µm, 0.1 µm, 0.2 µm and 0.45 µm.\nThe appropriate rating depends on the retention requirement and exact filter\ngrade.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eIs a 0.2 micron SIP PTFE capsule filter available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. A 0.2 µm configuration is documented. Where validated sterilizing-grade\nperformance is required, the supporting validation documentation for the exact\nconfiguration should also be confirmed.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich SIP capsule lengths are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented SIP capsule range includes 2.5-inch and 5-inch configurations,\nwith nominal lengths of approximately 84 mm and 159 mm respectively.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhy is PTFE used for sterile gas and vent filtration?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nPTFE is hydrophobic, allowing air and gas to pass through the membrane while\nresisting penetration by liquid water under suitable operating conditions.\nThis makes it useful for sterile gas and process vent filtration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eCan the SIP capsule be connected to an integrity tester?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nYes. The documented SIP capsule design supports connection to an automatic\nintegrity-testing system. Test parameters and acceptance limits depend on the\nselected membrane configuration.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhich vent connections are available?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented capsule platform includes Staubli and hose-barb vent\nconfigurations. Final connection arrangement depends on the selected capsule.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eAre the materials suitable for pharmaceutical applications?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe documented capsule materials include polypropylene support, end-cap,\ncore and cage components, with selected materials meeting USP Class VI-121°C\nbiological-safety requirements. Food-contact material compliance is also\ndocumented against relevant FDA 21 CFR and EU 10\/2011 requirements.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003cdetails\u003e\n\u003csummary\u003eWhat is the difference between an SIP PTFE capsule and a standard PTFE capsule?\u003c\/summary\u003e\n\u003cdiv\u003e\n\u003cp\u003e\nThe SIP capsule is specifically intended for processes requiring\nsteam-in-place sterilisation. A standard PTFE capsule is generally used for\ncompact gas, vent, solvent and laboratory filtration where an SIP-capable\nhousing design is not required.\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/details\u003e\n\n\u003c\/div\u003e\n\n\n\u003c!-- FAQ JSON-LD --\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\":\"https:\/\/schema.org\",\n  \"@type\":\"FAQPage\",\n  \"@id\":\"{{ request.origin }}{{ request.path }}#faq\",\n  \"url\":\"{{ request.origin }}{{ request.path }}\",\n  \"mainEntity\":[\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is a SIP PTFE capsule filter?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"A SIP PTFE capsule filter is a self-contained membrane filter designed for process systems using steam-in-place sterilisation. The PTFE configuration is particularly suited to critical air, gas and vent filtration.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which pore sizes are available for the SIP capsule platform?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Documented pore-size options include 0.04 µm, 0.1 µm, 0.2 µm and 0.45 µm. The appropriate rating depends on the retention requirement and exact filter grade.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Is a 0.2 micron SIP PTFE capsule filter available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. A 0.2 µm configuration is documented. Where validated sterilizing-grade performance is required, the supporting validation documentation for the exact configuration should also be confirmed.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which SIP capsule lengths are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented SIP capsule range includes 2.5-inch and 5-inch configurations, with nominal lengths of approximately 84 mm and 159 mm respectively.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Why is PTFE used for sterile gas and vent filtration?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"PTFE is hydrophobic, allowing air and gas to pass through the membrane while resisting penetration by liquid water under suitable operating conditions.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Can the SIP capsule be connected to an integrity tester?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"Yes. The documented SIP capsule design supports connection to an automatic integrity-testing system. Test parameters and acceptance limits depend on the selected membrane configuration.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"Which vent connections are available?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The documented capsule platform includes Staubli and hose-barb vent configurations.\"\n      }\n    },\n    {\n      \"@type\":\"Question\",\n      \"name\":\"What is the difference between an SIP PTFE capsule and a standard PTFE capsule?\",\n      \"acceptedAnswer\":{\n        \"@type\":\"Answer\",\n        \"text\":\"The SIP capsule is specifically intended for processes requiring steam-in-place sterilisation. A standard PTFE capsule is generally used for compact gas, vent, solvent and laboratory filtration where an SIP-capable housing design is not required.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e\n\n\u003c\/section\u003e","brand":"Filtra International","offers":[{"title":"0.04µm \/ 2.5\" \/ Staubli","offer_id":57329459200326,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.04µm \/ 2.5\" \/ Hose Barb","offer_id":57329459233094,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.04µm \/ 5\" \/ Staubli","offer_id":57329459265862,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.04µm \/ 5\" \/ Hose Barb","offer_id":57329459298630,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 2.5\" \/ Staubli","offer_id":56113421680966,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 2.5\" \/ Hose Barb","offer_id":56113421713734,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 5\" \/ Staubli","offer_id":56113421746502,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.1 µm \/ 5\" \/ Hose Barb","offer_id":56113421779270,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.2 µm \/ 2.5\" \/ Staubli","offer_id":56113421812038,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.2 µm \/ 2.5\" \/ Hose Barb","offer_id":56113421844806,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.2 µm \/ 5\" \/ Staubli","offer_id":56113421877574,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.2 µm \/ 5\" \/ Hose Barb","offer_id":56113421910342,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45µm \/ 2.5\" \/ Staubli","offer_id":57329459331398,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45µm \/ 2.5\" \/ Hose Barb","offer_id":57329459364166,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45µm \/ 5\" \/ Staubli","offer_id":57329459396934,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"0.45µm \/ 5\" \/ Hose Barb","offer_id":57329459429702,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/sip-sterile-gas-capsule-filter-PTFE.png?v=1772812726"},{"product_id":"single-use-fluoropolymer-freeze-bag","title":"Single-Use Fluoropolymer Freeze Bag Assembly","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Single-use fluoropolymer freeze bag assemblies are designed for the freezing,\n  storage, transport and handling of pharmaceutical and bioprocess liquids.\n  The fluid-contact bag is manufactured from a single-layer fluoropolymer material\n  and can be configured as part of a disposable fluid path with tubing and\n  connection components.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The combination of chemical resistance, low-temperature flexibility and\n  single-layer construction makes this type of process bag particularly suitable\n  for frozen drug substance, intermediates, cell culture materials and other\n  process fluids requiring controlled storage or transportation.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Unlike multilayer process films constructed from several polymers, adhesive\n  layers and barrier materials, the bag film consists of one fluoropolymer\n  material. This monolayer construction eliminates delamination between film\n  layers and avoids the use of interlayer adhesives within the bag film.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The specified working temperature range is approximately\n  \u003cstrong\u003e-85 °C to +40 °C\u003c\/strong\u003e. This allows the bag to remain suitable for\n  demanding low-temperature applications where conventional flexible materials\n  may become less elastic.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies can be supplied for gamma sterilisation and are intended for\n  pharmaceutical and bioprocess applications where cleanliness, material\n  compatibility and controlled fluid handling are important.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available test and conformity information includes biological safety,\n  endotoxin, particle and extractables data. Extractables and leachables test\n  data following BPOG guidelines can be made available for technical review.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bag functions as a flexible single-use process container within a closed\n  or controlled fluid path. Process liquid enters or leaves the bag through\n  tubing and connection components selected for the required application.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  During freezing, the liquid and flexible container are cooled together.\n  The fluoropolymer film is selected for its ability to remain functional at\n  low temperatures down to the specified operating limit. After freezing, the\n  assembly can be used for controlled storage and subsequent transport before\n  thawing or further downstream processing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the configuration, the bag may be supplied as a complete assembly\n  with tubing and connections or as a bag without tubing. The exact fluid path\n  should be defined around the intended filling, freezing, storage, transport\n  and discharge procedure.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bag film is manufactured from a\n  \u003cstrong\u003esingle-layer fluoropolymer material\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The monolayer construction does not rely on a combination of PE, EVOH,\n  nylon and adhesive layers commonly used in some multilayer process films.\n  The bag film also does not require plasticisers or colouring additives as\n  part of its stated construction.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Tubing, connectors and other assembly components are configuration-dependent.\n  Required component materials should therefore be specified and verified\n  during assembly selection.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e This product is a single-use process bag\n  assembly rather than a filtration medium and therefore does not have a micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where filtration is required within the same fluid path, a suitable filter\n  can be specified separately as part of the complete single-use assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  The process bag uses a monolayer fluoropolymer construction and is available\n  in multiple nominal volumes for laboratory, process development and production\n  applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard listed volumes range from \u003cstrong\u003e50 mL to 20 L\u003c\/strong\u003e.\n  Additional 20 mL and 50 L configurations are available on request.\n  Further sizes and assembly designs may also be specified according to the\n  application.\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Nominal volume\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Approx. length\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Approx. width\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e50 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e120 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e100 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e100 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e160 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e100 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e250 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e240 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e100 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e500 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e210 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e158 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e285 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e178 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e354 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e254 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e470 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e323 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e10 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e570 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e383 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e20 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e718 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e483 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003cp\u003e\n  Smaller bag assemblies from 50 mL to 250 mL and larger assemblies from\n  500 mL to 20 L can be configured with the required fluid-path components.\n  Bags without tubing are also available in non-sterile configurations.\n\u003c\/p\u003e\n\n\u003ch3\u003eCompliance and technical properties\u003c\/h3\u003e\n\n\u003cp\u003e\n  The available technical documentation for the fluoropolymer bag includes\n  the following stated tests and conformity references:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt;\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt;\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt;\u003c\/li\u003e\n  \u003cli\u003eEP 2.6.14 with stated endotoxin level below 0.125 EU\/mL\u003c\/li\u003e\n  \u003cli\u003eISO 10993-4, non-haemolytic\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;661\u0026gt; extractables testing\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; particle testing\u003c\/li\u003e\n  \u003cli\u003eEP 2.9.19 particle testing\u003c\/li\u003e\n  \u003cli\u003eCleanroom Class 5 production\u003c\/li\u003e\n  \u003cli\u003eGamma-sterilisable construction\u003c\/li\u003e\n  \u003cli\u003eSpecified working temperature: -85 °C to +40 °C\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact documentation requirements should be confirmed for the final assembly\n  configuration, including all tubing, connectors and other fluid-contact\n  components.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Single-use fluoropolymer freeze bag assemblies are primarily intended for\n  pharmaceutical and biotechnology processes involving low-temperature storage,\n  fluid handling and product transfer.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eFreezing of pharmaceutical intermediates\u003c\/li\u003e\n  \u003cli\u003eFrozen drug substance storage\u003c\/li\u003e\n  \u003cli\u003eDownstream bioprocessing\u003c\/li\u003e\n  \u003cli\u003eFreezing and storage of cell culture material\u003c\/li\u003e\n  \u003cli\u003eStem-cell freezing and storage\u003c\/li\u003e\n  \u003cli\u003eStorage and transport of active pharmaceutical ingredients\u003c\/li\u003e\n  \u003cli\u003eStorage and transport of chemically aggressive media\u003c\/li\u003e\n  \u003cli\u003eStorage and transportation of binding media\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical filling processes\u003c\/li\u003e\n  \u003cli\u003eCritical process sampling\u003c\/li\u003e\n  \u003cli\u003eLow-temperature product transfer\u003c\/li\u003e\n  \u003cli\u003eIntermediate storage before Fill \u0026amp; Finish\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eLow-temperature operation:\u003c\/strong\u003e\n    specified for use down to approximately -85 °C.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMonolayer fluoropolymer film:\u003c\/strong\u003e\n    constructed from a single polymer material rather than a multilayer\n    film system.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eNo film delamination:\u003c\/strong\u003e\n    the single-layer construction eliminates delamination between\n    individual bag-film layers.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eChemical resistance:\u003c\/strong\u003e\n    fluoropolymer construction supports applications involving demanding\n    pharmaceutical and process media.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eGamma sterilisation:\u003c\/strong\u003e\n    suitable configurations can be supplied for gamma-sterilised\n    single-use applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eClean manufacturing environment:\u003c\/strong\u003e\n    bag production is specified as taking place under ISO Class 5\n    cleanroom conditions.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eExtractables documentation:\u003c\/strong\u003e\n    test data following BPOG guidelines is available for technical review.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple process volumes:\u003c\/strong\u003e\n    standard sizes cover small laboratory volumes through larger\n    process-scale assemblies.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Freeze bag assemblies should be specified around the complete process rather\n  than bag volume alone. The required fluid path, storage conditions and\n  connection interfaces determine the final assembly configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired nominal bag volume\u003c\/li\u003e\n  \u003cli\u003eProcess fluid or product\u003c\/li\u003e\n  \u003cli\u003eMinimum and maximum operating temperature\u003c\/li\u003e\n  \u003cli\u003eFreezing and thawing procedure\u003c\/li\u003e\n  \u003cli\u003eRequired tubing type and dimensions\u003c\/li\u003e\n  \u003cli\u003eRequired inlet and outlet connections\u003c\/li\u003e\n  \u003cli\u003eNumber of fluid-path ports\u003c\/li\u003e\n  \u003cli\u003eFilling and discharge method\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation requirement\u003c\/li\u003e\n  \u003cli\u003eStorage and transport conditions\u003c\/li\u003e\n  \u003cli\u003eRequired technical or conformity documentation\u003c\/li\u003e\n  \u003cli\u003eAnnual demand and prototype quantity\u003c\/li\u003e\n  \u003cli\u003eExisting assembly drawing or process sketch, if available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Custom configurations and additional bag sizes can be evaluated where a\n  standard assembly does not match the required process.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a single-use fluoropolymer freeze bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A single-use fluoropolymer freeze bag is a disposable process container designed for freezing, storing, transporting and handling pharmaceutical or bioprocess liquids. The bag uses a monolayer fluoropolymer film and can form part of a configured single-use fluid path.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What temperature range can a fluoropolymer freeze bag operate at?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The specified working temperature range for this fluoropolymer bag is approximately -85 °C to +40 °C, making it suitable for low-temperature pharmaceutical storage and transport applications.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What material is the single-use freeze bag made from?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The bag film is manufactured from a single-layer fluoropolymer material rather than a multilayer film consisting of several polymers and adhesive layers.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sizes are available for single-use freeze bags?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Listed standard volumes include 50 mL, 100 mL, 250 mL, 500 mL, 1 L, 2 L, 5 L, 10 L and 20 L. Additional 20 mL and 50 L sizes are available on request.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can fluoropolymer freeze bag assemblies be gamma sterilised?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. The fluoropolymer bag construction is suitable for gamma sterilisation and can be configured as a pre-sterilised single-use assembly.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What are single-use fluoropolymer freeze bags used for?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Typical applications include frozen drug substance and intermediate storage, downstream processing, cell culture and stem-cell freezing, active ingredient storage and transport, filling, critical sampling and handling of chemically demanding process media.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"50 mL \/ Bag Assembly \/ Gamma Sterilised","offer_id":57300241580358,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 mL \/ Bag Assembly \/ Non-Sterile","offer_id":57300241613126,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"50 mL \/ Bag 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Connector","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  High-flow genderless sterile connectors are designed for aseptic fluid transfer\n  in pharmaceutical and bioprocess single-use systems. The large-bore connection\n  geometry supports high-volume liquid transfer where conventional small-bore\n  sterile connectors may restrict flow or increase transfer time.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The genderless connection design allows two compatible connector halves to be\n  joined without separate male and female configurations. Hose barb and sanitary\n  Tri-Clamp process connections are available for integration into tubing\n  assemblies, transfer lines and other single-use fluid paths.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  These sterile connectors are intended for high-volume biopharmaceutical\n  processes where a secure aseptic connection must be established between two\n  independent fluid paths. They can be incorporated into preconfigured\n  single-use assemblies for product transfer, fluid handling and other sterile\n  processing operations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The connector housing is manufactured from polycarbonate and incorporates\n  a silicone internal seal. The design is suitable for gamma irradiation as well\n  as autoclave sterilisation, allowing the connection technology to be integrated\n  into different single-use process strategies.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available technical documentation may include validation information,\n  extractables data and material conformity documentation for use in\n  biopharmaceutical applications.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The connector consists of two compatible genderless halves that are aligned\n  and mechanically joined. During connection, the sterile protective barriers\n  separating the internal fluid paths remain in place until the two connector\n  halves have been correctly mated.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Once the connector halves are secured, the protective membrane barriers are\n  removed together. This opens the internal fluid path while limiting exposure\n  of the sterile connection surfaces to the surrounding environment. The final\n  locking mechanism is then secured to complete the connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  No separate welding device or additional connection equipment is required\n  for normal operation of the connector.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The standard sterile connector construction uses the following materials:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n\u003cstrong\u003eHousing:\u003c\/strong\u003e Polycarbonate\u003c\/li\u003e\n  \u003cli\u003e\n\u003cstrong\u003eInternal seal:\u003c\/strong\u003e Silicone\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing, process bags, filters and other components connected to the sterile\n  connector may use different materials. Compatibility of the complete fluid\n  path should therefore be verified for the intended process fluid,\n  sterilisation method and operating conditions.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e This product is a sterile fluid connection\n  device rather than a filtration medium and therefore does not have a micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where sterile filtration is required, a suitable membrane or capsule filter\n  can be integrated separately into the same single-use assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  The connector uses a robust genderless design intended for large-volume\n  pharmaceutical and bioprocess fluid transfer. Both connector halves use the\n  same mating interface, simplifying fluid-path configuration and reducing the\n  need to manage separate male and female connector types.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available process-side connection configurations include:\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Process connection\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Housing material\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\" Hose Barb\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003ePolycarbonate\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1 1\/4\" Hose Barb\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003ePolycarbonate\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1 1\/2\" Hose Barb\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003ePolycarbonate\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e1 1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003ePolycarbonate\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003cp\u003e\n  The large-flow-path configuration is intended for processes involving\n  substantial transfer volumes where reducing restriction within the disposable\n  fluid path is important.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and conformity\u003c\/h3\u003e\n\n\u003cp\u003e\n  The connector is suitable for multiple pharmaceutical sterilisation strategies.\n  The stated sterilisation limits include gamma irradiation up to\n  \u003cstrong\u003e50 kGy\u003c\/strong\u003e and autoclaving at temperatures up to\n  \u003cstrong\u003e130 °C for 60 minutes\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity and technical documentation includes:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003eFDA-related material conformity\u003c\/li\u003e\n  \u003cli\u003eNo animal-derived ingredients (ADCF)\u003c\/li\u003e\n  \u003cli\u003eValidation documentation available\u003c\/li\u003e\n  \u003cli\u003eExtractables data available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Conformity of the complete single-use system should be confirmed based on\n  all components incorporated into the final assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  High-flow sterile connectors are primarily used where two preconfigured\n  bioprocess fluid paths must be connected aseptically while maintaining a\n  comparatively large internal flow path.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSterile fluid transfer\u003c\/li\u003e\n  \u003cli\u003eHigh-volume pharmaceutical liquid transfer\u003c\/li\u003e\n  \u003cli\u003eSingle-use bioprocess assemblies\u003c\/li\u003e\n  \u003cli\u003eUpstream processing\u003c\/li\u003e\n  \u003cli\u003eDownstream processing\u003c\/li\u003e\n  \u003cli\u003eBuffer and media transfer\u003c\/li\u003e\n  \u003cli\u003eBulk drug substance transfer\u003c\/li\u003e\n  \u003cli\u003eProcess vessel connections\u003c\/li\u003e\n  \u003cli\u003eBag-to-bag transfer\u003c\/li\u003e\n  \u003cli\u003eBag-to-vessel transfer\u003c\/li\u003e\n  \u003cli\u003eSingle-use manifolds\u003c\/li\u003e\n  \u003cli\u003eClosed fluid handling systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eHigh-flow design:\u003c\/strong\u003e\n    large connection geometry supports high-volume liquid transfer applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eGenderless connection:\u003c\/strong\u003e\n    both connector halves use a compatible mating interface, simplifying\n    single-use system configuration.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eAseptic connection:\u003c\/strong\u003e\n    protective sterile barriers are removed only after the connector halves\n    have been mechanically joined.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eNo separate connection equipment:\u003c\/strong\u003e\n    normal connection does not require a tube welder or additional connection device.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple process interfaces:\u003c\/strong\u003e\n    hose barb and sanitary Tri-Clamp configurations are available.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eGamma compatible:\u003c\/strong\u003e\n    suitable for gamma irradiation up to the stated maximum dose of 50 kGy.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eAutoclavable:\u003c\/strong\u003e\n    suitable for autoclave processing up to the stated maximum of 130 °C for 60 minutes.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSingle-use assembly integration:\u003c\/strong\u003e\n    suitable for incorporation into custom tubing, bag, bottle and transfer assemblies.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Sterile connectors should be selected as part of the complete fluid-path\n  specification. Connection size, tubing dimensions, process interface,\n  sterilisation method and operating requirements determine the appropriate\n  configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired process connection\u003c\/li\u003e\n  \u003cli\u003eTubing inner and outer diameter\u003c\/li\u003e\n  \u003cli\u003eRequired transfer flow rate\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eOperating pressure\u003c\/li\u003e\n  \u003cli\u003eGamma irradiation or autoclave requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and validation documentation\u003c\/li\u003e\n  \u003cli\u003eWhether the connector will be integrated into a complete single-use assembly\u003c\/li\u003e\n  \u003cli\u003eRequired quantity or annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting fluid-path drawing or assembly specification, if available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The connector can also be specified as part of a custom single-use bag,\n  bottle, tubing, sampling, filtration or product-transfer assembly.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a high-flow sterile connector?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A high-flow sterile connector is an aseptic connection device designed to join two sterile fluid paths while providing a relatively large internal flow path for high-volume pharmaceutical and bioprocess liquid transfer.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a genderless sterile connector?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A genderless sterile connector uses compatible mating interfaces on both connector halves rather than separate male and female connector types. This can simplify the configuration of single-use fluid paths.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What materials are used in the sterile connector?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The connector housing is manufactured from polycarbonate and the internal seal is silicone.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What connection sizes are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available process-side configurations include 1 inch, 1 1\/4 inch and 1 1\/2 inch hose barb connections, together with a 1 1\/2 inch Tri-Clamp connection.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can high-flow sterile connectors be gamma sterilised or autoclaved?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. The stated sterilisation limits include gamma irradiation up to 50 kGy and autoclaving up to 130 °C for 60 minutes.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Where are high-flow sterile connectors used?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Typical applications include sterile fluid transfer, high-volume product transfer, buffer and media handling, upstream and downstream processing, single-use manifolds and connections between bags, vessels and process equipment.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"1\" Hose Barb \/ Gamma Irradiated \/ Connector Only","offer_id":57300649869638,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"1\" Hose Barb \/ Gamma Irradiated \/ Integrated in Tubing Assembly","offer_id":57300649902406,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"1\" Hose Barb \/ Gamma 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with\n  permanently crimped stainless-steel end connections for hygienic fluid and\n  steam handling applications. Each assembly can be configured to match existing\n  process equipment, vessel connections and piping interfaces.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Different reinforced silicone and fluoropolymer hose constructions are\n  available for applications involving elevated pressure, temperature,\n  chemical exposure or demanding pharmaceutical processing conditions.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  A pharmaceutical hose assembly combines a flexible process hose with\n  hygienically crimped stainless-steel fittings. The assembly provides a flexible\n  connection between fixed vessels, process systems and pipework while avoiding\n  the need to modify the surrounding installation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Flexible hose assemblies can also accommodate limited movement and vibration\n  between connected equipment, which cannot be compensated for in the same way\n  by rigid process piping.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Typical configurations use sanitary Tri-Clamp connections, although weld ends\n  and hygienic coupling systems can also be specified. Standard stainless-steel\n  connection materials include \u003cstrong\u003e1.4404 \/ 1.4435\u003c\/strong\u003e, with other\n  materials available according to the process requirement.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Each supplied hose assembly can be pressure tested and provided with\n  batch-related conformity documentation. Applicable material declarations\n  depend on the selected hose construction.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The flexible hose forms the process fluid path between two pieces of\n  equipment. Stainless-steel fittings are permanently attached to the hose by\n  a controlled crimping process, creating a defined transition between the\n  flexible hose material and the hygienic process connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  During operation, the hose transports process liquid, purified water, steam\n  or another compatible medium while allowing flexibility between fixed\n  connection points. This makes assembled hoses particularly useful where\n  pipework, vessels or equipment cannot be connected conveniently using a\n  completely rigid piping system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Reinforced hose constructions can be selected for increased mechanical\n  stability under pressure, vacuum or elevated temperature conditions.\n  Fluoropolymer-lined configurations provide an alternative where additional\n  chemical resistance or a different product-contact surface is required.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Several hose constructions can be configured according to the operating\n  conditions and process medium:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eBraided silicone hose\u003c\/li\u003e\n  \u003cli\u003eBraided and wire-reinforced silicone hose\u003c\/li\u003e\n  \u003cli\u003eBraided and wire-reinforced silicone hose with PFA inner layer\u003c\/li\u003e\n  \u003cli\u003eAntistatic braided and wire-reinforced hose with PFA inner layer\u003c\/li\u003e\n  \u003cli\u003eAntistatic PFA hose for suitable ATEX-area applications\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Standard hygienic end connections are typically manufactured from\n  \u003cstrong\u003estainless steel 1.4404 \/ 1.4435\u003c\/strong\u003e. Alternative fitting\n  materials can be evaluated where required.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Material compatibility, pressure capability, temperature resistance and\n  applicable conformity documentation vary according to the selected hose\n  construction and should be confirmed for the final configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e Pharmaceutical hose assemblies are fluid\n  transfer components rather than filtration media and therefore do not have\n  a micron or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If particulate or sterile filtration is required within the process line,\n  an appropriate filter can be specified separately as part of the complete\n  fluid-handling system.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hose assemblies are manufactured to customer-specific dimensions so that\n  they can connect directly to existing equipment, vessels and process\n  pipework. Important configuration parameters include hose material,\n  reinforcement, internal diameter, overall length and end-connection type.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Sanitary Tri-Clamp connections are commonly used for pharmaceutical process\n  applications. Alternative configurations can include weld ends or hygienic\n  coupling systems where the existing installation requires a different\n  interface.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The standard stated internal surface quality of the stainless-steel\n  connection components is \u003cstrong\u003eRa \u0026lt; 0.8 µm\u003c\/strong\u003e. Electropolished\n  versions with surface roughness down to approximately\n  \u003cstrong\u003eRa 0.2 µm\u003c\/strong\u003e are available on request.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The transition between the flexible hose and stainless-steel fitting is\n  designed to provide a smooth hygienic junction. Assemblies are pressure\n  tested and can be supplied with batch-related certificates of conformance.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and conformity\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable hose configurations can be selected for\n  \u003cstrong\u003eSteam-in-Place (SIP)\u003c\/strong\u003e and autoclave applications. Clean-in-Place\n  applications are also possible where the selected materials and process\n  conditions are compatible.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the hose material and configuration, available conformity\n  references can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003eEuropean Pharmacopoeia 3.1.9\u003c\/li\u003e\n  \u003cli\u003eFDA CFR 177.1550\u003c\/li\u003e\n  \u003cli\u003e3-A requirements\u003c\/li\u003e\n  \u003cli\u003eAnimal-component-free material options\u003c\/li\u003e\n  \u003cli\u003ecGMP-related documentation\u003c\/li\u003e\n  \u003cli\u003eBatch traceability\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  These properties are configuration-dependent and should be verified for the\n  specific hose material, fitting material and intended process conditions.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Pharmaceutical process hose assemblies are used where hygienic equipment\n  requires a flexible connection capable of handling process fluids, cleaning\n  media or steam.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003ePharmaceutical process fluid transfer\u003c\/li\u003e\n  \u003cli\u003eBiotechnology process systems\u003c\/li\u003e\n  \u003cli\u003eVessel-to-vessel connections\u003c\/li\u003e\n  \u003cli\u003eProcess vessel connections\u003c\/li\u003e\n  \u003cli\u003eWFI distribution and transfer\u003c\/li\u003e\n  \u003cli\u003ePurified water systems\u003c\/li\u003e\n  \u003cli\u003eProcess tubing connections\u003c\/li\u003e\n  \u003cli\u003eSteam-in-Place applications\u003c\/li\u003e\n  \u003cli\u003eClean-in-Place applications\u003c\/li\u003e\n  \u003cli\u003eHigh-temperature fluid transfer\u003c\/li\u003e\n  \u003cli\u003eHigh-pressure process connections\u003c\/li\u003e\n  \u003cli\u003eChemically demanding process media\u003c\/li\u003e\n  \u003cli\u003eApplications requiring vibration or movement compensation\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eCustom configuration:\u003c\/strong\u003e\n    hose length, material and process connections can be selected to match\n    existing equipment.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible equipment connection:\u003c\/strong\u003e\n    provides a flexible alternative between fixed vessels, piping and process\n    systems.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eHigh-temperature capability:\u003c\/strong\u003e\n    suitable hose constructions can be selected for steam and elevated\n    temperature applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePressure-resistant constructions:\u003c\/strong\u003e\n    braided and wire-reinforced designs are available for mechanically\n    demanding applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eChemical compatibility options:\u003c\/strong\u003e\n    fluoropolymer-lined and PFA configurations are available for suitable\n    chemically demanding media.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eHygienic process connections:\u003c\/strong\u003e\n    Tri-Clamp, weld-end and hygienic coupling configurations can be specified.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eControlled surface finish:\u003c\/strong\u003e\n    standard stainless-steel fitting surfaces are specified at Ra \u0026lt; 0.8 µm,\n    with electropolished versions available down to approximately Ra 0.2 µm.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eTraceability:\u003c\/strong\u003e\n    assemblies can be pressure tested and supplied with batch-related\n    conformity documentation.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Pharmaceutical hose assemblies are configured around the process connection,\n  medium and operating conditions rather than supplied as one fixed design.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eProcess medium\u003c\/li\u003e\n  \u003cli\u003eRequired hose material or construction\u003c\/li\u003e\n  \u003cli\u003eHose inner diameter and outer diameter\u003c\/li\u003e\n  \u003cli\u003eRequired hose length\u003c\/li\u003e\n  \u003cli\u003eMaximum operating pressure\u003c\/li\u003e\n  \u003cli\u003eMaximum and minimum operating temperature\u003c\/li\u003e\n  \u003cli\u003eVacuum requirements, if applicable\u003c\/li\u003e\n  \u003cli\u003eRequired process connections\u003c\/li\u003e\n  \u003cli\u003eTri-Clamp size or alternative connection dimensions\u003c\/li\u003e\n  \u003cli\u003eRequired stainless-steel material\u003c\/li\u003e\n  \u003cli\u003eRequired surface finish\u003c\/li\u003e\n  \u003cli\u003eSIP, CIP or autoclave requirements\u003c\/li\u003e\n  \u003cli\u003eATEX requirements, where applicable\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and traceability documentation\u003c\/li\u003e\n  \u003cli\u003eRequired quantity or annual demand\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Existing hose drawings, equipment connection details or current hose\n  specifications can also be used as the basis for defining a replacement\n  or new process hose assembly.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a pharmaceutical process hose assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A pharmaceutical process hose assembly is a flexible hygienic hose fitted with permanently crimped stainless-steel process connections. It is used to connect vessels, process equipment and piping for pharmaceutical and biotechnology fluid handling.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What hose materials are available for pharmaceutical hose assemblies?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available constructions include braided silicone, braided and wire-reinforced silicone, reinforced silicone with a PFA inner layer and antistatic PFA-based configurations. The appropriate construction depends on pressure, temperature, chemical compatibility and process requirements.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Which process connections are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Sanitary Tri-Clamp connections are commonly used. Weld ends and hygienic coupling systems can also be specified according to the existing process installation.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can pharmaceutical hose assemblies be used for Steam-in-Place?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Suitable hose configurations can be selected for Steam-in-Place and autoclave applications. Material and temperature compatibility must be confirmed for the selected hose construction.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What surface finish is available on the stainless-steel fittings?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The stated standard surface finish is Ra below 0.8 micrometres. Electropolished versions with surface roughness down to approximately Ra 0.2 micrometres are available on request.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What information is required to specify a custom pharmaceutical hose assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Important parameters include process medium, hose material, inner and outer diameter, hose length, operating pressure and temperature, process connection type, connection size, surface finish and cleaning or sterilisation requirements.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"Braided Silicone \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404342598,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided Silicone \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404375366,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided Silicone \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404408134,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided Silicone \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404440902,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404473670,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404506438,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404539206,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404571974,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404604742,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404637510,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404670278,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404703046,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404735814,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404768582,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404801350,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic Braided \u0026 Wire-Reinforced Silicone with PFA Inner Layer \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404834118,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic PFA \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404866886,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic PFA \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404899654,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic PFA \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404932422,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Antistatic PFA \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404965190,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ Other \/ Tri-Clamp \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305404997958,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ Other \/ Weld End \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305405030726,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ Other \/ Hygienic Coupling \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305405063494,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ Other \/ Custom \/ Other \/ Custom – Please Specify Hose ID\/OD \u0026 Length","offer_id":57305405096262,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/pharmaceutical-process-hose-assembly.webp?v=1788945529"},{"product_id":"plastic-tri-clamp-adapter-integrated-gasket","title":"Plastic Tri-Clamp Adapter with Integrated Gasket","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Plastic Tri-Clamp adapters with an integrated gasket are designed for hygienic\n  fluid connections in pharmaceutical, biotechnology and single-use processing\n  systems. Unlike a conventional sanitary connection in which the flange and\n  gasket are handled as separate components, the gasket is permanently attached\n  to the plastic adapter.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The integrated-gasket design simplifies connection assembly, reduces the number\n  of loose components that must be positioned during installation and can help\n  reduce errors associated with gasket alignment or handling.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  A conventional Tri-Clamp connection normally requires two sanitary flanges,\n  a separate gasket and a clamp. With this type of plastic adapter, the gasket\n  is already fixed to the flange surface. This eliminates the need to manually\n  position a loose gasket between the mating sanitary connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The design is particularly suitable for preconfigured and ready-to-use\n  pharmaceutical fluid paths where consistent assembly and reduced handling\n  of individual connection components are desirable.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The fittings are produced and packaged in an ISO Class 7 cleanroom and are\n  available in both mini sanitary and 1-1\/2 inch Tri-Clamp configurations with\n  multiple hose-barb sizes.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The fitting connects flexible tubing to a hygienic Tri-Clamp process interface.\n  One side of the adapter incorporates a hose-barb connection for attachment to\n  the tubing, while the opposite side provides the sanitary flange.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The gasket is fixed directly to the flange. When the adapter is positioned\n  against the mating Tri-Clamp connection, the gasket is already aligned with\n  the sealing surface. A sanitary clamp is then installed around the two\n  mating flanges to compress the gasket and form the connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Because the gasket remains attached to the adapter, there is no separate\n  gasket that must be manually positioned, held in place or retrieved if it\n  is dropped during installation.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The product is manufactured as a \u003cstrong\u003eplastic sanitary fitting with an\n  integrated gasket\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The available source information does not specify the exact polymer grade\n  of the fitting body or the gasket material. These materials should therefore\n  be confirmed for the required configuration before specifying chemical,\n  temperature or process compatibility.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The stated material conformity includes USP Class VI and FDA CFR Title 21\n  Section 177.1520 requirements. The product is also specified as free from\n  animal-derived ingredients.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e This product is a hygienic fluid connection\n  component and does not contain filtration media. It therefore has no micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where filtration is required, an appropriate filter can be incorporated\n  elsewhere in the same single-use or pharmaceutical process assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  The adapter combines three functional elements in one connection component:\n  a plastic sanitary flange, an integrated sealing gasket and a hose-barb\n  connection for flexible tubing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Two sanitary flange formats are available: a compact mini sanitary\n  configuration and a standard 1-1\/2 inch sanitary configuration.\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Sanitary connection\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Hose barb size\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/8\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/16\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/4\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/8\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/2\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eMini Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/4\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1-1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/4\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1-1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/8\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1-1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/2\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1-1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/4\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e1-1\/2\" Tri-Clamp\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e1\"\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003eSterilisation and conformity\u003c\/h3\u003e\n\n\u003cp\u003e\n  The plastic sanitary adapters are suitable for integration into sterilised\n  pharmaceutical and single-use assemblies. The stated sterilisation methods\n  include gamma irradiation, ethylene oxide (ETO) and autoclaving.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity and production information includes:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003eFDA CFR Title 21 Section 177.1520\u003c\/li\u003e\n  \u003cli\u003eISO 10993\u003c\/li\u003e\n  \u003cli\u003eAnimal Derived Ingredients Free (ADIF \/ ADCF)\u003c\/li\u003e\n  \u003cli\u003eREACH conformity\u003c\/li\u003e\n  \u003cli\u003eCalifornia Proposition 65 conformity\u003c\/li\u003e\n  \u003cli\u003eNon-pyrogenic specification\u003c\/li\u003e\n  \u003cli\u003eProduced and packaged in an ISO Class 7 cleanroom\u003c\/li\u003e\n  \u003cli\u003eETO compatible\u003c\/li\u003e\n  \u003cli\u003eAutoclavable\u003c\/li\u003e\n  \u003cli\u003eGamma-sterilisable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The complete process assembly should still be evaluated as a system, because\n  tubing, clamps and other components may have different material and\n  sterilisation limitations.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Plastic Tri-Clamp adapters with integrated gaskets are intended for hygienic\n  and aseptic fluid connections where flexible tubing must interface with a\n  sanitary process connection.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSingle-use assemblies\u003c\/li\u003e\n  \u003cli\u003eWFI sampling\u003c\/li\u003e\n  \u003cli\u003eAseptic liquid transfer\u003c\/li\u003e\n  \u003cli\u003eCell cultivation\u003c\/li\u003e\n  \u003cli\u003eCell harvest\u003c\/li\u003e\n  \u003cli\u003eFermentation\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical filling\u003c\/li\u003e\n  \u003cli\u003eBag and tubing assemblies\u003c\/li\u003e\n  \u003cli\u003eProcess vessel connections\u003c\/li\u003e\n  \u003cli\u003ePreconfigured ready-to-use fluid paths\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eIntegrated gasket:\u003c\/strong\u003e\n    the sealing gasket remains attached to the sanitary flange instead of\n    being handled as a separate component.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSimplified assembly:\u003c\/strong\u003e\n    reduces the number of individual components that must be positioned when\n    making a Tri-Clamp connection.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eConsistent gasket positioning:\u003c\/strong\u003e\n    the attached gasket helps maintain alignment with the flange sealing surface.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eReduced handling:\u003c\/strong\u003e\n    operators do not need to separately position or hold the gasket while\n    installing the sanitary clamp.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSuitable for single-use assemblies:\u003c\/strong\u003e\n    can be incorporated into prefabricated fluid paths and gamma-sterilised\n    ready-to-use assemblies.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple tubing sizes:\u003c\/strong\u003e\n    mini and 1-1\/2 inch sanitary interfaces are available with several\n    hose-barb dimensions.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple sterilisation methods:\u003c\/strong\u003e\n    stated compatibility includes gamma irradiation, ETO and autoclaving.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCleanroom production:\u003c\/strong\u003e\n    manufactured and packaged under ISO Class 7 cleanroom conditions.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  The correct adapter should be selected according to both the sanitary\n  process interface and the tubing dimensions used in the fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired Tri-Clamp \/ sanitary connection size\u003c\/li\u003e\n  \u003cli\u003eRequired hose-barb size\u003c\/li\u003e\n  \u003cli\u003eTubing inner diameter and outer diameter\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eOperating pressure\u003c\/li\u003e\n  \u003cli\u003eRequired sterilisation method\u003c\/li\u003e\n  \u003cli\u003eRequired conformity documentation\u003c\/li\u003e\n  \u003cli\u003eWhether the fitting will be supplied individually or integrated into an assembly\u003c\/li\u003e\n  \u003cli\u003eRequired quantity or annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting assembly drawing or fluid-path specification, if available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The adapter can also be incorporated into custom bag, bottle, tubing,\n  sampling or other single-use assemblies.\n\u003c\/p\u003e\n\n  \u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a plastic Tri-Clamp adapter with an integrated gasket?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"It is a hygienic plastic fluid connection that combines a sanitary Tri-Clamp flange, an attached sealing gasket and a hose-barb connection in one component. The integrated gasket eliminates the need to manually position a separate gasket during connection.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Why use an integrated gasket on a Tri-Clamp fitting?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"An integrated gasket reduces the number of separate components that must be handled and helps maintain gasket alignment while the sanitary connection is assembled.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sizes are available for plastic Tri-Clamp hose barb adapters?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Mini Tri-Clamp adapters are available with 1\/8, 3\/16, 1\/4, 3\/8, 1\/2 and 3\/4 inch hose barbs. 1-1\/2 inch Tri-Clamp adapters are available with 1\/4, 3\/8, 1\/2, 3\/4 and 1 inch hose barbs.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can plastic Tri-Clamp adapters be sterilised?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. The stated sterilisation compatibility includes gamma irradiation, ethylene oxide and autoclaving.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Where are plastic Tri-Clamp adapters with integrated gaskets used?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Typical applications include single-use assemblies, WFI sampling, cell cultivation, cell harvest, fermentation, pharmaceutical filling and aseptic liquid transfer.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Do Tri-Clamp adapters have a micron rating?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"No. A Tri-Clamp adapter is a fluid connection component rather than filtration media and therefore does not have a micron or pore-size rating.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"Mini Tri-Clamp × 1\/8\" Hose Barb \/ Gamma Sterilised \/ 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Assembly","offer_id":57310388683078,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/mini-tri-clamp-hose-barb-adapters.webp?v=1788946782"},{"product_id":"single-use-bioprocess-bag-assemblies","title":"Custom Single-Use Bioprocess Bag Assemblies","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Custom single-use bioprocess bag assemblies are configurable disposable\n  fluid-handling systems for the storage, transfer and handling of pharmaceutical\n  and biotechnology process liquids.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies are available in compact 2D formats for smaller and intermediate\n  volumes and in 3D formats for large-volume storage and transfer. Standard\n  configurations can be selected for common applications, while tubing,\n  connectors, ports, sampling lines, filters and other fluid-path components\n  can be configured around the process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard 2D configurations are available from approximately 250 mL to 50 L,\n  while 3D systems cover large process volumes up to approximately 3,000 L.\n  Custom bag assemblies can be engineered for volumes up to approximately\n  4,000 L.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  A single-use bag assembly combines a flexible process container with the\n  tubing and connections required to introduce, remove, sample or transfer\n  process liquid.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Simple configurations may consist of a bag with two ports, while complete\n  assemblies can incorporate inlet and outlet tubing, sampling lines, sterile\n  connectors, quick couplings, sanitary interfaces, clamps and filtration\n  components.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This allows standard storage and transfer bags to be used where appropriate\n  while retaining the option to engineer the complete fluid path for more\n  application-specific processes.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The flexible bag acts as the disposable process container. Fluid enters and\n  leaves the system through heat-sealed or integrated bag ports connected to\n  tubing and the required process interfaces.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  In storage and transfer applications, the bag can receive buffer, media,\n  intermediates, stock solutions or filtered process liquids before subsequent\n  transfer to another process step.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies with a dedicated sampling line allow process samples to be taken\n  through a separate connection without using the main inlet or outlet line.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where filtration is incorporated, liquid passes through an integrated capsule\n  filter before entering or leaving the bag, creating a defined filtration and\n  storage fluid path within one preconfigured assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Several process-film constructions are available depending on the application,\n  required barrier properties, chemical compatibility and handling requirements.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available film concepts can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eMultilayer polyolefin process film\u003c\/strong\u003e with a polyethylene\n    product-contact layer and EVOH gas-barrier layer.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eReinforced multilayer film\u003c\/strong\u003e incorporating additional\n    mechanical protection for handling and transport.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eULDPE \/ EVA \/ EVOH \/ LDPE multilayer film\u003c\/strong\u003e for general\n    bioprocess storage and transfer applications.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePVDF-contact film\u003c\/strong\u003e for applications requiring different\n    chemical or temperature characteristics.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eFluoropolymer-contact film\u003c\/strong\u003e for specialised fluid-contact\n    requirements.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing can be configured independently of the bag film. Common options include\n  platinum-cured silicone and weldable TPE tubing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Final film and tubing selection should be based on the process fluid,\n  temperature, sterilisation requirements and required validation documentation.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable to the bag itself.\u003c\/strong\u003e A standard single-use\n  process bag does not contain filtration media and therefore has no micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filter-integrated bag assemblies can incorporate a separate capsule filter.\n  Standard sterile-filtration configurations are available with\n  \u003cstrong\u003e0.2 µm PES membrane filters\u003c\/strong\u003e. Other membrane materials,\n  filtration areas and micron ratings can be selected according to the\n  filtration requirement.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Bag assemblies can be based on standard 2D and 3D configurations or engineered\n  around a custom fluid-path design.\n\u003c\/p\u003e\n\n\n\u003ch3\u003e2D storage and transfer bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  Flat 2D bags are suitable for small and intermediate liquid volumes and are\n  commonly used for media, buffer, intermediates and process-liquid storage\n  and transfer.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Common standard volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e250 mL\u003c\/li\u003e\n  \u003cli\u003e500 mL\u003c\/li\u003e\n  \u003cli\u003e1 L\u003c\/li\u003e\n  \u003cli\u003e2 L\u003c\/li\u003e\n  \u003cli\u003e5 L\u003c\/li\u003e\n  \u003cli\u003e10 L\u003c\/li\u003e\n  \u003cli\u003e20 L\u003c\/li\u003e\n  \u003cli\u003e35 L\u003c\/li\u003e\n  \u003cli\u003e50 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Port-only configurations are also available where the user intends to define\n  the final tubing and fluid-path assembly separately.\n\u003c\/p\u003e\n\n\n\u003ch3\u003e3D large-volume bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  3D bag assemblies are designed for larger process volumes and are typically\n  used together with a suitable support container or handling system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available standard and configuration-to-order volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e50 L\u003c\/li\u003e\n  \u003cli\u003e100 L\u003c\/li\u003e\n  \u003cli\u003e200 L\u003c\/li\u003e\n  \u003cli\u003e250 L\u003c\/li\u003e\n  \u003cli\u003e500 L\u003c\/li\u003e\n  \u003cli\u003e650 L\u003c\/li\u003e\n  \u003cli\u003e1,000 L\u003c\/li\u003e\n  \u003cli\u003e1,500 L\u003c\/li\u003e\n  \u003cli\u003e2,000 L\u003c\/li\u003e\n  \u003cli\u003e2,500 L\u003c\/li\u003e\n  \u003cli\u003e3,000 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Custom engineered bag assemblies can be considered for volumes up to\n  approximately 4,000 L.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eBag ports\u003c\/h3\u003e\n\n\u003cp\u003e\n  Different bag-port arrangements can be selected according to the required\n  number of fluid connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard hose-barb port sizes can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/4\" hose barb\u003c\/li\u003e\n  \u003cli\u003e3\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/2\" hose barb\u003c\/li\u003e\n  \u003cli\u003eUp to approximately 1\" hose barb on suitable large-volume configurations\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Two-port and three-port layouts are available for common configurations,\n  while custom assemblies can incorporate additional ports where required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTubing and process connections\u003c\/h3\u003e\n\n\u003cp\u003e\n  Bag assemblies can be supplied with platinum-cured silicone or weldable\n  TPE tubing in dimensions selected according to the required flow rate and\n  connection technology.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available process interfaces can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSterile and aseptic connectors\u003c\/li\u003e\n  \u003cli\u003eQuick disconnect couplings\u003c\/li\u003e\n  \u003cli\u003eSanitary Tri-Clamp connections\u003c\/li\u003e\n  \u003cli\u003eHose barb fittings\u003c\/li\u003e\n  \u003cli\u003eTubing plugs\u003c\/li\u003e\n  \u003cli\u003eWeldable tubing ends\u003c\/li\u003e\n  \u003cli\u003eNeedle-free sampling valves\u003c\/li\u003e\n  \u003cli\u003eSampling plugs\u003c\/li\u003e\n  \u003cli\u003eLuer connections\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eSampling configurations\u003c\/h3\u003e\n\n\u003cp\u003e\n  A dedicated sampling line can be incorporated in addition to the main inlet\n  and outlet connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The sampling connection can be configured with a needle-free valve,\n  sampling plug, Luer interface or another suitable connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where a complete multi-sample system is required rather than a sampling\n  connection on a storage bag, a dedicated aseptic sampling assembly should\n  be specified separately.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eFilter-integrated bag assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Single-use bags can also be supplied as part of a filtration assembly.\n  These systems combine the process bag with tubing, connections and an\n  integrated capsule filter.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations are available with sterilising-grade\n  \u003cstrong\u003e0.2 µm PES capsule filters\u003c\/strong\u003e, while alternative filter\n  configurations can be selected for custom assemblies.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable standard storage and transfer bag assemblies can be supplied\n  gamma sterilised and ready to use.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard sterile configurations are available with gamma irradiation\n  in the \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e range. Other custom film and component\n  combinations may have different validated irradiation limits and should\n  be confirmed for the complete assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Non-sterile configuration-to-order bags are also available where the final\n  assembly or sterilisation strategy has not yet been defined.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProduction and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Bag assemblies are available from controlled cleanroom production\n  environments. Exact cleanroom classification depends on the selected\n  production route and assembly configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the selected materials and components, available documentation\n  can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eCertificate of Conformance\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis or Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eBatch traceability\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; cytotoxicity information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; biological reactivity information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; particulate information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA material conformity information\u003c\/li\u003e\n  \u003cli\u003eBSE \/ TSE or animal-derived component statements\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n  \u003cli\u003eExtractables and leachables documentation where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact conformity and validation documentation must be confirmed for the\n  final film, tubing, connectors, filters and other fluid-contact components.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eBuffer storage and transfer\u003c\/li\u003e\n  \u003cli\u003eMedia storage and transfer\u003c\/li\u003e\n  \u003cli\u003eProcess-liquid collection\u003c\/li\u003e\n  \u003cli\u003eFiltered liquid collection\u003c\/li\u003e\n  \u003cli\u003eIntermediate product storage\u003c\/li\u003e\n  \u003cli\u003eStock solution storage\u003c\/li\u003e\n  \u003cli\u003eProduct transfer\u003c\/li\u003e\n  \u003cli\u003eDownstream processing\u003c\/li\u003e\n  \u003cli\u003eUpstream processing\u003c\/li\u003e\n  \u003cli\u003eBuffer filling\u003c\/li\u003e\n  \u003cli\u003eWaste collection\u003c\/li\u003e\n  \u003cli\u003eRinsing and filter-wetting applications\u003c\/li\u003e\n  \u003cli\u003eFluid transfer between unit operations\u003c\/li\u003e\n  \u003cli\u003eFilter-integrated storage assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eWide volume range:\u003c\/strong\u003e\n    standard 2D and 3D configurations cover applications from 250 mL\n    through 3,000 L, with larger custom assemblies available.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eStandard and custom configurations:\u003c\/strong\u003e\n    common storage and transfer layouts can be selected directly while\n    specialised fluid paths can be engineered around the application.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple film constructions:\u003c\/strong\u003e\n    different product-contact and barrier materials can be selected\n    according to process requirements.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible tubing selection:\u003c\/strong\u003e\n    platinum-cured silicone and weldable TPE tubing configurations are available.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple connection technologies:\u003c\/strong\u003e\n    sterile connectors, quick couplings, Tri-Clamp interfaces and other\n    process connections can be incorporated.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSampling capability:\u003c\/strong\u003e\n    separate sampling lines and valves can be integrated where required.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFiltration integration:\u003c\/strong\u003e\n    suitable capsule filters can be incorporated into the fluid path.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSterile ready-to-use configurations:\u003c\/strong\u003e\n    standard assemblies can 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The tubing is pushed over\n  the barbed connection and mechanically retained using a suitable cable tie,\n  clamp or tubing-retention system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Straight connectors, reducing connectors and branching fittings are available\n  for connecting tubing with equal or different internal diameters. Sizes cover\n  tubing with internal diameters from approximately 1.6 mm to 25.4 mm\n  (1\/16\" to 1\").\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Hose barb fittings provide a simple mechanical method for creating fluid-path\n  connections without threaded or welded interfaces. Multiple fitting geometries\n  can be incorporated into disposable tubing assemblies, manifolds and\n  pharmaceutical process systems.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations include straight hose barb couplers, reducing couplers\n  and Wye connectors. Branching fittings can be used to divide or combine fluid\n  paths, while reducing connectors allow different tubing sizes to be joined\n  within the same assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Fittings are available in cleanroom-produced and standard production versions.\n  Cleanroom versions are manufactured and packaged under ISO Class 7 cleanroom\n  conditions. Batch-related conformity documentation is available for the\n  supplied components.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The flexible tubing is pushed over the tapered barbs of the fitting. The barb\n  geometry creates mechanical resistance against the tubing pulling away from\n  the connector while also supporting sealing between the tubing wall and the\n  fitting surface.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A suitable tubing-retention method is normally applied over the outside of the\n  tubing. Depending on the assembly requirements, this may include a cable tie,\n  stainless-steel tubing clamp or plastic retaining ring.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Straight couplers connect tubing sections of the same nominal size. Reducing\n  couplers provide a transition between two different tubing diameters, while\n  Wye fittings divide one fluid path into two branches or combine two lines into\n  one common line.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hose barb fittings are available in several polymer materials. The appropriate\n  material should be selected according to process-fluid compatibility,\n  sterilisation method, operating temperature and required technical\n  documentation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Common material options include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\u003cstrong\u003ePolypropylene (PP)\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003e\u003cstrong\u003ePVDF\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003e\u003cstrong\u003eHDPE\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003eAdditional polymer grades depending on fitting configuration\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  PVDF is particularly suitable for applications requiring increased chemical\n  and temperature resistance and can be considered for autoclavable process\n  configurations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Material options are available with USP Class VI conformity and are specified\n  as free from animal-derived components. Exact FDA and material documentation\n  should be confirmed for the selected fitting material.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e Hose barb fittings are fluid connection\n  components rather than filtration media and therefore do not have a micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If filtration is required within the same fluid path, a membrane, capsule,\n  vent or other suitable filter can be incorporated separately into the tubing\n  assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Plastic hose barb fittings are available in several geometries to support\n  different fluid-path layouts.\n\u003c\/p\u003e\n\n\u003ch3\u003eStraight hose barb couplers\u003c\/h3\u003e\n\n\u003cp\u003e\n  Straight couplers connect two tubing sections with the same nominal internal\n  diameter. Available listed tubing sizes range from 1\/16\" through 1\".\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Tubing ID\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Metric equivalent\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n  \u003ctbody\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/16\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 1.6 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/32\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 2.4 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/8\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 3.2 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5\/32\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 4.0 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/16\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 4.8 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/4\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 6.4 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5\/16\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 7.9 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/8\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 9.5 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1\/2\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 12.7 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5\/8\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 15.9 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3\/4\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003eApprox. 19.1 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n    \u003ctr\u003e\n\u003ctd style=\"padding:10px;\"\u003e1\"\u003c\/td\u003e\n\u003ctd style=\"padding:10px;\"\u003eApprox. 25.4 mm\u003c\/td\u003e\n\u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003eReducing hose barb couplers\u003c\/h3\u003e\n\n\u003cp\u003e\n  Reducing connectors provide different hose barb dimensions at each end,\n  allowing two different tubing IDs to be connected without a separate adapter.\n  Multiple combinations are available across the supported tubing range.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eWye and branching fittings\u003c\/h3\u003e\n\n\u003cp\u003e\n  Wye fittings provide three barbed connection points and are used to split,\n  combine or distribute process flow within a tubing assembly or manifold.\n  Multiple tubing sizes are available from small-bore fluid paths through\n  1-inch tubing systems.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Additional branching geometries can also be considered where the required\n  fluid-path layout cannot be achieved using a standard straight, reducing or\n  Wye connector.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProduction and sterilisation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Cleanroom versions are manufactured and packaged under\n  \u003cstrong\u003eISO Class 7 cleanroom conditions\u003c\/strong\u003e. Standard versions are\n  also available for applications that do not require cleanroom production.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the selected polymer, fittings can be incorporated into\n  gamma-sterilised single-use systems or autoclavable process assemblies.\n  PVDF configurations are particularly relevant for processes involving\n  elevated temperatures or chemically aggressive media.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity information includes:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003eFDA conformity for suitable material configurations\u003c\/li\u003e\n  \u003cli\u003eFree from animal-derived components\u003c\/li\u003e\n  \u003cli\u003eBatch-related certificate of compliance\u003c\/li\u003e\n  \u003cli\u003eISO Class 7 cleanroom production option\u003c\/li\u003e\n  \u003cli\u003eGamma-sterilisable configurations\u003c\/li\u003e\n  \u003cli\u003eAutoclavable material configurations\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Plastic hose barb fittings are widely used wherever flexible tubing needs to\n  be connected, reduced or divided within pharmaceutical and biotechnology\n  fluid-handling systems.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSingle-use tubing assemblies\u003c\/li\u003e\n  \u003cli\u003eSingle-use bag and bottle assemblies\u003c\/li\u003e\n  \u003cli\u003eMulti-use process assemblies\u003c\/li\u003e\n  \u003cli\u003eLiquid transfer\u003c\/li\u003e\n  \u003cli\u003eSampling systems\u003c\/li\u003e\n  \u003cli\u003eCell cultivation\u003c\/li\u003e\n  \u003cli\u003eCell harvest\u003c\/li\u003e\n  \u003cli\u003eFermentation\u003c\/li\u003e\n  \u003cli\u003ePharmaceutical filling\u003c\/li\u003e\n  \u003cli\u003eFluid distribution manifolds\u003c\/li\u003e\n  \u003cli\u003eBuffer and media transfer\u003c\/li\u003e\n  \u003cli\u003eGeneral bioprocess tubing connections\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eWide tubing range:\u003c\/strong\u003e\n    fittings are available for tubing IDs from approximately 1.6 mm to\n    25.4 mm.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple geometries:\u003c\/strong\u003e\n    straight, reducing and branching connectors support different fluid-path\n    layouts.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eDifferent tubing sizes can be connected:\u003c\/strong\u003e\n    reducing fittings provide direct transitions between different internal\n    diameters.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSimple tubing connection:\u003c\/strong\u003e\n    the tubing is pushed directly onto the barb and secured using an appropriate\n    retention method.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple polymer options:\u003c\/strong\u003e\n    materials can be selected according to temperature, chemical compatibility\n    and sterilisation requirements.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSingle-use compatibility:\u003c\/strong\u003e\n    fittings can be incorporated into gamma-sterilised disposable assemblies.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eAutoclave options:\u003c\/strong\u003e\n    suitable material configurations can be used in autoclavable process systems.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCleanroom option:\u003c\/strong\u003e\n    fittings can be manufactured and packaged under ISO Class 7 conditions.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Hose barb fittings should be selected according to the tubing dimensions,\n  process fluid, sterilisation method and required fluid-path geometry.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired fitting geometry: straight, reducing, Wye or other branching type\u003c\/li\u003e\n  \u003cli\u003eTubing inner diameter for each connection\u003c\/li\u003e\n  \u003cli\u003eTubing material and outer diameter\u003c\/li\u003e\n  \u003cli\u003ePreferred fitting material\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eOperating pressure\u003c\/li\u003e\n  \u003cli\u003eGamma irradiation or autoclave requirement\u003c\/li\u003e\n  \u003cli\u003eCleanroom or standard production requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity documentation\u003c\/li\u003e\n  \u003cli\u003eRequired quantity or annual demand\u003c\/li\u003e\n  \u003cli\u003eWhether the fitting will be integrated into a complete single-use assembly\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Fittings can also be supplied as part of a configured tubing, bag, bottle,\n  sampling or fluid-transfer assembly.\n\u003c\/p\u003e\n\n\n  \u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a plastic hose barb fitting?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A plastic hose barb fitting is a tubing connection component with ridged barbed ends. Flexible tubing is pushed over the barb and secured using a suitable cable tie, clamp or retaining system.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What tubing sizes are available for bioprocess hose barb fittings?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available fittings cover tubing internal diameters from approximately 1.6 mm to 25.4 mm, corresponding to 1\/16 inch through 1 inch tubing.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What types of hose barb fittings are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available configurations include straight couplers, reducing couplers and Wye branching connectors. 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Specified \/ 3\/32\"","offer_id":57318041092422,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ Other \/ Other \/ To Be Specified \/ 1\/8\"","offer_id":57318041125190,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/plastic-hose-barb-fittings-bioprocessing.webp?v=1788964634"},{"product_id":"single-use-bottle-assemblies","title":"Custom Single-Use Bottle Assemblies","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Custom single-use bottle assemblies combine a plastic process bottle with\n  tubing, closures, vent filters, connectors and other fluid-path components\n  for pharmaceutical and biotechnology applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard media bottle configurations are available in PETG and polycarbonate\n  from 30 mL to 2 L, including sealed bottles, two-port assemblies and\n  three-port assemblies. For applications outside these standard formats,\n  custom bottle systems can be configured using alternative bottle types,\n  materials, tubing and process connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Bottle assemblies can be used for media and buffer preparation, liquid\n  storage, aseptic sampling, intermediate-product handling, cell culture,\n  transfer, filling and other controlled fluid-handling processes.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  A bottle assembly provides a defined interface between the process container\n  and the surrounding fluid path. Depending on the configuration, the closure\n  can incorporate a feed line, dip tube, vent line, sterile connector, tubing\n  plug or additional process connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standardised PETG and polycarbonate assemblies provide practical options for\n  common media, buffer and biological-liquid applications. More specialised\n  systems can be engineered around different bottles, flasks, vials, carboys\n  or chemically resistant fluoropolymer containers.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies can therefore range from a simple sterile media bottle to a\n  multi-port bottle system or multi-container manifold.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bottle acts as the receiving, storage or supply container within the\n  fluid path. Liquid is introduced or removed through tubing connected to\n  ports in the bottle closure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A typical two-port configuration contains one process feed line and one\n  vent line. The feed line can extend into the bottle as a dip tube, allowing\n  fluid to be transferred into or withdrawn from the container.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The vent line allows pressure equalisation during filling or emptying and can\n  incorporate a hydrophobic vent filter to maintain a controlled gas interface.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Three-port configurations provide an additional process line and can be used\n  where two separate feed, transfer or connection points are required.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Custom assemblies can incorporate additional tubing, connectors, filters,\n  sampling interfaces and manifolds according to the process.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard bottle assemblies are available in\n  \u003cstrong\u003ePETG\u003c\/strong\u003e and \u003cstrong\u003epolycarbonate (PC)\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Their operating-temperature ranges differ:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePETG:\u003c\/strong\u003e approximately -40°C to +60°C\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePolycarbonate:\u003c\/strong\u003e approximately -80°C to +121°C\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  PETG is well suited to common media, buffer and liquid-storage applications,\n  while polycarbonate provides a wider temperature range for applications\n  involving low-temperature storage or suitable autoclave processing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Additional custom container materials can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003ePolypropylene (PP)\u003c\/li\u003e\n  \u003cli\u003ePFA\u003c\/li\u003e\n  \u003cli\u003eFEP\u003c\/li\u003e\n  \u003cli\u003eETFE\u003c\/li\u003e\n  \u003cli\u003eOther application-specific polymer containers\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing material is selected separately from the bottle. Common configurations\n  use platinum-cured silicone or weldable TPE tubing.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eThe bottle itself does not have a micron rating.\u003c\/strong\u003e\n  However, bottle assemblies can incorporate filtration components such as\n  vent filters.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard media bottle configurations are available with a\n  \u003cstrong\u003e0.2 µm hydrophobic PTFE vent filter\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Alternative vent or process filters can be specified separately where a\n  different membrane material, filter size or retention rating is required.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Bottle assemblies can be selected from standard media-bottle configurations\n  or designed as application-specific fluid paths.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eStandard bottle volumes\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard PETG bottle volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e30 mL\u003c\/li\u003e\n  \u003cli\u003e60 mL\u003c\/li\u003e\n  \u003cli\u003e125 mL\u003c\/li\u003e\n  \u003cli\u003e250 mL\u003c\/li\u003e\n  \u003cli\u003e500 mL\u003c\/li\u003e\n  \u003cli\u003e1 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Standard polycarbonate bottle volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e125 mL\u003c\/li\u003e\n  \u003cli\u003e250 mL\u003c\/li\u003e\n  \u003cli\u003e500 mL\u003c\/li\u003e\n  \u003cli\u003e1 L\u003c\/li\u003e\n  \u003cli\u003e2 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Other bottle sizes and container formats can be incorporated into custom\n  assemblies where required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSealed bottle configurations\u003c\/h3\u003e\n\n\u003cp\u003e\n  Bottles can be supplied with a sealing screw cap where no tubing ports are\n  required. This provides a simple single-use container for preparation,\n  handling or storage.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTwo-port bottle assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  A typical two-port configuration contains:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eOne feed or transfer line\u003c\/li\u003e\n  \u003cli\u003eOne vent line\u003c\/li\u003e\n  \u003cli\u003eAn internal dip tube\u003c\/li\u003e\n  \u003cli\u003eA hydrophobic vent filter\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Standard feed-line configurations can use 1\/4\" ID platinum-cured silicone\n  tubing with a process connector or 1\/4\" ID weldable TPE tubing with a\n  tubing closure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard vent configurations use flexible tubing connected to a\n  0.2 µm hydrophobic PTFE vent filter.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eThree-port bottle assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Three-port configurations provide two feed or process lines together with\n  a dedicated filtered vent line.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  These assemblies are useful where separate inlet and outlet connections,\n  multiple transfer paths or additional process interfaces are required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eCustom bottle assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Custom configurations can extend beyond standard PETG and polycarbonate\n  media bottles.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available container concepts can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eStandard process bottles\u003c\/li\u003e\n  \u003cli\u003eSampling bottles\u003c\/li\u003e\n  \u003cli\u003eErlenmeyer flasks\u003c\/li\u003e\n  \u003cli\u003eCentrifuge bottles\u003c\/li\u003e\n  \u003cli\u003eVials\u003c\/li\u003e\n  \u003cli\u003eCarboys\u003c\/li\u003e\n  \u003cli\u003ePFA bottles\u003c\/li\u003e\n  \u003cli\u003eFEP bottles\u003c\/li\u003e\n  \u003cli\u003eOther fluoropolymer containers\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The final configuration can include one container or several bottles\n  connected as part of a manifold system.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTubing and connection options\u003c\/h3\u003e\n\n\u003cp\u003e\n  Bottle assemblies can incorporate:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003ePlatinum-cured silicone tubing\u003c\/li\u003e\n  \u003cli\u003eWeldable TPE tubing\u003c\/li\u003e\n  \u003cli\u003eSterile and aseptic connectors\u003c\/li\u003e\n  \u003cli\u003eQuick disconnect couplings\u003c\/li\u003e\n  \u003cli\u003eTubing plugs\u003c\/li\u003e\n  \u003cli\u003eHose barb fittings\u003c\/li\u003e\n  \u003cli\u003eSanitary Tri-Clamp connections\u003c\/li\u003e\n  \u003cli\u003eVent filters\u003c\/li\u003e\n  \u003cli\u003eSampling connections\u003c\/li\u003e\n  \u003cli\u003eAdditional process filters\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eSterilisation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard PETG and polycarbonate bottle assemblies can be supplied gamma\n  sterilised using an irradiation range of approximately\n  \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  PETG configurations are intended for gamma sterilisation and are not suitable\n  for autoclaving.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable polycarbonate configurations can also be autoclaved at approximately\n  \u003cstrong\u003e121°C\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For custom bottle assemblies, sterilisation compatibility must be evaluated\n  across the complete container, cap, tubing, filter and connector configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Depending on the final bottle and assembly configuration, available quality\n  and conformity information can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI material conformity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; Bacterial Endotoxins\u003c\/li\u003e\n  \u003cli\u003eFDA CFR 21 material conformity where applicable\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component statements\u003c\/li\u003e\n  \u003cli\u003eBSE \/ TSE statements\u003c\/li\u003e\n  \u003cli\u003eCertificate of Conformance\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis or Certificate of Quality where applicable\u003c\/li\u003e\n  \u003cli\u003eBatch traceability\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact certificates and conformity statements depend on the materials and\n  components selected for the final bottle assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eCell culture media preparation and storage\u003c\/li\u003e\n  \u003cli\u003eBuffer preparation and storage\u003c\/li\u003e\n  \u003cli\u003eReagent preparation\u003c\/li\u003e\n  \u003cli\u003eBiological liquid storage\u003c\/li\u003e\n  \u003cli\u003eLiquid transfer\u003c\/li\u003e\n  \u003cli\u003eAseptic sampling\u003c\/li\u003e\n  \u003cli\u003eClosed process sampling\u003c\/li\u003e\n  \u003cli\u003eIntermediate-product storage\u003c\/li\u003e\n  \u003cli\u003eCell culture processes\u003c\/li\u003e\n  \u003cli\u003eMedia fill applications\u003c\/li\u003e\n  \u003cli\u003eFill \u0026amp; Finish\u003c\/li\u003e\n  \u003cli\u003eProcess manifolds\u003c\/li\u003e\n  \u003cli\u003eWaste collection\u003c\/li\u003e\n  \u003cli\u003eLow-temperature storage\u003c\/li\u003e\n  \u003cli\u003eFreeze-thaw applications with suitable container materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eStandard volume options:\u003c\/strong\u003e\n    defined PETG and polycarbonate bottle sizes provide a practical starting\n    point for common media and buffer applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple port configurations:\u003c\/strong\u003e\n    sealed, two-port and three-port designs cover common fluid-handling\n    requirements.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible material selection:\u003c\/strong\u003e\n    PETG and polycarbonate are available as standard, with PP and\n    fluoropolymer containers available for custom applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eIntegrated vent filtration:\u003c\/strong\u003e\n    standard configurations can incorporate a 0.2 µm hydrophobic PTFE\n    vent filter.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSilicone and TPE tubing options:\u003c\/strong\u003e\n    the fluid path can be selected according to connection and processing\n    requirements.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSterile ready-to-use configurations:\u003c\/strong\u003e\n    suitable assemblies can be supplied gamma irradiated.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eWide temperature range:\u003c\/strong\u003e\n    PETG and polycarbonate provide different operating ranges for ambient,\n    frozen and higher-temperature applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom engineering:\u003c\/strong\u003e\n    bottle type, tubing, ports, filters and connections can be configured\n    around the process.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Select a standard bottle material, volume and port configuration where these\n  match the application. If a different container, tubing layout or fluid-path\n  design is required, a custom bottle assembly can be configured.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired bottle or container type\u003c\/li\u003e\n  \u003cli\u003eNominal volume\u003c\/li\u003e\n  \u003cli\u003ePreferred bottle material\u003c\/li\u003e\n  \u003cli\u003eProcess application\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eNumber of process ports\u003c\/li\u003e\n  \u003cli\u003eFeed-line tubing material\u003c\/li\u003e\n  \u003cli\u003eTubing ID and OD\u003c\/li\u003e\n  \u003cli\u003eRequired tubing lengths\u003c\/li\u003e\n  \u003cli\u003eDip-tube requirement\u003c\/li\u003e\n  \u003cli\u003eVent-line and vent-filter requirement\u003c\/li\u003e\n  \u003cli\u003eRequired sterile connectors or couplings\u003c\/li\u003e\n  \u003cli\u003eSampling connection requirement\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eLow-temperature or freezing requirement\u003c\/li\u003e\n  \u003cli\u003eSterilisation method\u003c\/li\u003e\n  \u003cli\u003eRequired conformity or validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting drawing or process sketch where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  A finished assembly drawing is not required to begin. Bottle volume,\n  process application and required connection points usually provide enough\n  information for an initial technical review.\n\u003c\/p\u003e\n\n  \u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a single-use bottle assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A single-use bottle assembly combines a disposable plastic bottle with tubing, ports, vent filtration and process connections for pharmaceutical and biotechnology fluid handling.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What bottle volumes are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Standard PETG bottles are available from 30 mL to 1 L. Standard polycarbonate bottles are available from 125 mL to 2 L. Additional bottle types and volumes can be incorporated into custom assemblies.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the difference between PETG and polycarbonate bottle assemblies?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"PETG bottle assemblies are suitable for approximately -40°C to 60°C and can be gamma sterilised. Polycarbonate provides a wider operating range of approximately -80°C to 121°C and suitable configurations can also be autoclaved.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can single-use bottle assemblies include a vent filter?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Standard two-port and three-port bottle assemblies can incorporate a dedicated vent line with a 0.2 micron hydrophobic PTFE vent filter.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What tubing can be used with single-use bottle assemblies?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Common configurations use platinum-cured silicone or weldable TPE tubing. Other tubing materials can be selected for custom applications.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can custom bottle assemblies use containers other than PETG or polycarbonate?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. 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Specified","offer_id":57418820485446,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false},{"title":"Custom Container \/ Volume \/ Custom Multi-Port Configuration \/ Platinum-Cured Silicone","offer_id":57418820518214,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false},{"title":"Custom Container \/ Volume \/ Custom Multi-Port Configuration \/ Weldable TPE","offer_id":57418820550982,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false},{"title":"Custom Container \/ Volume \/ Custom Multi-Port Configuration \/ Custom \/ To Be Specified","offer_id":57418820583750,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/large-volume-single-use-bottle-assembly.webp?v=1788965554"},{"product_id":"reinforced-braided-silicone-tubing","title":"Reinforced Braided Silicone Tubing for Bioprocessing","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Reinforced braided silicone tubing is designed for pharmaceutical,\n  biotechnology and hygienic process applications requiring greater pressure\n  resistance than conventional unreinforced silicone tubing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The tubing consists of platinum-cured silicone with an integrated synthetic\n  fabric reinforcement. This construction combines the flexibility and\n  transparency of silicone with increased mechanical strength for fluid\n  transfer, manifolds and filtration processes.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Braided silicone tubing is used where a flexible process line must withstand\n  higher working pressures while maintaining visual access to the process fluid.\n  The transparent tubing allows operators to monitor liquid flow, bubbles and\n  process conditions during operation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The product-contact material is platinum-cured silicone rubber. A synthetic\n  fabric reinforcement is embedded in the tubing wall to increase pressure\n  resistance compared with standard silicone tubing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The smooth internal surface supports hygienic fluid handling and facilitates\n  cleaning where the tubing is used in reusable process applications.\n  Production takes place under ISO Class 7 cleanroom conditions.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  Process fluid flows through the smooth silicone inner bore while the braided\n  reinforcement within the tubing wall provides additional mechanical support.\n  As internal pressure increases, the reinforcement limits radial expansion of\n  the silicone and helps the tubing maintain its geometry.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This allows reinforced silicone tubing to operate at higher working pressures\n  than comparable non-reinforced silicone tubing while retaining the flexibility\n  required for routing between vessels, filters, pumps and process equipment.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The transparent construction also permits continuous visual monitoring of the\n  fluid path during transfer and processing.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The standard construction consists of:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n\u003cstrong\u003eProduct-contact material:\u003c\/strong\u003e platinum-cured silicone rubber\u003c\/li\u003e\n  \u003cli\u003e\n\u003cstrong\u003eReinforcement:\u003c\/strong\u003e synthetic fabric braid\u003c\/li\u003e\n  \u003cli\u003e\n\u003cstrong\u003eAppearance:\u003c\/strong\u003e transparent\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The silicone is specified as tasteless and odourless and is suitable for\n  pharmaceutical, biotechnology, food and cosmetic process applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If different chemical resistance, pressure capability or temperature\n  performance is required, alternative reinforced tubing constructions should\n  be considered separately.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e Reinforced silicone tubing is a fluid-transfer\n  component and does not contain filtration media. It therefore has no micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where filtration is required, the tubing can be connected to an appropriate\n  capsule, membrane or other process filter within the same fluid path.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  The tubing combines a smooth platinum-cured silicone fluid-contact layer with\n  an integrated braided reinforcement. The reinforced wall increases working\n  and burst-pressure capability while retaining flexibility for pharmaceutical\n  and bioprocess installations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available sizes range from approximately \u003cstrong\u003e3.18 mm to 31.75 mm internal\n  diameter\u003c\/strong\u003e. Working pressure depends on tubing size.\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Inner diameter\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Outer diameter\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Working pressure\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Burst pressure\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Minimum bend radius\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3.18 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e9.81 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e30 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e4.72 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e11.35 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e35 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e6.35 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e13.03 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e40 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e7.93 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e14.61 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e12 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e36 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e45 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e9.52 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e16.32 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e12 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e36 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e50 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e12.70 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e20.10 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e10 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e30 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e65 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15.87 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e24.37 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e8 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e24 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e75 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e19.05 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e27.91 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e8 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e24 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e80 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e22.20 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e31.12 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e100 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e25.40 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e34.50 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e120 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e31.75 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e40.80 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e4 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e12 bar\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e150 mm\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003ch3\u003eSterilisation and conformity\u003c\/h3\u003e\n\n\u003cp\u003e\n  The tubing is suitable for both gamma sterilisation and autoclaving and is\n  produced under ISO Class 7 cleanroom conditions.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity references include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI\u003c\/li\u003e\n  \u003cli\u003e3-A Standards\u003c\/li\u003e\n  \u003cli\u003eFDA conformity\u003c\/li\u003e\n  \u003cli\u003eEuropean Pharmacopoeia 3.1.9\u003c\/li\u003e\n  \u003cli\u003eISO 10993-4\u003c\/li\u003e\n  \u003cli\u003eISO 10993-5\u003c\/li\u003e\n  \u003cli\u003eISO 10993-11\u003c\/li\u003e\n  \u003cli\u003eBSE\/TSE conformity\u003c\/li\u003e\n  \u003cli\u003eNon-cytotoxic according to ISO 10993-5\u003c\/li\u003e\n  \u003cli\u003eGamma-sterilisable\u003c\/li\u003e\n  \u003cli\u003eAutoclavable\u003c\/li\u003e\n  \u003cli\u003eISO Class 7 cleanroom production\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Reinforced braided silicone tubing is used where flexible tubing must combine\n  hygienic product contact with increased pressure capability.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003ePharmaceutical fluid transfer\u003c\/li\u003e\n  \u003cli\u003eBioprocess liquid transfer\u003c\/li\u003e\n  \u003cli\u003eSingle-use and multi-use tubing assemblies\u003c\/li\u003e\n  \u003cli\u003eFluid distribution manifolds\u003c\/li\u003e\n  \u003cli\u003eFiltration processes\u003c\/li\u003e\n  \u003cli\u003eHigh-pressure tubing applications\u003c\/li\u003e\n  \u003cli\u003eProcess vessel connections\u003c\/li\u003e\n  \u003cli\u003eBuffer and media transfer\u003c\/li\u003e\n  \u003cli\u003eFood and beverage processing\u003c\/li\u003e\n  \u003cli\u003eCosmetic manufacturing\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eIncreased pressure capability:\u003c\/strong\u003e\n    braided reinforcement supports higher working pressures than standard\n    unreinforced silicone tubing.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eHigh flexibility:\u003c\/strong\u003e\n    suitable for routing flexible process connections between equipment.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eTransparent construction:\u003c\/strong\u003e\n    allows continuous visual monitoring of process fluid.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePlatinum-cured silicone:\u003c\/strong\u003e\n    suitable for demanding pharmaceutical and biotechnology fluid-contact\n    applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSmooth internal surface:\u003c\/strong\u003e\n    supports hygienic fluid transfer and facilitates cleaning in reusable\n    applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSterilisation flexibility:\u003c\/strong\u003e\n    suitable for gamma sterilisation and autoclaving.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eWide dimensional range:\u003c\/strong\u003e\n    available from approximately 3.18 mm to 31.75 mm inner diameter.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCleanroom production:\u003c\/strong\u003e\n    manufactured under ISO Class 7 cleanroom conditions.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Reinforced silicone tubing should be selected according to the required\n  dimensions, working pressure, bend radius, process fluid and sterilisation\n  method.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired inner diameter\u003c\/li\u003e\n  \u003cli\u003eRequired outer diameter\u003c\/li\u003e\n  \u003cli\u003eRequired tubing length\u003c\/li\u003e\n  \u003cli\u003eMaximum operating pressure\u003c\/li\u003e\n  \u003cli\u003eRequired burst-pressure margin\u003c\/li\u003e\n  \u003cli\u003eMinimum bend radius\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eGamma irradiation or autoclave requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity documentation\u003c\/li\u003e\n  \u003cli\u003eRequired quantity or annual demand\u003c\/li\u003e\n  \u003cli\u003eWhether the tubing will be supplied loose or integrated into an assembly\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The tubing can also be incorporated into custom transfer lines, manifolds,\n  filtration systems and other pharmaceutical or bioprocess tubing assemblies.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is reinforced braided silicone tubing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Reinforced braided silicone tubing is flexible platinum-cured silicone tubing with an integrated synthetic fabric reinforcement. The braid increases pressure resistance compared with standard unreinforced silicone tubing.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sizes are available for braided silicone tubing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available tubing sizes range from approximately 3.18 mm to 31.75 mm internal diameter, with outer diameters from approximately 9.81 mm to 40.80 mm.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What pressure can braided silicone tubing withstand?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Working pressure depends on tubing size. The listed range extends from 15 bar for smaller tubing sizes to 4 bar for the largest listed size. Burst pressures are higher and also vary by diameter.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can braided silicone tubing be gamma sterilised or autoclaved?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. The tubing is suitable for gamma sterilisation and autoclaving.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What material is braided silicone tubing made from?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The tubing is manufactured from platinum-cured silicone rubber with an integrated synthetic fabric reinforcement.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What applications use reinforced silicone tubing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Typical applications include pharmaceutical and bioprocess fluid transfer, filtration processes, manifolds and other applications requiring flexible tubing with increased working-pressure capability.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"3.18 × 9.81 mm \/ Gamma Sterilised \/ Custom Length \/ Please 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Specify","offer_id":57319132234054,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"7.93 × 14.61 mm \/ Gamma Sterilised \/ Custom Length \/ Please Specify","offer_id":57319132266822,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"7.93 × 14.61 mm \/ Autoclave \/ Ready-to-Autoclave \/ Custom Length \/ Please Specify","offer_id":57319132299590,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"7.93 × 14.61 mm \/ Non-Sterile \/ Custom Length \/ Please Specify","offer_id":57319132332358,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"7.93 × 14.61 mm \/ To Be Specified \/ Custom Length \/ Please Specify","offer_id":57319132365126,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"9.52 × 16.32 mm \/ Gamma Sterilised \/ Custom Length \/ Please Specify","offer_id":57319132397894,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"9.52 × 16.32 mm \/ Autoclave \/ 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Specify","offer_id":57319132954950,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"22.20 × 31.12 mm \/ Non-Sterile \/ Custom Length \/ Please Specify","offer_id":57319132987718,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"22.20 × 31.12 mm \/ To Be Specified \/ Custom Length \/ Please Specify","offer_id":57319133020486,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"25.40 × 34.50 mm \/ Gamma Sterilised \/ Custom Length \/ Please Specify","offer_id":57319133053254,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"25.40 × 34.50 mm \/ Autoclave \/ Ready-to-Autoclave \/ Custom Length \/ Please Specify","offer_id":57319133086022,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"25.40 × 34.50 mm \/ Non-Sterile \/ Custom Length \/ Please Specify","offer_id":57319133118790,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"25.40 × 34.50 mm \/ To Be Specified \/ Custom Length \/ Please Specify","offer_id":57319133151558,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"31.75 × 40.80 mm \/ Gamma Sterilised \/ Custom Length \/ Please Specify","offer_id":57319133184326,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"31.75 × 40.80 mm \/ Autoclave \/ Ready-to-Autoclave \/ Custom Length \/ Please Specify","offer_id":57319133217094,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"31.75 × 40.80 mm \/ Non-Sterile \/ Custom Length \/ Please Specify","offer_id":57319133249862,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"31.75 × 40.80 mm \/ To Be Specified \/ Custom Length \/ Please Specify","offer_id":57319133282630,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/reinforced-braided-silicone-tubing.webp?v=1788966719"},{"product_id":"non-invasive-bubble-detector-bioprocess-tubing","title":"Non-Invasive Bubble Detector for Bioprocess Tubing","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Non-invasive bubble detectors are designed to detect unwanted air or gas\n  bubbles in liquid-filled pharmaceutical, bioprocess and medical tubing.\n  Measurement takes place through the tubing wall, so the sensor does not come\n  into direct contact with the process medium.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The tubing is inserted directly into the detector, allowing continuous\n  monitoring of the fluid path without introducing an additional wetted\n  component. Depending on the configuration, the sensor can detect microbubbles,\n  larger gas inclusions, foam and whether the tubing is completely full or empty.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Bubble detection is particularly relevant in processes where uninterrupted\n  liquid flow must be verified and unwanted gas inclusions need to be detected\n  before they reach the next process step.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The non-invasive measuring principle keeps the sensor physically separated\n  from the product. This avoids adding another product-contact surface to the\n  fluid path and makes the detector particularly suitable for single-use tubing\n  systems and other hygienic process applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Clear flexible tubing materials such as silicone, TPE and PVC can be monitored.\n  Suitable reinforced transparent tubing can also be used. The detector is\n  intended primarily for water-like or low-viscosity liquids containing little\n  or no suspended solids.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bubble detector measures through the wall of the tubing rather than\n  contacting the liquid directly. The filled tubing is positioned inside the\n  sensor, which continuously monitors the condition of the fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Liquid and gas have different transmission characteristics. When an air or gas\n  bubble passes through the sensing area, the detector identifies the change and\n  generates the configured output signal.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the sensor configuration and sensitivity setting, the same\n  principle can be used for microbubble detection, general bubble monitoring,\n  foam detection and full-or-empty detection of the tubing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Because the tubing itself remains closed, the sensor can be installed without\n  creating an additional process connection, wetted fitting or penetration into\n  the fluid path.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bubble detector itself does not form part of the wetted process path.\n  Material compatibility therefore primarily concerns the tubing being monitored.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable transparent tubing materials include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSilicone tubing\u003c\/li\u003e\n  \u003cli\u003eTPE tubing\u003c\/li\u003e\n  \u003cli\u003ePVC tubing\u003c\/li\u003e\n  \u003cli\u003eSuitable transparent reinforced tubing\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing transparency, wall thickness, diameter, reinforcement and process-fluid\n  properties should be considered when selecting the appropriate sensor\n  configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e A bubble detector is a process-monitoring\n  sensor rather than filtration media and therefore does not have a micron or\n  pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The detector can, however, be configured for sensitive detection of small gas\n  inclusions or microbubbles. The required detection sensitivity should be\n  specified according to the application.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Non-invasive bubble detectors are available in different sizes and electronic\n  configurations to suit different tubing dimensions and process requirements.\n  The tubing is inserted into the sensor without requiring a separate mounting\n  or product-contact fitting.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the selected configuration, technical features can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eNon-invasive measurement through the tubing wall\u003c\/li\u003e\n  \u003cli\u003eMicrobubble detection\u003c\/li\u003e\n  \u003cli\u003eFull \/ empty tubing detection\u003c\/li\u003e\n  \u003cli\u003eFoam detection\u003c\/li\u003e\n  \u003cli\u003eAdjustable sensor sensitivity\u003c\/li\u003e\n  \u003cli\u003eIntegrated electronics\u003c\/li\u003e\n  \u003cli\u003eAutomatic or cyclic self-test functions\u003c\/li\u003e\n  \u003cli\u003eConfigurable electronic outputs\u003c\/li\u003e\n  \u003cli\u003eModular sensor configurations\u003c\/li\u003e\n  \u003cli\u003eOptional configurations for hazardous areas\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eElectrical and signal options\u003c\/h3\u003e\n\n\u003cp\u003e\n  The available sensor family supports several electronic interface options,\n  depending on the selected detector configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available signal and communication types can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eTTL logic\u003c\/li\u003e\n  \u003cli\u003eSerial communication\u003c\/li\u003e\n  \u003cli\u003ePWM output\u003c\/li\u003e\n  \u003cli\u003ePNP output\u003c\/li\u003e\n  \u003cli\u003e0–10 VDC analogue output\u003c\/li\u003e\n  \u003cli\u003e4–20 mA analogue output\u003c\/li\u003e\n  \u003cli\u003eRS485 communication\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Available supply voltages depend on the sensor configuration and can include\n  5 VDC or a wider 12–30 VDC supply range.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eCompliance and hazardous-area options\u003c\/h3\u003e\n\n\u003cp\u003e\n  Depending on the selected configuration, available conformity information\n  includes CE and RoHS \/ REACH documentation. Certain detector configurations\n  can also be supplied with an optional ATEX certificate for use in potentially\n  explosive environments.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Exact certifications, supply voltage and signal outputs should be confirmed\n  for the final sensor configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Non-invasive bubble detectors are used in processes where gas inclusion,\n  interrupted liquid supply or empty tubing could affect process control,\n  filling accuracy or equipment operation.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003ePharmaceutical filling processes\u003c\/li\u003e\n  \u003cli\u003eFill \u0026amp; Finish\u003c\/li\u003e\n  \u003cli\u003eSterile filtration\u003c\/li\u003e\n  \u003cli\u003eGeneral filtration applications\u003c\/li\u003e\n  \u003cli\u003eBioreactor processes\u003c\/li\u003e\n  \u003cli\u003eFermentation\u003c\/li\u003e\n  \u003cli\u003eLiquid dosing systems\u003c\/li\u003e\n  \u003cli\u003eMixing systems\u003c\/li\u003e\n  \u003cli\u003ePipetting systems\u003c\/li\u003e\n  \u003cli\u003eSingle-use tubing assemblies\u003c\/li\u003e\n  \u003cli\u003eFluid transfer systems\u003c\/li\u003e\n  \u003cli\u003eMedical pumps\u003c\/li\u003e\n  \u003cli\u003eDiagnostic systems\u003c\/li\u003e\n  \u003cli\u003eDialysis systems\u003c\/li\u003e\n  \u003cli\u003eBlood handling and separation systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eNon-invasive measurement:\u003c\/strong\u003e\n    the sensor monitors through the tubing wall without direct product contact.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eClosed fluid path:\u003c\/strong\u003e\n    no additional wetted sensor body or process penetration is required.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMicrobubble detection:\u003c\/strong\u003e\n    suitable configurations can detect small gas inclusions in the liquid stream.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple detection functions:\u003c\/strong\u003e\n    the sensor can also be used for foam monitoring and full-or-empty detection.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSimple tubing installation:\u003c\/strong\u003e\n    flexible tubing can be inserted into the sensing area without additional\n    product-contact fittings.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eAdjustable sensitivity:\u003c\/strong\u003e\n    sensor response can be adapted according to the application.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple electronic interfaces:\u003c\/strong\u003e\n    digital, serial and analogue output options are available depending on the\n    configuration.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSuitable for single-use systems:\u003c\/strong\u003e\n    the non-contact measuring principle allows the disposable tubing to remain\n    the complete product-contact surface.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  The correct bubble detector should be selected according to the tubing,\n  process liquid, required detection sensitivity and control-system interface.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical selection and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eTubing material\u003c\/li\u003e\n  \u003cli\u003eTubing inner diameter\u003c\/li\u003e\n  \u003cli\u003eTubing outer diameter\u003c\/li\u003e\n  \u003cli\u003eTubing wall thickness\u003c\/li\u003e\n  \u003cli\u003eWhether the tubing is reinforced\u003c\/li\u003e\n  \u003cli\u003eProcess liquid\u003c\/li\u003e\n  \u003cli\u003eLiquid viscosity\u003c\/li\u003e\n  \u003cli\u003ePresence of solids or suspended particles\u003c\/li\u003e\n  \u003cli\u003eRequired bubble detection sensitivity\u003c\/li\u003e\n  \u003cli\u003eMicrobubble detection requirement\u003c\/li\u003e\n  \u003cli\u003eFull \/ empty detection requirement\u003c\/li\u003e\n  \u003cli\u003eFoam detection requirement\u003c\/li\u003e\n  \u003cli\u003eRequired supply voltage\u003c\/li\u003e\n  \u003cli\u003eRequired electrical output or communication interface\u003c\/li\u003e\n  \u003cli\u003eATEX requirement, where applicable\u003c\/li\u003e\n  \u003cli\u003eRequired quantity\u003c\/li\u003e\n  \u003cli\u003eWhether the detector will be integrated with a single-use assembly\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the exact sensor configuration is not yet known, tubing dimensions and a\n  description of the process are usually sufficient as a starting point for\n  selection.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": 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Measurement takes place through the tubing wall.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can a bubble detector detect microbubbles?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable sensor configurations can detect small gas inclusions or microbubbles, with sensitivity adjusted according to the application.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What tubing materials can be used with a bubble detector?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Suitable clear tubing materials include silicone, TPE and PVC. Transparent reinforced tubing can also be monitored with suitable sensor configurations.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can a bubble sensor detect whether tubing is full or empty?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. 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The rigid metal enclosure supports the bag, tubing\n  and process connections and helps reduce the risk of mechanical\n  damage at very low temperatures.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The cassette is individually configured around the specific bag,\n  tubing layout and connectors. Standard configurations can accommodate\n  single-use bags from approximately 5 mL to 2 L, with larger sizes\n  available for custom applications.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Flexible single-use bags and tubing become more vulnerable to\n  mechanical stress when frozen. A rigid protection cassette provides\n  external support to the assembly and limits movement during freezing,\n  storage, handling and transport.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Internal form elements can be designed around the bag and fluid-path\n  geometry to secure the container, tubing and connectors. This is\n  particularly relevant for assemblies incorporating larger sterile\n  connectors or other components that require defined positioning.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The reusable metal construction is suitable for pharmaceutical\n  environments and can be cleaned between uses. Aluminum, stainless\n  steel and electropolished stainless-steel configurations are available.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The single-use bag assembly is placed inside the rigid cassette before\n  freezing. Internal contours and retaining features position the bag,\n  tubing and connectors so that movement is restricted during handling\n  and transportation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  As the product freezes, the cassette provides mechanical support around\n  the flexible assembly. This helps protect the bag and connection points\n  from impact, vibration and uncontrolled movement while the product is\n  in a frozen and potentially more fragile condition.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the freezing process, the cassette can be supplied with\n  openings in the housing to increase airflow around the bag or with a\n  closed housing where additional enclosure is preferred.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The flat cassette geometry is suitable for conventional freezer storage\n  and can also be configured for use with plate-freezing equipment.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Freeze bag protection cassettes are manufactured from metal rather\n  than disposable polymer materials. Available constructions include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\u003cstrong\u003eAluminum\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003e\u003cstrong\u003eStainless steel\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003e\u003cstrong\u003eElectropolished stainless steel\u003c\/strong\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Standard surfaces can be supplied cleaned and degreased, while\n  electropolished surfaces are available where a more refined stainless\n  steel surface is required.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The appropriate material should be selected according to handling,\n  cleaning, freezer environment, required durability and site-specific\n  operational requirements.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e A freeze bag protection cassette is\n  a mechanical handling and storage component and does not contain\n  filtration media. It therefore has no micron or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If the associated single-use assembly contains filtration components,\n  filter membrane and micron rating are specified separately as part of\n  the fluid-path configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Each cassette is configured around the required single-use bag and its\n  associated tubing and connection technology. The internal geometry can\n  therefore be adapted to the actual assembly rather than relying on a\n  universal cavity.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eBag size range\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard configurations are suitable for bag volumes from approximately\n  5 mL up to 2 L.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Typical supported volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e5 mL\u003c\/li\u003e\n  \u003cli\u003e50 mL\u003c\/li\u003e\n  \u003cli\u003e100 mL\u003c\/li\u003e\n  \u003cli\u003e250 mL\u003c\/li\u003e\n  \u003cli\u003e500 mL\u003c\/li\u003e\n  \u003cli\u003e1 L\u003c\/li\u003e\n  \u003cli\u003e2 L\u003c\/li\u003e\n  \u003cli\u003eLarger or custom bag sizes on request\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eTemperature capability\u003c\/h3\u003e\n\n\u003cp\u003e\n  The cassette is designed for pharmaceutical freezing applications at\n  temperatures down to approximately \u003cstrong\u003e−85°C and below\u003c\/strong\u003e.\n  Suitability of the complete system must also consider the bag film,\n  tubing, connectors and frozen product.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePerforated and closed designs\u003c\/h3\u003e\n\n\u003cp\u003e\n  Two principal housing concepts can be considered depending on the\n  freezing and transport process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003ePerforated or slotted housings\u003c\/strong\u003e allow increased air\n  circulation around the bag and can support efficient heat transfer\n  during freezing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eClosed housings\u003c\/strong\u003e provide a more enclosed cassette\n  construction and can help prevent materials such as dry-ice granulate\n  from entering the cassette during transport.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eBag, tubing and connector protection\u003c\/h3\u003e\n\n\u003cp\u003e\n  Internal contours can be designed to locate the bag and secure tubing\n  and process connections. This helps prevent components from moving\n  freely within the cassette during freezing, storage and transportation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Configurations can also accommodate relatively large sterile connectors\n  and other fluid-path components where sufficient internal space and\n  mechanical protection are required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical construction details\u003c\/h3\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eBag volume range\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Approx. 5 mL to 2 L, larger sizes on request\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eTemperature\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Down to approximately −85°C and below\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eMaterials\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Aluminum, stainless steel\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eSurface\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Cleaned and degreased; electropolished option available\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eSheet thickness\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Approx. 0.5–2.0 mm\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        \u003cstrong\u003eDimensional tolerances\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        According to DIN ISO 2768-cK\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003eIdentification and handling options\u003c\/h3\u003e\n\n\u003cp\u003e\n  Cassettes can be individually laser marked with identification such\n  as part numbers or QR codes. Sealing options can also be incorporated\n  where required for handling or traceability.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Dedicated freezer inserts, racks, holders and transport systems can\n  also be developed to accommodate multiple cassettes within a common\n  storage or logistics system.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cp\u003e\n  Freeze bag protection cassettes are intended for pharmaceutical and\n  biotechnology processes where frozen product must be stored or\n  transported in flexible single-use bags.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eDrug substance freezing\u003c\/li\u003e\n  \u003cli\u003eFrozen drug substance storage\u003c\/li\u003e\n  \u003cli\u003eFrozen pharmaceutical intermediate storage\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy processes\u003c\/li\u003e\n  \u003cli\u003eVaccine storage\u003c\/li\u003e\n  \u003cli\u003eCryogenic and low-temperature process handling\u003c\/li\u003e\n  \u003cli\u003eSingle-use freeze bag protection\u003c\/li\u003e\n  \u003cli\u003eFrozen product transportation\u003c\/li\u003e\n  \u003cli\u003eDry ice transportation\u003c\/li\u003e\n  \u003cli\u003ePlate freezer applications\u003c\/li\u003e\n  \u003cli\u003eConventional freezer storage\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eMechanical protection:\u003c\/strong\u003e\n    provides a rigid enclosure around flexible single-use bags,\n    tubing and connectors.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eLow-temperature capability:\u003c\/strong\u003e\n    designed for pharmaceutical applications at approximately\n    −85°C and below.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eApplication-specific design:\u003c\/strong\u003e\n    the internal geometry can be configured around the actual\n    bag assembly and connection layout.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eConnector protection:\u003c\/strong\u003e\n    internal contours can accommodate and secure larger sterile\n    connectors and other fluid-path components.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eReusable metal construction:\u003c\/strong\u003e\n    aluminum and stainless-steel cassettes can be cleaned and reused.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eDifferent freezing concepts:\u003c\/strong\u003e\n    perforated and closed housing configurations are available.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible freezer integration:\u003c\/strong\u003e\n    the flat design can be considered for conventional freezers\n    and plate-freezing systems.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eIdentification options:\u003c\/strong\u003e\n    laser marking with part numbers or QR codes can be incorporated.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Freeze bag protection cassettes are normally configured around the\n  actual bag assembly rather than selected only by nominal bag volume.\n  Bag dimensions, tubing routing and connector geometry all influence\n  the final cassette design.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following\n  information where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eBag manufacturer or bag drawing\u003c\/li\u003e\n  \u003cli\u003eNominal bag volume\u003c\/li\u003e\n  \u003cli\u003eFilled bag dimensions\u003c\/li\u003e\n  \u003cli\u003eBag film construction where relevant\u003c\/li\u003e\n  \u003cli\u003eTubing dimensions and routing\u003c\/li\u003e\n  \u003cli\u003eConnector types and dimensions\u003c\/li\u003e\n  \u003cli\u003eRequired minimum storage temperature\u003c\/li\u003e\n  \u003cli\u003eFreezing method\u003c\/li\u003e\n  \u003cli\u003eConventional freezer or plate freezer\u003c\/li\u003e\n  \u003cli\u003eStorage and transport method\u003c\/li\u003e\n  \u003cli\u003eDry ice transport requirement\u003c\/li\u003e\n  \u003cli\u003ePreferred cassette material\u003c\/li\u003e\n  \u003cli\u003ePerforated or closed housing\u003c\/li\u003e\n  \u003cli\u003eSurface-finish requirement\u003c\/li\u003e\n  \u003cli\u003eLaser marking or QR-code requirement\u003c\/li\u003e\n  \u003cli\u003eRack or multi-cassette handling requirement\u003c\/li\u003e\n  \u003cli\u003ePrototype quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Where no existing cassette design is available, a bag drawing or\n  physical bag assembly can provide the starting point for developing\n  a suitable protection system.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a freeze bag protection cassette?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A freeze bag protection cassette is a rigid reusable enclosure designed to support and protect pharmaceutical single-use bags, tubing and connectors during freezing, frozen storage and transportation.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What bag sizes can be used in a freeze protection cassette?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Standard configurations can accommodate single-use bags from approximately 5 mL up to 2 L. Larger custom bag sizes can also be considered.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What temperatures can a pharmaceutical freeze cassette withstand?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The cassette is designed for pharmaceutical freezing applications at temperatures down to approximately -85°C and below.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What materials are available for freeze bag protection cassettes?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available materials include aluminum and stainless steel, with electropolished stainless-steel surface options available where required.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the difference between perforated and closed freeze cassettes?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Perforated or slotted housings increase airflow around the bag during freezing, while closed housings provide a more enclosed design and can help prevent materials such as dry-ice granulate from entering the cassette.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can a freeze cassette be designed around a custom bag assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. The cassette can be configured around the specific bag, tubing layout and connector geometry so that the complete assembly is supported during freezing, storage and transportation.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"5 mL \/ Aluminum \/ Perforated \/ Slotted","offer_id":57319571620166,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"5 mL \/ Aluminum \/ Closed \/ Non-Perforated","offer_id":57319571652934,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"5 mL \/ Aluminum \/ Custom \/ To Be Specified","offer_id":57319571685702,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"5 mL \/ Stainless Steel \/ Perforated \/ Slotted","offer_id":57319571718470,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"5 mL \/ Stainless Steel \/ Closed \/ 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They combine a flexible process bag with an integrated mixing\n  element, inlet and outlet lines, sampling access and optional sensor\n  connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Mixing systems are available with different magnetic drive concepts to support\n  applications ranging from buffer and culture-media preparation to intermediate\n  product preparation and batch homogenisation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations cover nominal volumes from approximately\n  \u003cstrong\u003e20 L to 3,000 L\u003c\/strong\u003e. Tubing, connectors, powder ports, sampling\n  connections, sensors and other fluid-path components can be adapted to the\n  application.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Single-use mixing bags provide an alternative to reusable mixing vessels for\n  processes where a disposable product-contact path is preferred. The flexible\n  bag is installed in a compatible support container and connected to the\n  appropriate mixing drive.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Two principal mixing concepts are available:\n  \u003cstrong\u003emagnetically driven mixing\u003c\/strong\u003e for applications requiring\n  comparatively strong mixing action, and\n  \u003cstrong\u003emagnetic levitation mixing\u003c\/strong\u003e for applications where gentler,\n  lower-shear mixing is preferred.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard assemblies typically incorporate an inlet, bottom outlet, dedicated\n  sampling line and powder-addition port. Additional sensor interfaces, tubing,\n  connectors and filters can be configured according to the process.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The disposable mixing element is integrated into the bottom region of the\n  flexible bag. A reusable external drive transfers rotational energy to the\n  mixing element magnetically without requiring a conventional mechanical\n  shaft through the bag wall.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  As the impeller rotates, liquid circulates through the container and promotes\n  mixing throughout the bag volume.\n\u003c\/p\u003e\n\n\u003ch3\u003eMagnetic drive mixing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Magnetically driven impeller configurations provide strong mixing action and\n  are suitable for processes requiring effective liquid-liquid or solid-liquid\n  mixing. Typical reference rotational speeds depend on the selected impeller\n  and bag volume.\n\u003c\/p\u003e\n\n\u003ch3\u003eMagnetic levitation mixing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Magnetic levitation configurations suspend and drive the mixing element\n  magnetically. This provides a low-friction mixing concept that can be\n  considered for applications where gentler mixing and reduced mechanical\n  contact within the mixing system are desirable.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The appropriate mixing principle should be selected according to the process\n  fluid, required mixing intensity, shear sensitivity, powder-loading\n  requirements and batch volume.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard mixing bags use a multilayer co-extruded process film designed for\n  bioprocess fluid handling.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The film construction includes polymer layers based on:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eULDPE\u003c\/li\u003e\n  \u003cli\u003eEVA\u003c\/li\u003e\n  \u003cli\u003eEVOH barrier material\u003c\/li\u003e\n  \u003cli\u003eLDPE\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  This multilayer construction combines a suitable product-contact surface with\n  mechanical and gas-barrier properties required for bioprocess storage and\n  mixing applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Mixing-element materials depend on the selected mixing configuration and can\n  include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eHDPE\u003c\/li\u003e\n  \u003cli\u003ePolypropylene (PP)\u003c\/li\u003e\n  \u003cli\u003ePEEK components in suitable configurations\u003c\/li\u003e\n  \u003cli\u003eZirconia bearing components in certain mixing designs\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing and connection materials are configured separately according to the\n  fluid path and process requirements.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable to the mixing bag itself.\u003c\/strong\u003e A mixing bag is a\n  process container and mixing system rather than filtration media and therefore\n  has no micron or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where sterile filtration, vent filtration or another filtration step is\n  required, a suitable filter can be incorporated into the associated\n  single-use fluid path and specified separately.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Mixing bags are available in multiple impeller and drive configurations\n  covering small, intermediate and large production volumes.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eAvailable volumes\u003c\/h3\u003e\n\n\u003cp\u003e\n  Across the available mixing-system configurations, nominal bag volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e20 L\u003c\/li\u003e\n  \u003cli\u003e50 L\u003c\/li\u003e\n  \u003cli\u003e100 L\u003c\/li\u003e\n  \u003cli\u003e200 L\u003c\/li\u003e\n  \u003cli\u003e400 L\u003c\/li\u003e\n  \u003cli\u003e500 L\u003c\/li\u003e\n  \u003cli\u003e650 L\u003c\/li\u003e\n  \u003cli\u003e1,000 L\u003c\/li\u003e\n  \u003cli\u003e1,500 L\u003c\/li\u003e\n  \u003cli\u003e2,000 L\u003c\/li\u003e\n  \u003cli\u003e2,500 L\u003c\/li\u003e\n  \u003cli\u003e3,000 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Volume availability depends on the selected mixing technology and impeller\n  configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eWorking volume\u003c\/h3\u003e\n\n\u003cp\u003e\n  For complete mixing, the typical minimum working volume is approximately\n  \u003cstrong\u003e20% of the nominal bag volume\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  In applications where only a basic mixing effect is required, operation may\n  be possible at a lower volume provided that the liquid level sufficiently\n  covers the mixing element.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The maximum working volume can be up to approximately\n  \u003cstrong\u003e110% of nominal bag volume\u003c\/strong\u003e. Actual usable volume can be\n  influenced by air introduced during filling and by the required headspace.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eStandard fluid-path design\u003c\/h3\u003e\n\n\u003cp\u003e\n  A typical mixing bag configuration includes three process lines:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eOne inlet line\u003c\/li\u003e\n  \u003cli\u003eOne bottom outlet \/ drain line\u003c\/li\u003e\n  \u003cli\u003eOne dedicated sampling line\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  A \u003cstrong\u003e4-inch powder-addition port\u003c\/strong\u003e can be incorporated at the top\n  of the bag for introduction of media powder, buffer components or other dry\n  process materials.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eInlet and outlet tubing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard configurations use pharmaceutical-grade silicone tubing. Typical\n  standard dimensions include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003e50–200 L configurations:\u003c\/strong\u003e\n    3\/8\" ID × 5\/8\" OD silicone tubing\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003e500 L and larger configurations:\u003c\/strong\u003e\n    1\/2\" ID × 3\/4\" OD silicone tubing\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Typical inlet tubing length is approximately 150 cm. Outlet-line length can\n  vary according to bag volume, with longer drain lines available for\n  large-volume systems.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Different tubing materials, dimensions and lengths can be configured where\n  required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSampling line\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard configurations can incorporate a dedicated sampling line consisting\n  of approximately 20 cm of 1\/4\" ID × 7\/16\" OD silicone tubing with a\n  needle-free sampling valve.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Other sampling interfaces can be specified for custom configurations.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePowder addition\u003c\/h3\u003e\n\n\u003cp\u003e\n  A top-mounted sanitary powder port allows dry process materials to be\n  introduced directly into the mixing bag.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This configuration is particularly relevant for buffer and culture-media\n  preparation where powders must be dispersed and dissolved in the process\n  liquid.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSensor integration\u003c\/h3\u003e\n\n\u003cp\u003e\n  Sensor ports can be incorporated for online process monitoring.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available interface concepts can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eVertical threaded sensor ports\u003c\/li\u003e\n  \u003cli\u003eInclined threaded sensor ports\u003c\/li\u003e\n  \u003cli\u003eProtective sensor sleeves\u003c\/li\u003e\n  \u003cli\u003eHose-barb sensor ports\u003c\/li\u003e\n  \u003cli\u003ePG13.5-compatible interfaces\u003c\/li\u003e\n  \u003cli\u003eTemperature-sensor interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact sensor-port design depends on the measurement technology and mixing\n  system configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eOperating conditions\u003c\/h3\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003ctbody\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eNominal volume range\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Approx. 20 L to 3,000 L\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eTypical minimum mixing volume\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Approx. 20% of nominal volume\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eMaximum working volume\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Up to approx. 110% of nominal volume\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        \u003cstrong\u003eRecommended operating temperature\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Approx. 0°C to 40°C\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        \u003cstrong\u003eRecommended pH range\u003c\/strong\u003e\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        Approx. pH 2.5 to 11\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard mixing bags are supplied pre-sterilised and ready for integration\n  into the appropriate mixing system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Gamma sterilisation is performed using a validated irradiation range of\n  approximately \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Bags are individually protected using double-layer PE packaging.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Mixing bags are manufactured in controlled cleanroom production environments.\n  ISO Class 7 and ISO Class 8 production lines are used for suitable single-use\n  bag and assembly manufacturing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity and quality documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free material statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis \/ Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eBag integrity testing\u003c\/li\u003e\n  \u003cli\u003eSterility documentation\u003c\/li\u003e\n  \u003cli\u003eValidation documentation where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact conformity documentation should be confirmed for the selected bag,\n  mixing element and fluid-path configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eBuffer preparation\u003c\/li\u003e\n  \u003cli\u003eCulture-media preparation\u003c\/li\u003e\n  \u003cli\u003ePowder dissolution\u003c\/li\u003e\n  \u003cli\u003eSolid-liquid mixing\u003c\/li\u003e\n  \u003cli\u003eLiquid-liquid mixing\u003c\/li\u003e\n  \u003cli\u003eIntermediate-product preparation\u003c\/li\u003e\n  \u003cli\u003eBatch homogenisation\u003c\/li\u003e\n  \u003cli\u003eCombining liquid collections from different process batches\u003c\/li\u003e\n  \u003cli\u003eUpstream bioprocessing\u003c\/li\u003e\n  \u003cli\u003eDownstream bioprocessing\u003c\/li\u003e\n  \u003cli\u003eProcess-solution preparation\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eWide volume range:\u003c\/strong\u003e\n    mixing configurations cover applications from approximately 20 L\n    to 3,000 L.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple mixing technologies:\u003c\/strong\u003e\n    magnetic drive and magnetic levitation configurations allow the mixing\n    concept to be selected according to the process.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eLow-shear options:\u003c\/strong\u003e\n    magnetic levitation configurations can be selected for applications\n    requiring gentler mixing.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePowder addition:\u003c\/strong\u003e\n    suitable configurations incorporate a dedicated powder port for media,\n    buffer and other dry components.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eIntegrated sampling:\u003c\/strong\u003e\n    a dedicated sampling line can be incorporated without using the main\n    inlet or outlet.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eProcess monitoring:\u003c\/strong\u003e\n    sensor ports can be incorporated for online measurement.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom fluid path:\u003c\/strong\u003e\n    tubing, connectors, filters and sensor interfaces can be configured\n    according to the application.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePre-sterilised:\u003c\/strong\u003e\n    standard configurations are gamma irradiated and supplied ready for use.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Mixing-system selection should be based on the required batch volume,\n  process fluid and required mixing intensity rather than bag volume alone.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eNominal batch volume\u003c\/li\u003e\n  \u003cli\u003eMinimum operating volume\u003c\/li\u003e\n  \u003cli\u003eMaximum operating volume\u003c\/li\u003e\n  \u003cli\u003eLiquid-liquid or solid-liquid mixing requirement\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003ePowder type and approximate powder loading where applicable\u003c\/li\u003e\n  \u003cli\u003eRequired mixing time or process objective\u003c\/li\u003e\n  \u003cli\u003eShear sensitivity\u003c\/li\u003e\n  \u003cli\u003eProcess temperature\u003c\/li\u003e\n  \u003cli\u003eProcess pH\u003c\/li\u003e\n  \u003cli\u003eRequired inlet and outlet tubing\u003c\/li\u003e\n  \u003cli\u003eRequired process connectors\u003c\/li\u003e\n  \u003cli\u003ePowder-addition requirement\u003c\/li\u003e\n  \u003cli\u003eSampling requirement\u003c\/li\u003e\n  \u003cli\u003eRequired sensor interfaces\u003c\/li\u003e\n  \u003cli\u003eIntegrated filter requirement\u003c\/li\u003e\n  \u003cli\u003eExisting mixing hardware or support container where applicable\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the appropriate mixing technology has not yet been selected, the process\n  volume, liquid characteristics and mixing objective provide a suitable\n  starting point for technical selection.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a single-use mixing bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A single-use mixing bag is a disposable flexible bioprocess container with an integrated mixing element used for applications such as buffer preparation, culture-media preparation, liquid-liquid mixing and solid-liquid mixing.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What volumes are available for single-use mixing bags?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available mixing-system configurations cover nominal volumes from approximately 20 L to 3,000 L. Exact volume availability depends on the selected mixing technology and impeller configuration.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the difference between magnetic drive and magnetic levitation mixing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Magnetic drive configurations provide strong mixing action for demanding liquid-liquid and solid-liquid applications. Magnetic levitation systems provide a lower-friction and generally gentler mixing concept for applications where lower shear is preferred.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the minimum working volume of a single-use mixing bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"For complete mixing, a typical minimum working volume is approximately 20% of the nominal bag volume. Lower volumes may be possible where the liquid sufficiently covers the mixing element.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can powder be added directly to a single-use mixing bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable mixing-bag configurations incorporate a top-mounted powder port for introducing media powders, buffer components and other dry process materials.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can sensors be integrated into a single-use mixing bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. 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They provide the\n  sterile product-contact environment required for inoculation, feeding,\n  aeration, sampling, monitoring and harvesting without a reusable stainless\n  steel culture vessel forming the primary fluid-contact surface.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Configurations are available for both rocking-mode and stirred-tank\n  bioreactor systems, covering process development, seed train expansion\n  and larger-scale manufacturing applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the bioreactor platform, bags can incorporate optical pH and\n  dissolved-oxygen sensors, gas sparging, exhaust filtration, thermowells,\n  sampling lines, feed and harvest tubing and optional cell-retention\n  components for perfusion processes.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Rocking bioreactor bags are designed for installation on a rocking platform\n  where the movement of the tray generates mixing and gas transfer within the\n  flexible bag. Standard nominal bag volumes include 2 L, 10 L, 20 L and 50 L.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Stirred-tank single-use bioreactor bags are designed for larger-scale\n  cultivation and incorporate dedicated aeration, sensor and process-line\n  interfaces. Configurations cover nominal volumes from approximately\n  50 L to 2,000 L.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Both concepts can be configured around different cultivation strategies,\n  including seed expansion, batch, fed-batch and suitable perfusion processes.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003ch3\u003eRocking-mode bioreactor bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  The flexible bioreactor bag is installed on a compatible rocking platform.\n  Controlled rocking motion creates wave-induced circulation within the liquid,\n  providing mixing and supporting gas transfer without a conventional internal\n  stirred-tank impeller.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Rocking bags are particularly suited to smaller upstream volumes, seed train\n  expansion and applications where a compact single-use culture system is\n  preferred.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Configurations can range from a basic fluid-path design to systems with\n  integrated optical pH and dissolved-oxygen sensors. Perfusion configurations\n  can additionally incorporate a cell-retention membrane.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eStirred-tank bioreactor bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  Stirred-tank bioreactor bags are installed inside a compatible vessel or\n  support system and provide the disposable product-contact surface for\n  large-scale cell culture.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Gas is introduced through integrated sparging elements while dedicated\n  process lines provide inoculation, feed, sampling and harvest functions.\n  Exhaust gas is handled through a filtered exhaust line.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Integrated pH and dissolved-oxygen measurement interfaces support process\n  monitoring, while a thermowell provides a dedicated temperature-measurement\n  interface.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  The bioreactor bags are manufactured from a multilayer bioprocess film\n  developed for cell-culture applications requiring mechanical strength,\n  biocompatibility and compatibility with gamma sterilisation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The exact proprietary film formulation is configuration-specific and should\n  be confirmed as part of the technical documentation for the selected\n  bioreactor bag.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Additional fluid-path materials can include pharmaceutical-grade tubing,\n  polymer fittings, sensor interfaces, filters and connection components\n  selected according to the bioreactor configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable to the bioreactor bag itself.\u003c\/strong\u003e\n  The flexible bag is a cell-culture vessel rather than filtration media and\n  therefore does not have a filtration micron rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Stirred-tank configurations use dedicated gas-sparging elements. Available\n  aeration-hole sizes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e20 µm micro-sparging\u003c\/li\u003e\n  \u003cli\u003e0.5 mm macro-sparging\u003c\/li\u003e\n  \u003cli\u003e1 mm macro-sparging\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  These dimensions relate to aeration rather than liquid filtration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Perfusion configurations can also incorporate a cell-retention membrane.\n  Membrane selection should be specified separately according to the cell line,\n  cultivation mode and required retention performance.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003ch3\u003eRocking-mode configurations\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard rocking-mode bags are available in:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e2 L nominal volume\u003c\/li\u003e\n  \u003cli\u003e10 L nominal volume\u003c\/li\u003e\n  \u003cli\u003e20 L nominal volume\u003c\/li\u003e\n  \u003cli\u003e50 L nominal volume\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Nominal bag volume\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Minimum working volume\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Maximum working volume\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e0.2 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1 L\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e10 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e5 L\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e20 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e10 L\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e50 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e5 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e25 L\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003cp\u003e\n  Three principal rocking-mode configurations are available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eBasic:\u003c\/strong\u003e\n    standard process lines without integrated pH or dissolved-oxygen sensors.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eProcess monitoring:\u003c\/strong\u003e\n    configuration with integrated optical pH and dissolved-oxygen sensors.\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePerfusion:\u003c\/strong\u003e\n    process-monitoring configuration with an additional integrated\n    cell-retention membrane.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eOptical pH and dissolved-oxygen monitoring\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable rocking configurations can incorporate optical pH and dissolved\n  oxygen measurement.\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Parameter\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Control range\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Measurement range\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003epH\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e6.0–8.0\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e4.5–8.5\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003eDissolved oxygen\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e0–100%\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e0–250%\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003ePerfusion configurations\u003c\/h3\u003e\n\n\u003cp\u003e\n  Rocking bioreactor bags can be configured for perfusion culture using an\n  integrated cell-retention membrane.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This enables continuous or semi-continuous removal of spent medium while\n  retaining cells within the culture system. External hollow-fiber retention\n  concepts can also be considered depending on the process.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eStirred-tank configurations\u003c\/h3\u003e\n\n\u003cp\u003e\n  Stirred-tank single-use bioreactor bags are available across a scale range\n  from approximately 50 L to 2,000 L.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations incorporate process interfaces for:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eCell inoculation\u003c\/li\u003e\n  \u003cli\u003eMedia and nutrient feeding\u003c\/li\u003e\n  \u003cli\u003eSampling\u003c\/li\u003e\n  \u003cli\u003eProduct harvest\u003c\/li\u003e\n  \u003cli\u003eGas inlet and sparging\u003c\/li\u003e\n  \u003cli\u003eFiltered exhaust\u003c\/li\u003e\n  \u003cli\u003epH measurement\u003c\/li\u003e\n  \u003cli\u003eDissolved-oxygen measurement\u003c\/li\u003e\n  \u003cli\u003eTemperature measurement\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eAeration and sparging\u003c\/h3\u003e\n\n\u003cp\u003e\n  Stirred-tank configurations use dedicated aeration elements for gas delivery\n  into the culture.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available sparging concepts include combinations of micro- and macro-sparging,\n  with standard aeration-hole dimensions of 20 µm, 0.5 mm and 1 mm.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Sparger configuration and distribution are selected according to bioreactor\n  scale and process requirements such as oxygen transfer, carbon-dioxide\n  stripping, shear sensitivity and cell density.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProcess monitoring\u003c\/h3\u003e\n\n\u003cp\u003e\n  Stirred-tank configurations incorporate pH and dissolved-oxygen measurement\n  interfaces. Depending on vessel size, multiple sensor interfaces can be used\n  to support process monitoring.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A thermowell is also incorporated for process-temperature measurement.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePressure and exhaust management\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable configurations can incorporate a single-use pressure sensor and\n  dedicated filtered exhaust line.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Additional backup filtration or exhaust-port configurations can be included\n  where required by the process design.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Single-use bioreactor bags are supplied sterile and ready for installation\n  into the compatible bioreactor system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations are sterilised using gamma irradiation in the\n  \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e range and are individually protected using\n  double-layer PE packaging.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  The available bioreactor bags are manufactured under ISO Class 7 cleanroom\n  conditions and each bag is integrity tested prior to release.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available conformity and quality documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free material statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis \/ Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eBag integrity test documentation\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n  \u003cli\u003eValidation documentation where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact conformity and validation documentation should be confirmed for the\n  selected bioreactor platform and fluid-path configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSeed train expansion\u003c\/li\u003e\n  \u003cli\u003eBatch cell culture\u003c\/li\u003e\n  \u003cli\u003eFed-batch cell culture\u003c\/li\u003e\n  \u003cli\u003ePerfusion cell culture\u003c\/li\u003e\n  \u003cli\u003eSuspension cell culture\u003c\/li\u003e\n  \u003cli\u003eAdherent cell culture\u003c\/li\u003e\n  \u003cli\u003eCHO cell culture\u003c\/li\u003e\n  \u003cli\u003eHEK293 cell culture\u003c\/li\u003e\n  \u003cli\u003eBHK21 cell culture\u003c\/li\u003e\n  \u003cli\u003eHybridoma culture\u003c\/li\u003e\n  \u003cli\u003eSF9 insect-cell culture\u003c\/li\u003e\n  \u003cli\u003eVero cell culture\u003c\/li\u003e\n  \u003cli\u003eMonoclonal antibody production\u003c\/li\u003e\n  \u003cli\u003eVaccine manufacturing\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy processes\u003c\/li\u003e\n  \u003cli\u003eUpstream process development\u003c\/li\u003e\n  \u003cli\u003eCommercial upstream manufacturing\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple bioreactor platforms:\u003c\/strong\u003e\n    rocking-mode and stirred-tank bag configurations support different\n    upstream scales and cultivation strategies.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eScale range from development to manufacturing:\u003c\/strong\u003e\n    rocking bags cover small upstream volumes while stirred-tank\n    configurations extend to approximately 2,000 L.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eIntegrated process monitoring:\u003c\/strong\u003e\n    suitable configurations incorporate pH and dissolved-oxygen sensors.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePerfusion capability:\u003c\/strong\u003e\n    rocking bags can incorporate an integrated cell-retention membrane.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eControlled aeration:\u003c\/strong\u003e\n    stirred-tank configurations provide dedicated micro- and macro-sparging\n    options.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eComplete process fluid path:\u003c\/strong\u003e\n    inoculation, feeding, sampling, harvest and exhaust lines can be\n    incorporated into the disposable assembly.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePre-sterilised:\u003c\/strong\u003e\n    standard configurations are gamma irradiated and supplied ready for use.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSingle-use processing:\u003c\/strong\u003e\n    the disposable product-contact system reduces reliance on cleaning and\n    sterilisation of a reusable primary culture vessel.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Bioreactor bag selection should begin with the bioreactor platform and\n  required working volume rather than nominal bag size alone.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRocking-mode or stirred-tank bioreactor platform\u003c\/li\u003e\n  \u003cli\u003eExisting bioreactor equipment where applicable\u003c\/li\u003e\n  \u003cli\u003eNominal bag volume\u003c\/li\u003e\n  \u003cli\u003eMinimum working volume\u003c\/li\u003e\n  \u003cli\u003eMaximum working volume\u003c\/li\u003e\n  \u003cli\u003eCell line\u003c\/li\u003e\n  \u003cli\u003eSuspension or adherent culture\u003c\/li\u003e\n  \u003cli\u003eBatch, fed-batch or perfusion process\u003c\/li\u003e\n  \u003cli\u003eExpected cell density\u003c\/li\u003e\n  \u003cli\u003eRequired oxygen-transfer performance\u003c\/li\u003e\n  \u003cli\u003eCO₂ stripping requirement\u003c\/li\u003e\n  \u003cli\u003eShear-sensitivity considerations\u003c\/li\u003e\n  \u003cli\u003epH sensor requirement\u003c\/li\u003e\n  \u003cli\u003eDissolved-oxygen sensor requirement\u003c\/li\u003e\n  \u003cli\u003ePerfusion or cell-retention requirement\u003c\/li\u003e\n  \u003cli\u003eRequired feed lines\u003c\/li\u003e\n  \u003cli\u003eSampling configuration\u003c\/li\u003e\n  \u003cli\u003eHarvest configuration\u003c\/li\u003e\n  \u003cli\u003eRequired tubing and connectors\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype or qualification quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Where an existing bioreactor platform is already in use, equipment model,\n  required working volume and existing bag specification provide the best\n  starting point for technical review.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a single-use bioreactor bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A single-use bioreactor bag is a disposable sterile cell-culture vessel that provides the product-contact surface for upstream pharmaceutical and biotechnology processes.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sizes are available for single-use bioreactor bags?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Rocking-mode bioreactor bags are available in standard nominal volumes of 2 L, 10 L, 20 L and 50 L. Stirred-tank single-use bioreactor configurations are available from approximately 50 L to 2,000 L.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is the difference between rocking and stirred-tank single-use bioreactors?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Rocking bioreactor bags use controlled platform motion to generate mixing and are typically used at smaller upstream scales. Stirred-tank single-use bioreactor bags use a vessel-based system with dedicated aeration, monitoring and process interfaces for larger-scale cultivation.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can pH and dissolved oxygen sensors be integrated into a single-use bioreactor bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable rocking and stirred-tank configurations incorporate pH and dissolved-oxygen measurement interfaces for online cell-culture process monitoring.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can single-use bioreactor bags be used for perfusion culture?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Rocking-mode bioreactor bags are available with an integrated cell-retention membrane for suitable perfusion processes. External cell-retention systems can also be considered depending on the process.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Are single-use bioreactor bags supplied sterile?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Standard bioreactor bags are supplied sterile following gamma irradiation in the 25–45 kGy range and are individually protected in double-layer packaging.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"Rocking – 2 L \/ Standard Cell Culture \/ Batch \/ Fed-Batch","offer_id":57419007820102,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Rocking – 2 L \/ Standard Cell Culture \/ Perfusion","offer_id":57419007852870,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Rocking – 2 L \/ Standard Cell Culture \/ High Cell Density \/ Custom Process","offer_id":57419007885638,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Rocking – 2 L \/ Standard Cell Culture \/ To Be Specified","offer_id":57419007918406,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Rocking – 2 L \/ pH + DO Monitoring \/ Batch \/ 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Multi-sampling assemblies connect several sample\n  containers to a common process interface, allowing multiple samples to be\n  collected during different stages of a process or production run.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard bag-based configurations provide defined sample volumes and tubing\n  arrangements, while custom assemblies can be developed for applications\n  requiring different sample receivers, process connections, tubing dimensions\n  or numbers of sampling points.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The sampling assembly is connected to the process through a suitable sanitary,\n  sterile or aseptic interface. When a sample is required, the relevant fluid\n  path is opened and process liquid is transferred into the dedicated sample\n  container.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A single sampling bag normally receives one process sample and can then be\n  isolated from the process using the appropriate clamp, valve, tubing\n  disconnection method or connector.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Multi-sampling assemblies use a manifold to distribute the process line to\n  several individual sample bags. Each branch can be opened separately,\n  allowing sequential samples to be collected without replacing the complete\n  sampling assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Needle-free sampling valves can also be incorporated for controlled access to\n  specific sections of the assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard sampling bags use a multilayer bioprocess film suitable for\n  pharmaceutical fluid handling.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The film construction includes:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eULDPE fluid-contact layer\u003c\/strong\u003e for direct contact with the\n    process sample\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eEVOH gas-barrier layer\u003c\/strong\u003e\n  \u003c\/li\u003e\n  \u003cli\u003e\n    Intermediate polymer layers supporting the multilayer film construction\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Tubing options include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\u003cstrong\u003ePlatinum-cured silicone tubing\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003e\u003cstrong\u003eWeldable TPE tubing\u003c\/strong\u003e\u003c\/li\u003e\n  \u003cli\u003eApplication-specific tubing for custom assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The final material combination should be selected according to the process\n  fluid, temperature, sampling method, sterilisation requirements and required\n  validation documentation.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable to the sampling assembly itself.\u003c\/strong\u003e\n  Sampling bags and tubing are fluid-handling components and do not have a\n  filtration micron rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If sterile filtration, vent filtration or another filtration step is required\n  within the sampling fluid path, an appropriate filter can be incorporated and\n  specified separately.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Sampling assemblies are available as individual sampling bags, multi-sampling\n  manifolds and fully custom sampling configurations.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eIndividual sampling bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard sample volumes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e5 mL\u003c\/li\u003e\n  \u003cli\u003e50 mL\u003c\/li\u003e\n  \u003cli\u003e100 mL\u003c\/li\u003e\n  \u003cli\u003e250 mL\u003c\/li\u003e\n  \u003cli\u003e500 mL\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Small-volume sampling bags can be configured with one or more hose-barb ports\n  and with silicone or TPE tubing according to the required sampling method.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard port options include 1\/8\" and 1\/4\" hose-barb connections in\n  single-, double- and three-port layouts.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSmall-volume sampling lines\u003c\/h3\u003e\n\n\u003cp\u003e\n  Compact sampling assemblies can use 1\/8\" ID × 1\/4\" OD silicone or TPE tubing.\n  A typical 5 mL sampling configuration uses a male Luer Lock connection with\n  a protective plug.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Tubing length and connection technology can be modified where a different\n  distance from the process interface or different sampling method is required.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eMulti-sampling assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Multi-sampling assemblies combine several individual sample bags within one\n  manifold and provide a practical solution where multiple samples must be\n  collected from the same process connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations include:\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Configuration\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Sampling bags\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Tubing\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Additional container\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Standard 1\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        10 × 100 mL\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        1\/4\" ID × 7\/16\" OD TPE\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        2 L collection bag with vent filter\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Standard 2\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        15 × 50 mL\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        1\/8\" ID × 1\/4\" OD silicone\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        None\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        Standard 3\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        4 × 250 mL\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        1\/4\" ID × 7\/16\" OD silicone\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        None\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003cp\u003e\n  Custom assemblies can use a different number of sampling points, sample bag\n  volumes, tubing dimensions or branch arrangements.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSampling interfaces\u003c\/h3\u003e\n\n\u003cp\u003e\n  Available sampling and process interfaces can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eNeedle-free swabable valves\u003c\/li\u003e\n  \u003cli\u003eMale and female Luer Lock connections\u003c\/li\u003e\n  \u003cli\u003eSampling plugs\u003c\/li\u003e\n  \u003cli\u003eHose barb connections\u003c\/li\u003e\n  \u003cli\u003eSterile and aseptic connectors\u003c\/li\u003e\n  \u003cli\u003eQuick disconnect couplings\u003c\/li\u003e\n  \u003cli\u003eSanitary Tri-Clamp interfaces\u003c\/li\u003e\n  \u003cli\u003eWeldable tubing ends\u003c\/li\u003e\n  \u003cli\u003eCustom process connections\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eCustom sampling assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Where a standard sampling-bag configuration does not match the process,\n  a custom fluid path can be developed around the required process interface\n  and sampling procedure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Custom configurations can incorporate:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eDifferent quantities of sampling containers\u003c\/li\u003e\n  \u003cli\u003eDifferent sample volumes within one assembly\u003c\/li\u003e\n  \u003cli\u003eBag-based or suitable bottle-based sample collection\u003c\/li\u003e\n  \u003cli\u003eBranched sampling manifolds\u003c\/li\u003e\n  \u003cli\u003eDifferent tubing materials and dimensions\u003c\/li\u003e\n  \u003cli\u003eAdditional clamps and flow-control components\u003c\/li\u003e\n  \u003cli\u003eSterile connection technology\u003c\/li\u003e\n  \u003cli\u003eCustom labelling and sample identification\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eOperating conditions\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard sampling bags are suitable for a recommended operating-temperature\n  range of approximately \u003cstrong\u003e-80°C to 60°C\u003c\/strong\u003e and a recommended\n  process range of approximately \u003cstrong\u003epH 2.5 to 11\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitability for the actual process fluid and storage conditions should be\n  confirmed for the final assembly configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard sampling assemblies can be supplied pre-sterilised and ready to use\n  following gamma irradiation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The standard irradiation range is approximately\n  \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Configuration-to-order sampling bags can also be supplied non-sterile where\n  the final assembly or sterilisation strategy has not yet been defined.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Sampling bags are individually protected using double-layer PE packaging.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Sampling bags and assemblies are produced in controlled cleanroom\n  environments. Exact cleanroom classification depends on the selected\n  configuration and production route.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available quality and conformity documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free material statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis \/ Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eIntegrity-test documentation where applicable\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n  \u003cli\u003eValidation documentation where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact conformity documentation should be confirmed for the final sample bag,\n  tubing, connectors and other fluid-contact components.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAseptic process sampling\u003c\/li\u003e\n  \u003cli\u003eClosed process sampling\u003c\/li\u003e\n  \u003cli\u003eBioreactor sampling\u003c\/li\u003e\n  \u003cli\u003eCell-culture sampling\u003c\/li\u003e\n  \u003cli\u003eUpstream process monitoring\u003c\/li\u003e\n  \u003cli\u003eDownstream process monitoring\u003c\/li\u003e\n  \u003cli\u003eBuffer and media sampling\u003c\/li\u003e\n  \u003cli\u003eIntermediate-product sampling\u003c\/li\u003e\n  \u003cli\u003eSampling before and after filtration\u003c\/li\u003e\n  \u003cli\u003eBatch sampling\u003c\/li\u003e\n  \u003cli\u003eMultiple time-point sampling\u003c\/li\u003e\n  \u003cli\u003eQuality-control sample collection\u003c\/li\u003e\n  \u003cli\u003eSample storage and transport\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eDefined sample volumes:\u003c\/strong\u003e\n    standard individual sampling bags are available from 5 mL to 500 mL.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSingle and multi-sampling options:\u003c\/strong\u003e\n    one-time sampling bags and multi-point manifold systems can be selected\n    according to the process.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eClosed sampling capability:\u003c\/strong\u003e\n    sterile connection technology and dedicated sampling branches support\n    controlled sample collection from a closed process.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple tubing options:\u003c\/strong\u003e\n    silicone and weldable TPE tubing are available for different connection\n    and handling requirements.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible sampling interfaces:\u003c\/strong\u003e\n    needle-free valves, Luer connections, sterile connectors and other\n    interfaces can be incorporated.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom manifold design:\u003c\/strong\u003e\n    the number of sampling points, sample volumes and branch configuration can\n    be adapted to the sampling plan.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePre-sterilised options:\u003c\/strong\u003e\n    suitable configurations are gamma irradiated and supplied ready to use.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom engineering:\u003c\/strong\u003e\n    assemblies can be developed around existing process connections,\n    sampling procedures and sample-receiver requirements.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Sampling-system selection should begin with the required sample volume,\n  number of samples and process connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired sample volume\u003c\/li\u003e\n  \u003cli\u003eNumber of samples required per assembly\u003c\/li\u003e\n  \u003cli\u003eSingle or multi-sampling configuration\u003c\/li\u003e\n  \u003cli\u003eProcess application\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eProcess connection\u003c\/li\u003e\n  \u003cli\u003eTubing material\u003c\/li\u003e\n  \u003cli\u003eTubing ID and OD\u003c\/li\u003e\n  \u003cli\u003eRequired branch lengths\u003c\/li\u003e\n  \u003cli\u003eSampling valve or connector requirement\u003c\/li\u003e\n  \u003cli\u003eBag-based or bottle-based sample collection\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eRequired sample-storage temperature\u003c\/li\u003e\n  \u003cli\u003eSterilisation requirement\u003c\/li\u003e\n  \u003cli\u003eSample-labelling requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity or validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting sampling drawing or process sketch where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the final sampling manifold has not yet been defined, the required sample\n  volume, number of sampling points and process connection usually provide\n  enough information for an initial technical review.\n\u003c\/p\u003e\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is an aseptic single-use sampling assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"An aseptic single-use sampling assembly is a preconfigured disposable fluid path used to collect process samples through dedicated tubing, sample containers and connection technology while supporting controlled or closed process sampling.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sample volumes are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Standard single-use sampling bags are available in 5 mL, 50 mL, 100 mL, 250 mL and 500 mL volumes. Custom multi-sampling systems can combine multiple sample containers in one assembly.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can multiple samples be collected using one sampling assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Multi-sampling manifold assemblies connect several individual sampling bags to one process fluid path, allowing sequential samples to be collected from the same process connection.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What tubing materials can be used in sampling assemblies?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Common tubing options include platinum-cured silicone and weldable TPE. Tubing size, length and material can be selected according to the sampling application.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sampling connections are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available sampling interfaces can include needle-free swabable valves, Luer connections, sampling plugs, hose barbs, sterile connectors, aseptic connectors and sanitary process connections.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can sampling assemblies be supplied sterile?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable standard sampling assemblies are supplied gamma sterilised and ready to use. The standard irradiation range is approximately 25–45 kGy.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"Single Bag – 5 mL \/ Platinum-Cured Silicone \/ Male Luer Lock","offer_id":57419030659398,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false},{"title":"Single Bag – 5 mL \/ Platinum-Cured Silicone \/ Needle-Free Swabable Valve","offer_id":57419030692166,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Single Bag – 5 mL \/ Platinum-Cured Silicone \/ Sampling Plug","offer_id":57419030724934,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Single Bag – 5 mL \/ Platinum-Cured Silicone \/ Sterile \/ Aseptic Connector","offer_id":57419030757702,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Single Bag – 5 mL \/ Platinum-Cured Silicone \/ Custom \/ To Be 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Connector","offer_id":57419035017542,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom Sampling Assembly \/ Custom \/ To Be Specified \/ Custom \/ To Be Specified","offer_id":57419035050310,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/aseptic-single-use-sampling-assembly.webp?v=1790014284"},{"product_id":"single-use-filling-assemblies","title":"Custom Single-Use Filling Assemblies","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Custom single-use filling assemblies are preconfigured disposable fluid paths\n  designed for aseptic transfer and final filling of pharmaceutical and\n  biopharmaceutical products.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A typical filling assembly combines a sterile filling bag with pump tubing,\n  aseptic process connections and one or more disposable filling needles.\n  Standard configurations are available with 3 L and 5 L filling bags and\n  between 1 and 12 filling needles, while the complete fluid path can be\n  adapted to the filling process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filling assemblies can be configured for applications involving monoclonal\n  antibodies, vaccines, recombinant proteins, gene therapies, blood products\n  and other liquid pharmaceutical products.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  The filling bag acts as an intermediate product reservoir between the upstream\n  process and the filling machine. Product enters the bag through an aseptic\n  process connection and is transferred through dedicated pump tubing to one\n  or more filling needles.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The complete assembly can be supplied preassembled and gamma sterilised,\n  reducing the need to assemble individual tubing, connectors, bags and filling\n  needles at the point of use.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard filling-bag systems provide a defined starting configuration, while\n  tubing dimensions, inlet connections, number of filling lines, needle size\n  and other process interfaces can be configured according to the required\n  filling machine and dosage range.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  Bulk product is transferred into the single-use filling bag through the inlet\n  line. The bag functions as a temporary sterile reservoir immediately upstream\n  of the filling operation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Product is then transferred from the bag through dedicated pump tubing.\n  A peristaltic filling pump can control the volume delivered through each\n  filling line without introducing a reusable pump component into the\n  product-contact path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Each filling line terminates in a disposable filling needle. Needle internal\n  diameter is selected according to the required filling volume, product\n  properties and filling-machine configuration.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies can use a single filling needle or multiple parallel filling lines\n  where the equipment supports multi-head filling.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filling assemblies combine several product-contact materials selected\n  according to their function within the fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eMultilayer bioprocess film\u003c\/strong\u003e for the disposable filling bag\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePlatinum-cured silicone pump tubing\u003c\/strong\u003e for controlled\n    peristaltic filling\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003e316L stainless steel\u003c\/strong\u003e for the product-contact section of\n    suitable disposable filling needles\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePolysulfone (PSF)\u003c\/strong\u003e in suitable filling-needle components\n  \u003c\/li\u003e\n  \u003cli\u003e\n    Polymer aseptic connectors and fluid-path fittings according to the\n    selected assembly\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Alternative tubing and connection materials can be evaluated where required\n  by chemical compatibility, process conditions or an existing filling-machine\n  specification.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable to the filling assembly itself.\u003c\/strong\u003e\n  Filling bags, tubing and filling needles are fluid-transfer components and\n  therefore do not have a filtration micron rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A vent filter can be incorporated into suitable filling-bag configurations.\n  Where sterile product filtration is required upstream of final filling,\n  the required sterilising-grade filter can be specified separately as part\n  of the complete single-use fluid path.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003cp\u003e\n  Single-use filling assemblies can be based on standard filling-bag\n  configurations or developed as a customised final-filling fluid path.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eFilling bag volumes\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard filling bags are available in:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e3 L\u003c\/li\u003e\n  \u003cli\u003e5 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Other bag volumes can be considered for custom filling assemblies where the\n  standard reservoir volumes do not match the batch size or filling equipment.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eNumber of filling lines\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard filling bags can be configured with between\n  \u003cstrong\u003e1 and 12 filling needles\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The number of filling lines should be selected according to the filling\n  machine, number of pump channels, required throughput and container format.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eFilling needle sizes\u003c\/h3\u003e\n\n\u003cp\u003e\n  Disposable filling needles are available in several internal diameters to\n  support different dosage volumes.\n\u003c\/p\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Needle ID\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Needle OD\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Reference filling volume\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Reference accuracy\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e0.6 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2.0 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;0.1 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤2%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1.2 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1.7 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;0.5 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e1.6 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2.1 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;1.5 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2.1 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2.8 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;3 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3.0 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3.8 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;5 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e3.8 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e4.6 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;10 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e4.6 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e6.2 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\u0026gt;30 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e5.5 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e8.6 mm\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\u0026gt;50 mL\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e≤1%\u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\u003cp\u003e\n  These accuracy figures are reference values obtained from laboratory filling\n  tests using WFI. Actual filling accuracy depends on the complete filling\n  system, pump configuration, fluid characteristics, process parameters and\n  equipment settings.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eFilling needle design\u003c\/h3\u003e\n\n\u003cp\u003e\n  Available needle configurations include hose-barb and straight-end\n  connection designs depending on needle diameter and filling-system layout.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The product-contact needle section is manufactured from 316L stainless\n  steel. Filling is designed to take place from the bottom upwards, supporting\n  controlled liquid dispensing into the receiving container.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePump tubing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Platinum-cured silicone pump tubing can be incorporated between the filling\n  bag and disposable needles for use with peristaltic filling pumps.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Tubing dimensions and length should be selected according to the filling\n  machine, pump head, filling volume, required accuracy and number of filling\n  lines.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eBag ports and connections\u003c\/h3\u003e\n\n\u003cp\u003e\n  Filling bags can use low-residual-volume bag-port designs to support efficient\n  product recovery.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available process interfaces can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAseptic inlet connectors\u003c\/li\u003e\n  \u003cli\u003eTubing ports\u003c\/li\u003e\n  \u003cli\u003eLow-residual bag ports\u003c\/li\u003e\n  \u003cli\u003eDispensing connections\u003c\/li\u003e\n  \u003cli\u003eOptional vent filtration\u003c\/li\u003e\n  \u003cli\u003eCustom process interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eIntegration with filling equipment\u003c\/h3\u003e\n\n\u003cp\u003e\n  Filling-bag and needle configurations can be adapted for integration with\n  different pharmaceutical filling-machine platforms.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The required bag geometry, hanging-hole position, number of filling lines,\n  tubing routing and needle dimensions should therefore be specified according\n  to the actual filling equipment.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard filling-bag assemblies are supplied sterile following gamma\n  irradiation in the \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e range.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filling bags are individually protected in double PE packaging.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Disposable filling needles are available either pre-sterilised by gamma\n  irradiation or non-sterile for suitable steam sterilisation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable non-sterile needle configurations can be autoclaved for up to\n  approximately \u003cstrong\u003e90 minutes at 135°C\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Filling-system related products are produced in a controlled ISO Class 4.8\n  cleanroom environment. The filling bags are integrity tested before release.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free material statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis \/ Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n  \u003cli\u003eExtractables and leachables support where applicable\u003c\/li\u003e\n  \u003cli\u003eChemical-compatibility evaluation where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact documentation depends on the final bag, tubing, needle, connector\n  and fluid-path configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAseptic final filling\u003c\/li\u003e\n  \u003cli\u003eMonoclonal antibody filling\u003c\/li\u003e\n  \u003cli\u003eRecombinant protein filling\u003c\/li\u003e\n  \u003cli\u003eVaccine filling\u003c\/li\u003e\n  \u003cli\u003emRNA product filling\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy filling\u003c\/li\u003e\n  \u003cli\u003eLiquid injectable product filling\u003c\/li\u003e\n  \u003cli\u003eBlood-product filling\u003c\/li\u003e\n  \u003cli\u003ePre-lyophilisation filling\u003c\/li\u003e\n  \u003cli\u003eSterile bulk drug substance transfer\u003c\/li\u003e\n  \u003cli\u003eSmall-volume pharmaceutical filling\u003c\/li\u003e\n  \u003cli\u003eMulti-head filling processes\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eComplete disposable filling fluid path:\u003c\/strong\u003e\n    bag, tubing, process connections and filling needles can be supplied\n    as one configured system.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple filling lines:\u003c\/strong\u003e\n    standard configurations support between 1 and 12 disposable filling\n    needles.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eDefined needle sizes:\u003c\/strong\u003e\n    multiple needle diameters support a broad range of filling volumes.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePeristaltic pump compatibility:\u003c\/strong\u003e\n    platinum-cured silicone pump tubing can be integrated for controlled\n    filling.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eLow residual volume:\u003c\/strong\u003e\n    suitable bag-port configurations are designed to reduce retained product\n    after filling.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eEquipment-specific configuration:\u003c\/strong\u003e\n    bag geometry, tubing, hanging position and filling lines can be adapted\n    to the filling-machine layout.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePre-sterilised option:\u003c\/strong\u003e\n    standard filling assemblies can be supplied gamma sterilised and ready\n    for use.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom engineering:\u003c\/strong\u003e\n    the complete assembly can be configured around dosage volume, process\n    fluid and filling equipment.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Filling assemblies should be configured around the filling machine,\n  required dosage range and number of filling channels rather than the bag\n  volume alone.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eFilling machine manufacturer and model\u003c\/li\u003e\n  \u003cli\u003eRequired filling-bag volume\u003c\/li\u003e\n  \u003cli\u003eProduct or process fluid\u003c\/li\u003e\n  \u003cli\u003eMinimum filling volume\u003c\/li\u003e\n  \u003cli\u003eMaximum filling volume\u003c\/li\u003e\n  \u003cli\u003eTarget filling accuracy\u003c\/li\u003e\n  \u003cli\u003eNumber of filling needles\u003c\/li\u003e\n  \u003cli\u003eRequired filling-needle diameter\u003c\/li\u003e\n  \u003cli\u003eNeedle connection type\u003c\/li\u003e\n  \u003cli\u003ePump type and pump-head configuration\u003c\/li\u003e\n  \u003cli\u003ePump tubing dimensions\u003c\/li\u003e\n  \u003cli\u003eRequired tubing lengths\u003c\/li\u003e\n  \u003cli\u003eInlet process connection\u003c\/li\u003e\n  \u003cli\u003eVent-filter requirement\u003c\/li\u003e\n  \u003cli\u003eUpstream sterile-filtration requirement\u003c\/li\u003e\n  \u003cli\u003eRequired hanging-hole or bag-support geometry\u003c\/li\u003e\n  \u003cli\u003eSterilisation requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype or qualification quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting filling-system drawing or process sketch where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the final fluid path has not yet been defined, filling-machine model,\n  dosage range, number of filling heads and process-fluid information provide\n  a suitable starting point for technical configuration.\n\u003c\/p\u003e\n\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  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Other configurations can be evaluated for custom filling assemblies.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"How many filling needles can be incorporated into one assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Standard filling-bag configurations can incorporate between 1 and 12 filling needles depending on the filling-machine configuration.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What filling needle sizes are available?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available disposable filling-needle internal diameters range from approximately 0.6 mm to 5.5 mm. 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fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations are available for single filtration and redundant\n  filtration arrangements, while custom assemblies can be engineered around\n  the required filter train, wetting strategy, process connections and final\n  filling process.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  PUPSIT is used to verify the integrity of a sterilized sterilizing-grade\n  filter assembly before process filtration begins. The test is performed after\n  sterilization and before the filter is exposed to the product filtration step.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A PUPSIT assembly provides the tubing, filters, containers and process\n  interfaces required to wet, test and subsequently use the sterilizing-grade\n  filter within a controlled single-use fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the filtration strategy, the assembly can contain a single\n  sterilizing-grade filter, serial filtration stages or a redundant\n  sterilizing-filter arrangement.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  The sterilizing-grade filter is first prepared using an appropriate wetting\n  liquid and then connected to an integrity-testing system.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A validated non-destructive integrity test is performed before product\n  filtration. Suitable test methods can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eDiffusive-flow testing\u003c\/li\u003e\n  \u003cli\u003eBubble-point testing\u003c\/li\u003e\n  \u003cli\u003ePressure-hold testing where appropriate\u003c\/li\u003e\n  \u003cli\u003eOther validated integrity-test methods suitable for the selected filter\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The applicable integrity-test method and acceptance criteria must correlate\n  with the microbial-retention capability established during filter validation.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  After a successful pre-use integrity test, the filtration fluid path can be\n  prepared for process filtration according to the validated operating\n  procedure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Following product filtration, the sterilizing-grade filter is normally\n  integrity tested again using the validated post-use integrity-test method.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePUPSIT and EU GMP Annex 1\u003c\/h3\u003e\n\n\u003cp\u003e\n  EU GMP Annex 1 states that the integrity of the sterilized filter assembly\n  should be verified by integrity testing before use to check for damage or\n  loss of integrity caused during filter preparation and sterilization.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Annex 1 also requires a non-destructive integrity test after use for a\n  sterilizing-grade filter used to sterilize a fluid.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The guidance recognizes that PUPSIT may not always be possible because of\n  process constraints. Where an alternative approach is used, this should be\n  supported by a thorough risk assessment and appropriate controls.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard PUPSIT configurations combine several fluid-contact materials,\n  each selected according to its function within the filtration assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Typical standard components include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePES membrane\u003c\/strong\u003e for the sterilizing-grade liquid filter\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePTFE membrane\u003c\/strong\u003e for hydrophobic gas filtration\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003ePlatinum-cured silicone tubing\u003c\/strong\u003e\n  \u003c\/li\u003e\n  \u003cli\u003e\n    Single-use process bags selected according to the required fluid volume\n  \u003c\/li\u003e\n  \u003cli\u003e\n    Polymer aseptic connectors, fittings and instrumentation components\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Reinforced silicone tubing can also be incorporated where a section of the\n  assembly requires increased pressure capability.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Alternative filter membranes, tubing materials, bag constructions and\n  connection technologies can be evaluated for custom assemblies.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard PUPSIT configurations use:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003e0.2 µm PES sterilizing-grade liquid filter\u003c\/strong\u003e\n  \u003c\/li\u003e\n  \u003cli\u003e\n    \u003cstrong\u003e0.2 µm hydrophobic PTFE gas filter\u003c\/strong\u003e\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  A standard sterilizing-grade capsule configuration is available with an\n  effective filtration area of approximately \u003cstrong\u003e660 cm²\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A standard hydrophobic gas-filter configuration is available with an\n  effective filtration area of approximately \u003cstrong\u003e640 cm²\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Other filter sizes, filtration areas and membrane materials can be selected\n  for custom PUPSIT assemblies according to required batch volume, flow rate,\n  product compatibility and validated filtration parameters.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003ch3\u003eSingle-filter PUPSIT assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  A single-filter configuration is designed around one sterilizing-grade\n  process filter together with the required wetting, testing, venting and\n  process-transfer fluid paths.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This configuration can be used where the validated sterile-filtration\n  process contains a single final sterilizing-grade filter.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSerial filtration assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Serial filtration configurations can incorporate a bioburden-reduction or\n  prefiltration stage upstream of the final sterilizing-grade filter.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Filter selection and integrity-testing requirements must be defined according\n  to the function of each filtration stage and the validated process.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eRedundant sterilizing-filter assemblies\u003c\/h3\u003e\n\n\u003cp\u003e\n  Redundant filtration configurations use two sterilizing-grade filters within\n  the filtration train.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where both filters form part of the validated sterilizing filtration\n  strategy, the integrity-testing arrangement must allow the applicable filters\n  to be tested according to the validated PUPSIT procedure.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSingle-use bag integration\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard PUPSIT configurations are available with:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e500 mL single-use bag\u003c\/li\u003e\n  \u003cli\u003e5 L single-use bag\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Other bag volumes can be incorporated into custom assemblies according to the\n  required wetting-liquid volume, flushing procedure and filtration process.\n\u003c\/p\u003e\n\n\n\u003ch3\u003ePressure monitoring\u003c\/h3\u003e\n\n\u003cp\u003e\n  Single-use pressure sensors, pressure gauges or instrumentation tees can be\n  incorporated at suitable positions within the assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Pressure monitoring can support integrity testing and process control while\n  helping confirm that the assembly remains within the validated operating\n  limits of the selected filters and tubing.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTubing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Platinum-cured silicone tubing is used in standard configurations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Reinforced silicone tubing can be incorporated where higher pressure\n  resistance is required. Tubing dimensions and lengths can be configured\n  around the required flow, filter connections, integrity tester and filling\n  equipment.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eConnection technology\u003c\/h3\u003e\n\n\u003cp\u003e\n  PUPSIT assemblies can incorporate:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eAseptic and sterile connectors\u003c\/li\u003e\n  \u003cli\u003eSanitary Tri-Clamp connections\u003c\/li\u003e\n  \u003cli\u003eHose barb fittings\u003c\/li\u003e\n  \u003cli\u003eTee, cross and Y fittings\u003c\/li\u003e\n  \u003cli\u003eInstrumentation tees\u003c\/li\u003e\n  \u003cli\u003eTubing clamps\u003c\/li\u003e\n  \u003cli\u003ePressure-sensor interfaces\u003c\/li\u003e\n  \u003cli\u003eConnections to integrity-testing equipment\u003c\/li\u003e\n  \u003cli\u003eCustom process interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eWetting strategy\u003c\/h3\u003e\n\n\u003cp\u003e\n  The integrity-test procedure can be designed around a suitable validated\n  wetting liquid.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the filter and process, this can include WFI or the process\n  liquid itself.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Wetting-fluid selection affects the integrity-test procedure, acceptance\n  criteria, flushing requirements and potential product dilution and should\n  therefore be defined as part of process validation.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard PUPSIT assemblies are supplied sterile and ready for integration\n  into the filtration process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations are gamma irradiated using an irradiation range of\n  \u003cstrong\u003e25–45 kGy\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Assemblies are individually protected using double-layer PE packaging.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For custom assemblies, gamma compatibility must be confirmed for every\n  component incorporated into the final fluid path.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProduction and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable PUPSIT assemblies are produced and assembled in controlled cleanroom\n  environments, with ISO Class 4.8 production available for PUPSIT assemblies.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Each finished assembly is integrity tested prior to release.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eCertificate of Analysis or Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eBatch traceability\u003c\/li\u003e\n  \u003cli\u003eFilter validation documentation\u003c\/li\u003e\n  \u003cli\u003eExtractables data where applicable\u003c\/li\u003e\n  \u003cli\u003eSystem design information\u003c\/li\u003e\n  \u003cli\u003eApplication and operating documentation\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity information\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information where applicable\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact conformity, validation and integrity-test documentation depends on the\n  filters and components selected for the final assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eFinal sterile filtration\u003c\/li\u003e\n  \u003cli\u003eSterilizing-grade filtration prior to aseptic filling\u003c\/li\u003e\n  \u003cli\u003ePre-Use Post-Sterilization Integrity Testing\u003c\/li\u003e\n  \u003cli\u003eFinal filling filtration systems\u003c\/li\u003e\n  \u003cli\u003eBiopharmaceutical manufacturing\u003c\/li\u003e\n  \u003cli\u003eMonoclonal antibody processing\u003c\/li\u003e\n  \u003cli\u003eVaccine manufacturing\u003c\/li\u003e\n  \u003cli\u003eRecombinant protein processing\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy manufacturing\u003c\/li\u003e\n  \u003cli\u003eSmall-molecule sterile pharmaceutical processing\u003c\/li\u003e\n  \u003cli\u003eSingle-use sterile filtration trains\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eDesigned for PUPSIT:\u003c\/strong\u003e\n    the fluid path is configured specifically for integrity testing of\n    sterilized sterilizing-grade filters before use.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eStandard and custom configurations:\u003c\/strong\u003e\n    single-filter, serial and redundant filtration strategies can be supported.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eIntegrated filtration:\u003c\/strong\u003e\n    sterilizing-grade liquid filters and hydrophobic gas filters can be\n    incorporated within one assembly.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePressure monitoring:\u003c\/strong\u003e\n    pressure sensors and instrumentation interfaces can be incorporated where\n    required.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eClosed single-use fluid path:\u003c\/strong\u003e\n    bags, tubing, filters and aseptic connections can be supplied as one\n    preassembled filtration system.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003ePre-sterilised supply:\u003c\/strong\u003e\n    standard assemblies are gamma irradiated and supplied ready for use.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFlexible process integration:\u003c\/strong\u003e\n    tubing, filter size, bag volume and connection technology can be configured\n    around the existing integrity tester and filtration process.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eEU GMP Annex 1 support:\u003c\/strong\u003e\n    the assembly architecture can support implementation of a validated PUPSIT\n    strategy for sterilizing-grade filtration.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  PUPSIT assemblies should be configured around the complete sterile filtration\n  process rather than the filter alone.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSingle, serial or redundant filtration strategy\u003c\/li\u003e\n  \u003cli\u003eProcess application\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eRequired sterilizing-grade membrane\u003c\/li\u003e\n  \u003cli\u003eRequired micron rating\u003c\/li\u003e\n  \u003cli\u003eRequired filtration area\u003c\/li\u003e\n  \u003cli\u003eExpected batch volume\u003c\/li\u003e\n  \u003cli\u003eRequired process flow rate\u003c\/li\u003e\n  \u003cli\u003eMaximum operating pressure\u003c\/li\u003e\n  \u003cli\u003eIntegrity-test method\u003c\/li\u003e\n  \u003cli\u003eIntegrity tester manufacturer and model\u003c\/li\u003e\n  \u003cli\u003eWetting liquid\u003c\/li\u003e\n  \u003cli\u003eRequired wetting or flush volume\u003c\/li\u003e\n  \u003cli\u003eSingle-use bag volume\u003c\/li\u003e\n  \u003cli\u003eTubing ID and OD\u003c\/li\u003e\n  \u003cli\u003eRequired tubing lengths\u003c\/li\u003e\n  \u003cli\u003eProcess connection types\u003c\/li\u003e\n  \u003cli\u003ePressure-sensor requirement\u003c\/li\u003e\n  \u003cli\u003eFinal filling equipment connection\u003c\/li\u003e\n  \u003cli\u003eSterilisation requirement\u003c\/li\u003e\n  \u003cli\u003eRequired validation documentation\u003c\/li\u003e\n  \u003cli\u003eExisting filtration drawing or process sketch where available\u003c\/li\u003e\n  \u003cli\u003ePrototype or qualification quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the complete assembly has not yet been defined, the filtration strategy,\n  filter specification, integrity-test method and existing process connections\n  provide a suitable starting point for technical design.\n\u003c\/p\u003e\n\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a PUPSIT assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A PUPSIT assembly is a single-use filtration fluid path designed to support Pre-Use Post-Sterilization Integrity Testing of a sterilized sterilizing-grade filter before product filtration.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What filter configurations can be used for PUPSIT?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"PUPSIT assemblies can be configured for a single sterilizing-grade filter, serial filtration with an upstream filtration stage, or redundant sterilizing-grade filtration.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What filters are used in a standard single-use PUPSIT assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A standard configuration can incorporate a 0.2 micron PES sterilizing-grade liquid filter and a 0.2 micron hydrophobic PTFE gas filter. Other filter configurations can be specified for custom assemblies.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Which filter integrity tests can be used for PUPSIT?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Depending on the filter and validated process, non-destructive integrity testing can include methods such as diffusive-flow, bubble-point or pressure-hold testing.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can pressure sensors be incorporated into a PUPSIT assembly?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Single-use pressure sensors, instrumentation tees and other monitoring components can be incorporated according to the integrity-test and sterile-filtration process.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can PUPSIT assemblies be supplied sterile?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Standard assemblies can be supplied preassembled and gamma sterilised using an irradiation range of approximately 25–45 kGy.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"PUPSIT Test Assembly \/ 500 mL \/ No Pressure Sensor","offer_id":57419221139782,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"PUPSIT Test Assembly \/ 500 mL \/ Single-Use Pressure Sensor","offer_id":57419221172550,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"PUPSIT Test Assembly \/ 500 mL \/ Custom Instrumentation \/ To Be Specified","offer_id":57419221205318,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"PUPSIT Test Assembly \/ 5 L \/ No Pressure Sensor","offer_id":57419221238086,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"PUPSIT Test Assembly \/ 5 L \/ Single-Use Pressure 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The product-contact layer is based on EVA,\n  providing flexibility and resistance to the mechanical stresses associated\n  with freezing and thawing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard configurations are available from small-volume 30 mL bags through\n  12 L freeze-thaw systems. Larger configurations incorporate a protective\n  shell that supports the bag, tubing and connections during freezing,\n  handling, storage and transport.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  Freezing a liquid inside a flexible bioprocess bag creates mechanical stress\n  as the liquid expands and the film becomes less flexible at low temperature.\n  A dedicated freeze-thaw system is therefore designed around both the flexible\n  container and the protection required during frozen handling.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Small-volume configurations are available as standalone bags, while larger\n  2 L, 6 L and 12 L systems integrate the bag with a protective structure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Tubing and process connections can be configured for filling, draining,\n  sterile connection and transfer before or after the freeze-thaw process.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  Process fluid is transferred into the flexible bag through the configured\n  inlet connection. The bag is then positioned correctly within its protective\n  system before freezing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  During freezing, the bag and fluid path remain supported to reduce uncontrolled\n  movement and mechanical impact. The protective structure also provides fixed\n  locations for the tubing and connections.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Once frozen, the complete system can be stored or transported under the\n  validated low-temperature conditions of the process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  During thawing, the frozen product is allowed to return to the required\n  processing temperature using the validated thawing procedure. Product can\n  subsequently be transferred through the existing tubing and connections\n  without transferring the frozen material to another container.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Standard freeze-thaw bags use a\n  \u003cstrong\u003e360 µm multilayer co-extruded freeze-resistant film\u003c\/strong\u003e\n  manufactured using a blown-film process.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The construction uses an\n  \u003cstrong\u003eEVA product-contact layer\u003c\/strong\u003e, selected for flexibility and\n  low-temperature performance.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Tubing and fluid-path options can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eEVA tubing for suitable small-volume configurations\u003c\/li\u003e\n  \u003cli\u003eWeldable TPE tubing\u003c\/li\u003e\n  \u003cli\u003eSilicone tubing for suitable custom configurations\u003c\/li\u003e\n  \u003cli\u003eAseptic connection technology\u003c\/li\u003e\n  \u003cli\u003eQuick-connect process connections\u003c\/li\u003e\n  \u003cli\u003eLuer connections for small-volume systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Final material selection should be confirmed against the process fluid,\n  freezing temperature, thawing conditions and required connection technology.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e Freeze-thaw bags are storage and fluid-handling\n  containers rather than filtration media and therefore do not have a micron\n  or pore-size rating.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Where filtration is required before filling or after thawing, a suitable\n  filtration assembly can be connected or incorporated into the overall\n  single-use fluid path.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\u003ch3\u003eAvailable volumes\u003c\/h3\u003e\n\n\u003cp\u003e\n  Published freeze-thaw bag configurations include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e30 mL\u003c\/li\u003e\n  \u003cli\u003e60 mL\u003c\/li\u003e\n  \u003cli\u003e100 mL\u003c\/li\u003e\n  \u003cli\u003e2 L\u003c\/li\u003e\n  \u003cli\u003e6 L\u003c\/li\u003e\n  \u003cli\u003e12 L\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  The currently standard selectable configurations include 30 mL, 100 mL,\n  2 L, 6 L and 12 L. Other volumes should be confirmed during configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSmall-volume freeze-thaw bags\u003c\/h3\u003e\n\n\u003cp\u003e\n  30 mL and 100 mL configurations are available without an external protective\n  shell and are intended for small-volume frozen storage applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable configurations can use EVA tubing with Luer connections for compact\n  filling and transfer fluid paths.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eIntegrated protected freeze-thaw systems\u003c\/h3\u003e\n\n\u003cp\u003e\n  The 2 L, 6 L and 12 L configurations combine the flexible freeze-thaw bag\n  with an external protective structure.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The protection system helps:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSupport the flexible bag during freezing\u003c\/li\u003e\n  \u003cli\u003eProtect the frozen bag during handling\u003c\/li\u003e\n  \u003cli\u003eFix tubing and connections in defined positions\u003c\/li\u003e\n  \u003cli\u003eReduce impact on the frozen fluid container\u003c\/li\u003e\n  \u003cli\u003eSupport stacking during storage\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Up to four suitable systems can be stacked to improve utilisation of frozen\n  storage space.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eDimensions\u003c\/h3\u003e\n\n\u003ctable style=\"width:100%; border-collapse:collapse; margin:24px 0;\"\u003e\n  \u003cthead\u003e\n    \u003ctr\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Volume\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Configuration\n      \u003c\/th\u003e\n      \u003cth style=\"text-align:left; padding:10px; border-bottom:1px solid #ddd;\"\u003e\n        Approximate dimensions\n      \u003c\/th\u003e\n    \u003c\/tr\u003e\n  \u003c\/thead\u003e\n\n  \u003ctbody\u003e\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e2 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Bag + protective shell\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        430 × 360 × 122 mm\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e6 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        Bag + protective shell\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px; border-bottom:1px solid #eee;\"\u003e\n        605 × 480 × 128 mm\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n\n    \u003ctr\u003e\n      \u003ctd style=\"padding:10px;\"\u003e12 L\u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        Bag + protective shell\n      \u003c\/td\u003e\n      \u003ctd style=\"padding:10px;\"\u003e\n        690 × 530 × 130 mm\n      \u003c\/td\u003e\n    \u003c\/tr\u003e\n  \u003c\/tbody\u003e\n\u003c\/table\u003e\n\n\n\u003ch3\u003eTubing and connection options\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard configurations include several tubing and process-connection\n  concepts.\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    EVA tubing with 1\/4\" female Luer Lock and matching closure for\n    suitable small-volume systems\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    3\/8\" ID × 5\/8\" OD TPE tubing with quick-connect interfaces\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    3\/8\" ID × 5\/8\" OD TPE tubing with aseptic connectors\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    Custom silicone or TPE fluid paths where required\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact tubing length, number of lines and connection technology can be adapted\n  to the filling, storage and post-thaw transfer process.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eOperating temperature\u003c\/h3\u003e\n\n\u003cp\u003e\n  The freeze-thaw system is designed for low-temperature applications down to\n  approximately \u003cstrong\u003e-80°C\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For normal freeze-thaw process applications, a working range of approximately\n  \u003cstrong\u003e-80°C to 40°C\u003c\/strong\u003e should be used as the initial design range.\n  Any requirement above this range should be technically confirmed for the\n  complete bag, tubing and connection configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eFrozen transport and handling\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable freeze-thaw configurations are designed not only for freezing and\n  storage but also for low-temperature transport.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Performance testing for the system includes:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e-80°C freezing testing\u003c\/li\u003e\n  \u003cli\u003eTransport testing\u003c\/li\u003e\n  \u003cli\u003eStacking testing\u003c\/li\u003e\n  \u003cli\u003eDrop testing under frozen conditions\u003c\/li\u003e\n  \u003cli\u003eSimulated manual-handling drop testing\u003c\/li\u003e\n  \u003cli\u003eISTA-3A transport testing\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  These tests support evaluation of the complete protection concept during\n  frozen handling and distribution.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eIntegrity testing\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard freeze-thaw bags are subject to 100% leak testing prior to release.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Integrity requirements for a custom assembly should be confirmed for the\n  complete bag, tubing and connection configuration.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation and supply condition\u003c\/h3\u003e\n\n\u003cp\u003e\n  The published standard freeze-thaw bag configurations are supplied\n  \u003cstrong\u003enon-sterile\u003c\/strong\u003e.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Custom configurations with aseptic connection technology are available.\n  Where a sterile or irradiated assembly is required, compatibility and\n  sterilisation conditions should be confirmed for the complete assembly\n  before specification.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProduction and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Standard freeze-thaw bags are manufactured in a controlled\n  \u003cstrong\u003eISO Class 4.8 cleanroom\u003c\/strong\u003e environment and are produced for\n  use in cGMP manufacturing processes.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available quality and conformity documentation can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP \u0026lt;788\u0026gt; Particulate Matter\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;87\u0026gt; Cytotoxicity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;88\u0026gt; Biological Reactivity\u003c\/li\u003e\n  \u003cli\u003eUSP \u0026lt;85\u0026gt; bacterial endotoxin information\u003c\/li\u003e\n  \u003cli\u003eFDA 21 CFR 177–182 material conformity information\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free material statements\u003c\/li\u003e\n  \u003cli\u003eTSE \/ BSE documentation\u003c\/li\u003e\n  \u003cli\u003eCertificate of Analysis or Certificate of Quality\u003c\/li\u003e\n  \u003cli\u003eIntegrity-test documentation\u003c\/li\u003e\n  \u003cli\u003eFreeze, transport and handling validation documentation where applicable\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact documentation should be confirmed for the final bag and fluid-path\n  configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eFrozen drug substance storage\u003c\/li\u003e\n  \u003cli\u003eBiopharmaceutical intermediate storage\u003c\/li\u003e\n  \u003cli\u003eBulk biological product storage\u003c\/li\u003e\n  \u003cli\u003eMonoclonal antibody storage\u003c\/li\u003e\n  \u003cli\u003eVaccine intermediate storage\u003c\/li\u003e\n  \u003cli\u003eRecombinant protein storage\u003c\/li\u003e\n  \u003cli\u003eBlood-product processing\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy processing\u003c\/li\u003e\n  \u003cli\u003eLow-temperature process-fluid storage\u003c\/li\u003e\n  \u003cli\u003eFreeze-thaw process development\u003c\/li\u003e\n  \u003cli\u003eFrozen product transport\u003c\/li\u003e\n  \u003cli\u003eCold-chain bioprocess logistics\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eDesigned for low-temperature processing:\u003c\/strong\u003e\n    dedicated multilayer film supports freezing applications down to\n    approximately -80°C.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eEVA product-contact layer:\u003c\/strong\u003e\n    the freeze-resistant film construction provides flexibility for repeated\n    freezing and thawing conditions.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eProtected large-volume configurations:\u003c\/strong\u003e\n    2 L, 6 L and 12 L systems combine the bag and protective structure.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eTubing protection:\u003c\/strong\u003e\n    tubing and connections can be fixed within the protective structure to\n    reduce movement during frozen handling.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eStackable design:\u003c\/strong\u003e\n    suitable protected systems can be stacked to improve frozen-storage\n    utilisation.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eFrozen transport capability:\u003c\/strong\u003e\n    system performance has been evaluated through transport, stacking,\n    freezing and drop testing.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple connection options:\u003c\/strong\u003e\n    Luer, quick-connect and aseptic connection configurations are available.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eCustom fluid paths:\u003c\/strong\u003e\n    tubing material, dimensions and process connections can be configured\n    around filling and post-thaw transfer requirements.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Freeze-thaw bag selection should be based on working volume, freezing\n  temperature, storage method and handling requirements rather than nominal\n  bag volume alone.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eRequired working volume\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eMinimum freezing temperature\u003c\/li\u003e\n  \u003cli\u003eMaximum thawing temperature\u003c\/li\u003e\n  \u003cli\u003eNumber of expected freeze-thaw cycles\u003c\/li\u003e\n  \u003cli\u003eStatic storage or frozen transport requirement\u003c\/li\u003e\n  \u003cli\u003eRequired tubing material\u003c\/li\u003e\n  \u003cli\u003eTubing ID and OD\u003c\/li\u003e\n  \u003cli\u003eRequired tubing lengths\u003c\/li\u003e\n  \u003cli\u003eInlet and outlet connection types\u003c\/li\u003e\n  \u003cli\u003eAseptic connection requirement\u003c\/li\u003e\n  \u003cli\u003eRequired protective shell or handling system\u003c\/li\u003e\n  \u003cli\u003eFreezer type and available dimensions\u003c\/li\u003e\n  \u003cli\u003eStorage and stacking requirements\u003c\/li\u003e\n  \u003cli\u003eSterilisation requirement\u003c\/li\u003e\n  \u003cli\u003eRequired conformity and validation documentation\u003c\/li\u003e\n  \u003cli\u003ePrototype or qualification quantity\u003c\/li\u003e\n  \u003cli\u003eEstimated annual demand\u003c\/li\u003e\n  \u003cli\u003eExisting freeze-thaw specification or process drawing where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the final system has not yet been defined, working volume, minimum\n  temperature, process fluid and required process connections provide a\n  suitable starting point for technical selection.\n\u003c\/p\u003e\n\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a single-use freeze-thaw bag?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A single-use freeze-thaw bag is a flexible disposable bioprocess container designed for freezing, frozen storage, thawing and low-temperature transport of pharmaceutical and biopharmaceutical process fluids.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What volumes are available for single-use freeze-thaw bags?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Published configurations include 30 mL, 60 mL, 100 mL, 2 L, 6 L and 12 L. Currently selectable standard configurations include 30 mL, 100 mL, 2 L, 6 L and 12 L.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What temperature can single-use freeze-thaw bags withstand?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"The freeze-thaw system is designed for low-temperature applications down to approximately -80°C. The complete bag, tubing and connection configuration should be reviewed for the required freezing and thawing temperatures.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Which freeze-thaw bag sizes include a protective shell?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Standard 2 L, 6 L and 12 L freeze-thaw systems incorporate a protective structure around the flexible bag. Smaller 30 mL and 100 mL configurations are available without this external shell.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What connections are available for freeze-thaw bags?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available configurations include Luer connections, quick-connect interfaces and aseptic connectors. Tubing and process connections can also be customised for the application.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can single-use freeze-thaw bags be used for frozen transport?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable protected freeze-thaw systems are designed for low-temperature transport and have been evaluated through freezing, transport, stacking and frozen-condition drop testing.\"\n      }\n    }\n  ]\n}\n\u003c\/script\u003e","brand":"Filtra International","offers":[{"title":"30 mL – Bag Only \/ EVA Tubing + 1\/4\" Female Luer Lock","offer_id":57419704435014,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"30 mL – Bag Only \/ 3\/8\" ID × 5\/8\" OD TPE + Quick Connectors","offer_id":57419704467782,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"30 mL – Bag Only \/ 3\/8\" ID × 5\/8\" OD TPE + Aseptic Connectors","offer_id":57419704500550,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"30 mL – Bag Only \/ Custom \/ To Be Specified","offer_id":57419704533318,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"100 mL – Bag Only \/ EVA Tubing + 1\/4\" Female Luer 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Female Luer Lock","offer_id":57419704959302,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"12 L – Bag + Protective Shell \/ 3\/8\" ID × 5\/8\" OD TPE + Quick Connectors","offer_id":57419704992070,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"12 L – Bag + Protective Shell \/ 3\/8\" ID × 5\/8\" OD TPE + Aseptic Connectors","offer_id":57419705024838,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"12 L – Bag + Protective Shell \/ Custom \/ To Be Specified","offer_id":57419705057606,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ To Be Specified \/ EVA Tubing + 1\/4\" Female Luer Lock","offer_id":57419705090374,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ To Be Specified \/ 3\/8\" ID × 5\/8\" OD TPE + Quick Connectors","offer_id":57419705123142,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ To Be Specified \/ 3\/8\" ID × 5\/8\" OD TPE + Aseptic Connectors","offer_id":57419705155910,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Custom \/ To Be Specified \/ Custom \/ To Be Specified","offer_id":57419705188678,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0975\/2985\/6326\/files\/single-use-freeze-thaw-bags.webp?v=1790017517"},{"product_id":"single-use-sterile-aseptic-connectors","title":"Sterile \u0026 Aseptic Connectors for Single-Use Bioprocessing","description":"\u003ch2\u003eProduct description\u003c\/h2\u003e\n\n\u003cp\u003e\n  Sterile and aseptic connectors are used to join separate single-use fluid\n  paths while maintaining the required process boundary in pharmaceutical\n  and biotechnology applications.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Connection technologies are available for applications ranging from\n  small-volume cell and gene therapy processes to production-scale transfer\n  of buffers, media, intermediates and bulk pharmaceutical liquids.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available configurations include small-bore and standard sterile connectors,\n  genderless connector systems, male\/female sterile connectors, high-flow\n  connectors, sterile disconnect couplings and interfaces for connecting\n  pre-sterilised single-use assemblies to steam-sterilised stainless-steel\n  equipment.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Hose barb connections range from approximately 1\/16\" through 1 1\/2\",\n  with sanitary Tri-Clamp interfaces available for suitable configurations.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\n\u003cp\u003e\n  A sterile connector allows two previously separated fluid paths to be joined\n  without requiring open handling of the internal product-contact surfaces.\n  Suitable designs use protective barriers that remain in position until the\n  connector halves have been mechanically joined.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Different connector geometries are available according to tubing size,\n  process volume, flow requirement, sterilisation strategy and whether the\n  connection must subsequently be disconnected.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Genderless designs use identical mating halves, simplifying component\n  selection within complex single-use assemblies. Male\/female connector\n  systems are also available where an established process already uses that\n  connection architecture.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\n\u003cp\u003e\n  A sterile connection system typically consists of two protected connector\n  halves. The connector halves are first mechanically joined while the sterile\n  barriers continue to isolate the internal fluid path from the surrounding\n  environment.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Once the mechanical connection has been secured, the protective barrier\n  membranes are removed according to the connector-specific operating\n  procedure. This opens a continuous fluid path between the two pre-sterilised\n  systems.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  This principle allows separately prepared bags, tubing assemblies, filters,\n  bottles or other process systems to be connected during operation without\n  requiring a tube welder for the connection.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Other connection technologies provide specific functions such as sterile\n  disconnection or transition between a steam-sterilised stainless-steel system\n  and a pre-sterilised single-use assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\n\u003cp\u003e\n  Materials depend on the required connector function and sterilisation method.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Common connector materials include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n\u003cstrong\u003ePolycarbonate\u003c\/strong\u003e for many sterile and aseptic connector housings\u003c\/li\u003e\n  \u003cli\u003e\n\u003cstrong\u003ePlatinum-cured silicone\u003c\/strong\u003e for suitable internal seals\u003c\/li\u003e\n  \u003cli\u003e\n\u003cstrong\u003ePolysulfone\u003c\/strong\u003e for higher-temperature and sterile-disconnect applications\u003c\/li\u003e\n  \u003cli\u003eApplication-specific polymer seals and internal valve components\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Suitable connector families are available with USP Class VI and\n  pharmaceutical material-conformity documentation. Exact conformity,\n  animal-derived component statements and validation documentation depend on\n  the selected connector family and configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\n\u003cp\u003e\n  \u003cstrong\u003eNot applicable.\u003c\/strong\u003e Sterile connectors and couplings are\n  fluid-path connection components and do not contain filtration media.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  If sterile filtration is required within the same process, a suitable capsule\n  filter can be incorporated separately into the single-use assembly.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\n\n\u003ch3\u003eSmall-bore sterile connectors\u003c\/h3\u003e\n\n\u003cp\u003e\n  Small-bore genderless sterile connectors are available for low-volume fluid\n  paths where conventional bioprocess connector dimensions would be unnecessarily\n  large.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard hose barb sizes include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\/16\"\u003c\/li\u003e\n  \u003cli\u003e3\/32\"\u003c\/li\u003e\n  \u003cli\u003e1\/8\"\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  These configurations are suitable for tubing with internal diameters from\n  approximately 1.6 mm to 3.2 mm and are particularly relevant to small-volume\n  bioprocess, cell and gene therapy and sampling applications.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eStandard genderless sterile connectors\u003c\/h3\u003e\n\n\u003cp\u003e\n  Genderless sterile connectors provide identical mating interfaces on both\n  sides of the connection. This eliminates the need to manage separate male\n  and female connector halves within the same connector family.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard connection sizes can include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/4\" hose barb\u003c\/li\u003e\n  \u003cli\u003e3\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/2\" hose barb\u003c\/li\u003e\n  \u003cli\u003e3\/4\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\" hose barb\u003c\/li\u003e\n  \u003cli\u003e3\/4\" Tri-Clamp\u003c\/li\u003e\n  \u003cli\u003e1 1\/2\" Tri-Clamp\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  This provides a scalable connection concept from relatively small tubing\n  assemblies through production-scale transfer systems.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eMale \/ female sterile connectors\u003c\/h3\u003e\n\n\u003cp\u003e\n  Male\/female sterile connection systems are also available for processes where\n  this connection architecture is already established.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Common process interfaces include 3\/8\" and 1\/2\" hose barbs together with\n  sanitary Tri-Clamp configurations.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard and higher-temperature versions can be selected according to the\n  required sterilisation method.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eHigh-flow sterile connectors\u003c\/h3\u003e\n\n\u003cp\u003e\n  High-flow genderless connectors provide a larger internal flow path for\n  production-scale transfer applications where reducing connection restriction\n  is important.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Available high-flow process connections include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1 1\/4\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1 1\/2\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1 1\/2\" Tri-Clamp\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  These connectors are suitable for high-volume buffer, media, intermediate\n  and bulk-product transfer applications.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterile disconnect couplings\u003c\/h3\u003e\n\n\u003cp\u003e\n  Sterile disconnect couplings provide controlled separation of a fluid path\n  after processing.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Internal valves automatically close the fluid path when the coupling halves\n  are separated, helping reduce product leakage and protecting the disconnected\n  system from external contamination.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard hose barb configurations include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\/4\"\u003c\/li\u003e\n  \u003cli\u003e3\/8\"\u003c\/li\u003e\n  \u003cli\u003e1\/2\"\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Valved female and male couplings are available, together with suitable\n  non-valved configurations, caps and closure plugs.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable sterile disconnect configurations are rated from vacuum up to\n  approximately 8.6 bar. The complete tubing assembly must also be suitable\n  for the required process pressure.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSteam-to-single-use connections\u003c\/h3\u003e\n\n\u003cp\u003e\n  Steam-compatible transition connectors provide an interface between\n  steam-sterilised stainless-steel process equipment and a pre-sterilised\n  single-use assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  The connector incorporates separate interfaces for the stainless-steel\n  process system, steam exhaust and the downstream single-use fluid path.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  During the SIP cycle, the stainless-steel equipment and connection interface\n  are exposed to steam while the pre-sterilised single-use side remains\n  isolated. After the sterilisation cycle, the connector is activated to open\n  the sterile product path into the single-use assembly.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard connection combinations include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e3\/4\" sanitary process connections\u003c\/li\u003e\n  \u003cli\u003e1 1\/2\" sanitary process connections\u003c\/li\u003e\n  \u003cli\u003e3\/8\" hose barb to the single-use fluid path\u003c\/li\u003e\n  \u003cli\u003e1\/2\" hose barb to the single-use fluid path\u003c\/li\u003e\n  \u003cli\u003e3\/4\" Tri-Clamp single-use-side configurations\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003ch3\u003eQuick-disconnect couplings\u003c\/h3\u003e\n\n\u003cp\u003e\n  Quick-disconnect couplings can also be incorporated into single-use fluid\n  paths where rapid mechanical connection and disconnection is required but\n  creation of a new sterile connection in a non-sterile environment is not\n  required.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Standard tubing interfaces cover approximately:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003e1\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/4\" hose barb\u003c\/li\u003e\n  \u003cli\u003e3\/8\" hose barb\u003c\/li\u003e\n  \u003cli\u003e1\/2\" hose barb\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Polycarbonate configurations are suitable for many gamma-sterilised\n  single-use systems, while polysulfone configurations provide additional\n  temperature capability for suitable autoclave processes.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  A standard quick coupling should not be treated as equivalent to an aseptic\n  connector where a sterile connection must be established in an uncontrolled\n  environment.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSterilisation compatibility\u003c\/h3\u003e\n\n\u003cp\u003e\n  Sterilisation capability depends on the selected connector family.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Suitable sterile connector configurations are available for:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eGamma irradiation up to approximately 50 kGy\u003c\/li\u003e\n  \u003cli\u003eAutoclave processing with suitable high-temperature configurations\u003c\/li\u003e\n  \u003cli\u003eSteam-in-place connection to stainless-steel equipment\u003c\/li\u003e\n  \u003cli\u003ePre-sterilised ready-to-use single-use assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Certain polycarbonate sterile connector configurations can be autoclaved up\n  to approximately 130°C for 60 minutes. Suitable sterile disconnect\n  configurations can withstand approximately 132°C for 60 minutes.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Sterilisation limits must always be confirmed for the selected connector and\n  complete single-use assembly rather than applied universally to all\n  connection technologies.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eSingle-use assembly integration\u003c\/h3\u003e\n\n\u003cp\u003e\n  Sterile connectors can be incorporated directly into:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSingle-use tubing assemblies\u003c\/li\u003e\n  \u003cli\u003eBioprocess bag assemblies\u003c\/li\u003e\n  \u003cli\u003eBottle assemblies\u003c\/li\u003e\n  \u003cli\u003eSampling assemblies\u003c\/li\u003e\n  \u003cli\u003eFiltration assemblies\u003c\/li\u003e\n  \u003cli\u003ePUPSIT assemblies\u003c\/li\u003e\n  \u003cli\u003eFilling assemblies\u003c\/li\u003e\n  \u003cli\u003eBioreactor fluid paths\u003c\/li\u003e\n  \u003cli\u003eMedia and buffer transfer sets\u003c\/li\u003e\n  \u003cli\u003eCustom manifolds\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Connector selection can therefore be considered as part of the complete\n  fluid-path design rather than as an isolated component.\n\u003c\/p\u003e\n\n\n\u003ch3\u003eProduction and documentation\u003c\/h3\u003e\n\n\u003cp\u003e\n  Suitable sterile connector families are available from controlled\n  ISO Class 7 cleanroom production and packaging environments.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  Depending on the selected connector family, available documentation can\n  include:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eUSP Class VI material conformity\u003c\/li\u003e\n  \u003cli\u003eFDA-related material conformity information\u003c\/li\u003e\n  \u003cli\u003eBSE \/ TSE statements\u003c\/li\u003e\n  \u003cli\u003eAnimal-derived component-free statements\u003c\/li\u003e\n  \u003cli\u003eCertificate of Conformance\u003c\/li\u003e\n  \u003cli\u003eValidation documentation\u003c\/li\u003e\n  \u003cli\u003eExtractables data where available\u003c\/li\u003e\n  \u003cli\u003eGamma sterilisation compatibility information\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  Exact documentation should be confirmed for the selected connector and final\n  assembly configuration.\n\u003c\/p\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSterile fluid transfer\u003c\/li\u003e\n  \u003cli\u003eAseptic connection of independent single-use assemblies\u003c\/li\u003e\n  \u003cli\u003eBag-to-bag transfer\u003c\/li\u003e\n  \u003cli\u003eBag-to-vessel transfer\u003c\/li\u003e\n  \u003cli\u003eBottle and container connections\u003c\/li\u003e\n  \u003cli\u003eBuffer and media transfer\u003c\/li\u003e\n  \u003cli\u003eCell-culture fluid paths\u003c\/li\u003e\n  \u003cli\u003eCell and gene therapy processing\u003c\/li\u003e\n  \u003cli\u003eSampling assemblies\u003c\/li\u003e\n  \u003cli\u003eSterile filtration systems\u003c\/li\u003e\n  \u003cli\u003ePUPSIT assemblies\u003c\/li\u003e\n  \u003cli\u003eFill \u0026amp; Finish\u003c\/li\u003e\n  \u003cli\u003eBulk drug substance transfer\u003c\/li\u003e\n  \u003cli\u003eUpstream processing\u003c\/li\u003e\n  \u003cli\u003eDownstream processing\u003c\/li\u003e\n  \u003cli\u003eSterile disconnection\u003c\/li\u003e\n  \u003cli\u003eStainless-steel to single-use transfer\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\n\u003cul\u003e\n  \u003cli\u003e\n    \u003cstrong\u003eBroad connection range:\u003c\/strong\u003e\n    connection technologies cover fluid paths from approximately 1\/16\"\n    small-bore tubing through 1 1\/2\" high-flow applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eGenderless options:\u003c\/strong\u003e\n    identical mating halves simplify connector management within complex\n    single-use systems.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSmall-volume configurations:\u003c\/strong\u003e\n    dedicated connectors are available for low-volume tubing and cell and gene\n    therapy applications.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eHigh-flow configurations:\u003c\/strong\u003e\n    large-bore connectors support production-scale pharmaceutical liquid\n    transfer.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eSterile disconnect capability:\u003c\/strong\u003e\n    valved coupling technology allows controlled separation of process lines.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eHybrid process integration:\u003c\/strong\u003e\n    steam-compatible connection technology enables transition between\n    stainless-steel equipment and pre-sterilised single-use fluid paths.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eMultiple sterilisation strategies:\u003c\/strong\u003e\n    suitable configurations are available for gamma irradiation,\n    autoclaving and SIP-based processes.\n  \u003c\/li\u003e\n\n  \u003cli\u003e\n    \u003cstrong\u003eAssembly integration:\u003c\/strong\u003e\n    connectors can be incorporated directly into ready-to-use tubing, bag,\n    bottle, filtration and filling assemblies.\n  \u003c\/li\u003e\n\u003c\/ul\u003e\n\n\n\u003chr\u003e\n\n\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\n\u003cp\u003e\n  Connector selection should begin with the required connection function,\n  tubing size and sterilisation strategy.\n\u003c\/p\u003e\n\n\u003cp\u003e\n  For technical configuration and quotation, provide the following information\n  where available:\n\u003c\/p\u003e\n\n\u003cul\u003e\n  \u003cli\u003eSterile connection or sterile disconnection requirement\u003c\/li\u003e\n  \u003cli\u003eGenderless or male\/female connection preference\u003c\/li\u003e\n  \u003cli\u003eTubing material\u003c\/li\u003e\n  \u003cli\u003eTubing ID and OD\u003c\/li\u003e\n  \u003cli\u003eRequired hose barb or sanitary connection size\u003c\/li\u003e\n  \u003cli\u003eProcess fluid\u003c\/li\u003e\n  \u003cli\u003eExpected flow rate\u003c\/li\u003e\n  \u003cli\u003eMaximum operating pressure\u003c\/li\u003e\n  \u003cli\u003eOperating temperature\u003c\/li\u003e\n  \u003cli\u003eGamma irradiation requirement\u003c\/li\u003e\n  \u003cli\u003eAutoclave requirement\u003c\/li\u003e\n  \u003cli\u003eSIP interface requirement\u003c\/li\u003e\n  \u003cli\u003eNeed for sterile disconnection after processing\u003c\/li\u003e\n  \u003cli\u003eIntegration into a tubing, bag, bottle or other assembly\u003c\/li\u003e\n  \u003cli\u003eRequired validation and conformity documentation\u003c\/li\u003e\n  \u003cli\u003eEstimated annual quantity\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003e\n  If the exact connector technology has not yet been selected, the tubing\n  dimensions, process function and sterilisation method normally provide enough\n  information for an initial technical selection.\n\u003c\/p\u003e\n\n\n\u003cscript type=\"application\/ld+json\"\u003e\n{\n  \"@context\": \"https:\/\/schema.org\",\n  \"@type\": \"FAQPage\",\n  \"mainEntity\": [\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a sterile connector for single-use bioprocessing?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A sterile connector joins two separately prepared single-use fluid paths while maintaining the required sterile process boundary. Suitable designs allow the connection to be made without a tube welder.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What sizes are available for single-use sterile connectors?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Available connector technologies cover small-bore tubing from approximately 1\/16 inch through high-flow connections up to 1 1\/2 inch. Exact sizes depend on the connector family.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"What is a genderless sterile connector?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"A genderless sterile connector uses identical compatible mating halves rather than separate male and female connector components. This can simplify component selection and inventory within single-use assemblies.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can sterile connectors be gamma sterilised?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. Suitable sterile connector configurations are compatible with gamma irradiation up to approximately 50 kGy. Compatibility should be confirmed for the selected connector and complete assembly.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can a single-use tubing line be disconnected aseptically?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Suitable sterile disconnect couplings use internal valves that close automatically when the coupling halves are separated, supporting controlled separation of the fluid path.\"\n      }\n    },\n    {\n      \"@type\": \"Question\",\n      \"name\": \"Can a single-use assembly be connected to steam-sterilised stainless-steel equipment?\",\n      \"acceptedAnswer\": {\n        \"@type\": \"Answer\",\n        \"text\": \"Yes. 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Each material provides different characteristics for fluid transfer, sterile welding, pumping, pressure resistance and process compatibility.\u003c\/p\u003e\n\u003cp\u003eTubing can be supplied as individual lengths or incorporated into complete single-use assemblies with sterile connectors, fittings, filters, bags, bottles and process instrumentation.\u003c\/p\u003e\n\u003ch3\u003eTechnical overview\u003c\/h3\u003e\n\u003cp\u003eTubing selection should be based on more than internal diameter alone. Material compatibility, wall thickness, pump requirements, pressure, sterilisation method, connection technology and the required flexibility of the fluid path all influence the appropriate tubing construction.\u003c\/p\u003e\n\u003cp\u003ePlatinum-cured silicone provides a flexible and transparent fluid path for general pharmaceutical transfer and pumping. Weldable TPE allows tubing sections to be aseptically welded and heat sealed. Dedicated pump tubing is designed for extended use in peristaltic pumping applications, while braided silicone provides increased pressure capability where conventional unreinforced tubing is insufficient.\u003c\/p\u003e\n\u003chr\u003e\n\u003ch2\u003eOperating principle\u003c\/h2\u003e\n\u003cp\u003eProcess fluid flows through the internal bore of the flexible tubing between the connected process components.\u003c\/p\u003e\n\u003cp\u003eIn gravity- or pressure-driven transfer applications, tubing acts as the flexible connection between containers, equipment and other unit operations.\u003c\/p\u003e\n\u003cp\u003eIn peristaltic pumping applications, the tubing is repeatedly compressed between the pump rollers and pump housing. Tubing construction and wall thickness are therefore important for maintaining flow performance and tubing life.\u003c\/p\u003e\n\u003cp\u003eWeldable TPE tubing provides an additional function: compatible tubing sections can be joined using suitable sterile tube-welding equipment or permanently closed using a compatible tube sealer.\u003c\/p\u003e\n\u003cp\u003eReinforced tubing uses an integrated textile braid to restrict radial expansion under pressure, allowing higher working pressures while retaining the flexibility of silicone.\u003c\/p\u003e\n\u003chr\u003e\n\u003ch2\u003eMaterial options\u003c\/h2\u003e\n\u003ch3\u003ePlatinum-cured silicone tubing\u003c\/h3\u003e\n\u003cp\u003eClear platinum-cured silicone tubing provides high flexibility and allows visual observation of process liquid, bubbles and other conditions within the fluid path.\u003c\/p\u003e\n\u003cp\u003eIt is suitable for:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eGeneral pharmaceutical fluid transfer\u003c\/li\u003e\n\u003cli\u003eMedia and buffer transfer\u003c\/li\u003e\n\u003cli\u003eCell-culture processes\u003c\/li\u003e\n\u003cli\u003ePeristaltic pumping\u003c\/li\u003e\n\u003cli\u003eFilling applications\u003c\/li\u003e\n\u003cli\u003eSingle-use tubing assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eStandard silicone tubing is suitable for ETO treatment, autoclaving and gamma sterilisation. Published material documentation includes USP Class VI, ISO 10993, FDA 21 CFR 177.2600 and animal-derived ingredient-free information.\u003c\/p\u003e\n\u003ch3\u003eWeldable TPE tubing\u003c\/h3\u003e\n\u003cp\u003eWeldable thermoplastic elastomer tubing is designed for single-use processes requiring sterile tube welding and heat sealing.\u003c\/p\u003e\n\u003cp\u003eCompatible tubing sections can be connected using suitable sterile tube welders without introducing a separate connector into the fluid path. The tubing can also be permanently sealed using compatible thermal sealing equipment.\u003c\/p\u003e\n\u003cp\u003eTypical applications include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSingle-use fluid-transfer assemblies\u003c\/li\u003e\n\u003cli\u003eAseptic connection and disconnection\u003c\/li\u003e\n\u003cli\u003eSampling assemblies\u003c\/li\u003e\n\u003cli\u003eFilling systems\u003c\/li\u003e\n\u003cli\u003eCell-culture processes\u003c\/li\u003e\n\u003cli\u003eFermentation\u003c\/li\u003e\n\u003cli\u003ePeristaltic pumping\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe clear tubing construction allows visual monitoring of the fluid path. Available material documentation includes USP Class VI, ISO 10993, REACH, RoHS and animal-derived component-free information.\u003c\/p\u003e\n\u003ch3\u003ePeristaltic pump tubing\u003c\/h3\u003e\n\u003cp\u003eDedicated pump tubing is manufactured from a thermoplastic elastomer formulated for repeated compression in peristaltic tubing pumps.\u003c\/p\u003e\n\u003cp\u003eCompared with general transfer tubing, this construction is intended to provide extended pump life, chemical resistance, low spallation and flexibility during demanding pumping applications.\u003c\/p\u003e\n\u003cp\u003eThe tubing is opaque, which can also provide additional protection for light-sensitive process fluids.\u003c\/p\u003e\n\u003cp\u003eTypical applications include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePeristaltic transfer pumps\u003c\/li\u003e\n\u003cli\u003eBioreactor feed systems\u003c\/li\u003e\n\u003cli\u003eFilling applications\u003c\/li\u003e\n\u003cli\u003eVaccine manufacturing\u003c\/li\u003e\n\u003cli\u003eProcess-fluid transfer\u003c\/li\u003e\n\u003cli\u003eSingle-use pump assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eReinforced braided silicone tubing\u003c\/h3\u003e\n\u003cp\u003eReinforced braided silicone tubing combines a platinum-cured silicone product-contact surface with an integrated synthetic fabric reinforcement.\u003c\/p\u003e\n\u003cp\u003eThe reinforcement increases working and burst-pressure capability compared with conventional unreinforced silicone tubing while maintaining flexibility and visual access to the process fluid.\u003c\/p\u003e\n\u003cp\u003eThis construction is particularly suitable for:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePressurised pharmaceutical fluid transfer\u003c\/li\u003e\n\u003cli\u003eFiltration assemblies\u003c\/li\u003e\n\u003cli\u003eFluid-distribution manifolds\u003c\/li\u003e\n\u003cli\u003eHigher-pressure pump applications\u003c\/li\u003e\n\u003cli\u003eTransfer between single-use and stainless-steel equipment\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr\u003e\n\u003ch2\u003eAvailable micron ratings\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eNot applicable.\u003c\/strong\u003e Bioprocess tubing is a fluid-transfer component and does not contain filtration media.\u003c\/p\u003e\n\u003cp\u003eWhere filtration is required, a suitable capsule filter can be incorporated into the same single-use fluid path. Filter membrane material and micron rating are then selected separately according to the process.\u003c\/p\u003e\n\u003chr\u003e\n\u003ch2\u003eDesign and construction\u003c\/h2\u003e\n\u003ch3\u003eStandard silicone tubing sizes\u003c\/h3\u003e\n\u003cp\u003ePlatinum-cured silicone tubing is available across a wide dimensional range from approximately \u003cstrong\u003e0.02\" ID to 1\" ID\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003eFrequently used bioprocess dimensions include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e1\/8\" ID × 1\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 3\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 7\/16\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 9\/16\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 5\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/2\" ID × 3\/4\" OD\u003c\/li\u003e\n\u003cli\u003e5\/8\" ID × 7\/8\" OD\u003c\/li\u003e\n\u003cli\u003e3\/4\" ID × 1 1\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\" ID × 1 1\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\" ID × 1 3\/8\" OD\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eDifferent wall thicknesses are available for several internal diameters, allowing tubing geometry to be selected according to pumping, pressure and connection requirements.\u003c\/p\u003e\n\u003ch3\u003eWeldable TPE tubing sizes\u003c\/h3\u003e\n\u003cp\u003eWeldable TPE tubing is available from approximately \u003cstrong\u003e1\/8\" ID to 1\" ID\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003eStandard dimensions include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e1\/8\" ID × 1\/4\" OD\u003c\/li\u003e\n\u003cli\u003e3\/16\" ID × 5\/16\" OD\u003c\/li\u003e\n\u003cli\u003e3\/16\" ID × 3\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 3\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 7\/16\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e5\/16\" ID × 7\/16\" OD\u003c\/li\u003e\n\u003cli\u003e5\/16\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 9\/16\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 5\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/2\" ID × 3\/4\" OD\u003c\/li\u003e\n\u003cli\u003e5\/8\" ID × 7\/8\" OD\u003c\/li\u003e\n\u003cli\u003e3\/4\" ID × 1\" OD\u003c\/li\u003e\n\u003cli\u003e3\/4\" ID × 1 1\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\" ID × 1 1\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\" ID × 1 3\/8\" OD\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePump tubing sizes\u003c\/h3\u003e\n\u003cp\u003eDedicated pump tubing is available in both inch and metric dimensions. Published inch sizes cover approximately \u003cstrong\u003e1\/32\" ID through 1\" ID\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003eFrequently used configurations include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e1\/8\" ID × 1\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 3\/8\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 7\/16\" OD\u003c\/li\u003e\n\u003cli\u003e1\/4\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 1\/2\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 9\/16\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 5\/8\" OD\u003c\/li\u003e\n\u003cli\u003e3\/8\" ID × 3\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\/2\" ID × 3\/4\" OD\u003c\/li\u003e\n\u003cli\u003e1\/2\" ID × 7\/8\" OD\u003c\/li\u003e\n\u003cli\u003e5\/8\" ID × 7\/8\" OD\u003c\/li\u003e\n\u003cli\u003e3\/4\" ID × 1 1\/8\" OD\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eMetric pump-tubing configurations are also available for equipment requiring metric pump-head dimensions.\u003c\/p\u003e\n\u003ch3\u003eReinforced braided silicone sizes\u003c\/h3\u003e\n\u003ctable style=\"width: 100%; border-collapse: collapse; margin: 24px 0;\"\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth style=\"text-align: left; padding: 10px; border-bottom: 1px solid #ddd;\"\u003eID\u003c\/th\u003e\n\u003cth style=\"text-align: left; padding: 10px; border-bottom: 1px solid #ddd;\"\u003eOD\u003c\/th\u003e\n\u003cth style=\"text-align: left; padding: 10px; border-bottom: 1px solid #ddd;\"\u003eWorking pressure\u003c\/th\u003e\n\u003cth style=\"text-align: left; padding: 10px; border-bottom: 1px solid #ddd;\"\u003eBurst pressure\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e3.18 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e9.81 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e4.72 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e11.35 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e6.35 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e13.03 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e45 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e7.93 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e14.61 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e12 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e36 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e9.52 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e16.32 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e12 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e36 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e12.70 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e20.10 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e10 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e30 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15.87 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e24.37 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e8 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e24 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e19.05 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e27.91 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e8 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e24 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e22.20 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e31.12 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e5 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e25.40 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e34.50 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e5 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px; border-bottom: 1px solid #eee;\"\u003e15 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 10px;\"\u003e31.75 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px;\"\u003e40.80 mm\u003c\/td\u003e\n\u003ctd style=\"padding: 10px;\"\u003e4 bar\u003c\/td\u003e\n\u003ctd style=\"padding: 10px;\"\u003e12 bar\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003cp\u003ePressure ratings above apply to the published reinforced tubing construction. The allowable pressure of a complete fluid path may be lower and is determined by the lowest-rated tubing, fitting, connector or other component in the assembly.\u003c\/p\u003e\n\u003ch3\u003eSterilisation compatibility\u003c\/h3\u003e\n\u003cp\u003eSuitable tubing constructions can support:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eGamma sterilisation\u003c\/li\u003e\n\u003cli\u003eAutoclave sterilisation\u003c\/li\u003e\n\u003cli\u003eETO treatment\u003c\/li\u003e\n\u003cli\u003eIntegration into pre-sterilised ready-to-use assemblies\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eWeldable TPE and suitable pump tubing can also be incorporated into processes using tube welding and sealing equipment.\u003c\/p\u003e\n\u003cp\u003eSterilisation compatibility must be confirmed for the selected tubing construction and complete single-use assembly.\u003c\/p\u003e\n\u003ch3\u003eQuality and documentation\u003c\/h3\u003e\n\u003cp\u003eAvailable pharmaceutical tubing configurations are produced under controlled cleanroom conditions and can be supplied with material and validation documentation appropriate to the selected construction.\u003c\/p\u003e\n\u003cp\u003eDepending on tubing type, available documentation can include:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUSP Class VI conformity\u003c\/li\u003e\n\u003cli\u003eISO 10993 information\u003c\/li\u003e\n\u003cli\u003eFDA 21 CFR material conformity\u003c\/li\u003e\n\u003cli\u003eBSE \/ TSE statements\u003c\/li\u003e\n\u003cli\u003eAnimal-derived component-free statements\u003c\/li\u003e\n\u003cli\u003eREACH conformity\u003c\/li\u003e\n\u003cli\u003eRoHS conformity\u003c\/li\u003e\n\u003cli\u003eEuropean Pharmacopoeia information\u003c\/li\u003e\n\u003cli\u003eSterilisation compatibility information\u003c\/li\u003e\n\u003cli\u003eExtractables and leachables information where available\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eExact documentation depends on the tubing material and final configuration.\u003c\/p\u003e\n\u003chr\u003e\n\u003ch2\u003eTypical applications\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eSingle-use fluid transfer\u003c\/li\u003e\n\u003cli\u003eBuffer and media transfer\u003c\/li\u003e\n\u003cli\u003eCell-culture processes\u003c\/li\u003e\n\u003cli\u003eBioreactor feed lines\u003c\/li\u003e\n\u003cli\u003ePeristaltic pumping\u003c\/li\u003e\n\u003cli\u003eSampling assemblies\u003c\/li\u003e\n\u003cli\u003eFilling assemblies\u003c\/li\u003e\n\u003cli\u003eSterile filtration systems\u003c\/li\u003e\n\u003cli\u003eTangential flow filtration\u003c\/li\u003e\n\u003cli\u003ePUPSIT assemblies\u003c\/li\u003e\n\u003cli\u003eBag and bottle assemblies\u003c\/li\u003e\n\u003cli\u003eSingle-use manifolds\u003c\/li\u003e\n\u003cli\u003eAseptic tube welding\u003c\/li\u003e\n\u003cli\u003eAseptic tube sealing\u003c\/li\u003e\n\u003cli\u003eUpstream processing\u003c\/li\u003e\n\u003cli\u003eDownstream processing\u003c\/li\u003e\n\u003cli\u003ePharmaceutical fluid transfer\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr\u003e\n\u003ch2\u003eKey benefits\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eMultiple tubing technologies:\u003c\/strong\u003e silicone, weldable TPE, dedicated pump tubing and reinforced silicone cover different single-use processing requirements.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eWide dimensional range:\u003c\/strong\u003e tubing is available from small-bore laboratory and sampling dimensions through production-scale fluid-transfer sizes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSterile welding capability:\u003c\/strong\u003e suitable TPE tubing can be joined and sealed using compatible tube welding and sealing equipment.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePeristaltic pump options:\u003c\/strong\u003e dedicated tubing constructions are available for demanding pumping applications.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHigher-pressure options:\u003c\/strong\u003e braided silicone provides increased working-pressure capability compared with conventional unreinforced silicone tubing.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eTransparent fluid paths:\u003c\/strong\u003e clear silicone and TPE configurations allow visual monitoring of the process liquid.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSterilisation compatibility:\u003c\/strong\u003e suitable tubing materials can be gamma sterilised, autoclaved or supplied as part of a ready-to-use assembly.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eAssembly integration:\u003c\/strong\u003e tubing can be combined with bags, bottles, filters, sterile connectors, sensors and other components within a complete custom fluid path.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr\u003e\n\u003ch2\u003eConfiguration and quotation\u003c\/h2\u003e\n\u003cp\u003eTubing selection should begin with the process function and fluid characteristics rather than tubing dimensions alone.\u003c\/p\u003e\n\u003cp\u003eFor technical selection and quotation, provide the following information where available:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eRequired tubing material\u003c\/li\u003e\n\u003cli\u003eTubing ID and OD\u003c\/li\u003e\n\u003cli\u003eRequired length\u003c\/li\u003e\n\u003cli\u003eProcess fluid\u003c\/li\u003e\n\u003cli\u003eRequired flow rate\u003c\/li\u003e\n\u003cli\u003eOperating temperature\u003c\/li\u003e\n\u003cli\u003eMaximum operating pressure\u003c\/li\u003e\n\u003cli\u003ePeristaltic pump requirement\u003c\/li\u003e\n\u003cli\u003ePump manufacturer and pump-head type where applicable\u003c\/li\u003e\n\u003cli\u003eSterile welding requirement\u003c\/li\u003e\n\u003cli\u003eTube sealing requirement\u003c\/li\u003e\n\u003cli\u003eGamma sterilisation requirement\u003c\/li\u003e\n\u003cli\u003eAutoclave requirement\u003c\/li\u003e\n\u003cli\u003eRequired connectors or fittings\u003c\/li\u003e\n\u003cli\u003eIntegration into a complete single-use assembly\u003c\/li\u003e\n\u003cli\u003eRequired material and validation documentation\u003c\/li\u003e\n\u003cli\u003eEstimated annual quantity\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIf the exact tubing grade has not yet been selected, process fluid, ID and OD, pressure, temperature and pumping requirements normally provide enough information for an initial technical selection.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Filtra International","offers":[{"title":"Platinum-Cured Silicone \/ 1\/8\" × 1\/4\" \/ Bulk Tubing \/ Custom Length","offer_id":57419799626054,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Platinum-Cured Silicone \/ 1\/8\" × 1\/4\" \/ Cut Lengths","offer_id":57419801264454,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":true},{"title":"Platinum-Cured Silicone \/ 1\/8\" × 1\/4\" \/ Integrated in Single-Use 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