Select a Size
About This Item
Product Name
Opticap® XLT 20 CapsuleMedia: Durapore® 0.1 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)Inlet: 1-1/2 in. Sanitary FlangeOutlet: 5/8 in. Hose BarbT-lineMax Operating Pressure: 80 psi @ 25 °C
Quality Level
material
polypropylene filter, polypropylene housing, polypropylene support, silicone seal
reg. compliance
FDA 21CFR177-182 (all component materials)
sterility
non-sterile
sterilization compatibility
autoclavable compatible
product line
Opticap® XLT 20
feature
hydrophilic
manufacturer/tradename
Opticap®
parameter
≤40 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water), 1 bar max. inlet pressure (15 psi) at 80 °C, 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward:), 2.8 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent), 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward:), 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure
technique(s)
sterile filtration: suitable
W
6.9 in.
cartridge nominal length
20 in. (50 cm)
device L
62.5 cm (24.6 in.)
device size
20 in.
filter diam.
4.2 in. (10.7 cm)
filtration area
1.4 m2
inlet connection diam.
1-1/2 in.
inlet to outlet width
17.5 cm (6.9 in.)
outlet connection diam.
5/8 in.
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction), <0.5 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
matrix
Durapore®
pore size
0.1 μm pore size
bubble point
≥4830 mbar (70 psig), air with water at 23 °C
fitting
16 mm (5/8 in.) fitting (hose barb inlet/oulet), 38 mm (1 1/2 in.) fitting (sanitary flange inlet/oulet), 1/4 in. fitting (vent/drain hose barb with double O-ring seal), (38 mm (1 1/2 in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet)
General description
Packaging
Preparation Note
3 autoclave cycles of 60min at 126°C; not in-line steam sterilizable
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).
Analysis Note
Other Notes
- Organism Retention: Microorganism
- Mode of Action: Filtration (size exclusion)
- Application: BioProcessing
- Intended Use: Reduction or removal of microorganism/bioburden
- Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore® Membrane user guide
- Storage Statement: Store in dry location
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
Legal Information
Still not finding the right product?
Explore all of our products under Opticap® XLT 20 CapsuleMedia: Durapore® 0.1 µm
Regulatory Information
This item has
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Before adoption of single-use technologies in biomanufacturing, manufacturers must assess the risk to the drug product from potential leachables. This article highlights a general approach based on the United States Pharmacopeia (USP).
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| KVVLA2TTH1 | 04053252656835 |