KVVLA2TTH1
Durapore® 0.1 µm, Opticap® XLT Capsule
Opticap® XLT 20, cartridge nominal length 20 in. (50 cm), filter diam. 4.2 in. (10.7 cm)
material
polypropylene filter
polypropylene housing
polypropylene support
silicone seal
Quality Level
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)
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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
Regulatory Information
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