KVVLA02FH3
Durapore® 0.1 µm, Opticap® XL Capsule
Opticap® XL 2, cartridge nominal length 2 in. (5 cm), filter diam. 5.7 in. (14.5 cm)
동의어(들):
Durapore® 0.1 µm, Opticap® XL Capsule
크기 선택
제품정보 (DICE 배송 시 비용 별도)
제품 이름
Opticap® XL 2 CapsuleMedia: Durapore® 0.1 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)Inlet: 3/4 in. Sanitary FlangeOutlet: 9/16 in. Hose BarbMax Operating Pressure 80 psi @ 25 °C
Quality Segment
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® XL 2
feature
hydrophilic
manufacturer/tradename
Opticap®
parameter
≤3.5 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, 1.0 bar max. differential pressure (15 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
cartridge nominal length
2 in. (5 cm)
device L
14.0 cm (5.5 in.)
device size
2 in.
filter diam.
5.7 in. (14.5 cm)
filter filtration area
0.2 m2
inlet connection diam.
3/4 in.
inlet to outlet width
14 cm (5.5 in.)
outlet connection diam.
9/16 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
19 mm (3/4 in.) fitting (sanitary flange inlet/oulet), 1/4 in. fitting (vent/drain hose barb with double O-ring seal), (19 mm (3/4 in.) Sanitary Flange Inlet and 14 mm (9/16 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
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