K002A05HH1
Opticap® XL Capsule Filter
pore size 0.2 μm, cartridge nominal length 5 in. (12.5 cm), filter diam. 4.2 in. (10.7 cm)
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About This Item
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material
polypropylene filter
polypropylene housing
polypropylene support
silicone seal
Quality Level
reg. compliance
meets FDA 21 CFR 177-182 (all component materials)
manufacturer/tradename
Opticap®
parameter
max. inlet temp. at 25 °C
1.0 bar max. inlet pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
4.8 bar max. differential pressure (70 psid) at 20 °C
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure
cartridge nominal length
5 in. (12.5 cm)
device size
5 in.
filter L
8.5 in. (21.6 cm)
filter diam.
4.2 in. (10.7 cm)
inlet connection diam.
9/16 in. , hose barb
inlet to outlet width
21.6 cm (8.5 in.)
impurities
≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)
matrix
Clarigard®
pore size
0.2 μm pore size
fitting
inlet/outlet connection for 14 mm (9/16 in.) hose barb
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This Item | K003A05TT1 | KHGES3TTH1 | KHGES2TTH1 |
|---|---|---|---|
| fitting inlet/outlet connection for 14 mm (9/16 in.) hose barb | fitting inlet/outlet connection for 38 mm (1 1/2 in.) sanitary flange | fitting (38 mm (1 ½ in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet) | fitting (38 mm (1 ½ in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet) |
| material polypropylene filter, polypropylene support, polypropylene housing, silicone seal | material polypropylene filter, polypropylene housing, polypropylene support, silicone seal | material polyester support, polypropylene device, polypropylene housing, polypropylene vent cap, polysulfone device, silicone seal | material polyester support, polypropylene device, polypropylene housing, polypropylene vent cap, polysulfone device, silicone seal |
| impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction) | impurities ≤0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction) | impurities ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction), <0.25 EU/mL USP bacterial endotoxins (sample aqueous extraction) | impurities ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction), <0.25 EU/mL USP bacterial endotoxins (sample aqueous extraction) |
| parameter max. inlet temp. at 25 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 80 psig max. inlet pressure | parameter max. inlet temp. at 25 °C, 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 4.8 bar max. differential pressure (70 psid) at 20 °C, 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure | parameter ≤93.7 mL/min air diffusion at 2.8 bar (40 psig) (in water), 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 100 psi max. differential pressure (6.9 bar) (intermittent), 2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent), 2.75 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward), 5.5 bar max. inlet pressure (80 psi) at 25 °C, 6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent), 6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent), 80 psi max. differential pressure (5.5 bar) (continuous), 80 psig max. inlet pressure | parameter ≤62.5 mL/min air diffusion at 2.8 bar (40 psig) (in water), 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 100 psi max. differential pressure (6.9 bar) (intermittent), 2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent), 2.75 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward), 5.5 bar max. inlet pressure (80 psi) at 25 °C, 6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent), 6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent), 80 psi max. differential pressure (5.5 bar) (continuous), 80 psig max. inlet pressure |
| reg. compliance meets FDA 21 CFR 177-182 (all component materials) | reg. compliance meets FDA 21 CFR 177-182 (all component materials) | reg. compliance meets FDA 21 CFR 177-182 (all component materials) | reg. compliance meets FDA 21 CFR 177-182 (all component materials) |
| manufacturer/tradename Opticap® | manufacturer/tradename Opticap® | manufacturer/tradename Millipore Express® | manufacturer/tradename Millipore Express® |
General description
Packaging
Preparation Note
3 autoclave cycles of 30min at 126°C; not in-line steam sterilizable
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 installation section of OPTICAP® XL Capsules and OPTICAP® XLT Capsules user guide
- Storage Statement: Store in dry location
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
Legal Information
Storage Class Code
10-13 - German Storage Class 10 to 13
Certificates of Analysis (COA)
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