KWSSA1ZTT1
Milligard® 0.5/0.2 µm nominal, Opticap® XLT Capsule
pore size 0.5/0.2 μm, Opticap® XLT 10, cartridge nominal length 10 in. (25 cm)
About This Item
material
mixed cellulose esters (MCE) membrane
polyester support
polypropylene filter
polypropylene housing
silicone seal
Quality Level
reg. compliance
FDA 21CFR177-182 (all component materials)
sterility
non-sterile
Sterilization Compatibility
autoclavable compatible
product line
Opticap® XLT 10
feature
hydrophilic
manufacturer/tradename
Opticap®
parameter
1 bar max. inlet pressure (15 psi) at 80 °C
2.75 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
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure
technique(s)
prefiltration: suitable
cartridge nominal length
10 in. (25 cm)
device size
10 in.
inlet connection diam.
1-1/2 in.
outlet connection diam.
1-1/2 in.
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction)
<0.5 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
matrix
Milligard®
pore size
0.5/0.2 μm nominal pore size
0.5/0.2 μm pore size
fitting
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)
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General description
Features and Benefits
Packaging
Preparation Note
3 autoclave cycles of Sterilization Method: 30min at 121°C; not in-line steam sterilizable
This product was manufactured with a media combination 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 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
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Certificates of Analysis (COA)
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