CGW1M4S03
Polysep™ II 1.0/0.2/0.1 µm nominal, Cartridge
pore size 1.0/0.2/0.1 μm, cartridge nominal length 10 cm (4 in.), filter diam. 7.1 cm (2.8 in.)
About This Item
material
borosilicate glass fiber (BGF) membrane
mixed cellulose esters (MCE) membrane
polypropylene prefilter
polypropylene support
silicone seal
Quality Level
reg. compliance
meets FDA 21 CFR 177-182 (all component materials)
sterility
non-sterile
Sterilization Compatibility
autoclavable compatible
steam-in-place compatible
product line
Polysep™
feature
hydrophilic
manufacturer/tradename
Polysep™
parameter
3.5 bar max. differential pressure (50 psid) at 25 °C
3.5 bar max. inlet pressure (50 psi) at 25 °C
technique(s)
prefiltration: suitable
L
4 in.
W
2.7 in.
cartridge nominal length
10 cm (4 in.)
filter diam.
7.1 cm (2.8 in.)
filter filtration area
0.17 m2
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction )
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction )
matrix
Polysep™ II
pore size
1.0/0.2/0.1 μm nominal pore size
1.0/0.2/0.1 μm pore size
cartridge code
Code M
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General description
Features and Benefits
Packaging
Preparation Note
Analysis Note
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 2 L
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 first page of Visual Inspection Guide and introduction section of Mixed cellulose esters Tech Brief
- Storage Statement: Please refer Mixed cellulose esters Tech Brief
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
Legal Information
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