material
borosilicate glass fiber (BGF) membrane, mixed cellulose esters (MCE) membrane, polypropylene prefilter, polypropylene support, silicone seal
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.)
filtration area
0.19 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
1.0/1.2 μm nominal pore size, 1.2/1.0 μm pore size
cartridge code
Code M
Quality Level
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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
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B Inhalation - Flam. Sol. 1
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 3
法规信息
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