SI1M142A7
Durapore® 0.22 µm, Millipak® Capsule
Millipak® 20
Synonym(s):
MPGL02GH2 Non Sterile
About This Item
material
PVDF
PVDF vent cap
polycarbonate
polycarbonate support
Quality Level
sterility
irradiated
sterile
product line
Millipak® 20
feature
hydrophilic
manufacturer/tradename
Millipak®
parameter
0.35 bar max. differential pressure (5 psid) at 123 °C (Forward)
0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse)
1.5 L/min flow rate at 1.75 bar (ΔP
ΔP)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
10 L process volume
4.1 bar max. differential pressure (60 psid) at 25 °C (Forward)
5.2 bar max. inlet pressure (75 psi) at 25 °C
technique(s)
sterile filtration: suitable
L
9.4 cm
diam.
6.9 cm (2.7 in.)
filtration area
100 cm2
inlet connection diam.
1/4 in.
outlet connection diam.
1/4 in.
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
matrix
Durapore®
pore size
0.22 μm
bubble point
≥3450 mbar (50 psig), air with water at 23 °C
fitting
inlet hose barb
outlet hose barb
(14 mm (9/16 in.) Hose Barb Inlet and Outlet)
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General description
Preparation Note
3 autoclave cycles of 90 min @ 123 °C; not in-line steam sterilizable
Analysis Note
Quantitative retention of 107 CFU/cm2Brevundimonas diminuta (ATCC® 19146) per ASTM F838-83 methodology
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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Certificates of Analysis (COA)
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