MPGL06CB1
Durapore® 0.22 µm, Millipak® Capsule
sterile, filtration area 300 cm2, matrix Durapore®
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material
PVDF membrane
PVDF vent cap
polycarbonate
polycarbonate support
Quality Level
sterility
irradiated
sterile
product line
Millipak®
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)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
30 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
7.6 L/min flow rate at 2.9 bar (ΔP)
technique(s)
sterile filtration: suitable
filtration area
300 cm2
inlet connection diam.
1/4 in.
outlet connection diam.
1/4 in.
impurities
≤0.5 EU/mL (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
gravimetric extractables
≤2 mg/device
matrix
Durapore®
pore size
0.22 μm
bubble point
≥3450 mbar (50 psig), air with water at 23 °C
fitting
NPT inlet connection
outlet hose barb
(6 mm (1/4 in.) NPTM Inlet and Outlet)
shipped in
ambient
Related Categories
General description
Packaging
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.
Preparation Note
3 autoclave cycles of 90 min @ 123°C; not in-line steam sterilizable
Analysis Note
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Legal Information
Certificates of Analysis (COA)
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