MFGL06ST3
Durapore® 0.22 µm, Millipak® Final Fill Capsule
Millipak® Final Fill 60, sterile; γ-irradiated
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+49 6151 3599 399or
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About This Item
+49 6151 3599 399or
This item is not able to be purchased as a guest user. For further information, please contact us at .Recommended Products
material
polysulfone device
polysulfone support
Quality Level
Agency
meets EP 2.6.14
meets JP 4.01
meets USP 85
sterility
irradiated
sterile; γ-irradiated
product line
Millipak® Final Fill 60
feature
hydrophilic
manufacturer/tradename
Millipak®
parameter
1.51 L/min flow rate at 0.86 bar (ΔP)
10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse)
5.5 bar max. inlet pressure (80 psi) at 25 °C
60 L process volume
80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
technique(s)
sterile filtration: suitable
filter filtration area
300 cm2
impurities
<0.25 EU/mL USP bacterial endotoxins (LAL test, per device; aqueous extraction)
<0.25 EU/mL bacterial endotoxins (LAL test, per device; aqueous extraction)
matrix
Durapore®
pore size
0.22 μm pore size
bubble point
≥50 psi (3450 mbar), air with water
fitting
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)
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General description
Packaging
Preparation Note
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b)(6), validated based on large volume parenteral specifications as detailed in USP 788 Particulate Matter in Injections
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 general guidelines section of user guide shipped with this product
- Storage Statement: Please refer user guide shipped with this product
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
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