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MSP010012

Millipore

Hydrophilic/Hydrophobic Durapore® 0.22 µm, Millipak® Barrier 200 Capsule

Millipak® Barrier 200

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Synonym(s):
Durapore Millipak Barrier 200, 0.22 m, Hydrophobic/Hydrophilic, HB/HB
eCl@ss:
32031690

material

PVDF

Quality Level

description

hydrophobic/hydrophilic

sterility

irradiated
non-sterile

Sterilization Compatibility

gamma compatible

product line

Millipak® Barrier 200

feature

hydrophilic
hydrophobic

manufacturer/tradename

Durapore®

technique(s)

sterile filtration: suitable

L

6.1 in.

W

3.0 in.

filtration area

1000 cm2

inlet connection diam.

9/16 in.

outlet connection diam.

9/16 in.

impurities

<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

matrix

Durapore®

pore size

0.22 μm

fitting

inlet hose barb
outlet hose barb
(14 mm (9/16 in.) Hose Barb Inlet and Outlet)

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This Item
MPGL2GCA3MSP010013MPVL2GCA3
sterility

irradiated, non-sterile

sterility

irradiated, sterile

sterility

irradiated, non-sterile

sterility

irradiated, sterile

product line

Millipak® Barrier 200

product line

EMPROVE® Filter

product line

Millipak® Barrier 200

product line

Millipak® 200

feature

hydrophilic, hydrophobic

feature

hydrophilic

feature

hydrophilic, hydrophobic

feature

hydrophilic

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

filtration area

1000 cm2

filtration area

1000 cm2

filtration area

1000 cm2

filtration area

1000 cm2

General description

Device Configuration: Capsule

Other Notes

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Directions for Use

  • 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

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).

Analysis Note

Bacterial Retention
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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