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MilliporeSigma

MSP000812

Durapore® 0.22 µm, Cartridge

cartridge nominal length 10 in. (25 cm), Code 7 (2-226; O-rings w/locking-tabs)

Synonym(s):

Durapore Cartridge Filter 10 in. 0.22 μm Code 7

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About This Item

eCl@ss:
27293007
UNSPSC Code:
23151806

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material

PVDF

reg. compliance

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

sterility

non-sterile

sterilization compatibility

autoclavable compatible
steam-in-place compatible

product line

Durapore®, EMPROVE® Filter

feature

hydrophilic

manufacturer/tradename

Durapore®

technique(s)

sterile filtration: suitable

L

10 in.

W

2.7 in.

cartridge nominal length

10 in. (25 cm)

filtration area

0.69 m2

impurities

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

gravimetric extractables

≤20 mg/cartridge

matrix

Durapore®

pore size

0.22 μm

input

sample type liquid

cartridge code

Code 7 (2-226; O-rings w/locking-tabs)

Quality Level

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This Item
MSP000941MSP000950MSP000953
pore size

0.22 μm

pore size

0.1 μm

pore size

0.22 μm

pore size

0.22 μm

product line

Durapore®, EMPROVE® Filter

product line

Durapore®

product line

Durapore®, EMPROVE® Filter

product line

Durapore®, EMPROVE® Filter

filtration area

0.69 m2

filtration area

0.69 m2

filtration area

1.38 m2

filtration area

2.07 m2

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

material

PVDF

material

PVDF

material

PVDF

material

PVDF

manufacturer/tradename

Durapore®

manufacturer/tradename

Durapore®

manufacturer/tradename

Durapore®

manufacturer/tradename

Durapore®

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.
Gravimetric Extractables: after 24 hours in water at controlled room temperature

General description

Device Configuration: Cartridge

Other Notes

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.

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

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).

Legal Information

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

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