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CLGL72TP3

Durapore® 0.22 µm, High Area, Cartridge

pore size 0.22 μm, cartridge nominal length 20 in. (50 cm), Code 7 (2-226; O-rings w/locking-tabs)

Synonim(y):

Durapore® II Cartridge Filter 20 in. 0.22 m Code 7, Durapore® 0.22 µm, High Area, Cartridge

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Rozmiar/SKUDostępnośćCena netto
3 ea

Informacje o tej pozycji

eCl@ss:
27293007
UNSPSC Code:
23151806

Tego produktu nie można kupić jako gość. Aby uzyskać więcej informacji, skontaktuj się z nami pod adresem +48 225 844 261lub

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Nazwa produktu

Durapore® High Area Cartridge, Chemistry: 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 20 in. Code 7

material

PVDF

Quality Segment

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®

feature

hydrophilic

manufacturer/tradename

Durapore® II

technique(s)

sterile filtration: suitable

L

20 in.

W

2.7 in.

cartridge nominal length

20 in. (50 cm)

filtration area

2.2 m2

impurities

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

gravimetric extractables

≤60 mg/cartridge

matrix

Durapore® High Area  

pore size

0.22 μm pore size

input

sample type liquid

cartridge code

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

General description

Device Configuration: Cartridge

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.
Gravimetric Extractables: after a 1.5 L flush and 24 hours in water at controlled room temperature

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.

Legal Information

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

Chemistry: 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 20 in. Code 7

description

Chemistry: 0.1 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 20 in. Code 7

description

Chemistry: 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 20 in. Code 0

description

Chemistry: 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 30 in. Code 7

pore size

0.22 μm pore size

pore size

0.1 μm pore size

pore size

0.22 μm pore size

pore size

0.22 μm pore size

filtration area

2.2 m2

filtration area

2.2 m2

filtration area

2.2 m2

filtration area

3.3 m2

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

product line

Durapore®

product line

Durapore®

product line

Durapore®

product line

Durapore®

manufacturer/tradename

Durapore® II

manufacturer/tradename

Durapore® II

manufacturer/tradename

Durapore® II

manufacturer/tradename

Durapore®

matrix

Durapore® High Area  

matrix

Durapore® High Area  

matrix

Durapore® High Area  

matrix

Durapore® High Area  


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