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CLVL03TP3

Durapore® 0.1 µm, High Area, Cartridge

pore size 0.1 μm, cartridge nominal length 30 in. (75 cm), Code 0

Synonim(y):

Durapore® 0.1 µm, High Area, Cartridge

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Rozmiar/SKUDostępnośćCena netto
3 pkg

Informacje o tej pozycji

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: 0.1 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 30 in. Code 0

Quality Segment

material

PVDF membrane, polypropylene support, silicone O-ring

reg. compliance

meets FDA 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

30 in.

W

2.7 in.

cartridge nominal length

30 in. (75 cm)

device size

30 in.

filtration area

3.3 m2

impurities

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

gravimetric extractables

≤30 mg/cartridge

matrix

Durapore® High Area  

pore size

0.1 μm pore size

code

Code 0

General description

Device configuration: Cartridge
Cartridge type: Liquid

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: The extractables level was ≤ 30 mg per 10-inch cartridge 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 to 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

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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CLGL03TP3CLVL02TP3CLVL01TP3
description

Chemistry: 0.1 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 30 in. Code 0

description

Chemistry: 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 30 in. Code 0

description

Chemistry: 0.1 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 20 in. Code 0

description

Chemistry: 0.1 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 10 in. Code 0

pore size

0.1 μm pore size

pore size

0.22 μm pore size

pore size

0.1 μm pore size

pore size

0.1 μm pore size

filtration area

3.3 m2

filtration area

3.3 m2

filtration area

2.2 m2

filtration area

1.1 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® II

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile


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