Skip to Content
MilliporeSigma
All Photos(1)

Documents

CVGB75S01

Millipore

Hydrophobic Durapore® 0.22 µm, Cartridge

pore size 0.22 μm, cartridge nominal length 5 in. (12.5 cm), Code 7

Synonym(s):

Durapore Cartridge Filter 5 in. 0.22 µm hydrophobic Code 7

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

UNSPSC Code:
23151806
eCl@ss:
27293007

material

PVDF
polypropylene
polypropylene support
silicone seal

Quality Level

400

sterility

non-sterile

sterilization compatibility

steam-in-place compatible

product line

Durapore®

feature

hydrophobic

manufacturer/tradename

Durapore®

parameter

≤5 mL/min nitrogen diffusion at 1.7 bar (25 psig) and 23 °C (with water)
0.35 bar max. differential pressure (5 psid) at 135 °C (Forward)
0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward)
3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse)
3.5 bar max. inlet pressure (50 psi) at 25 °C (Reverse)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward)

technique(s)

sterile filtration: suitable

L

5 in.

W

2.7 in.

cartridge nominal length

5 in. (12.5 cm)

diam.

6.9 cm (2.7 in.)

filtration area

0.35 m2

impurities

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

gravimetric extractables

≤10 mg

matrix

Durapore®

pore size

0.22 μm pore size

bubble point

≥1240 mbar (18 psig), nitrogen with 60/40% IPA/water at 23 °C

cartridge code

Code 7

Related Categories

General description

Device Configuration: Cartridge

Packaging

Double Easy-Open bag

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

Sterilization Method
30 SIP cycles of 30 min @ 126 °C; 30 autoclave cycles of 60 min @ 126 °C
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 24 hours in a 70/30% IPA/water mixture at controlled room temperature

Legal Information

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

Not finding the right product?  

Try our Product Selector Tool.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service