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CVHL72TP3

Millipore

Durapore® (w/Prefilter) 0.45 µm, Cartridge

pore size 0.45 μm, cartridge nominal length 20 in. (50 cm), Code 7 (2-226; O-rings w/locking-tabs)

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Synonym(s):
Durapore Cartridge Filter with prefilter 20 in. 0.45 μm Code 7
eCl@ss:
32031690

material

PVDF
mixed cellulose esters (MCE) prefilter
polypropylene
polypropylene support
silicone seal

Quality Level

reg. compliance

meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food)
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®

parameter

≤30 mL/min air diffusion at 1.5 bar (22 psig) and 23 °C (in 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)

bioburden reduction: suitable

L

20 in.

W

2.7 in.

cartridge nominal length

20 in. (50 cm)

diam.

6.9 cm (2.7 in.)

filtration area

1.38 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

≤90 mg/cartridge

matrix

Durapore® (w/Prefilter)

pore size

0.45 μm pore size

input

sample type liquid

bubble point

≥1930 mbar (28 psig), air with water at 23 °C

cartridge code

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

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CVHL71TP3CVHL73TP3CVHL01TP3
sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

product line

Durapore®

product line

Durapore®

product line

Durapore®

product line

Durapore®

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

filtration area

1.38 m2

filtration area

0.69 m2

filtration area

2.07 m2

filtration area

0.69 m2

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
10 SIP cycles of 30 min or 10 autoclave cycles of 60 min @ 121 °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

Gravimetric Extractables: after 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L

Legal Information

Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 2


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