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Merck
CN

CVHL03PP3

Durapore 筒式过滤器，无预滤器 30 in.0.45 µm 0 号

pore size 0.45 μm, cartridge nominal length 30 in. (75 cm), Code 0 (2-222; O-rings)

别名:

Durapore® 0.45 µm，小柱

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eCl@ss:
32031690
UNSPSC Code:
23151806

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产品名称

Durapore 筒式过滤器，无预滤器 30 in.0.45 µm 0 号, pore size 0.45 μm, cartridge nominal length 30 in. (75 cm), Code 0 (2-222; O-rings)

material

PVDF
polypropylene
polypropylene support
silicone seal

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

≤45 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

30 in.

W

2.7 in.

cartridge nominal length

30 in. (75 cm)

diam.

6.9 cm (2.7 in.)

filtration area

2.07 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

≤60 mg/cartridge

matrix

Durapore®

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 0 (2-222; O-rings)

Quality Level

400

General description

Device Configuration: Cartridge

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 ≥3 L

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.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
30 SIP cycles of 30 min @ 135 °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).

Legal Information

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

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