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Merck
CN

KHGLG10TH1

Multilayer Durapore® 0.45/0.22 µm, Opticap® XL Capsule

Opticap® XL 10, cartridge nominal length 10 in. (25 cm), filter diam. 4.2 in. (10.7 cm)

别名:

Opticap XL 10 CapsuleMedia: Multilayer Durapore 0.45 / 0.22 µm

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UNSPSC Code:
23151806

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产品名称

多层Durapore® 0.45/0.22 µm，Opticap® XL囊式, Opticap® XL 10, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)Inlet: 1-1/2 in. Sanitary FlangeOutlet: 9/16 in. Hose BarbMax Operating Pressure: 80 psi @ 25 °C, cartridge nominal length 10 in. (25 cm), filter diam. 4.2 in. (10.7 cm)

material

polyester support, polyethylene support, polypropylene filter, polypropylene housing, silicone outer O-ring, silicone-coated EPDM rubber lead O-ring

reg. compliance

FDA 21CFR177-182 (all component materials)

Quality Level

400

sterility

non-sterile

sterilization compatibility

gamma compatible

product line

Opticap® XL 10

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

≤15.0 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water), 1 bar max. inlet pressure (15 psi) at 80 °C, 1.05 bar max. differential pressure (15 psid) at 80 °C (Forward:), 2.75 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent), 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward:), 5.5 bar max. inlet pressure (80 psi) at 23 °C, 80 psig max. inlet pressure

technique(s)

sterile filtration: suitable

W

4.2 in.

cartridge nominal length

10 in. (25 cm)

device L

33.5 cm (13.2 in.)

device size

10 in.

filter diam.

4.2 in. (10.7 cm)

filter filtration area

1.86 m2

inlet connection diam.

1-1/2 in.

inlet to outlet width

33.5 cm (13.2 in.)

outlet connection diam.

9/16 in.

impurities

≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction), <0.25 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)

matrix

Multilayer Durapore®

pore size

0.45/0.22 μm pore size

bubble point

≥3450 mbar (50 psig), air with water at 23 °C

fitting

1/4 in. fitting (vent/drain hose barb with double O-ring seal), (38 mm (1 1/2 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

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General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method:
Gamma compatible to 45 kGy; 3 autoclave cycles of 60min at 3°C; not in-line steam sterilizable

This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).

Analysis Note

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 1.5 L
Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 107 CFU/cm2 using ASTM® F838 methodology.
TOC/Conductivity: After sterilization and a controlled water flush, samples exhibited less than 500ppb TOC per USP < 643 > and less than 1.3μS/cm per USP < 645 > at 25°C.

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

Legal Information

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

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