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KVGLA04HH3

Durapore® 0.22 µm, Opticap® XL Capsule

Opticap® XL, inlet connection diam. 9/16 in.

Synonym(s):

Opticap XL4 Durapore 0.22 μm 9/16 in. HB/HB, Durapore® 0.22 µm, Opticap® XL Capsule

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About This Item

UNSPSC Code:
23151806
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Product Name

Opticap® XL 4 CapsuleMedia: Durapore® 0.22 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF)Inlet: 9/16 in. Hose BarbOutlet: 9/16 in. Hose BarbMax Operating Pressure: 80 psi @ 25 °C

Quality Level

400

material

silicone seal, PVDF membrane, polypropylene housing, polypropylene support, polypropylene vent cap, silicone O-ring

reg. compliance

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap® XL

feature

hydrophilic

manufacturer/tradename

Durapore®

parameter

1 bar max. differential pressure (15 psid) at 80 °C (Forward), 1 bar max. inlet pressure (15 psi) at 80 °C, 3.4 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 25 °C

technique(s)

sterile filtration: suitable

L

4 in. (10 cm)

filtration area

0.19 m2

inlet connection diam.

9/16 in.

inlet to outlet W

19.3 cm (7.6 in.)

outlet connection diam.

9/16 in.

impurities

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

gravimetric extractables

≤10 mg/capsule

matrix

Durapore®

pore size

0.22 μm

input

sample type liquid

bubble point

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

fitting

14 mm (9/16 in.) inlet hose barb, 14 mm (9/16 in.) outlet hose barb

General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 60 min @ 126 °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 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 water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL

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.

Replaces: KVGL04HB3
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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

Disclaimer

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.

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Global Trade Item Number

SKUGTIN
KVGLA04HH304053252495052