KVGBA10TT1

Hydrophobic Durapore^® 0.22 µm, Opticap^® XL Capsule

Opticap^® XL 10, inlet connection diam. 1.5 in., pore size 0.22 μm, cartridge nominal length 10 in. (25 cm)

• Synonym(s): Opticap Sterilizing Grade XL10 Durapore Hydrophobic 0.22 µm 1-1/2 in. TC/TC
• UNSPSC Code: 23151806

Properties

• material: PVDF , polypropylene , polypropylene housing, polypropylene support, polypropylene vent cap, silicone seal
• 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 10
• feature: hydrophobic
• manufacturer/tradename: Opticap^®
• parameter: ≤10 mL/min nitrogen diffusion at 1.7 bar (25 psig) and 23 °C (with 60/40% IPA/water), 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 2.8 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 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 23 °C, 80 psig max. inlet pressure
• technique(s): sterile filtration: suitable
• L: 33.5 cm (13.2 in.)
• W: 4.2 in.
• cartridge nominal length: 10 in. (25 cm)
• diam.: 14.5 cm (5.7 in.)
• filtration area: 0.69 m²
• inlet connection diam.: 1.5 in.
• inlet to outlet W: 33.5 cm (13.2 in.)
• outlet connection diam.: 1.5 in.
• impurities: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction), <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Durapore^®
• pore size: 0.22 μm pore size
• bubble point: ≥1240 mbar (18 psig), nitrogen with 60/40% IPA/water at 23 °C
• fitting: 1/4 in. drain/vent hose barb (with double O-ring Seal), (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)
• Quality Level: 400

Description

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.

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.

General description

Device Configuration: Capsule

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 installation section of OPTICAP^® XL Capsules and OPTICAP^® XLT Capsules user guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Replaces: SN2M027A6

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

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
20 autoclave cycles of 30 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).

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