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Multilayer Durapore^® 0.45/0.22 µm, Opticap^® XLT Capsule

Opticap^® XLT 20, cartridge nominal length 20 in. (50 cm), filter diam. 4.2 in. (10.7 cm)

• UNSPSC Code: 23151806

Properties

• material: polyester support; polyethylene support; polypropylene filter; polypropylene housing; silicone seal
• Quality Level: 400
• reg. compliance: FDA 21CFR177-182 (all component materials)
• sterility: non-sterile
• sterilization compatibility: gamma compatible
• product line: Opticap^® XLT 20
• feature: hydrophilic
• manufacturer/tradename: Opticap^®
• parameter: ≤30.0 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: 20 in. (50 cm)
• device L: 62.5 cm (24.6 in.)
• device size: 20 in.
• filter diam.: 4.2 in. (10.7 cm)
• filtration area: 1.1 m²
• inlet connection diam.: 5/8 in.
• inlet to outlet width: 19.8 cm (7.8 in.)
• outlet connection diam.: 5/8 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); (16 mm (5?8 in.) Hose Barb Inlet and Outlet)

Description

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

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.

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

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