KPHLG1TTT1

Durapore^® 0,45 µm, Opticap^® XLT Cápsula

Opticap^® XLT 10, cartridge nominal length 14.8 in. (37.6 cm), filter diam. 4.2 in. (10.7 cm)

• UNSPSC Code: 23151806

Propiedades

• 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 10
• feature: hydrophilic
• manufacturer/tradename: Opticap^®
• parameter: ≤15.0 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water); 1 bar max. inlet pressure (15 psi) at 80 °C; 2.1 bar max. differential pressure (30 psid) at 4-40 °C (Reverse:); 2.8 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward:); 5.5 bar max. inlet pressure (80 psi) at 23 °C; 80 psig max. inlet pressure
• technique(s): bioburden reduction: suitable
• W: 6.0 in.
• cartridge nominal length: 14.8 in. (37.6 cm)
• device L: 37.6 cm (14.8 in.)
• device size: 10 in.
• filter diam.: 4.2 in. (10.7 cm)
• filtration area: 0.62 m²
• inlet connection diam.: 1-1/2 in.
• inlet to outlet width: 37.6 cm (14.8 in.)
• outlet connection diam.: 1-1/2 in.
• impurities: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Durapore^®
• pore size: 0.45 μm pore size
• bubble point: ≥1930 mbar (28 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 Outlet)

Descripción

General description

Device Configuration: Capsule

Preparation Note

Sterilization Method:
Gamma compatible to 40 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

Gravimetric Extractables: ≤ 25 mg per capsule after 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 1500 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 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

Legal Information

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

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