KPHLG3TTT1

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

Opticap^® XLT 30, cartridge nominal length 34.3 in. (87.1 cm), filter diam. 4.2 in. (10.7 cm)

• Código UNSPSC: 23151806

Propiedades

• Materiales: polyester support; polyethylene support; polypropylene filter; polypropylene housing; silicone seal
• Nivel de calidad: 400
• cumplimiento norm.: FDA 21CFR177-182 (all component materials)
• esterilidad: non-sterile
• Compatibilidad de esterilización: gamma compatible
• Línea del producto: Opticap^® XLT 30
• Características: hydrophilic
• fabricante / nombre comercial: Opticap^®
• Parámetros: ≤45.0 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
• técnicas: bioburden reduction: suitable
• Anchura: 6.0 in.
• longitud nominal del cartucho: 34.3 in. (87.1 cm)
• device L: 87.1 cm (34.3 in.)
• device size: 30 in.
• diám. del filtro: 4.2 in. (10.7 cm)
• filter filtration area: 1.86 m²
• diám. conexión a entrada: 1-1/2 in.
• inlet to outlet width: 87.1 cm (34.3 in.)
• diám. conexión a salida: 1-1/2 in.
• impurezas: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• matriz: Durapore^®
• tamaño de poro: 0.45 μm pore size
• punto de burbuja: ≥1930 mbar (28 psig), air with water at 23 °C
• Adaptador: 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

Descripción general

Device Configuration: Capsule

Nota de preparación

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).

Nota de análisis

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 ≥ 4500 mL

Otras notas

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

Información legal

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

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