KVVLA2TTH1

Durapore^® 0,1 µm, Opticap^® XLT Cápsula

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

• Código UNSPSC: 23151806

Propiedades

• Materiales: polypropylene filter; polypropylene housing; polypropylene support; silicone seal
• Nivel de calidad: 400
• cumplimiento norm.: FDA 21CFR177-182 (all component materials)
• esterilidad: non-sterile
• Compatibilidad de esterilización: autoclavable compatible
• Línea del producto: Opticap^® XLT 20
• Características: hydrophilic
• fabricante / nombre comercial: Opticap^®
• Parámetros: ≤40 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; 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward:); 2.8 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
• técnicas: sterile filtration: suitable
• Anchura: 6.9 in.
• longitud nominal del cartucho: 20 in. (50 cm)
• device L: 62.5 cm (24.6 in.)
• device size: 20 in.
• diám. del filtro: 4.2 in. (10.7 cm)
• filtración área: 1.4 m²
• diám. conexión a entrada: 1-1/2 in.
• inlet to outlet width: 17.5 cm (6.9 in.)
• diám. conexión a salida: 5/8 in.
• impurezas: ≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.5 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• matriz: Durapore^®
• tamaño de poro: 0.1 μm pore size
• punto de burbuja: ≥4830 mbar (70 psig), air with water at 23 °C
• Adaptador: 16 mm (5/8 in.) fitting (hose barb inlet/oulet); 38 mm (1 1/2 in.) fitting (sanitary flange inlet/oulet); 1/4 in. fitting (vent/drain hose barb with double O-ring seal); (38 mm (1 1/2 in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet)

Descripción

Descripción general

Device Configuration: Capsule

Envase

Double Easy-Open bag

Nota de preparación

Sterilization Method:
3 autoclave cycles of 60min at 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 21CFR210.3(b)(6).

Nota de análisis

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: ≤ 50 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 ≥ 2 L

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 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

Información legal

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