KPHLG10HH1

Cápsula Durapore^® 0,45 µm. Opticap^® XL

Opticap^® XL 10, cartridge nominal length 13.2 in. (33.5 cm), filter diam. 4.2 in. (10.7 cm)

• Código UNSPSC: 23151806

Propriedades

• Materiais: polyester support; polyethylene support; polypropylene filter; polypropylene housing; silicone outer O-ring; silicone-coated EPDM rubber lead O-ring
• Nível de qualidade: 400
• conformidade reg.: FDA 21CFR177-182 (all component materials)
• esterilidade: non-sterile
• Compatibilidade de esterilização: gamma compatible
• linha de produto: Opticap^® XL 10
• Características: hydrophilic
• fabricante/nome comercial: Opticap^®
• Parâmetros: ≤15.0 mL/min air diffusion at 3.9 bar (22 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
• técnica(s): bioburden reduction: suitable
• Largura: 4.2 in.
• comprimento nominal do cartucho: 13.2 in. (33.5 cm)
• device L: 33.5 cm (13.2 in.)
• device size: 10 in.
• diâmetro do filtro: 4.2 in. (10.7 cm)
• área de filtração: 0.62 m²
• diâm. conexão de entrada: 9/16 in.
• inlet to outlet width: 33.5 cm (13.2 in.)
• diam. conexão de saída: 9/16 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^®
• tamanho de poro: 0.45 μm pore size
• ponto de bolha: ≥1930 mbar (28 psig), air with water at 23 °C
• conector: 1/4 in. fitting (vent/drain hose barb with double O-ring seal); (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Descrição

Descrição geral

Device Configuration: Capsule

Nota de preparo

Sterilization Method:
Gamma compatible to 40 kGy. 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 análise

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

Outras 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

Informações legais

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

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