KGEPS1THH1

Millipore Express^® SHF 0.2µm, Opticap^® XLT 10 Capsule

Fittings 5/8 in. HB, Sterile

• Código UNSPSC: 23151806

Propiedades

• Nombre del producto: Millipore Express^® SHF, Opticap^® XLT Cápsula, sterile, Opticap^® XLT 10, cartridge nominal length 10 in. (25 cm), filter diam. 10.7 cm (4.2 in.)
• Materiales: polyester support; polypropylene device (gamma stable); polypropylene housing; polypropylene vent cap; polysulfone device; silicone seal
• Nivel de calidad: 400
• cumplimiento norm.: meets FDA 21 CFR 177-182 (all component materials)
• esterilidad: irradiated; sterile
• Línea del producto: Opticap^® XLT 10
• Características: hydrophilic
• fabricante / nombre comercial: Millipore Express^®
• Parámetros: ≤32.7 mL/min air diffusion at 2.8 bar (40 psig) (in water); 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward); 1.0 bar max. inlet pressure (15 psi) at 80 °C; 100 psi max. differential pressure (6.9 bar) (intermittent); 2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward); 5.5 bar max. inlet pressure (80 psi) at 25 °C; 6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent); 6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent); 80 psi max. differential pressure (5.5 bar) (continuous); 80 psig max. inlet pressure
• técnicas: sterile filtration: suitable
• longitud nominal del cartucho: 10 in. (25 cm)
• L unidad: 37.6 cm (14.8 in.)
• Tamaño de la unidad: 10 in.
• diám. del filtro: 10.7 cm (4.2 in.)
• Área de filtración del filtro: 0.57 m²
• impurezas: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (sample aqueous extraction)
• Matriz: Millipore Express^® SHF
• tamaño de poro: 0.2 μm pore size
• punto de burbuja: ≥4000 mbar (58 psig), air with water
• Adaptador: (16 mm (5?8 in.) Hose Barb Inlet and Outlet)

Descripción

Descripción general

Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle.

Envase

Double Easy-Open bag

Nota de preparación

Sterilization Method:
3 autoclave cycles of 60 min at 123 °C; not in-line steam sterilizable

This product was manufactured with a MILLIPORE EXPRESS^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (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.

TOC/Conductivity: After sterilization and a controlled water flush of 11 L, samples exhibited &#x3C 500 ppb TOC per USP &#x3C 643 &#x3C and &#x3C 1.3 μS/cm per USP &#x3C 645 &#x3C at 25 °C.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 1.5 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 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

ASTM is a registered trademark of American Society for Testing and Materials

MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany

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