MPVL20CL3

Durapore^® 0,1 µm, Cápsula Millipak^®

Millipak^® 200, filtration area 1000 cm², matrix Durapore^®

• Sinónimos: Gamma Compatible Millipak -200 Filter Unit 0.1 μm 1-1/2 in. TC/TC
• Código UNSPSC: 23151806

Propiedades

• Materiales: PVDF ; PVDF vent cap; polycarbonate ; polycarbonate support
• Nivel de calidad: 400
• esterilidad: irradiated; non-sterile
• Compatibilidad de esterilización: gamma compatible; gamma compatible
• Línea del producto: Millipak^® 200
• Características: gamma compatible; hydrophilic
• fabricante / nombre comercial: Millipak^®
• Parámetros: 0.35 bar max. differential pressure (5 psid) at 123 °C (Forward); 0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 100 L process volume; 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward); 5.2 bar max. inlet pressure (75 psi) at 25 °C; 8.5 L/min flow rate at 2.45 bar (ΔP)
• técnicas: sterile filtration: suitable
• Longitud: 6.0 in.
• Anchura: 3.0 in.
• Diámetro: 7.6 cm (3.0 in.)
• filtración área: 1000 cm²
• diám. conexión a entrada: 1.5 in.
• diám. conexión a salida: 1.5 in.
• impurezas: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• extraíbles gravimétricos: ≤5 mg/device
• matriz: Durapore^®
• tamaño de poro: 0.1 μm
• punto de burbuja: ≥4830 mbar (70 psig), air with water at 23 °C
• Adaptador: inlet sanitary flange; outlet sanitary flange; (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Descripción

Descripción general

Device Configuration: Capsule

Envase

Double Easy-Open bag

Otras notas

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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.

Nota de preparación

Sterilization Method
3 autoclave cycles of 90 min @ 123°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 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.

Gravimetric Extractables: after 24 hours in water at controlled room temperature

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥200 mL

Información legal

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

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

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