MPVL02GH2

Durapore^® 0,1 µm, Cápsula Millipak^®

Millipak^® 20, sterile

• Sinónimos: Sterile Millipak-20 Filter Unit 0.1 μm 1/4 in. HB/HB w/bell
• Código UNSPSC: 23151806
• eCl@ss: 32031690
• NACRES: NB.24

Propiedades

• Materiales: PVDF membrane; PVDF vent cap; polycarbonate ; polycarbonate support
• Nivel de calidad: 400
• esterilidad: irradiated; sterile
• Línea del producto: Millipak^® 20
• Características: hydrophilic
• fabricante / nombre comercial: Millipak^®
• Parámetros: 0.35 bar max. differential pressure (5 psid) at 123 °C (Forward); 0.7 L/min flow rate at 1.75 bar (ΔP); 0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 10 L process volume; 25 °C max. temp.; 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward); 5.2 bar max. inlet pressure (75 psi) at 25 °C
• técnicas: sterile filtration: suitable
• filtración área: 100 cm²
• diám. conexión a entrada: 1/4 in.
• diám. conexión a salida: 1/4 in.
• impurezas: ≤0.5 EU/mL (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• extraíbles gravimétricos: ≤1 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 hose barb; outlet hose barb (with bell); (6 mm (1/4 in.) Hose Barb Inlet and Outlet with filling bell)
• Condiciones de envío: ambient

Descripción

Descripción general

Device Configuration: Gamma Gold Capsule

Envase

Blister

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: using sterilized device after a 200 mL flush and 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