MPVL10CA3

Durapore^® 0.1 µm, Millipak^® Capsule

filtration area 500 cm², matrix Durapore^®

• Synonim(y): Gamma Compatible Millipak -100 Filter Unit 0.1 μm 9/16 in. HB/HB
• Kod UNSPSC: 23151806

Właściwości

• Materiały: PVDF ; PVDF vent cap; polycarbonate ; polycarbonate support
• Poziom jakości: 400
• sterylność: irradiated; non-sterile
• Kompatybilność ze sterylizacją: gamma compatible; gamma compatible
• linia produktu: Millipak^®
• Właściwości: gamma compatible; hydrophilic
• producent / nazwa handlowa: Millipak^®
• Parametry: 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); 3.8 L/min flow rate at 2.45 bar (ΔP); 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward); 5.2 bar max. inlet pressure (75 psi) at 25 °C; 50 L process volume
• metody: sterile filtration: suitable
• Długość: 5.1 in.
• Szerokość: 3.0 in.
• Średnica: 7.6 cm (3.0 in.)
• powierzchnia filtracyjna: 500 cm²
• śr. przyłącza doprowadzającego: 9/16 in.
• śr. przyłącza odprowadzającego: 9/16 in.
• zanieczyszczenia: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• substancje ekstrahujące się grawimetrycznie: ≤2.5 mg/device
• macierz: Durapore^®
• wielkość porów: 0.1 μm
• punkt pęcherzykowania: ≥4830 mbar (70 psig), air with water at 23 °C
• dopasowywanie: inlet hose barb; outlet hose barb; (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Opis

Opis ogólny

Device Configuration: Capsule

Opakowanie

Double Easy-Open bag

Inne uwagi

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.

Uwaga dotycząca przygotowania

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).

Komentarz do analizy

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

Informacje prawne

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

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