MPVL2GCF3

Millipak^® 200 Gamma Gold Capsule Media: Sterile Durapore^® 0.1 µm

Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 3/4 in. Sanitary Flange Outlet: 3/4 in. Sanitary Flange

• Synonim(y): Sterile Millipak-200 Filter Unit 0.1 μm 3/4 in. TC/TC, Millipak^®-200 Capsule Filter Unit
• UNSPSC Code: 23151806

Właściwości

• Nazwa produktu: Millipak^® 200 Gamma Gold Capsule Media: Sterile Durapore^® 0.1 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 3/4 in. Sanitary Flange Outlet: 3/4 in. Sanitary Flange
• Quality Segment: 400
• material: PVDF vent cap, polycarbonate support, PVDF membrane, polycarbonate housing
• sterility: sterile
• product line: Millipak^®
• feature: hydrophilic
• manufacturer/tradename: Durapore^®
• parameter: 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), 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward)
• technique(s): sterile filtration: suitable
• filter diam.: 7.6 cm (3.0 in.)
• filtration area: 1000 cm²
• inlet connection diam.: 3/4 in.
• outlet connection diam.: 3/4 in.
• impurities: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetric extractables: ≤5 mg/device
• matrix: Durapore^®
• pore size: 0.1 μm
• bubble point: ≥70 psi (4830 mbar), air with water at 23 °C
• fitting: 19 mm (3/4 in.) inlet sanitary flange, 19 mm (3/4 in.) outlet sanitary flange

Opis

General description

Device Configuration: Gamma Gold Capsule

Packaging

Double Easy-Open bag

Preparation Note

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).

Analysis Note

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

Other Notes

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.

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

Legal Information

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

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

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

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