MPVL20CA3

Millipak^® 200 Capsule Media: Durapore^® 0.1 µm

Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 9/16 in. Hose Barb Outlet: 9/16 in. Hose Barb

• Synonim(y): Gamma Compatible Millipak -200 Filter Unit 0.1 μm 9/16 in. HB/HB, Durapore^® 0.1 µm, Millipak^® Capsule
• UNSPSC Code: 23151806

Właściwości

• Nazwa produktu: Millipak^® 200 Capsule Media: Durapore^® 0.1 µm, Chemistry: Hydrophilic Polyvinylidene Fluoride (PVDF) Inlet: 9/16 in. Hose Barb Outlet: 9/16 in. Hose Barb
• material: PVDF vent cap, polycarbonate support, polycarbonate housing, PVDF membrane
• Quality Segment: 400
• sterility: non-sterile
• sterilization compatibility: gamma compatible; x-ray compatible
• 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
• L: 6.0 in.
• W: 3.0 in.
• filter diam.: 7.6 cm (3.0 in.)
• filtration area: 1000 cm²
• inlet connection diam.: 9/16 in.
• outlet connection diam.: 9/16 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: 14 mm (9/16 in.) inlet hose barb, 14 mm (9/16 in.) outlet hose barb

Opis

General description

Device Configuration: 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: after 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

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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