MFGL10GL3

Durapore^®, 0,22 µm, Millipak^®-Kapsel für Endabfüllung

Millipak^® Final Fill 100

• UNSPSC Code: 23151806

Eigenschaften

• Produktname: Durapore^®, 0,22 µm, Millipak^®-Kapsel für Endabfüllung, Millipak^® Final Fill 100
• material: polysulfone device; polysulfone support
• agency: meets EP 2.6.14; meets JP 4.01; meets USP 85
• sterility: irradiated; non-sterile
• sterilization compatibility: gamma compatible
• product line: Millipak^® Final Fill 100
• feature: hydrophilic
• manufacturer/tradename: Millipak^®
• parameter: 10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse); 100 L process volume; 3.81 L/min flow rate at 1.1 bar (ΔP); 5.5 bar max. inlet pressure (80 psi) at 25 °C; 80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
• technique(s): sterile filtration: suitable
• L: 4.7 in.
• W: 3.0 in.
• filter filtration area: 500 cm²
• impurities: <0.25 EU/mL USP bacterial endotoxins (LAL test, per device; aqueous extraction); <0.25 EU/mL bacterial endotoxins (LAL test, per device; aqueous extraction)
• matrix: Durapore^®
• pore size: 0.22 μm pore size
• bubble point: ≥50 psi (3450 mbar), air with water
• fitting: (38 mm (1 1/2 in.) Sanitary Flange Inlet and 13 mm (1/2 in.) Hose Barb Outlet)
• Quality Level: 400

Beschreibung

Analysis Note

Bacterial Grow-Through: Quantitative retention of 1 x 10⁷ CFU/cm² Brevundimonas diminuta ATCC^® 19146 per ASTM^® F838 methodology.

General description

Device Configuration: Capsule

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 general guidelines section of user guide shipped with this product
• Storage Statement: Please refer user guide shipped with this product
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

These products are manufactured in a facility which is certified to ISO 9001:2015 Quality Management Systems.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method: Device integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126  °C. Devices can withstand a dose ≤40  kGy gamma exposure.

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), validated based on large volume parenteral specifications as detailed in USP 788 Particulate Matter in Injections

Legal Information

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

ATCC is a registered trademark of American Type Culture Collection

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

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