MPVL06GH2

Durapore^® 0.1 µm, Millipak^® Capsule

sterile, Millipak^® 60

• Synonym(s): Sterile Millipak-60 Filter Unit 0.1 μm 1/4 in. HB/HB w/bell
• UNSPSC Code: 23151806
• NACRES: NB.24
• eCl@ss: 32031690

Properties

• Product Name: Durapore^® 0.1 µm, Millipak^® Capsule, sterile, Millipak^® 60
• material: PVDF membrane; PVDF vent cap; polycarbonate ; polycarbonate support
• sterility: irradiated; sterile
• product line: Millipak^® 60
• feature: hydrophilic
• manufacturer/tradename: Millipak^®
• 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); 1.9 L/min flow rate at 1.75 bar (ΔP); 25 °C max. temp.; 30 L process volume; 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward); 5.2 bar max. inlet pressure (75 psi) at 25 °C
• technique(s): sterile filtration: suitable
• filtration area: 300 cm²
• inlet connection diam.: 1/4 in.
• outlet connection diam.: 1/4 in.
• impurities: ≤0.5 EU/mL (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetric extractables: ≤2 mg/device
• matrix: Durapore^®
• pore size: 0.1 μm
• bubble point: ≥4830 mbar (70 psig), air with water at 23 °C
• fitting: inlet hose barb; outlet hose barb (with bell); (6 mm (1/4 in.) Hose Barb Inlet and Outlet with filling bell)
• shipped in: ambient
• Quality Level: 400

Description

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

General description

Device Configuration: Gamma Gold 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 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.

Packaging

Blister

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).

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