MPHL10CA3

Durapore^® 0.45 µm, Millipak^® Capsule

filtration area 500 cm², matrix Durapore^®

• Szinonimák: Gamma Compatible Millipak -100 Filter Unit 0.45 μm 9/16 in. HB/HB
• UNSPSC kód: 23151806

Tulajdonságok

• material: PVDF ; PVDF vent cap; polycarbonate ; polycarbonate support
• Minőségi szint: 400
• sterilitás: irradiated; non-sterile
• Sterilizálási kompatibilitás: gamma compatible
• termékcsalád: Millipak^®
• Jellemzők: gamma compatible; hydrophilic
• gyártó/kereskedő neve: 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); 23 L/min flow rate at 2.6 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
• technika/technikák: bioburden reduction: suitable
• Hosszúság: 5.1 in.
• Szélesség: 3.0 in.
• szűrőfelület: 500 cm²
• bemeneti csatl. átmérője: 9/16 in.
• kimeneti csatl. átmérője: 9/16 in.
• szennyeződések: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetriás extrahálható anyagok: ≤2.5 mg/device
• matrix: Durapore^®
• pórusméret: 0.45 μm
• buborékpont: ≥1790 mbar (26 psig), air with water at 23 °C
• szerelvény: inlet hose barb; outlet hose barb; (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Leírás

Általános leírás

Device Configuration: Capsule

Kiszerelés

Double Easy-Open bag

Egyéb megjegyzések

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.

Elkészítési megjegyzés

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).

Analízis megjegyzés

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

Jogi információk

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

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