CHGL03TP3

Multilayer Durapore^® 0.45/0.22 µm, Cartridge

cartridge nominal length 30 in. (75 cm), filter diam. 2.7 in. (6.9 cm), Code 0

• Synonim(y): Multilayer Durapore^® 0.45/0.22 µm, Cartridge
• UNSPSC Code: 23151806

Właściwości

• Nazwa produktu: Multilayer Durapore^® Cartridge, Chemistry: 0.45 / 0.22 µm Hydrophilic Polyvinylidene Fluoride (PVDF) Configuration: 30 in. Code 0
• Quality Segment: 400
• material: polypropylene device, polypropylene support, silicone seal
• reg. compliance: meets FDA 21 CFR 177-182 (all component materials)
• sterility: non-sterile
• sterilization compatibility: autoclavable compatible; steam-in-place compatible
• product line: Durapore^®
• feature: hydrophilic
• manufacturer/tradename: Durapore^®
• parameter: ≤32.4 mL/min air diffusion at 2.75 bar (40 psig) (in water), 0.35 bar max. differential pressure (5 psid) at 135 °C (forward), 0.35 bar max. inlet pressure (5 psi) at 135 °C (forward), 1.7 bar max. differential pressure (25 psid) at 80 °C (forward), 1.7 bar max. inlet pressure (25 psi) at 80 °C (forward), 3.5 bar max. differential pressure (50 psid) at 25 °C (reverse; intermittent), 3.5 bar max. inlet temp. (50 psi) at 25 °C (reverse; intermittent), 5.5 bar max. differential pressure (80 psid) at 25 °C (forward), 5.5 bar max. inlet pressure (80 psi) at 25 °C (forward)
• technique(s): sterile filtration: suitable
• L: 30 in.
• W: 2.7 in.
• cartridge nominal length: 30 in. (75 cm)
• device size: 30 in.
• filter diam.: 2.7 in. (6.9 cm)
• filter filtration area: 1.65 m²
• impurities: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction), <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Multilayer Durapore^®
• pore size: 0.45/0.22 μm pore size
• bubble point: ≥3450 mbar (50 psig), air with water
• code: Code 0

Opis

General description

Device configuration: Cartridge
Cartridge type: Liquid

Preparation Note

Sterilization Method: 30 SIP cycles of 30 min at 135°C; 30 autoclave cycles of 60 min at 126°C

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.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 4.5L

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 to 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

Legal Information

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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