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Multilayer Durapore^® 0.45/0.22 µm, Opticap^® XLT Capsule

Opticap^® XLT 30, cartridge nominal length 30 in. (75 cm), filter diam. 4.2 in. (10.7 cm)

• Kod UNSPSC: 23151806

Właściwości

• Materiały: polyester support; polyethylene support; polypropylene filter; polypropylene housing; silicone seal
• Poziom jakości: 400
• zgodność regionalna: FDA 21CFR177-182 (all component materials)
• sterylność: non-sterile
• Kompatybilność ze sterylizacją: gamma compatible
• linia produktu: Opticap^® XLT 30
• Właściwości: hydrophilic
• producent / nazwa handlowa: Opticap^®
• Parametry: ≤45.0 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water); 1 bar max. inlet pressure (15 psi) at 80 °C; 1.05 bar max. differential pressure (15 psid) at 80 °C (Forward:); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 3.5 bar max. differential pressure (50 psid) 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 23 °C; 80 psig max. inlet pressure
• metody: sterile filtration: suitable
• Szerokość: 7.8 in.
• długość nominalna kartridża: 30 in. (75 cm)
• device L: 87.1 cm (34.3 in.)
• device size: 30 in.
• śr. filtra: 4.2 in. (10.7 cm)
• powierzchnia filtracyjna: 1.81 m²
• śr. przyłącza doprowadzającego: 5/8 in.
• inlet to outlet width: 19.8 cm (7.8 in.)
• śr. przyłącza odprowadzającego: 5/8 in.
• zanieczyszczenia: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• macierz: Multilayer Durapore^®
• pore size: 0.45/0.22 μm pore size
• punkt pęcherzykowania: ≥3450 mbar (50 psig), air with water at 23 °C
• dopasowywanie: 1/4 in. fitting (vent/drain hose barb with double O-ring seal); (16 mm (5?8 in.) Hose Barb Inlet and Outlet)

Opis

Opis ogólny

Device Configuration: Capsule

Opakowanie

Double Easy-Open bag

Uwaga dotycząca przygotowania

Sterilization Method:
Gamma compatible to 45 kGy; 3 autoclave cycles of 60min at 3°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 21CFR210.3(b)(6).

Komentarz do analizy

Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.

TOC/Conductivity: After sterilization and a controlled water flush, samples exhibited less than 500ppb TOC per USP < 643 > and less than 1.3μS/cm per USP < 645 > at 25°C.

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

Inne uwagi

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

Informacje prawne

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

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

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

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