KGEPG3FBB1

Millipore Express^® SHF 0.2µm, Opticap^® XLT 30 Capsule

Fittings 1 in. HB/HB, Gamma Compatible

• Kod UNSPSC: 23151806

Właściwości

• Nazwa produktu: Millipore Express^® SHF, Opticap^® XLT Capsule, Opticap^® XLT 30, cartridge nominal length 30 in. (75 cm), filter diam. 19.8 cm (7.8 in.)
• Materiały: polyester support; polypropylene device; polypropylene housing; polypropylene vent cap; polysulfone device; silicone seal
• Poziom jakości: 400
• zgodność regionalna: meets FDA 21 CFR 177-182 (all component materials)
• sterylność: non-sterile
• Kompatybilność ze sterylizacją: gamma compatible
• linia produktu: Opticap^® XLT 30
• Właściwości: hydrophilic
• producent / nazwa handlowa: Millipore Express^®
• Parametry: 1.0 bar max. inlet pressure (15 psi) at 80 °C; 1000 mbar max. differential pressure (15 psi) at 80 °C (Forward); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 2100 bar max. differential pressure (30 psi) at 25 °C (Reverse; intermittent); 25 °C max. inlet temp.; 5.5 bar max. inlet pressure (80 psi) at 23 °C; 5500 mbar max. differential pressure (80 psi) at 25 °C (Forward); 6.9 bar max. inlet pressure (100 psi) at 23 °C (intermittent); 6900 mbar max. differential pressure (100 psi) at 25 °C (Forward; intermittent); 80 psig max. inlet pressure
• metody: sterile filtration: suitable
• Szerokość: 7.8 in.
• długość nominalna kartridża: 30 in. (75 cm)
• Dł. urządzenia: 87.2 cm (34.3 in.)
• Rozmiar urządzenia: 30 in.
• śr. filtra: 19.8 cm (7.8 in.)
• Powierzchnia filtracyjna filtra: 1.71 m²
• zanieczyszczenia: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (sample aqueous extraction)
• Matryca: Millipore Express^® SHF
• wielkość porów: 0.2 μm pore size
• punkt pęcherzykowania: ≥4000 mbar (58 psig), air with water
• dopasowywanie: (25 mm (1 in.) Hose Barb Inlet and Outlet)

Opis

Opis ogólny

Device Configuration: Capsule

T-line/Gauge Port: T-line with 3/4 in. Gauge Port

Opakowanie

Double Easy-Open bag

Uwaga dotycząca przygotowania

Sterilization Method:
3 autoclave cycles of 60 min at 126 °C; capable of 45 kilogray (4.5 Megarad) gamma exposure; not in-line steam sterilizable

This product was manufactured with a MILLIPORE EXPRESS^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (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 of 33 L, samples exhibited &#x3C 500 ppb TOC per USP &#x3C 643 &#x3C and &#x3C 1.3 μS/cm per USP &#x3C 645 &#x3C 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 installation section of OPTICAP^® XL Capsules and OPTICAP^® XLT Capsules 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

MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany

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

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