CVBW01PK1

Vitipore^® II Cartridge Filter

sterile, pore size 0.22 μm, cartridge nominal length 10 in. (25 cm), Code 0 (2-222; O-rings)

• Synonim(y): Vitipore^® II Cartridge Filter 10 in. 0.22 μm Code 0
• Kod UNSPSC: 23151806
• eCl@ss: 32031690

Właściwości

• Materiały: PVDF ; polypropylene ; polypropylene support; silicone seal
• zgodność regionalna: meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food); meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• sterylność: sterile
• Właściwości: hydrophilic
• producent / nazwa handlowa: Vitipore^®
• Parametry: ≤15.2 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water); 0.35 bar max. differential pressure (5 psid) at 135 °C (Forward); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 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)
• długość nominalna kartridża: 10 in. (25 cm)
• Średnica: 6.9 cm (2.7 in.)
• powierzchnia filtracyjna: 0.78 m²
• substancje ekstrahujące się grawimetrycznie: ≤23 mg/cartridge
• macierz: Vitipore^® II
• wielkość porów: 0.22 μm nominal pore size; 0.22 μm pore size
• moc wejściowa: sample type liquid; sample type food(s); sample type beverage(s); sample type bottled water; sample type beer; sample type wine
• punkt pęcherzykowania: ≥3100 mbar (45 psig), air with water at 23 °C
• kod wkładu: Code 0 (2-222; O-rings)

Opis

Opis ogólny

Device Configuration: Cartridge

Inne uwagi

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.

Uwaga dotycząca przygotowania

Sterilization Method
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 30 times for 30 min @ 80 °C maximum

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).

Komentarz do analizy

Gravimetric Extractables: after 24 hours in water at controlled room temperature

Informacje prawne

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

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

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