CGW204S03

Polysep^™ II 1.0/1.2 µm nominal, Cartridge

pore size 1.2/1.0 μm, filter diam. 7.1 cm (2.8 in.), cartridge nominal length 100 cm (40 in.)

• UNSPSC-Code: 23151806

Eigenschaften

• Materialien: borosilicate glass fiber (BGF) prefilter; polypropylene prefilter; polypropylene support; silicone seal
• Qualitätsniveau: 400
• Einhaltung gesetzlicher Vorschriften: meets FDA 21 CFR 177-182 (all component materials)
• Sterilität: non-sterile
• Kompatibilität mit Sterilisationsverfahren: autoclavable compatible; steam-in-place compatible
• Produktlinie: Polysep^™
• Leistungsmerkmale: hydrophilic
• Hersteller/Markenname: Polysep^™
• Parameter: 3.5 bar max. differential pressure (50 psid) at 25 °C; 3.5 bar max. inlet pressure (50 psi) at 25 °C
• Methode(n): prefiltration: suitable
• Länge: 40 in.
• Breite: 2.7 in.
• Nennlänge Kartusche: 100 cm (40 in.)
• Filterdurchm.: 7.1 cm (2.8 in.)
• filter filtration area: 1.84 m²
• Verunreinigungen: ≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction ); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction )
• Matrix: Polysep^™ II
• pore size: 1.0/1.2 μm nominal pore size; 1.2/1.0 μm pore size
• Kartuschencode: Code 0

Beschreibung

Allgemeine Beschreibung

Device Configuration: Cartridge

Leistungsmerkmale und Vorteile

Double Layer

Verpackung

Double Easy-Open bag

Angaben zur Herstellung

Non-Fiber Releasing: This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).

Sterilization Method: 10 autoclave cycles or SIP for 30 min at 121 °C

Hinweis zur Analyse

Gravimetric Extractables: the extractables level was equal to or less than 140 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 20 L

Sonstige Hinweise

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 first page of Visual Inspection Guide and introduction section of Mixed cellulose esters Tech Brief
• Storage Statement: Please refer Mixed cellulose esters Tech Brief
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Rechtliche Hinweise

Polysep is a trademark of Sigma-Aldrich Co. LLC