CGW172S48

Polysep^™ II 1.0/0.2/0.1 µm nominal, Cartridge

pore size 1.0/0.2/0.1 μm, cartridge nominal length 50 cm (20 in.)

• UNSPSC Code: 23151806

Properties

• material: borosilicate glass fiber (BGF) membrane; fluoroelastomer O-ring; mixed cellulose esters (MCE) membrane; polypropylene support
• Quality Level: 400
• reg. compliance: meets FDA 21 CFR 177-182 (all component materials)
• sterility: non-sterile
• Sterilization Compatibility: autoclavable compatible; steam-in-place compatible
• product line: Polysep^™
• feature: hydrophilic
• manufacturer/tradename: Polysep^™
• technique(s): prefiltration: suitable
• L: 20 in.
• W: 2.7 in.
• cartridge nominal length: 50 cm (20 in.)
• filtration area: 0.84 m²
• matrix: Polysep^™ II
• pore size: 1.0/0.2/0.1 μm nominal pore size; 1.0/0.2/0.1 μm pore size
• cartridge code: Code 7

Description

General description

Device Configuration: Cartridge

Features and Benefits

Triple Layer

Preparation Note

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).

Analysis Note

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.

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 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.

Legal Information

Polysep is a trademark of Sigma-Aldrich Co. LLC