CVSS71TP3

Multimedia Durapore^® 0.5/0.2/0.22 µm, Cartridge

pore size 0.5/0.2/0.22 μm, cartridge nominal length 10 in. (25 cm), Code 7 (2-226; O-rings w/locking-tabs)

• Synonym(e): Durapore Multimedia Cartridge Filter 10 in. 0.5+0.2+0.22 μm Code 7, Multimedia Durapore^® 0.5/0.2/0.22 µm, Cartridge
• eCl@ss: 32031690
• UNSPSC Code: 23151806

Eigenschaften

• Produktname: Multimedia Durapore^® Cartridge, Chemistry: 0.5 / 0.2 / 0.22 µm Hydrophilic Mixed Cellulose Esters / Polyvinylidene Fluoride (MCE / PVDF)Configuration: 10 in. Code 7
• Quality Segment: 400
• material: PVDF , mixed cellulose esters (MCE) , mixed cellulose esters (MCE) prefilter, polypropylene , polypropylene support, silicone seal
• reg. compliance: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• sterility: non-sterile
• sterilization compatibility: autoclavable compatible; steam-in-place compatible
• product line: Durapore^®
• feature: hydrophilic
• manufacturer/tradename: Durapore^®
• parameter: ≤10.8 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), 0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward), 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward), 1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward), 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent), 3.5 bar max. inlet pressure (50 psi) 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 25 °C (Forward)
• technique(s): sterile filtration: suitable
• W: 2.7 in.
• cartridge nominal length: 10 in. (25 cm)
• diam.: 6.9 cm (2.7 in.)
• filtration area: 0.56 m²
• impurities: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction), <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetric extractables: ≤70 mg/cartridge
• matrix: Multimedia Durapore^®
• pore size: 0.5/0.2/0.22 μm pore size
• input: sample type liquid
• bubble point: ≥3450 mbar (50 psig), air with water at 23 °C
• cartridge code: Code 7 (2-226; O-rings w/locking-tabs)

Beschreibung

General description

Device Configuration: Cartridge

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
6 autoclave or SIP cycles of 30 min @ 123 °C

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).

Analysis Note

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

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

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥5 L

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 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.

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

Legal Information

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

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

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 2