CVML72TP3

Durapore^® 0.1 µm, Cartridge

cartridge nominal length 20 in. (50 cm), Code 7 (2-226; O-rings w/locking-tabs)

• Sinónimos: Durapore CVML Cartridge Filter 20 in. 0.1 μm Code 7, Durapore^® 0.1 µm, Cartridge
• eCl@ss: 27293007
• UNSPSC Code: 23151806

Propiedades

• Nombre del producto: Durapore^® 0,1 µm, Cartucho, Chemistry: 0.1 µm Hydrophilic Modified Polyvinylidene Fluoride (PVDF)Configuration: 20 in. Code 7
• material: PVDF
• Quality Segment: 400
• 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^®
• technique(s): sterile filtration: suitable
• L: 20 in.
• W: 2.7 in.
• cartridge nominal length: 20 in. (50 cm)
• filtration area: 1.38 m²
• impurities: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetric extractables: ≤48 mg/cartridge
• matrix: Durapore^®
• pore size: 0.1 μm pore size
• input: sample type liquid
• cartridge code: Code 7 (2-226; O-rings w/locking-tabs)

Descripción

General description

Device Configuration: Cartridge

Preparation Note

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

Other Notes

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