VBMSPDKNB9

Viresolve^® Barrier Capsule

Process Development Kit

• Sinonimo/i: Viresolve^® Barrier Micro Process Development Kit
• Codice UNSPSC: 23151806
• eCl@ss: 32031690

Proprietà

• Materiali: molded polypropylene component(s); polyethersulfone membrane; teal device
• Produttore/marchio commerciale: Viresolve^®
• Parametri: 4.1 bar max. inlet pressure (60 psig)
• dilution: (process development studies)
• Alt. × Diam.: 3.83 cm (1.51 in.) × 3.07 cm (1.21 in.)
• Altezza: 3.83 cm (1.51 in.)
• Diametro: 3.07 cm (1.21 in.)
• Superficie filtrante: 3.3 cm²
• Impurezze: <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Raccordi: female Luer inlet fitting; male Luer outlet fitting

Descrizione

Descrizione generale

Device Configuration: Micro

Applicazioni

Process Development Kit

Altre note

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

Directions for Use

• Organism Retention: Parvovirus
• Mode of Action: Filtration (size exclusion)
• Application: Protein purification
• Intended Use: Viral clearance
• Instructions for Use: Please see the user guide shipped with this product
• Storage Statement: Store at room temperature
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Nota sulla preparazione

This product was manufactured with materials that meet the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Risultati analitici

TOC/Conductivity
After a controlled water flush of 40 L/m², samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64>.

Note legali

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