VBMSPDKNB9

Viresolve^® Barrier Capsule

Process Development Kit

• Synonyme(s) : Viresolve^® Barrier Micro Process Development Kit
• Code UNSPSC : 23151806
• eCl@ss : 32031690

Propriétés

• Matériaux: molded polypropylene component(s); polyethersulfone membrane; teal device
• Fabricant/nom de marque: Viresolve^®
• Paramètres: 4.1 bar max. inlet pressure (60 psig)
• dilution: (process development studies)
• H × Diam.: 3.83 cm (1.51 in.) × 3.07 cm (1.21 in.)
• Hauteur: 3.83 cm (1.51 in.)
• Diamètre: 3.07 cm (1.21 in.)
• Surface de filtration: 3.3 cm²
• Impuretés: <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Raccords: female Luer inlet fitting; male Luer outlet fitting

Description

Description générale

Device Configuration: Micro

Application

Process Development Kit

Autres remarques

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.

Notes préparatoires

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).

Remarque sur l'analyse

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>.

Informations légales

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