KZRVA10TT1

Opticap^® XL Viresolve^® NFR

Retrovirus removal

• Synonyme(s) : Opticap XL10 Viresolve NFR 1-1/2 in. TC/TC
• Code UNSPSC : 23151806
• eCl@ss : 32031690

Propriétés

• Matériaux: polyethersulfone ; polypropylene ; polypropylene support; polypropylene vent cap; silicone seal
• Niveau de qualité: 400
• Caractéristiques: holdup volume 175 mL
• Fabricant/nom de marque: Viresolve^®
• Paramètres: ≤16 mL/min air diffusion at 3.45 bar (50 psig) and 23 °C (in water); 25 °C max. inlet temp.; 3.4 bar max. differential pressure (50 psid) (Reverse); 5.5 bar max. differential pressure (80 psid) (Forward); 600-1200 L process volume; 80 psig max. inlet pressure
• Technique(s): protein purification: suitable
• Longueur: 33 cm (13 in.)
• device size: 10 in.
• Surface de filtration: 0.43 m²
• Diam. du raccord d'entrée: 1.5 in.
• Diam. du raccord de sortie: 1.5 in.
• Impuretés: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Extractibles par gravimétrie: ≤35 mg
• Matrice: Viresolve^® NFR
• Raccords: 1/4 in. drain/vent hose barb (with double O-ring Seal); inlet sanitary flange; 38 mm (1 1/2 in.) inlet/outlet sanitary flange; outlet sanitary flange

Description

Description générale

Device Configuration: Capsule

Application

Retrovirus removal

Conditionnement

Double Easy-Open bag

Autres remarques

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

Directions for Use

• Organism Retention: Retrovirus
• Mode of Action: Filtration (size exclusion)
• Application: Protein purification
• Intended Use: Viral clearance
• Instructions for Use: Please see the user guide (pg. 3) 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

Sterilization Method
After wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C, using liquid cycle, slow exhaust.

This product was manufactured with a Viresolve^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Remarque sur l'analyse

Gravimetric Extractables: after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4 L

Informations légales

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

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

Clause de non-responsabilité

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.