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Merck
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KVPVA1TTT1

Millipore

Opticap® XLT Viresolve® NFP

Parvovirus removal

Synonyme(s) :

Opticap XLT10 Viresolve NFP 1-1/2 in. TC/TC

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About This Item

Code UNSPSC :
23151806
eCl@ss :
32031690

Matériaux

PVDF (modified)
polypropylene
polypropylene support
polypropylene vent cap
silicone O-ring (for vent)
silicone seal

Fabricant/nom de marque

Viresolve®

Paramètres

≤10 mL/min air diffusion at 3.45 bar (50 psig) and 23 °C (in water)
25 °C max. inlet temp.
250 L process volume
3.4 bar max. differential pressure (50 psid) (Reverse)
5.5 bar max. differential pressure (80 psid) (Forward)
80 psig max. inlet pressure

Technique(s)

protein purification: suitable

Longueur

38.1 cm (15 in.)

device size

10 in.

Surface de filtration

0.42 m2

Diam. du raccord d'entrée

1.5 in.

Largeur, de l'entrée à la sortie

15.2 cm (6.0 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)

Matrice

Viresolve® NFP

Raccords

1/4 in. drain/vent hose barb (with double O-ring Seal)
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

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Description générale

Device Configuration: Capsule
T-line/Gauge Port: T-line

Application

Parvovirus 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: 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

Sterilization Method
Water wet filter for 5 min @ 3.4 bar (50 psi); liquid cycle, slow exhaust @ 123 °C maximum 60 min
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

TOC/Conductivity
After sterilization and a controlled water flush of 12 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.

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.

Certificats d'analyse (COA)

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