KZRVA10TH1

Opticap XL 10 Viresolve NFR TC/HB

• Code UNSPSC : 23151806
• eCl@ss : 32031690

Propriétés

• Matériaux: polyethersulfone ; polypropylene
• Niveau de qualité: 400
• Paramètres: 25 °C max. inlet temp.; 80 psig max. inlet pressure
• device size: 10 in.
• Diam. du raccord d'entrée: 1 1/2 in.
• Diam. du raccord de sortie: 9/16 in.
• Matrice: Viresolve^® NFR
• Raccords: 16 mm (5/8 in.) hose barb; 1/4 in. hose barb (double O-ring Seal); inlet sanitary flange; outlet hose barb; 38 mm (1 1/2 in.) sanitary flange drain/vent
• Adéquation: suitable for endotoxin (A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.)

Description

Description générale

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

The extractables level was equal to or less than 35 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.

Autres remarques

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.

Informations légales

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

Clause de non-responsabilité

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