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Merck
CN

KZRVA10TH1

Opticap® XL 10 Capsule Media: Viresolve® NFR

Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 9/16 in. Hose Barb Max Operating Pressure: 80 psi @ 25 °C

Synonym(s):

Opticap XL 10 Viresolve NFR TC/HB

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About This Item

eCl@ss:
32031690
UNSPSC Code:
23151806

Key Documents

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Product Name

Opticap® XL 10 Capsule Media: Viresolve® NFR, Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 9/16 in. Hose Barb Max Operating Pressure: 80 psi @ 25 °C

parameter

25 °C max. inlet temp., 80 psig max. inlet pressure

device size

10 in.

inlet connection diam.

1 1/2 in.

outlet connection diam.

9/16 in.

matrix

Viresolve® NFR

fitting

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

suitability

suitable for endotoxin

material

polyethersulfone , polypropylene

Quality Level

400

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General description

A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.

Analysis Note

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.

Other Notes

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.

Legal Information

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

Disclaimer

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

Regulatory Information

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