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Opticap^® XLT 20 Capsule Media: Viresolve^® NFR

Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange T-line with 1-1/2 in. Gauge Port Max Operating Pressure: 80 psi @ 25 °C

• Synonym(s): Opticap XLT 20 Viresolve NFR TC/TC
• eCl@ss: 32031690
• UNSPSC Code: 23151806

Properties

• Product Name: Opticap^® XLT 20 Capsule Media: Viresolve^® NFR, Chemistry: Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange T-line with 1-1/2 in. Gauge Port Max Operating Pressure: 80 psi @ 25 °C
• material: polyethersulfone
• Quality Level: 400
• description: T-line with 3/4 in. Gauge Port
• parameter: 25 °C max. inlet temp., 80 psig max. inlet pressure
• device size: 20 in.
• inlet connection diam.: 1 1/2 in.
• outlet connection diam.: 1-1/2 in.
• matrix: Viresolve^® NFR
• fitting: inlet sanitary flange, outlet sanitary flange
• suitability: suitable for endotoxin

Description

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 70 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.