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Opticap® XLT 10 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
동의어(들):
Opticap XLT 10 Viresolve NFR TC/TC
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크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
eCl@ss:
32031690
UNSPSC Code:
23151806
제품 이름
Opticap® XLT 10 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 Segment
description
T-line with 1-1/2 in. Gauge Port
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.
1-1/2 in.
matrix
Viresolve® NFR
fitting
inlet sanitary flange, outlet sanitary flange
suitability
suitable for endotoxin
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.
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