material
polyethersulfone
polypropylene
Quality Level
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
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
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.
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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