Viresolve Pro Modus 1.1 护罩 H

32031690

Device Configuration: Modus 1.1 Shield H

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

This product was manufactured with materials that meet the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

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

400

PVDF housing
polyethersulfone membrane
silicone O-ring
white device

EMPROVE^® Filter

Viresolve^®

4.1 bar max. inlet pressure (60 psig)

5.92 cm (2.33 in.)

5.9 cm (2.3 in.) × 18.2 cm (7.3 in.) × 9.2 cm (3.6 in.)

18.62 cm (7.33 in.)

9.22 cm (3.63 in.)

0.017 m²

0.017 m²

0.37 kg (0.81 lb)

<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

3/4 in. inlet/outlet sanitary fitting(s)
1/8 in. integrated vent hose barb (with double O-ring seal)

4°C - 30°C

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.