Merck - VPMD101NB1 - VPMD101NB1, Viresolve(R) Pro Modus 1.1

ITEM #: 11570572
Catalogue Number VPMD101NB1
Trade Name

• Viresolve ®

Viresolve® Pro Modus 1.1 Device
Device Configuration Modus 1.1 Device
Connections, Inlet/Outlet Inlet/outlet: 3/4" sanitary TC fittings
Connections, Vent/Drain Integrated vent: 1/4" Hose barb with double O-ring seal
European Pressure Equipment Directive 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.
Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Quality Level MQ400
Key Applications

• Scale studies/Pilot

Maximum Inlet Pressure (psig) 60 psig
Non-Fiber Releasing 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).
TOC/Conductivity After a controlled water flush of 50 L/m², samples exhibited less than 500 ppb TOC per USP and less than 1.3 µS/cm per USP .
USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Height 5.92 cm (2.33 in.)
Width 9.22 cm (3.63 in.)
Length 18.62 cm (7.33 in.)
Filtration Area 0.017 m²
Device Size 1.1 in.
Chemistry

• Polyvinylidene Fluoride (PVDF)

Materials of Construction Membrane: Polyethersulfone (PES); Gaskets: Silicone; Housing: Polyvinylidene fluoride (PVDF)
Material Size 1