VPMD103NB1 Viresolve® Pro Modus 1.3 Device

Retrieving price...
Price could not be retrieved
Minimum Quantity needs to be mulitiple of
Upon Order Completion More Information
You Saved ()
Request Pricing
Limited AvailabilityLimited Availability
Limited Quantities Available
    Remaining : Will advise
      Remaining : Will advise
      Will advise
      Contact Customer Service
      Contact Customer Service


      Contact Customer Service


      Replacement Information

      Key Specifications Table

      Catalogue NumberVPMD103NB1
      Trade Name
      • Viresolve®
      DescriptionViresolve® Pro Modus 1.3 Device
      Product Information
      Device ConfigurationModus 1.3 Device
      Connections, Inlet/OutletInlet/outlet: 3/4" sanitary TC fittings
      Connections, Vent/DrainIntegrated vent: 1/4" Hose barb with double O-ring seal
      European Pressure Equipment DirectiveEMD 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 PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
      Quality LevelMQ400
      Key Applications
      • Pilot/small volumes
      Biological Information
      Physicochemical Information
      Maximum Inlet Pressure (psig)60 psig
      Non-Fiber ReleasingThis 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/ConductivityAfter a controlled water flush of 50 L/m², samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645>.
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Height13.56 cm (5.34 in.)
      Width9.22 cm (3.63 in.)
      Length18.62 cm (7.33 in.)
      Filtration Area0.22 m²
      Device Size1.3 in.
      Materials Information
      • Polyvinylidene Fluoride (PVDF)
      Materials of ConstructionMembrane: Polyethersulfone (PES); Gaskets: Silicone; Housing: Polyvinylidene fluoride (PVDF)
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Packaging Information
      Material Size1
      Transport Information
      Supplemental Information


      Material Qualification Dossier


      Quality Management Dossier


      Operational Excellence Dossier


      Viresolve® Pro Modus 1.3 Device SDS


      Safety Data Sheet (SDS) 

      Certificates of Quality

      Viresolve Pro Magnus 1.3 Device C0AB23121
      Viresolve Pro Magnus 1.3 Device C9JA67595
      Viresolve Pro Magnus 1.3 Device C9PA15736
      Viresolve Pro Magnus 1.3 Device C9SA43605
      Viresolve Pro Modus 1.3 C7EA20251
      Viresolve Pro Modus 1.3 Device
      Viresolve Pro Modus 1.3 Device
      Viresolve Pro Modus 1.3 Device C0KB03633
      Viresolve Pro Modus 1.3 Device C5DA84803
      Viresolve Pro Modus 1.3 Device C5PA87559

      User Guides

      Viresolve® Pro Modus and Magnus Devices User Guide