VPMG202NB1 Viresolve® Pro Magnus 2.2 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 NumberVPMG202NB1
      Trade Name
      • Viresolve®
      DescriptionViresolve® Pro Magnus 2.2 Device
      Product Information
      Device ConfigurationMagnus 2.2 Device
      Connections, Inlet/OutletDisposable 1.5" sanitary TC fittings
      Connections, Vent/DrainVent: disposable 3/4" sanitary TC fitting for the port
      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
      • Large volume processing
      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.
      Height9.50 cm (3.74 in.)
      Width20.96 cm (8.25 in.)
      Length34.29 cm (13.50 in.)
      Filtration Area1.53 m²
      Device Size2.2 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 Magnus 2.2 Device SDS


      Safety Data Sheet (SDS) 

      Certificates of Quality

      Viresilve Pro Magnus 2.2 Device C8MA24274
      Viresolve Pro Magnun 2.2 Device C5EA96238
      Viresolve Pro Magnus 2.2 Device C0HB77145
      Viresolve Pro Magnus 2.2 Device C9HA45311
      Viresolve Pro Magnus 2.2 - C3SA69986
      Viresolve Pro Magnus 2.2 Device
      Viresolve Pro Magnus 2.2 Device
      Viresolve Pro Magnus 2.2 Device
      Viresolve Pro Magnus 2.2 Device C0BB03063
      Viresolve Pro Magnus 2.2 Device C0BB33753

      User Guides

      Viresolve® Pro Modus and Magnus Devices User Guide