Millipore Sigma Vibrant Logo

VPMD103NB1 Viresolve® Pro Modus 1.3 Device

Viresolve® Pro Modus 1.3 Device MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
View Products on Sigmaaldrich.com
VPMD103NB1
1  
Retrieving price...
Price could not be retrieved
Minimum Quantity is a multiple of
Maximum Quantity is
Upon Order Completion More Information
You Saved ()
 
—
Request Pricing
—
Limited Availability Limited Availability
In Stock 
Discontinued
Limited Quantities Available
Availability to be confirmed
    Remaining : Will advise
      Remaining : Will advise
      Will advise
      Contact Customer Service
      Contact Customer Service

       

      Contact Customer Service

      Overview

      Replacement Information
      Description
      Catalogue NumberVPMD103NB1
      Trade Name
      • Viresolve®
      DescriptionViresolve® Pro Modus 1.3 Device
      References
      Product Information
      HS Code8421 29 90
      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
      Applications
      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.
      Dimensions
      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
      Chemistry
      • 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
      Specifications
      Global Trade Item Number
      Catalogue Number GTIN
      VPMD103NB1 04053252720550

      Documentation

      Material Qualification Dossier

      TitleVersion
      5.0

      Quality Management Dossier (Open Access)

      Title

      Operational Excellence Dossier

      Title

      Certificates of Quality

      Title
      Viresolv Pro Modus 1.3 Device C2JB24711
      Viresolve Pro Magnus 1.3 Device C0AB23121
      Viresolve Pro Magnus 1.3 Device C1HB71062
      Viresolve Pro Magnus 1.3 Device C9JA67595
      Viresolve Pro Magnus 1.3 Device C9PA15736
      Viresolve Pro Magnus 1.3 Device C9SA43605
      Viresolve Pro Modos 1.3 Device C1KB71110
      Viresolve Pro Modus 1.3 Device C1MB71086
      Viresolve Pro Modus 1.2 Device C2AB70448
      Viresolve Pro Modus 1.3 C7EA20251
      Show more

      User Guides

      Title
      Viresolve® Pro Modus and Magnus Devices User Guide