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VPMD102NB1 Viresolve® Pro Modus 1.2 Device

Viresolve® Pro Modus 1.2 Device : FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.
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VPMD102NB1
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      Aperçu

      Replacement Information
      Description
      Catalogue NumberVPMD102NB1
      Trade Name
      • Viresolve®
      DescriptionViresolve® Pro Modus 1.2 Device
      References
      Product Information
      HS Code8421 29 90
      Device ConfigurationModus 1.2 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
      Height7.85 cm (3.09 in.)
      Width9.22 cm (3.63 in.)
      Length18.62 cm (7.33 in.)
      Filtration Area0.07 m²
      Device Size1.2 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
      Référence GTIN
      VPMD102NB1 04053252450624

      Documentation

      Material Qualification Dossier

      TitreVersion
      5.0

      Quality Management Dossier (Open Access)

      Title

      Operational Excellence Dossier

      Title

      Certificats de qualité

      Titre
      Viresolove Pro Modus 1.2 Device C8KA16595
      Viresolve Pro Modus 1.2 Devicce - C8AA03919V
      Viresolve Pro Modus 1.2 Device C0DB58383
      Viresolve Pro Modus 1.2 Device C0KB01520
      Viresolve Pro Modus 1.2 Device C0NB37195
      Viresolve Pro Modus 1.2 Device C1AB86864
      Viresolve Pro Modus 1.2 Device C1DB08847
      Viresolve Pro Modus 1.2 Device C1EB91617
      Viresolve Pro Modus 1.2 Device C1EB91625
      Viresolve Pro Modus 1.2 Device C1HB71076
      Show more

      Manuels d'utilisation

      Titre
      Viresolve® Pro Modus and Magnus Devices User Guide