Depth & Pod Filtration

ViresolvePro Magnus 2.2 Device 요약정보 및 구매

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제조사 Merck
원산지 USA

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Description
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
Applications
Key Applications
  • Large volume processing
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
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
Chemistry
  • Polyvinylidene Fluoride (PVDF)
Materials of ConstructionMembrane: Polyethersulfone (PES); Gaskets: Silicone; Housing: Polyvinylidene fluoride (PVDF)
Packaging Information
Material Size1

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