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KVPVA3TTT1 Opticap XLT30 Viresolve NFP 1-1/2 in. TC/TC

Parvovirus removal

Opticap XLT30 Viresolve NFP 1-1/2 in. TC/TC MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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KVPVA3TTT1
1  Double Easy-Open bag
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      Overview

      Replacement Information
      Description
      Catalogue NumberKVPVA3TTT1
      Trade Name
      • Viresolve®
      DescriptionOpticap XLT30 Viresolve NFP 1-1/2 in. TC/TC
      References
      Product Information
      Device ConfigurationCapsule
      Connections, Inlet/Outlet38 mm (1-1/2 in.) Sanitary Flange
      Connections, Vent/Drain1/4 in. Hose Barb with double O-ring Seal
      Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid). Reverse: 3.4 bar (50 psid)
      Maximum Inlet Pressure, bar (psi)5.5 bar (80 psi) @ 23 °C
      Good Manufacturing PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
      T-line/Gauge PortT-line
      Quality LevelMQ400
      Applications
      ApplicationParvovirus removal
      Key Applications
      • Protein Purification
      Biological Information
      Bacterial EndotoxinsAqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaViresolve® NFP
      SterilizationWater wet filter for 5 min @ 3.4 bar (50 psi); liquid cycle, slow exhaust @ 123 °C maximum 60 min
      Physicochemical Information
      Inlet ConnectionSanitary Flange
      Outlet ConnectionSanitary Flange
      Air Diffusion at 23 °C≤30 mL/min @ 3.45 bar (50 psig) in water
      Maximum Inlet Pressure (psig)80 psig
      Maximum Inlet Temperature25 °C
      Non-Fiber ReleasingThis product was manufactured with a Viresolve® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
      TOC/ConductivityAfter sterilization and a controlled water flush of 36 L, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 °C.
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Dimensions
      Length86.4 cm (34 in.)
      Filtration Area1.26 m²
      Inlet to Outlet Width15.2 cm (6.0 in.)
      Process Volume750 L
      Device Size30 in.
      Inlet Connection Diameter1-1/2 in.
      Outlet Connection Diameter1-1/2 in.
      Materials Information
      Chemistry
      • Modified Polyvinylidene Fluoride (Modified PVDF)
      Device Material
      • Polypropylene
      Seal MaterialSilicone (SI)
      Support MaterialPolypropylene
      Vent Cap MaterialPolypropylene (PP)
      Vent O-ring MaterialSilicone (SI)
      Vent/Drain1/4 in. hose barb with double O-ring seal
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Packaging Information
      Material Size1
      Material PackageDouble Easy-Open bag
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Catalog Number GTIN
      KVPVA3TTT1 04053252606274

      Documentation

      Opticap XLT30 Viresolve NFP 1-1/2 in. TC/TC SDS

      Title

      Safety Data Sheet (SDS) 

      Certificates of Quality

      Title
      Opticap XLT 30 Capsule Viresolve NFP Media C7NA71259
      Opticap XLT 30 Capsule Viresolve NFP Media C8SA57003
      Opticap XLT 30 Capsule Viresolve NFP Media C0AB88213
      Opticap XLT 30 Capsule Viresolve NFP Media C0DB22024
      Opticap XLT 30 Capsule Viresolve NFP Media C0JB64908
      Opticap XLT 30 Capsule Viresolve NFP Media C0KB89721
      Opticap XLT 30 Capsule Viresolve NFP Media C0SB36246
      Opticap XLT 30 Capsule Viresolve NFP Media C7EA95944
      Opticap XLT 30 Capsule Viresolve NFP Media C7HA25769
      Opticap XLT 30 Capsule Viresolve NFP Media C7HA28110
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