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KHGLG1THH1 Opticap® Gamma Compatible Multilayer XLT10 Durapore® 0.45/0.22 µm 5/8 in. HB

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.
KHGLG1THH1
1  Double Easy-Open bag
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      Replacement Information
      Description
      Catalogue NumberKHGLG1THH1
      Trade Name
      • Opticap®
      DescriptionOpticap® Gamma Compatible Multilayer XLT10 Durapore® 0.45/0.22 µm 5/8 in. HB
      References
      Product Information
      Device ConfigurationCapsule
      Connections, Inlet/Outlet16 mm (5/8 in.) Hose Barb
      Connections, Vent/Drain1/4 in. Hose Barb with double O-ring Seal
      Housing MaterialPolypropylene (PP)
      Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.05 bar (15 psid) @ 80 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
      Maximum Inlet Pressure, bar (psi)5.5 bar (80 psi) @ 23 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
      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.
      T-line/Gauge PortT-line
      Quality LevelMQ400
      Applications
      Biological Information
      Bacterial EndotoxinsAqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaMultilayer Durapore®
      SterilityGamma
      SterilizationGamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
      Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
      WettabilityHydrophilic
      Physicochemical Information
      Pore Size0.45 / 0.22 µm
      Inlet ConnectionHose Barb
      Outlet ConnectionHose Barb
      Air Diffusion at 23 °C≤15.0 mL/min @ 2.75 bar (40 psig) in water
      Bubble Point at 23 °C≥3450 mbar (50 psig) air with water
      Indirect Food AdditiveAll component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
      Maximum Inlet Pressure (psig)80 psig
      Maximum Inlet Temperature25 °C
      Non-Fiber ReleasingThis product was manufactured with a Durapore® 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, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 ºC.
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Dimensions
      Cartridge Nominal Length10 in. (25 cm)
      Length37.6 cm (14.8 in.)
      Diameter10.7 cm (4.2 in.)
      Filtration Area0.55 m²
      Inlet to Outlet Width19.8 cm (7.8 in.)
      Device Size10 in.
      Inlet Connection Diameter5/8 in.
      Outlet Connection Diameter5/8 in.
      Materials Information
      Chemistry
      • Polyvinylidene Fluoride (PVDF)
      Device Material
      • Polypropylene
      Seal MaterialSilicone (SI)
      Support MaterialPolypropylene
      Vent Cap MaterialPolypropylene (PP)
      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
      Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥1.5 L
      Global Trade Item Number
      Référence GTIN
      KHGLG1THH1 04053252573262

      Documentation

      Material Qualification Dossier

      TitreVersion
      2.0

      Certificats de qualité

      Titre
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C1HB80659
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C7EA07406
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C2EB67292
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C3SB68111
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C4AB73543
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C4CB03589
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C4DB14698
      Opticap XLT 10 Capsule Multilayer Durapore Membrane C9EA85465
      Opticap XLT 10 Capsule Multilayer Durapore Membrane- C4DB17293

      Informations techniques

      Titre
      Autoclaving Guidelines for Opticap® XL and XLT Disposable Capsule Filters

      Fiche technique

      Titre
      Durapore® Family Guide

      Manuels d'utilisation

      Titre
      Opticap® XL Capsules and Opticap® XLT Capsules