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KHGLS10FF1 Opticap® Sterile Multilayer XL10 Durapore® 0.45/0.22 µm 3/4 in. TC/TC

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KHGLS10FF1
1  Double Easy-Open bag
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      Übersicht

      Replacement Information
      Description
      Catalogue NumberKHGLS10FF1
      Trade Name
      • Opticap®
      DescriptionOpticap® Sterile Multilayer XL10 Durapore® 0.45/0.22 µm 3/4 in. TC/TC
      References
      Product Information
      Device ConfigurationCapsule
      Connections, Inlet/Outlet19 mm (3/4 in.) Sanitary Flange
      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.
      Quality LevelMQ400
      Applications
      Biological Information
      Bacterial EndotoxinsAqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaMultilayer Durapore®
      SterilitySterile
      Sterilization3 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 ConnectionSanitary Flange
      Outlet ConnectionSanitary Flange
      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)
      Length33.5 cm (13.2 in.)
      Diameter10.7 cm (4.2 in.)
      Filtration Area0.55 m²
      Inlet to Outlet Width33.5 cm (13.2 in.)
      Device Size10 in.
      Inlet Connection Diameter3/4 in.
      Outlet Connection Diameter3/4 in.
      Materials Information
      Chemistry
      • Polyvinylidene Fluoride (PVDF)
      Device Material
      • Polypropylene
      Seal MaterialLead O-ring: Silicone-coated EPDM, Outer O-ring: Silicone
      Support MaterialPolyester/Polyethylene
      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
      Bestellnummer GTIN
      KHGLS10FF1 04053252260001

      Documentation

      Material Qualification Dossier

      TitelVersion
      2.0

      Operational Excellence Dossier

      Title

      Qualitätszertifikate

      Titel
      OPTICAP XL 10 Capsule Multilayer Durapore Membrane C3NB56500
      Opticap XL 10 Capsule Multilayer Durapore Membrane C0DB49502Z
      Opticap XL 10 Capsule Multilayer Durapore Membrane C0SB83109Z
      Opticap XL 10 Capsule Multilayer Durapore Membrane C1AB03941
      Opticap XL 10 Capsule Multilayer Durapore Membrane C7HA24937
      Opticap XL 10 Capsule Multilayer Durapore Membrane C7KA50825
      Opticap XL 10 Capsule Multilayer Durapore Membrane C9DA17652
      Opticap XL 10 Capsule Multilayer Durapore Membrane - C0BB37996Z
      Opticap XL 10 Capsule Multilayer Durapore Membrane - C0DB60704Z
      Opticap XL 10 Capsule Multilayer Durapore Membrane - C9HA52399
      Show more

      Technische Informationen

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

      Datenblatt

      Titel
      Durapore® Family Guide

      Gebrauchsanleitungen

      Titel
      Opticap® XL Capsules and Opticap® XLT Capsules