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CVGB53TP3 Durapore Cartridge Filter 30 in. 0.22 µm hydrophobic Code 5

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CVGB53TP3
3  Double Easy-Open bag
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      Overview

      Replacement Information

      Key Specifications Table

      Description
      Catalogue NumberCVGB53TP3
      Trade Name
      • Durapore®
      DescriptionDurapore Cartridge Filter 30 in. 0.22 µm hydrophobic Code 5
      References
      Product Information
      Device ConfigurationCartridge
      Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C
      Maximum Inlet Pressure, bar (psi)Forward - 5.5 bar (80 psi) @ 25 °C; 1.7 bar (25 psi) @ 80 °C; 0.35 bar (5 psi) @ 135 °C; Reverse - 3.5 bar (50 psi) @ 25 °C
      Cartridge CodeCode 5 (2-222) O-rings and spear
      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 ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaDurapore®
      Sterilization30 SIP cycles of 30 min @ 126 °C; 30 autoclave cycles of 60 min @ 126 °C
      Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
      WettabilityHydrophobic
      Physicochemical Information
      Pore Size0.22 µm
      Bubble Point at 23 °C≥1240 mbar (18 psig) nitrogen with 60/40 % IPA/water
      Gravimetric ExtractablesThe extractables level was equal to or less than 20 mg per 10-inch cartridge after 24 hours in a 70/30% IPA/water mixture at controlled room temperature.
      Nitrogen Diffusion at 23 °C≤30 mL/min @ 1.7 bar (25 psig) with water
      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).
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Dimensions
      Cartridge Nominal Length30 in. (75 cm)
      Diameter6.9 cm (2.7 in.)
      Filtration Area2.07 m²
      Device Size30 in.
      Materials Information
      Chemistry
      • Polyvinylidene Fluoride (PVDF)
      Device Material
      • Polypropylene
      Seal MaterialSilicone (SI)
      Support MaterialPolypropylene
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Packaging Information
      Material Size3
      Material PackageDouble Easy-Open bag
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      Certificates of Quality

      Title
      Durapore Cartridge - C4CA40626
      Durapore Cartridge - C6AA10484
      Durapore Cartridge C5KA47793
      Durapore Cartridge C6KA00074
      Durapore Cartridge C8DA64179

      Technical Info

      Title
      Application Note: Integrity Test Troubleshooting - Beyond Rewet and Retest
      Establishing Product Specific Bubble Point Specifications For Sterilizing-Grade Filters
      Filter Integrity Test Methods

      Data Sheet

      Title
      Millidisk® Cartridges and Millipak® Disposable Capsules (MilliporeSigma)
      Sterile and Gamma Compatible Sterilizing-grade Durapore® 0.1 μm and 0.22 μm Filters (MilliporeSigma)
      Sterilizing-grade Durapore® 0.22 µm Hydrophobic Filters