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CCGL03TP1 Charged Durapore® Cartridge 30 in. 0.22 µm Code 0

Charged Durapore® Cartridge 30 in. 0.22 µm Code 0 MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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CCGL03TP1
1  Double Easy-Open bag
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      Overview

      Replacement Information
      Description
      Catalogue NumberCCGL03TP1
      Trade Name
      • Durapore®
      DescriptionCharged Durapore® Cartridge 30 in. 0.22 µm Code 0
      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 0 (2-222) O-rings
      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
      MediaCharged Durapore®
      SterilityOther
      Sterilization10 SIP cycles of 30 min @ 135 °C
      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 Size0.22 µm
      Air Diffusion at 23 °C≤30 mL/min @ 2.1 bar (30 psig) in water
      Bubble Point at 23 °C≥3100 mbar (45 psig) air with water
      Flow Rate45 L/min @ 400 mbar ΔP
      Gravimetric ExtractablesThe extractables level was equal to or less than 20 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
      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 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 ≥500 mL
      Global Trade Item Number
      Catalogue Number GTIN
      CCGL03TP1 04053252487521

      Documentation

      Certificates of Quality

      Title
      Charged Durapore Cartridge C0CB42324
      Charged Durapore Cartridge C0DB55513
      Charged Durapore Cartridge C4AB04793
      Charged Durapore Cartridge - C0HB81439
      Charged Durapore Cartridge C1SB07229
      Charged Durapore Cartridge C8MA25770
      Charged Durapore Cartridge- C9KA74336
      Charged Durapore Cartridge- C9MA93839

      Technical Info

      Title
      Bubble Point Test Method Using Durapore® 0.22 µm Hydrophilic Membrane with 60/40 IPA
      Integrity Test Troubleshooting - Beyond Rewet and Retest

      Data Sheet

      Title
      Charged Durapore® Hydrophilic 0.22 μm Cartridge Filters
      Durapore® Family Guide

      User Guides

      Title
      Hydrophilic Durapore® Cartridges and Capsules User Guide
      Wetting Instructions for Filter Units with Durapore Membrane