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MCE 0.45μm Cartridge Filters

Product Introduction
Alioth Aligard® MHF Single-layer Cartridge Filter is made from mixed cellulose ester. It has a nominal filtration accuracy of 0.2 μm, a sturdy structure and stable material. It can efficiently retain pollutants, effectively remove particles and colloidal contaminants, block no important active ingredients, protect downstream filtration equipment, and prevent premature clogging.

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    • Fast flow rate.

    • High capacity.

    • No fiber release.

    • Can withstand multiple cycles of high-temperature sterilization.

     

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    • Pre-filtration of culture media and buffer solutions

    • Pre-filtration of LVP/SVP

    • Pre-filtration of blood products

    • Pre-filtration for column protection, etc.

     

  • Product Specifications

      10 inch 20 inch 30 inch

    Dimensions

    Diameter
    Maximum Length

     

    69 mm
    320 mm

     

    69 mm
    560 mm

     

    69 mm
    800 mm
    Filtration Area 0.68 m2 1.32 m2 1.98 m2
    Pore Size 0.2 μm
    Materials of Construction

    Filter membrane:Mixed Cellulose Ester                     

    Supporting Layer: Polypropylene (PP)
    O-rings of capsules vent: Silicone                             

    Liner / Cartridge body: Polypropylene (PP)
    End caps: Polypropylene/ Polycarbonate (PP/PC)
    Maximum Differential
    Pressure    		 Forward: 5 bar ( 72.5 psi ) @ 25℃ / 1.5 bar ( 21.75 psi ) @ 80℃ / Reverse: 2 bar ( 29 psi ) @ 25℃
    Sterilization Parameters 121℃, 30 minutes, 5 cycles of high-pressure sterilizations or 5 cycles of sterilization in place
    Extractable Water: ~20 mg / 10 inch
    Ethanol: water ( 50：50 ): ~55 mg / 10 inch
    Biological Safety All the construction components of this cartridge comply with the requirements for biological safety of Class VI plastics in current USP < 88 >
    Indirect Food Additive The primary construction components of this cartridge comply with the reguirements for food contact materials as stipulated in EU 1935 / 2004 / EC and FDA 21 CFR 177-182
    Cleanliness Cleanliness meets the requirements for nonfiber releasing filter as specified in FDA 21 CFR 211.72 and 210.3 (b) (5) (6), and the level of insoluble particles in rinsing liquid meets the
    requirements of USP < 788 >
    Endotoxin The endotoxin level of cartridge rinsing liquid is < 0.25 EU/mL as indicated by gel method, which complies with the requirements of USP < 85 >
    Integrity Each filter has passed the integrity test
    TOC / Conductivity TOC < 0.5 mg/L, Conductivity < 1.3 μS/cm
    Manufacturing environment Manufactured in conformance with cGMP

     

     

    Test Results of Flow Differential Pressure