Home  ꄲ  预过滤  ꄲ  MCE 0.45μm Cartridge Filters
4
넳 넲

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.

Data Download：

Depth Stacked DataSheet
넳 넲

  • 我是段落。点击这儿添加你的文字并编辑它，非常容易。-双击进行编辑

     

    • Fast flow rate.

    • High capacity.

    • No fiber release.

    • Can withstand multiple cycles of high-temperature sterilization.

     

  •  

    • 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

    Product Specifications

     

    5 inch

    10 inch

    20 inch

    30 inch

    Diameter
    Maximum Length

    69 mm
    150 mm

    69 mm
    320 mm

    69 mm
    560 mm

    69 mm
    800 mm

    Materials of

    Construction

    Membrane

    Mixed Cellulose Ester (MCE)

    Supporting Layer

    Polypropylene (PP)

    O-rings

    Silicone、Ethylene propylene diene monomer（EPDM）

    Core/Cage/End caps/Housing

    Polypropylene (PP)

    Working characteristics

    Maximum Differential

    Pressure

    Forward: 5.0 bar（72.5 psi）@ 25°C/1.5 bar（21.75 psi）@ 80°C

    Reverse: 2.0 bar（29.0 psi）@ 25°C

    Sterilization

    Resistance

    In-line steam: 121℃, 30 min,5 cycles

    Autoclave: 121℃, 30 min,5 cycles

    Filtration Area

    0.32 m2

    0.68 m2

    1.32 m2

    2.04 m2

    Pore Size

    0.45 μm

    Biological Safety

    All construction components meet the biological safety requirements refering to USP<88> Class VI plastic and USP<87>

    Indirect Food Additive

    All component materials meet the requirements of Indirect Food Additive cited in EU 1935/2004/EC and FDA 21 CFR 177-182

    Cleanliness

    Meets the requirements for a ‘non-fiber releasing’ filter defined in FDA 21 CFR 211.72 and 210.3 (b) (5) (6), and particulate matter meets the requirements of USP<788>

    Endotoxin

    Endotoxin﹤0.25 EU/mL by LAL test method, which complies with the requirements of USP<85>

    TOC/Conductivity

    TOC﹤0.5 mg/L, Conductivity﹤1.3 μS/cm

    Manufacturing Integrity

    100% integrity test passed

    Manufacturing Environment

    Manufactured in conformance with cGMP

     

     

    Test Results of Flow Differential Pressure