PES 0.2μm Cartridge Filters
Product Specifications
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Product Specifications |
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5 inch |
10 inch |
20 inch |
30 inch |
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Diameter |
69 mm |
69 mm |
69 mm |
69 mm |
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Materials of Construction |
Membrane |
Hydrophilic polyethersulfone (PES) |
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Supporting Layer |
Polypropylene (PP) |
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O-rings |
Silicone、Ethylene propylene diene monomer（EPDM） |
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Core/Cage/End caps/Housing |
Polypropylene (PP) |
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Integrity testing |
Bubble Point |
≥3180 mbar（46 psi）(wetted with H2O, 20℃, compressed air） |
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Working characteristics |
Maximum Differential Pressure |
Forward: 5.0 bar（72.5 psi）@ 25℃/1.5 bar（21.75 psi）@ 80℃ Reverse: 2.0 bar（29 psi）@ 25℃ |
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Sterilization Resistance |
In-line steam: 135℃, 30 min,10 cycles Autoclave: 135℃, 30 min, 20 cycles |
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Filtration Area |
0.32 m2 |
0.66 m2 |
1.32 m2 |
1.98 m2 |
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Pore Size |
0.2 μm |
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Bacterial Retention |
TR﹥106 B. diminuta ( ATCC® 19146TM ) |
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Biological Safety |
All construction components meet the biological safety requirements refering to USP<88> Class VI plastic and USP<87> |
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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 |
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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> |
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Endotoxin |
Endotoxin﹤0.25 EU/mL by LAL test method, which complies with the requirements of USP<85> |
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TOC/Conductivity |
TOC﹤0.5 mg/L, Conductivity﹤1.3 μS/cm |
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Manufacturing Integrity |
100% integrity test passed |
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Manufacturing Environment |
Manufactured in conformance with cGMP |
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Test Results of Flow Differential Pressure
