Cobetter Aegivast® Vent Filter is a sterilizing-grade gas filter with high retention specifically developed for biopharmaceutical applications, available in both syringe and disc filters. The ACEB vent filter is made of a 0.2μm hydrophobic PTFE membrane composite with a polyester support layer and housed in a high-purity polypropylene casing. With a complete range of product specifications, it is highly suitable for sterile venting of small containers, bioreactors, and tubings.
Specifications
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Connections |
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Inlet |
1/4''-3/8'' Stepped HB |
1/4''-3/8'' Stepped HB |
1/4''-1/2'' Stepped HB |
1/4''-1/2'' Stepped HB |
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Outlet |
1/4''-3/8'' Stepped HB |
1/4''-3/8'' Stepped HB |
1/4''-1/2'' Stepped HB |
1/4''-1/2'' Stepped HB |
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Physical Properties |
Filtration Area |
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Max. Differential Pressure@25°C |
0.24 MPa |
0.24 MPa |
0.24 MPa |
0.42 MPa |
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Max. Operating Temp. |
50°C |
Material |
Housing
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PP |
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Membrane |
Hydrophobic PTFE |
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Pore Size |
0.2 μm |
Sterility |
Delivery Condition
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Nonsterile, can be autoclaved for 30 mins at 130 °C, 20 circles (cannot be steam sterilized in-line) |
Package |
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Individually packaged by double PE Bag, 10pcs/pk |
Features
- Natural hydrophobic PTFE membrane
- Low pressure drop
- Reliable bacteria and fine particle retention capability
- Unique product serial number tracking system
- Can be sterilized by gamma irradiation or autoclaved
Applications
- Vent filter for fermenters, storage tanks
- Sterilization filtration of compressed air, O2, N2
- Venting filtration for single-use systems
Regulatory Compliance
- Particulate matter in injections meet the requirements in USP <788> for large volume parenterals
- Meet the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6)
Fully validated as sterilizing grade filters according to ASTM F-838 guidelines, retaining a minimum of 1 x 107 CFU/cm2 Brevundimonas diminuta (ATCC™ No. 19146)
- Endotoxin limit of WFI System< 0.25 EU/mL with the Limulus Amebocyte Lysate (LAL), USP <85>
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Meet the criteria of USP <88> Class VI, Biological Reactivity Test, In Vivo
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Complies with FDA 21 CFR Part 177-182 (Indirect food additives)
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All component materials do not contain animal derived components