AseptiVent® TF 5", 10", 20", 30"
mdi AseptiVent® TF PTFE large capsule filters offer absolute retention and wide chemical compatibility for sterile filtration of air/gases as well as aggressive solvents in large volume.
Consistent and Reliable Quality: | AseptiVent® capsule filters are produced with ISO 9001 certified quality management systems. |
Regulatory Compliance: | Meet all pharmacopeial and compendia requirements and are registered with USFDA DMF No. 015554 |
Air Flow rates/ Hydrophobicity: | Translates to lower filtration costs, less number of filter changes and overall economy of operations. |
- Fermentor / Bioreactor sparging
- Sterilization of environmental air in isolators
- Venting of sterile collection vessels
- Cleaning sterile surfaces
Construction | |||||
Membrane | Hydrophobic PTFE | ||||
Pore size |
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Support Layers | Polypropylene | ||||
Body and Core | Polypropylene | ||||
Size | |||||
Size |
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Effective Filtration Area |
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Dimension (End to End) - 1½" Sanitary Flange Inlet ½" Hose Barb Outlet |
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Dimension (End to End) - ¾" Sanitary Flange I/O |
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Dimension (End to End) - 1½" Sanitary Flange I/O |
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Dimension (End to End) - ½" Single Step Hose Barb |
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Dimension (End to End) - 1" Hose Barb I/O |
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Operational Radius (with Vent/ Drain) |
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Dimension (End to End) - 3/8" Hose Barb I/O |
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Integrity Testing / Retention | |||||
Air Diffusion Flow per 10" Capsule Filter (70% IPA/Water Wetted) |
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Microbial Retention |
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Operational | |||||
Max. Operating Temperature | 80 °C @ <30psi (2Kg/cm²) | ||||
Max. Differential Pressure | < 60psi (4Kg/cm²) @ 30 °C | ||||
Sterilization By Gas | Sterilizable by Ethylene Oxide | ||||
Sterilization By Autoclave | Autoclavable at 125°C for 30minute, 30 cycles and it cannot be in-line steam sterilized | ||||
Shelf Life | 3 years after Ethylene Oxide sterilization | ||||
Assurance | |||||
Toxicity | Passes Bioreactivity test, In Vivo, as per USP <88> for Class VI plastics | ||||
Cytotoxicity | Passes Biological Reactivity Tests, In vitro, USP <87> for cytotoxicity | ||||
Microbial Bacterial Retention | Validated as per ASTM F 838-05 | ||||
Bacterial Endotoxin | Aqueous extracts exhibit < 0.5 EU/ml as established by Limulus Amebocyte Lysate (LAL) Test | ||||
Bioburden | Bioburden level is < 1000 cfu/filter device as per ISO 11737-1 : 2018 | ||||
Non Fiber Releasing | Passes test as per USP and comply with USFDA 21 CFR Part 210.3 (b)(6) for fiber release | ||||
Indirect Food Additive | All Polypropylene components meet the FDA Indirect Food Additive requirements cited in 21 CFR 177.1520 | ||||
Good Manufacturing Practice | These products are manufactured in a facility which adheres to Good Manufacturing Practices | ||||
Oxidizable Substances | Within limits as specified in USP <1231> | ||||
Particle Shedding | Passes USP test for particulates in injectables | ||||
Quality Management System | ISO-9001 Certified | ||||
USFDA | DMF No. 015554 |
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*T-line is not available in 5" Capsule filter
*T-line Capsule filter are available with 1½" Sanitary Flange I/O connection only
***3/8" Hose Barb is available only with inline capsule filters
**3/4" Sanitary Flange end connection is available only in 5" and 10" capsule filters
Example :
LTLX | 54 | 01 | EE | XX | X | 1 | 01 |