- Sterile venting of filling vessels and fermentation carboys, including culture vessels and CO2 incubators （6 to 120l）
- Venting of holding tanks for sterile, distilled water and liquid culture media
- Autoclave venting
- In-line sterilization of and particulate removal from air and gases, such as sterilization of air for small fermenters
Product attributes
| Filtration area | 0.002 m² |
| Membrane | PTFE （Polytetrafluorethylene） |
| pore size Final-Filter | 0.2 µm |
Quantity
General specifications
| Filtration area | 20 cm² | 3 square inch |
| Filter Material | PTFE （Polytetrafluorethylene） |
| Housing Material | Polypropylene |
| Max. operating pressure | 3 bar | 44 psi |
| Bacterial Retention | Quantitative retention of 1 x E7 CFU/cm² Brevundimonas diminuta ATCC® 19146 per ASTM methodology |
| Bacterial Endotoxins | <0.18 EU/mL as determined by the LAL test |
| Extractables | Product meets or exceeds the Quality standards set for "Sterile Water for Injection" by the current USP. |
| Biosafety | All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI, （Systemic Injection, Intracutaneous and Implantation tests）. |
| Sterilization | Autoclaving: max. 20 cycles at max. 134 °C, 2 bar | 29 psi |
| Non-Fiber Releasing | This filter product complies with the title 21 of the Code of Federal Regulations （CFR）, section 210.3（b）（6） and 211.72. |
| GMP Compliance | The product was manufactured in conformance with established Current Good Manufacturing Practice （cGMP） standards. |
| Pore size | 0.2 |
| Filtration area | 20 cm² | 3 square inch |
| Filter Material | PTFE （Polytetrafluorethylene） |
| Housing Material | Polypropylene |
| Max. operating pressure | 3 bar | 44 psi |
| Bacterial Retention | Quantitative retention of 1 x E7 CFU/cm² Brevundimonas diminuta ATCC® 19146 per ASTM methodology |
| Bacterial Endotoxins | <0.18 EU/mL as determined by the LAL test |
| Extractables | Product meets or exceeds the Quality standards set for "Sterile Water for Injection" by the current USP. |
| Biosafety | All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI, （Systemic Injection, Intracutaneous and Implantation tests）. |
| Sterilization | Autoclaving: max. 20 cycles at max. 134 °C, 2 bar | 29 psi |
| Non-Fiber Releasing | This filter product complies with the title 21 of the Code of Federal Regulations （CFR）, section 210.3（b）（6） and 211.72. |
| GMP Compliance | The product was manufactured in conformance with established Current Good Manufacturing Practice （cGMP） standards. |
| Pore size | 0.2 |
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