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17805E Midisart 2000，空气过滤器的价格，滤器的使用方法，PTFE

产品信息
  • 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
Pack size 12 pc.

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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