We use cookies to help provide you with the best possible online experience. Please read our Privacy Policy for information about which cookies we use and what information we collect on our site. By continuing to use this site, you agree that we may store and access cookies on your device.
One More Step to Finalize Your Registration
An activation link has been sent to your email address.
Please check the email and activate your account now. It might take few minutes to get the email.
If you did not find it, please check your spam box.
Having problem receiving the email? Send again
Still cannot receive? Contact us
Email ：PharmaSources@imsinoexpo.com
Whatsapp ：+86-13621645194
Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa
Sample Provided: no
Imported PES filter membrane is adopted in the product as filter media. The product is produced by overall structure sweat welding. The filter element is produced through optimum filter membrane matching mode, thereby the product has higher pollutant containing ability and longer service life, which is suitable for terminal filtration of high viscosity material fluid. Features:
●The filter membrane is hydrophilic with absolute filtration accuracy;
● Low protein adsorption performance;
● High pollutant containing ability;
● Long service life and economic use;
Typical applications:
● Sterile filtration of vaccine;
●Sterile filtration of blood products;
● Sterile filtration of raw material medicine, injections and other drugs;
● Filter elements are flushed and pass integrity test before filter elements are left from the factory;
● The batch passes through bacterial challenge test for confirming 100% bacteria interception ability;
Biological safety:
Biological Safety: The product materials comply with USP in-vivo VI-121 ℃ plastic biological response test.
Endotoxin: <0.25EU/ml;
Cleanliness: The product is in line with 2010 GMP requirements on injection of particles;
Readily oxidizable substance: the substance should be in line with 2010 GMP test requirements of particle contents in injections after water rinsing for 2000ml;
TOC/conductivity: after the product is flushed with 20L injection water at 25 ℃ (10〃) . It is in line with requirements of 2010 GMP on total organic carbon contents and conductivity in injection water.
Five years of qualification
Audited Supplier
Pharma Sources Insight June 2024: Globalization on the Go
