Sanitary direct flow cartridges Robust size exclusion mechanism ≥ 3 log TR for > 20 nm viruses ≥ 6 log TR for > 50 nm viruses Low binding for high protein yields High transmission of albumin and IgG Very low extractables Autoclavable and Steamable in situ (SIP) 100% integrity-tested (correlated to virus retention) Manufactured for use in conformance with cGMP Pharmaceutical P optimized with Certificate of Test provided Validation Guide availableClaims based on challenges with bacteriophage (bacterial viruses) PP7 (25 nm) and PR772 (53 nm) in 1% Bovine Serum Albumin in phosphate-buffered saline at pH 7.4, 20 °C (68 °F).Note: These filters are also available in Kleenpak Nova capsule format.
Every DV20 grade filter integrity tested during manufacture. Test correlated to viral (phage) removal
Meets USP Biological Reactivity Test, in vivo, for Class VI-121 °C Plastics
Meets Cleanliness per USP Particulates in Injectables Non-Fiber-Releasing Non-Pyrogenic per USP Bacterial Endotoxins (< 0.25 EU/mL) Meets Total Organic Carbon and Conductivity per USP Purified Water; pH per Sterile Purified Water
Lot samples multi-cycle autoclave challenged* Per lot sample or rinse-flush aliquots.
Diffusional flow integrity test, carried out by standard upstream or downstream methods Correlated to 3 log TR for 25 nm PP7 phage and ≥ 6 log TR for 53 nm PR772 phage Test Wetting Fluid: 30% IPA (20% EtOH values also available) Water or buffer-wet values for installation confirmation can also be provided Test Pressure: 85 psi (air test gas) Contact Pall for cartridge values and correlation data
• Validation Guide available