Pall™ Supor™ EAV membrane in Mini Kleenpak™ syringe filter
The Supor™ EAV membrane in Mini Kleenpak™ syringe filter, part of our Pall filtration portfolio, is designed for effective bioburden and particle control of buffers and biological process fluids in volumes up to 100 mL.
Pall™ Supor™ EAV membrane in Mini Kleenpak™ syringe filter
The Supor™ EAV membrane in Mini Kleenpak™ syringe filter, part of our Pall filtration portfolio, is designed for effective bioburden and particle control of buffers and biological process fluids in volumes up to 100 mL.
Overview
The Supor™ EAV membrane in Mini Kleenpak™ syringe filter, part of our Pall filtration portfolio, is designed for effective bioburden and particle control of buffers and biological process fluids in volumes up to 100 mL.
- Titer reduction claim in excess of 6 log guarantees excellent microbial filtration efficiency in processes with variable bioburden
- Broad pH compatibility PES membrane means Supor™ EAV filters are suitable for processing a wide range of fluids
- Polyethersulfone membrane has low adsorption profile for maximum transmission of proteins
- Supplied pre-sterilized for immediate use
- Built-in, MachV asymmetric prefilter layer for long-life and low filtration costs
- PFAS free filter
Supor™ EAV filters include the Pall-patented Supor™ machV membrane to ensure high throughputs and flow rates when utilized for the protection of buffers and biological process fluids. Supor™ EAV filters allow for reduced sizing of filter systems with improved process efficiencies when use of validated sterilizing grade filters is not essential, but reliable bioburden control is. The filters are also effective prefilters for protection and extended life of 0.2 µm sterilizing grade and finer membrane filters where required..
The Mini Kleenpak™ syringe filter capsule format is designed for use in the laboratory, ideal for filtering small quantities of fluids (up to 100 mL) with minimal losses.
Quality Standards
- Meet USP biological reactivity tests in-vivo, in accordance with USP Class VI 121°C for biological safety
- Endotoxin Level < 0.25 EU/mL using Limulus Amoebocyte Lysate (LAL) test
- Cleanliness per USP particulates in injectables
- Non fiber releasing per CFR 211.72 and CFR 210.3(b)(6)
