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GVS Polyethersulfone (PES) Membrane

  • £18400
  • Save £12400


Buy GVS products from MSE Supplies at the best value. 

MSE Supplies is an authorized distributor of GVS

This strong, microporous film asymmetric membrane is constructed from a high-temperature polyethersulfone polymer that is acid and base resistant. Its strength and durability are advantageous during usage that involves aggressive handling or automated equipment. GVS PES Filtration Membrane is naturally hydrophilic without added wetting agents and has low extractables.

Hydrophilic: eliminates the need for wetting agents that can potentially interfere with analyses.

Low extractables: ensures test results will not be compromised by wetting agents or other extractables.

Low drug and protein binding: maximizes recovery of critical drugs or proteins.

Wide range of pore sizes: pore size range of 0.03 μm to 5.0 μm enables specific pore size selection for given applications.

Superior burst strength: protects the integrity of the membrane under high pressure.

Quality checks ensure lot-to-lot consistency, both down and across the polyester web, for dependable results every time.

Product Characteristics

  • Pore Size: 0.03μm - 5.0μm
  • Thickness: 110μm - 150μm
  • Membrane material: PES

Applications

  • Biological fluid sterilization
  • Environmental water studies
  • Pharmaceutical sterilization
  • Protein and enzyme filtration

GVS was founded in 1979 and is headquartered out of Bologna, Italy. GVS has a rich history of responsible innovation and a commitment to a future in which good health is a universally reachable target. In over 40 years of history, GVS has evolved from a supplier of components for the healthcare sector to a global group that produces highly technological diversified filtration solutions. 

In the Healthcare & Life Sciences area, the GVS plants operate with ISO 13485 certifications and are compliant with the European Guide to Good Manufacturing Practice. Many of the products in this division have the CE certification, are registered with FDA in the United States or have registrations for the specific countries where the group operates.


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