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Regulatory Approved Porous Plastics for Medical Applications

Regulatory Approved Porous Plastics for Medical Applications

Porvair Filtration Group, an international leader in high performance filtration and separation materials and products for the medical industry has announced its presence  at the forthcoming Medical Design & Manufacturing (MD&M) West in Anaheim, CA (7-10th February 2011).

At MD&M West - Porvair Filtration Group will showcase regulatory-approved materials based upon its proprietary BioVyon™ sintered porous plastic technology, for filtration, separation, venting and wicking applications in the medical industry. Manufactured to current good manufacturing practices (cGMP) in ISO-accredited cleanrooms, the ultra-clean BioVyon™ materials meet USP and FDA approvals for biocompatibility and bio-safety. Visitors to Booth 346 will have immediate, hands-on access to Porvair specialists to discuss the latest BioVyon™ materials including composites and surface modified functionality with chemically active or biologically active species such as antibodies or proteins for novel filtration and separation opportunities in medical devices.
 
Driven by market requirements, the Porvair range of BioVyon™ materials and applications is continuously expanding and is available to both OEM and end user customers. To discuss your application please visit our booth at MD&M West 2011 or contact Porvair Filtration Group on +44-1489-864330 / +1-804-550-1600, or email info@porvairfiltration.com.

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