Medical Device Packaging and Next Generation Tyvek®

medical device packaging and next generation tyvek®

A significant modification in the technology used in the manufacture of Tyvek® material will now require manufacturers of currently approved Tyvek®-based products to re-evaluate them for continued compliance with applicable standards and regulations. This white paper presents the details of the production transition regarding Tyvek®, and summarises the likely steps necessary to ensure the continued recognition of previously approved medical devices and packaging that incorporate Tyvek® material.

Why download this white paper?

• Learn more about Tyvek® material, its uses and applications
  
• Understand Tyvek®'s production transition to its new process
  
• Understand the steps involved in ensuring recognition of medical devices and packaging using the new Tyvek® material

Related Services: Medical Device Regulation (MDR) | EU In Vitro Diagnostic Medical Device Regulation (IVDR) | Medical Device Single Audit Program (MDSAP)