The EU Medical Devices Regulation (MDR) will improve patient safety 

EU MDR icon

At Gore, we prioritize reliability and quality in supplying patients with the devices they need. With production facilities in the U.S. and Europe, we can respond promptly to market demands. Committed to patient safety, we achieved compliance with the EU's Medical Device Regulation (MDR) program in August 2021, with all Gore devices* MDR certified by May 2023.  

100%*

of the products within our program are MDR certified

Gore information for health care providers that are involved in the purchasing of medical devices

 

* Part of Gore’s MDR program. 

25PR2021-EN01