MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...

The overarching principles of the regulation of medical devices are similar, but not identical, across the US, EU, and UK. Medical devices are classified according to the level of risk they pose ...

“At a high level, new transparencies required under the Act relate to safety, which was already there in the EU’s Medical Device Regulation (MDR), and a more explicit focus on fairness.

proudly announces successful certification under the European Medical Device Regulation (MDR, Regulation (EU) 2017/745) by notified body TÜV SÜD Product Service. This certification marks a ...