2024-04

The European Commission published the final report on the Study on the implementation of Article 17 of Regulation (EU) 2017/745 on medical devices on the EU market.

The study started in December 2022 and was performed over 14 months.  The study main objective was to evaluate how the provisions established in the MDR have been implemented in European countries and how such provisions operate.

In the context of the study, a dashboard has been developed. The dashboard (click on the arrows at the bottom of the dashboard to scroll through the different pages) presents an overview of the mapping activities within the study regarding the reprocessing and reuse of single-use-devices in the EU.

The final report can be downloaded in our library

Source: European Commission