EU Commission Release Report from Study Conducted Regarding the Implementation of Article 17 of Regulation (EU) 2017/745 on medical devices on the EU market
The EU Commission has released a report from a study that they have conducted concerning the reprocessing and reuse of single-use-devices in the EU. The study aimed to evaluate how the provisions that have been established in Article 17 of the MDR, which regulates the reprocessing of Single Use Devices (SUD’s), have been implemented and ...
