The EU Commission’s Q&A

The EU Commission’s Q&A

The EU Commission’s Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices that were released in July has a handy set of questions you can use to check the applicability of your device.

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