EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in-vitro diagnostics… Read More »How to read the SRN correctly
understanding the classification rules The In-Vitro Diagnostics Regulation (MDR) EU 2017/746 defines in its Annex VIII the classification rules for in-vitro diagnostics. Read here how… Read More »Classification Rules under the IVDR
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