
EUDAMED registration becomes mandatory
From 28 May 2026, manufacturers are required to register medical devices covered by certificates under the Medical Devices Regulation (EU) 2017/745 (MDR) in the European Database on Medical Devices (EUDAMED).
Mandatory EUDAMED registration will provide regulators, market operators, and stakeholders with a much clearer picture of the European dental amalgam market — including which manufacturers are active, which products are certified, and whether regulatory obligations are being met.










