Under EEA law, the use of the following four modules of the European Database on Medical Devices (EUDAMED) will be mandatory as of 28 May 2026: Actor registration, UDI/device registration, Notified Bodies and Certificates and Market Surveillance.
Under customs treaty law, device registration in the swiss database on medical devices (swissdamed) will be mandatory as of 1 July 2026.
Further information can be found on our website.