EUDAMED – European Database for Medical Devices

EUDAMED is an upcoming part of the newly enforce European (EU) Regulations 2017/745. EUDAMED database will be a transparent system aiming at coordinating information regarding medical devices available in the EU market. EU Commission in co-ordination with MDCG is currently working on the database planning, creation, and implementation. The new MDR based requirements will be imposed once EUDAMED becomes fully function in the market.
Please find our blog discussing upcoming information on MDR EUDAMED.