Launching EU dashboard monitoring the availability of medical devices and in vitro diagnostic medical devices
10 January 2024
Following the entry into force of Regulations (EU) 2017/745 and (EU) 2017/746, the European Commission (EC) initiated an EU-wide study in late 2022 to monitor and analyse the availability of medical devices (MD) and in vitro diagnostic medical devices (IVDR) on the EU market. As part of the ongoing project, a dashboard with an overview of the recently collected data has been established. The dashboard will be further expanded as the study continues. Alongside recent data, it contains comparable results from previous surveys on the availability of MD and IVDR. The dashboard can be viewed on the EC website.