Important notice: The following information is not completely up to date (due to the current dynamic situation) and is currently under revision.
EUR-Lex - the access to European Union law - and the European Commission - DG for Enterprise and Industry offer an overall view on medical devices, e.g. Directives, Guidelines, harmonised standards and other important documents.
This website uses session cookies to ensure certain functionalities such as downloads or login to closed areas. In order to optimize the website, we use the analysis tool Matomo. Our Matomo installation works without tracking cookies. You will find more detailed information and the possibilities to object to the use of Matomo in our data privacy declaration.