Guides MEDDEVs The guidelines aim at promoting a common approach by manufacturers and Notified Bodies involved in the conformity assessment procedures according to the relevant annexes of the Directives, and by the Competent Authorities charged with safeguarding Public Health. They have been carefully drafted through a process of consultation with various interested parties during which intermediate drafts were circulated and comments were taken up in the documents. Therefore, they reflect positions taken in particular by representatives of Competent Authorities and Commission Services, Notified Bodies, industry and other interested parties in the medical devices sector. The guidelines are not legally binding. It is recognised that under given circumstances, for example, as a result of scientific developments, an alternative approach may be possible or appropriate to comply with the legal requirements.
Medical Devices Law DIMDI - Medical Devices Law Within-Page Navigation Accesskeys end of section: to within-page navigation Global Servicelinks Navigation Local Servicelinks Servicelinks Quicklinks content print version (opens new window) Your position: Homepage » Medical Devices » Medical Devices Law Medical Devices Law 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. German Laws European Directives EUR-Lex provides direct access to European Union law including the Official Journal of the European Union. EUR-Lex Guidelines and Standards to top of the page Sitemap | Imprint | Privacy© DIMDI 2014last modified: 3/7/14