The following documents are the official European Commission consolidated versions of the Medical Devices Directives, which regulate European market access for medical devices.
The first two documents below are the official consolidated versions of the Active Implantable Medical Devices Directive (AIMDD) and Medical Devices Directive (MDD) incorporating Directive 2007/47/EC, which became fully effective on 21 March 2010.
The third document is in In Vitro Diagnostic Devices Directive (IVDDD), which remains unchanged by Directive 2007/47/EC.
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