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for economic operators, to facilitate free movement of goods inside the EU.

The previous core legal framework consisted of three directives:
* Directive 90/385/EEC regarding active implantable medical devices
* Directive 93/42/EEC regarding medical devices
* Directive 98/79/EC regarding in vitro diagnostic medical devices (Until 2022, the In Vitro Diagnosis Regulation (IVDR) will replace the EU's current Directive on In-Vitro Diagnostic (98/79/EC)).

They aim

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