Member States overview: Implementation of EU legislation on CE marking of medical devices
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This document provides an overview of the implementation of EU legislation on CE marking of medical devices by the 27 Member States. All EU countries implemented the relevant EU Directive. As a result the legislation on CE marking of medical devices is harmonised throughout the EU.
Download Member States overview: Implementation of EU legislation on CE marking of medical devices
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Related Documents
- Norway legislation on CE marking: Medical devices
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On market access requirements: marketaccess@cbi.eu
On CBI market information: marketinfo@cbi.eu
