Regulation (EU) 2185/2017 (OJ:L309/7/2017) on the list of codes and types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 and in vitro diagnostic medical devices under Regulation (EU) 2017/746

Applies to: Europe
Updated: 30/01/2018

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