Italian Device Registration

The Italian Ministry of Health (MOH) has implemented mandatory procedures for the Italian registration of medical devices as of 1 May 2007. == Overview == Placing a Medical Device into the European market is contingent upon compliance with the Medical Device Regulation (EU 2017/745), While this directive applies in all member states of the European Union, each member state has its own way of implementing the directive within their country, essentially adding regulations to the directive and creating local legislation.

Source: Wikipedia — Italian Device Registration (CC BY-SA 4.0)