National and International Registrations and Notifications
Products Registration in Italy
According to existing procedures for the registration of medical devices in Italy, all products falling within the scope of Directives 90/385/EEC, 93/42/EEC and 98/79/CEE must be registered in the databank of the MoH before they can be placed on the market.
Thanks to our long-term relationships with the Italian Health Institutions, we know how to complete registrations and obtain approval for medical devices in the most efficient possible way.
International Registrations and Notifications
Some European countries require that even CE-marked medical products be registered with the National Competent Authority before they can be placed on the local market.
Merc will assist you through the notification process and answer all your questions about national and international registrations.