The advertising of certain devices mentioned in Article 1 of Regulation (EU) 2017/746, the failure of which is likely to cause a serious risk to health and the list of which is set by order of the Minister for Health, is subject to prior authorisation issued by the National Agency for the Safety of Medicines and Health Products.
This authorisation is issued for a renewable period of five years.
This authorisation may be suspended or withdrawn by reasoned decision of the Agency.