The advertising defined in Article L. 5213-1 relates to the devices mentioned in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 which have the EU declaration of conformity provided for in Article 19 of that Regulation.
Advertising shall objectively define the device and, where applicable, its performance and compliance with general safety and performance requirements, as attested by the declaration referred to in the previous paragraph, and promote its proper use.
Advertising may not present a risk to public health. It may not, under the conditions laid down in Article 7 of the same Regulation, contain content likely to mislead the user or the patient.
All advertising must comply with the obligation to mention the identification number of the notified body responsible for the conformity assessment of the device, as provided for in Article 20(5) of Regulation (EU) 2017/745.