I. – Advertising for the devices referred to in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 means any form of information, including canvassing, canvassing or inducement that is intended to promote the prescription, supply, sale or use of these devices, with the exception of information provided as part of their duties by pharmacists managing an in-house pharmacy.
II – The following are not included in the scope of this definition:
1° The label and instructions for use of these devices ;
2° Correspondence, accompanied, where appropriate, by any non-promotional document required to answer a specific question about a particular device;
3° Information relating to warnings, precautions for use and undesirable effects noted in the context of materiovigilance, as well as sales catalogues and price lists if they do not contain any information about the device;
4° Information relating to human health or human diseases, provided that there is no reference, even indirect, to a device.