Article L5462-2 of the French Public Health Code
I.-If the manufacturer of a device referred to in Article 1 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 or, where applicable, its authorised representative, having become aware of a serious incident occurring on French territory, concerning this device, fails to notify the National Agency for the Safety of Medicines and Health Products in accordance with the procedures and deadlines laid down…