This document describes the intended use, content and information to be provided by the manufacturer together on the IC and a definition of fields to be completed by the implanting healthcare institutions or healthcare providers according to national law in Member States.

Medical Devices: Guidance document Implant Card relating to the application of Article 18 Regulation (EU) 2017:745 of the European Parliament and of the Council of 5 April 2017 on medical devices.pdf

Example of IC Leaflet