PART 2 Making available on the market and putting into service under Regulation (EU) 2017/745

Requirement on health institutions to provide information relating to implanted devices

6.  A health institution which has implanted a device to which Article 18 applies, must make available to the patient in whom the device has been implanted—

(a) the implant card for the device bearing the health institution’s identity, and

(b) the information provided by the manufacturer with the device pursuant to Article 18(1), by any means that allow rapid access to that information.