Implant Information

Implant Card and Patient Information acc. requirements of Article 18 of MDR (EU) 2017/745

In accordance with new Regulation (EU) 2017/745 of the European Parliament and the Council of 5 April 2017 on medical devices manufacturers of implantable medical devices are obliged to provide an implant card and information for patients with an implanted device.

The relevant information and downloads will be available to you shortly.