CamNtech has completed the transition of its medical devices to full compliance with the Medical Device Regulation 2017/745 (MDR).
All systems and processes have been revised where appropriate and new Technical Files created to meet the requirements of the MDR.
In accordance with the MDR, CamNtech has appointed Qarad BV to act as the EC Representative:
Qarad EC-REP BV
Qarad has completed a high level technical review of the relevant CamNtech MDR documentation.