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

PAS257

2440 Geel

Belgium

Qarad has completed a high level technical review of the relevant CamNtech MDR documentation.

 

UK & International customers

CamNtech Ltd.
Manor Farm
Fenstanton
Cambridgeshire
PE28 9JD, UK

US customers

CamNtech Inc.
630 Boerne Stage Airfield,
Boerne,
Texas 78006,
USA

Copyright

© 2020 CamNtech Ltd and CamNtech Inc

Company information

Registered in England No. 2221302
VAT No: GB486 3019 34

Company information

VAT No: GB486 3019 34

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