C3+ IFU - 0723 01140 (70048) UK Page 17 of 18
6.3 Serious Incidents
In case of serious incidents in relation to the device, please contact your local competent authority as
well as Cortrium support@cortrium.com without undue delay.
6.4 Declaration of conformity
The C3+ is in conformity with the essential requirements and provisions of the EU Medical Device
Regulation (MDR).
2
2
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
of 5 April 2017.
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