![]() ![]() ![]() ![]() This technical documentation must be prepared according to Annex II and III and prior to drawing up the EU declaration of conformity.The device(s) covered by the present declaration arein conformity with the MDR 2017/745 and, if applicable, with any other relevant Union legislation that provides for the issuing of an EU declaration of conformity. Device(s) meet(s) the provisions of the Medical Device Regulation 2017/745/EU (MDR) which apply to them.
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