CHF19.00
The Medical Device Regulation MDR 2017/745, Article 19 defines requirements for manufacturers to draw up a Declaration of Conformity (DoC) prior affixing the CE-mark and making the device available on the market. Find here the template for the DoC delivered as:
The MDR 2017/745 defines in its Article 19 the requirements for a Declaration of Conformity prior affixing the CE-mark and makeing the medical device available on the market. Find here the template establish the Declaration of Conformity (DoC).
