Items list
Click to enlarge
DMP Dental Industry S.A. is pleased to announce the achievement of the certification of its medical devices under the demanding European Union’s MDR (Regulation (EU) 2017/745). DMP remains committed to the safety, quality and performance of its medical devices enhancing customer confidence and patient satisfaction. MDR EU 2017/745 enforces the most stringent requirements compared to the previous MDD (medical device directive).
Consequently, we are thrilled to be among the limited number of companies completing the process smoothly and obtaining the certification without using the extension period. This is a significant milestone as DMP ensures continued market access and has the ability to enhance its portfolio with new products.
