Are you asking yourself if your product is considered as a Medical Device within the new EU MDR 2017/745?
Then here is the tool to help you answer this question.
Latest News, Official Information, Experts Information. MedBoard organises information in the medical device industry, and make it fast accessible, integrated, and useful, creating also tools and analyses that medical devices companies – professionals need.
Do you need a tool to perform Gap Assessment for MDR, MDSAP, ISO 13485 and others…
I propose you to test this tool from Regulatory Globe.
Check the offer