This means that the BuddyCare has been certified as a product that now meets all essential requirements of all relevant European Medical Device Directives. The Directives outline the safety and performance requirements for medical solutions in the European Union. The CE mark is a legal requirement to place a device on the market in Europe.
This is a huge step for us in commercializing the solution. Now we can move on with enhancing surgery care and patient experience together with our customers!