We are proud to announce that Micropos Medical AB has received the MDR as well as the UKCA certificate for the Raypilot System. This certification confirms that Micropos Medical’s Raypilot System is now fully compliant with the European Union’s regulation MDR 2017/745 and UK MDR 2002 for medical devices.
The new regulations represents a substantial shift in the requirements for medical devices ensures that the medical devices used in healthcare and care environments meet the highest safety and quality standards. Achieving this certification has required extensive work, significant effort, and substantial resources across the entire organization.
“Achieving MDR certification is a major milestone and clear proof that our products meet stringent regulatory requirements. It is vital for our company, our customers, and—most importantly—patient safety, while also enabling further product development and expansion,” says Hanna Syrén, COO and QA/RA.
