Sedana Medical’s products receive MDR certification
Sedana Medical AB (publ) (SEDANA: FN Stockholm) today announces that the company has received Medical Device Regulation (MDR) certification, which secures EU market access for Sedaconda® ACD under the new MDR regulation, well ahead of the deadline in 2024."The new EU Medical Device Regulation (MDR) was implemented to ensure an even higher level of quality and safety for medical devices in Europe. This approval is the final and very important step for Sedana Medical in the transition into the new regulation. Therefore, while this outcome was expected, I am proud of Sedana Medical’s efforts