EU MDR 2017/745

Regen Lab Announces the Obtention of the New CE Certification Under Medical Device Regulation (EU MDR 2017/745) Validating the Safety and Performance of Its Proprietary Best-in-class PRP Solutions, Alone or Combined With Hyaluronic Acid

• Obtaining the CE certification under Medical Device Regulation reinforces Regen Lab's positioning as a leading innovator of medical devices in the field of autologous tissue engineering therapies
• This regulatory achievement highlights Regen Lab's patented technologies which are available in over 90 countries and have been used to treat patients in various therapeutic areas (musculoskeletal, dermo-esthetics, wound care and urogenital) leading to the publication of over 200 clinical studies