Agfa Radiology Solutions is proud to receive the new European Medical Device Regulation (MDR) certification, which was issued by Intertek on 21 June 2022.

This certification allows Agfa to continue expanding its Radiology solutions and release innovations in due course. This includes making significant changes to the solutions and adding new functionalities to meet the evolving needs of our customers and the market, as well as allowing them to benefit from state-of-the-art X-ray technologies.

“This certification, which covers Agfa’s Class IIb X-ray rooms, ensures that Agfa can continue to deliver innovative solutions that help our customers face their real challenges and address their needs and requirements on a day-to-day basis,” says Georges Espada, Global Head of Digital Radiography Business Unit of Agfa.

“The MDR certification is testimony to Agfa’s purpose to provide patients and caregivers with the highest quality healthcare solutions” says Pascal Juéry, President and CEO of Agfa.

Read the full press release here