South Korean digital radiography (DR) manufacturer DRGEM has obtained CE Medical Device Regulation certification for its Raymo mobile system, enabling the company to commercialize the product across Europe.
The certification follows U.S. Food and Drug Administration clearance for Raymo in May, the company noted. Raymo features radio frequency identification-based user recognition technology that automatically applies personalized settings for individual healthcare professionals. The platform also includes a range of smart features to improve mobility, ease of use, and workflow efficiency in clinical settings, according to the firm.
