DR. INFO Secures CE Marking Under EU MDR - Ready for Regulated European Deployment

Munich, Germany - March 26, 2026: Synduct GmbH today announced that DR. INFO has been CE-marked under the European Union Medical Device Regulation (EU MDR) for its intended use.

Built for Healthcare, Grounded in Science

DR. INFO was developed to support healthcare professionals with structured access to medical information in a way that is transparent, traceable, and aligned with the realities of clinical practice. The product was built at the intersection of healthcare and rigorous computer science, with the goal of helping doctors and clinics reduce friction, save time, and focus more attention on patient care.

What CE Marking Means

The CE certification confirms that the product meets the essential safety and performance requirements set out under EU MDR for medical devices in its classification. For Synduct, this represents an important step in building the regulatory foundation for long-term institutional adoption across European healthcare systems.

Performance and Focus

DR. INFO has shown strong performance in internal and external evaluations, including comparisons with other widely used systems. At the same time, the company states that its primary focus remains practical usefulness in day-to-day care environments, ongoing product improvement, and close collaboration with physicians.

Synduct will continue to develop DR. INFO with emphasis on transparency, quality, and responsible deployment in healthcare settings.

Media Contact

news@synduct.com