EXIAS Medical has achieved the in vitro diagnostic (IVD) Medical Devices Regulation (IVDR) certification from the notified body. The certification highlights the company’s commitment to quality and safety in in-vitro diagnostics, ensuring compliance with EU regulations.
This milestone reinforces EXIAS Medical’s position as a trusted player in the global market, emphasizing its dedication to delivering reliable and advanced in-vitro diagnostic solutions.
Stay informed with the latest updates from EXIAS. Discover news, insights, and publications that highlight our projects, innovations, and industry developments. Keep up to date with everything happening at EXIAS and never miss an important announcement.
In response to substantial feedback and high demand, EXIAS has introduced new Cartridge versions for the e|1 Analyzer to enhance flexibility for laboratories and point-of-care environments of all sizes.
