Medistim receives EU MDR certificates for MiraQ systems and TTFM probes

Today, Medistim announces that it has received EU Medical Device Regulation (MDR) certification for its MiraQ™ ultrasound systems and Transit Time Flow Measurement (TTFM) probes.

After years of preparation, Medistim has successfully obtained its first CE certificates under the latest EU Medical Device Regulation (EU MDR 2017/745).

This achievement represents a key milestone, affirming Medistim’s compliance with the most rigorous medical device standards set by the European Union. The new EU MDR imposes stricter requirements on safety, performance, and traceability of medical devices, with the goal of enhancing patient protection. Medistim’s successful certification underscores its dedication to excellence and itsmission to deliver high-impact solutions that make a clinically significant difference in healthcare worldwide.

“Receiving the CE certificate under the EU MDR for our MiraQ™ system platform is atestament to the dedication and hard work of our entire team,"said Kari E. Krogstad, President and CEO at Medistim. "This accomplishment reflects our unwavering commitment to delivering safe and reliable medical devices to our customers worldwide."