Lifemotion ECMO System Granted European MDR CE Mark Certification

February 6, 2025—CBM Lifemotion recently announced it received European Union Medical Device Regulation (MDR) CE Mark certification for the Lifemotion extracorporeal membrane oxygenation (ECMO) system and extracorporeal life support (ECLS) technology. The company is headquartered in Shenzhen, China, and has an international office in Mirandola, Italy.

As noted in the company’s press release, the entire Lifemotion ECMO system—including its individual components—has been approved for extended 14-day use to provide sustained critical care support. The Lifemotion ECMO system includes a stand-alone centrifugal pump; an ECLS membrane oxygenator; an integrated tubing set; and a dedicated trolley/cart for effective setup and easy transportation

The Lifemotion ECMO system features an intuitive full-size touchscreen interface that enhances clinical control and monitoring. Additionally, advanced mobility features enable seamless patient transport across care settings. A versatile design supports rapid deployment in emergency situations, stated CBM Lifemotion.