Medtronic plc, a global leader in medical technology, has announced that its VitalFlow™ Extracorporeal Membrane Oxygenation (ECMO) System has received CE Mark approval in Europe. This significant regulatory milestone marks a major advancement in critical care, allowing Medtronic to offer a fully integrated ECMO portfolio designed to meet the complex needs of modern intensive care units. The CE Mark approval represents a leap forward in delivering seamless, life-saving support to critically ill patients across Europe. Medtronic's VitalFlow ECMO technology, stemming from its acquisition of MC3 Cardiopulmonary, aims to simplify ECMO therapy and improve patient outcomes.
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