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Bmeye receives FDA clearance for hemodynamic monitor

Netherlands-based Bmeye has received 510(K) clearance from the FDA to market Nexfin, its newly developed line of hemodynamic monitors.

The Nexfin monitors are said to provide provide precise and easy to use continuous non-invasive blood pressure and cardiac output monitoring. Bmeye received CE market approval earlier this year.

Bill Bednarski, CEO of Bmeye, said: “The Nexfin is cost effective and will significantly improve patient care.”