Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform
GOTEBORG, Sweden, April 22, 2021 /PRNewswire/ — Today, Getinge announces clearance from the US FDA of several new software options for the Servo-u and Servo-n ventilators. In addition to the latest ...
GETINGE, Sweden, April 10, 2019 /PRNewswire/ -- Getinge is today announcing clearance from the US Food & Drug Administration (FDA) for a new software version for the Servo-u® and Servo-n® mechanical ...
In a study published last September in clinical medical journal Critical Care, Maquet’s SERVO-U ventilator outperformed other ventilators in seven out of nine comparisons on use safety, perceived ...
WAYNE, New Jersey, July 7, 2020 /PRNewswire/ -- US Food & Drug Administration (FDA) clears Servo-air® mechanical ventilator for use with adult and pediatric patients dependent on intensive care ...
As the demand for ventilators increased due to the ongoing COVID-19 pandemic, Getinge, a global supplier of mechanical ventilators, was faced with the challenge of ramping its production up 160 ...
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