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 ...
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 ...
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 ...
Please provide your email address to receive an email when new articles are posted on . Treatment with adaptive servo-ventilation for 12 months improved disease-specific quality of life scores. At 12 ...
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 ...
Getinge, a Swedish public limited company, announces clearance from the US FDA for Servo-air Lite, a wall gas independent non-invasive mechanical ventilator. “We are happy to broaden our ventilator ...
To the Editor: Cowie et al. (Sept. 17 issue) 1 report on the results of the Treatment of Sleep-Disordered Breathing with Predominant Central Sleep Apnea by Adaptive Servo Ventilation in Patients with ...
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