The Maquet SERVO-i ventilator battery module has been recalled due to the battery having a shorter run time than expected, according to the American Society of Anesthesiologists. The FDA assigned a ...
GALWAY, Ireland--(BUSINESS WIRE)--Swedish based Maquet Critical Care and Aerogen, Ireland, have today announced the release of their partnered product, an integrated unit which provides state of the ...
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 ...
The Maquet Getinge Group is recalling 90,000 defective batteries used with the SERVO-i ventilator system, the US Food and Drug Administration (FDA) announced May 7. The FDA said some battery modules ...
Troubled Maquet's woes continue. On the heels of a permanent injunction from the Department of Justice that resulted in the halt of manufacturing at one of its facilities, the suspension of 5 of its ...
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 ...
Interstate Batteries announced a partnership today with Maquet Medical Systems USA (now Getinge Group) to provide original equipment manufacturer (OEM) batteries to the health care industry through ...
Bridgewater, N.J. (January 6, 2009) — MAQUET Inc., a subsidiary of the Swedish-based Getinge Group and one of the oldest and largest surgical equipment companies in the world, has announced that it ...
Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform
GÖTEBORG, 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 ...
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