Frost & Sullivan honors Dräger for the third time based on best practices in ventilation therapyTelford, PA, Oct. 21, 2020 (GLOBE NEWSWIRE) -- Dräger, an international leader in the fields of ...

The 402 affected Oxylog 3000 and Oxylog 3000 Plus ventilators are distributed throughout the U.S., the FDA said. They were distributed between April 2007 and December 2015.

Dräger recognized for pioneering innovations in respiratory care, delivering measurable improvements in patient outcomes, clinical efficiency, cost-effectiveness and critical care training ...

TELFORD, PA — Dräger has announced that its Evita V800/V600, Babylog VN800, and Savina 300 ventilators have received Authority to Operate ... President and CEO of Draeger, Inc.

The recall spans more than 11,600 ventilators, according to its entry in the FDA’s recall database. They were distributed over the span of more than a decade, from March of 2009 through this year.

New certifications follow Dräger's previous ATO certification for a critical care ventilator. Dräger Evita V800/V600 and Babylog VN800 family of devices, effective 1/23/2025 and expiring on 1/21 ...

The Fabius MRI anesthesia machine features our precision E-Vent piston ventilator technology, renowned for both performance and safety. It has been tested for use with MRI systems of 1.5 and 3 ...

For questions regarding the operation and/or servicing of affected Draeger ventilators in the United States, call DraegerService Technical Support at 1-800-543-5047 (press 4 at the prompt) between ...

German medical device manufacturer Dräger has voluntarily recalled the optional PS500 Power Supply Unit used with the Evita V500 and Babylog VN500 ventilators following complaints that the ...