In less than a month, engineers at Sandia National Laboratories converted 100 respiratory machines New Mexico hospitals had on hand into machines that can safely be used as ventilators to treat ...
Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...
In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...
Despite the U.S. government issuing guidelines to allow re-engineering of CPAP sleep apnea machines into ventilators, a major manufacturer stresses the units would need considerable work. However, a ...
In the race to provide the ventilators needed to treat COVID-19, several companies have developed new devices. But there may be a simpler approach. Formlabs has received an emergency use authorization ...
A court has ordered the Dutch medical device company Philips and its subsidiary, Respironics, to stop making sleep apnea machines in the US until they resolve a slew of manufacturing issues. The case ...
(RTTNews) - Royal Philips (PHG) announced the launch of Philips Ventilator BiPAP A40 EFL which comes with a new ventilation therapy feature for chronic obstructive pulmonary disease (COPD) patients to ...
(RTTNews) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently conducted an ...
To continue reading this content, please enable JavaScript in your browser settings and refresh this page. The BiPAP A40, which is only available in Europe, treats ...
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