Inspira Tech Granted Patent for Convertible Dual Lumen Cannula Device, Method of Use
Inspira Technologies' convertible dual lumen cannula device has been granted a patent by the U.S. Patent and Trademark Office.
Inspira Technologies' convertible dual lumen cannula device has been granted a patent by the U.S. Patent and Trademark Office.
Philips' recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.
Roy Jakobs is tapped to succeed Frans van Houten as Royal Philips’ president and CEO, effective October 15. Jakobs has been critical in helping Philips address ongoing medical device recall challenges, the company says.
Inspira Technologies' convertible dual lumen cannula device has been granted a patent by the U.S. Patent and Trademark Office.
Certain Philips ventilators that were recalled last year may lead to injuries or death, according to a new classification of the recall by the FDA.
Read MoreComplications involving a recall for certain sleep and respiratory care devices are causing some to make difficult personal health decisions.
Read MoreHenley Ion reports positive testing results of their respiratory protection device, without the use of conventional filtration.
Read MoreN95 respirators met the primary endpoints of function and effectiveness, in addition to maintaining filtration efficiencies of 95% or more in the study.
Read MoreResearchers reprocessed respirators using vaporized hydrogen peroxide and found that the devices maintained effectiveness with up to 25 cycles of re-use.
Read MorePhilips Respironics has been conducting comprehensive testing to address potential health risks related to the PE-PUR sound abatement foam in the devices.
Read MorePhilips is scrutinizing a recall of its ventilators and respiratory devices from the U.S. FDA.