The Food and Drug Administration (FDA) is warning consumers that some models of HeartStart automated external defibrillators (AED) may not work during a cardiac emergency. The devices, which are made ...
Philips receives FDA premarket approval for its HeartStart OnSite and HeartStart Home defibrillators
Amsterdam, the Netherlands –Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices and Radiological Health (CDRH) of the Food and Drug ...
Emirates Airline has placed a further order for the Philips Automated External Defibrillator (AED) device, FR2 AED, for the new fleet of Emirates planes that have already been ordered from Boeing and ...
Amsterdam, the Netherlands and Cambridge, MA – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices and Radiological Health (CDRH) of ...
Royal Philips Electronics, a pioneer in developing treatments to combat sudden cardiac arrest, and Air France-KLM Group, one of the leading European air transport group, today announced an agreement ...
Since officers are often first to arrive at the scene of a cardiac emergency, it is crucial to have immediate access to an AED in the event the victim is experiencing SCA. Defibrillation is recognized ...
OpenMarkets, a collaborative marketplace for capital medical equipment, has announced multiple providers have already taken advantage of its recently launched OpenMarkets MarketBuy for Philips ...
Philips recently announced that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a ...
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