New technology integrates seamlessly into IntelliVue Patient Monitoring system to deliver real-time data records and enhance clinical decision support Royal Philips (NYSE: PHG AEX: PHIA), a global ...
Royal Philips Electronics (NYSE: PHG, AEX: PHI) today introduced the IntelliVue MX800 patient monitoring system, a new dimension in patient care that provides immediate access to comprehensive patient ...
Philips’ IntelliVue Patient Monitors MX750/MX850, IntelliVue 4-Slot Module Rack FMX-4 and IntelliVue Active Displays AD75/AD85 receive FDA Emergency Use Authorization for use in the US during the ...
Philips is introducing its IntelliVue X3 patient monitoring system in Europe. The device is designed to monitor vitals at the bedside and when patients are being moved between locations to cut the ...
Medasense Biometrics Ltd., developer of the physiological pain-response monitoring technology (NOL® ‒- the Nociception Level Index), now supports Philips IntelliVue Patient Monitors for anesthesia and ...
Dutch health tech giant Royal Philips has scored FDA 510(k) clearance for its IntelliVue MX750 and MX850 patient monitors. The monitors, which received an FDA emergency use authorization in 2020 and ...
New technology integrates seamlessly into IntelliVue Patient Monitoring system to deliver real-time data records and enhance clinical decision support Royal Philips, a global health technology company ...
Medasense Biometrics Ltd, a developer of the physiological pain-response monitoring technology (NOL ?- the Nociception Level Index), now supports Philips IntelliVue Patient Monitors for anaesthesia ...
FDA 510(k) clearance of latest Philips IntelliVue patient monitor software helps drive alarm management strategies toward a more peaceful, healing environment for patients and caregivers Noise in ...
AMSTERDAM & DALLAS--(BUSINESS WIRE)--Royal Philips (NYSE: PHG, AEX: PHIA) and Children’s Health SM today announced an up to 15-year, long-term, strategic agreement worth up to USD $75 million to ...
More than a year after doling out an emergency use authorization for a handful of Philips’ IntelliVue patient monitoring devices, the FDA is doubling down on the regulatory nod. Two of the patient ...