Philips Launches Telemetry Platform to Address Alarm Fatigue
The new system, featuring the Telemetry Monitor 5500, is designed to streamline alarm management and provide data-driven operational insights for cardiac monitoring.
The new system, featuring the Telemetry Monitor 5500, is designed to streamline alarm management and provide data-driven operational insights for cardiac monitoring.
Summary: Mindset Medical has received FDA 510(k) clearance for its Informed Vital Core (IVC) App,...
US Med-Equip has partnered with Gentherm to expand the distribution of Gentherm's Blanketrol System in the U.S. healthcare market, providing hospitals with advanced temperature management devices and comprehensive service plans.
The new system, featuring the Telemetry Monitor 5500, is designed to streamline alarm management and provide data-driven operational insights for cardiac monitoring.
Huma has received FDA Class II clearance for its disease-agnostic Software as a Medical Device (SaMD) platform.
Read MoreRoyal Philips and Masimo announce U.S. FDA clearance allowing the activation of SedLine Brain Function Monitoring, Regional Oximetry (O3), and CO₂ measurements in Philips patient monitors: IntelliVue MX750 and MX850.
Read MoreGE HealthCare announced US FDA 510(k) clearance of its Carescape Canvas patient monitoring platform for precise, flexible patient care.
Read MoreIcentia has received U.S. FDA clearance for CardioSTAT, an ambulatory, continuous ECG monitoring solution that uses a wireless, single-use recorder.
Read MoreRoyal Philips and Northwell Health have entered into a seven-year agreement to help the health system standardize patient monitoring.
Read MoreLaborie launched the alpHaONE system which is designed to diagnose GERD and offers up to 96 hours of monitoring data.
Read MoreThe FDA granted marketing authorization for a device that recognizes when someone experiences opioid-induced respiratory depression.