FDA-Cleared Pediatric Body Coil Now Available for Philips 3.0T MRI
The pediatric body array coil, developed to offer a more flexible alternative to rigid devices, is optimized and validated for use on 3.0T MRI systems.
The pediatric body array coil, developed to offer a more flexible alternative to rigid devices, is optimized and validated for use on 3.0T MRI systems.
The platforms feature AI-powered imaging, helium-free MR technology, and designs focused on long-term operational value and efficiency.
Updated guidance addresses ventilator inoperative alarm failures that may lead to therapy loss, with 13 injuries and eight deaths reported.
The pediatric body array coil, developed to offer a more flexible alternative to rigid devices, is optimized and validated for use on 3.0T MRI systems.
AWS’ AI services and global infrastructure support the expansion of Philips’ healthcare informatics portfolio and product development for interoperable healthcare.
Read MorePhilips integrates AI algorithms into its MRI systems and showcases its AI-enabled software to streamline workflows and new wide-bore scanner at ECR 2025.
Read MoreBy streaming data from medical devices and other sources, Philips and Mass General Brigham aim to create a scalable, unified, near real-time data and insights ecosystem.
Read MorePhilips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Read MorePhilips has updated instructions for several ventilators to address aerosol deposits on internal sensors when used with in-line nebulizers.
Read MorePhilips’ Spectral CT 7500 RT, now FDA-cleared, integrates spectral CT into radiotherapy, enhancing tumor visualization and targeting.
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Philips has introduced a 160cm FDA-approved version of its LumiGuide navigation wire, powered by FORS technology.