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.
New MRI systems at Mansfield Hospital and Ontario Health Center aim to improve scan quality, reduce imaging time, and enhance patient comfort.
Hyperfine, in collaboration with the Medical University of South Carolina, will use the Swoop Portable MR Imaging system to scan astronauts.
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.
Royal Philips and Nicklaus Children’s Health System began a 10-year collaboration on pediatric care with new MR and ultrasound technology.
Read MoreA fire broke out near the MRI room at the Jamaica Plain VA Medical Center in Boston, Mass. No injuries or deaths were reported.
Read MoreSiemens Healthineers has nabbed U.S. FDA clearance for the Magnetom Terra.X, a second-generation 7-tesla MRI scanner with Ultra IQ Technology and improved hardware, including XA60A software, enhancing image quality, enabling advanced clinical imaging and research capabilities.
Read MoreClear Guide Medical announced the FDA clearance for the Clear Guide Scenergy computer aided instrument guidance system.
Read MoreSiemens Healthineers showcased its Magnetom Flow, 1.5 tesla platform for MRI with a closed helium circuit and no quench pipe.
Read MoreHyperfine has launched the eighth generation of its Swoop system MR brain imaging device software, featuring an FDA-cleared AI denoising feature for diffusion-weighted imaging.
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Philips is recalling the Panorama 1.0T HFO due to risk of explosion during a quench procedure caused by excessive pressure buildup.