Konica Minolta Healthcare Americas Inc. introduced the Sonimage MX1 portable ultrasound system, optimized for musculoskeletal (MSK) and orthopedic practices, interventional guidance and outpatient centers. Sonimage MX1 delivers the power, ease-of-use and portability that physicians need to make a confident and efficient diagnosis at the point-of-care. Designed for MSK, anesthesia and pain management exams, the new ultrasound system provides high-resolution image quality and simplified workflow with an intuitive touchscreen interface.

Dictum Health Inc., creators of the Virtual Exam Room (VER) telehealth technology, announced the release of their Care Central advanced telestroke module. The module provides neurological images viewing capability for use with the VER to reduce door-to-needle time, improve patient outcomes and lower costs.

June 27, 2018 — Zetta Medical Technologies announced the release of Zoom, its latest magnetic resonance imaging (MRI) software algorithm for image quality enhancement and image optimization of short scanning techniques.

Zoom is vendor-neutral and works with all MRI models from all major manufacturers. Its core algorithm was designed to help MRI imaging departments to automatically process all MRI imaging techniques, including time-sensitive short scans.

A recent study conducted with the Minneapolis Heart Institute found that Bay Labs’ EchoMD AutoEF deep learning software has less variability in evaluating left ventricular ejection fraction (EF) than the average variability of cardiologists reported in literature. Results of the study were presented at the 2018 American Society of Echocardiography (ASE) Annual Scientific Sessions, June 22-26 in Nashville.

At the 2018 Association for Medical Imaging Management (AHRA) Annual Meeting, July 22-25 in Orlando, Fla., Neusoft Medical Systems USA will introduce its latest computed tomography (CT) innovation, the NeuViz 16 Essence. The NeuViz 16 Essence is a 16-slice CT system designed to elevate routine imaging for exceptional results, ideally suited for U.S. healthcare providers. It has received U.S. Food and Drug Administration (FDA) 510(k) clearance.

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