MRS (Mammography Reporting System Inc.) has earned the top ranking in the Mammography Information Systems (MIS) vendor category in the newly released KLAS report entitled Women's Imaging 2013: Measuring the Options. The Women’s Imaging 2013 report is an independent overview of industry trends and advancements among key vendors conducted by KLAS, which is an independent research firm that is widely recognized in the healthcare industry. 

 

Unisyn Medical Technologies Inc. announced the sale of its Transactional business to GE Healthcare, including its ultrasound probe repair, multi-modality part and proprietary test equipment businesses.

 

GE Healthcare announced that it has agreed to acquire certain Mammography assets of Rayence, a subsidiary of Vatech Co. Ltd., a Korean X-Ray manufacturer. The Mammography assets of Rayence will, at closing, become part of the Detection and Guidance Solutions (DGS) business unit of GE Healthcare.

Digisonics will exhibit its No. 1 KLAS rated cardiology picture archive and communications system (PACS) and structured reporting solutions at this year’s American Society of Echocardiography (ASE) Scientific Sessions in Minneapolis, Minn. 

More than 54 companies will display their latest products and services at the American Society of Echocardiography’s (ASE) 24th Annual Scientific Sessions, planned for June 29-July 2 at the Minneapolis Convention Center in Minneapolis, Minn. This year, the conference theme is “a disease-based focus on the role of echocardiography in diagnosis and guiding therapy”. 

June 25, 2013 — Siemens Healthcare announced that the U.S. Food and Drug Administration (FDA) has cleared the Virtual Touch imaging ultrasound application, Siemens’ first commercially available implementation of Acoustic Radiation Force Impulse (ARFI) technology.

Magnetic resonance imaging (MRI) may be an effective way to diagnose mental illnesses such as bipolar disorder, according to experts from the Icahn School of Medicine at Mount Sinai.

iCAD, Inc. announced approval by the U.S. Food and Drug Administration (FDA) for use of the company’s SecondLook mammography computer-aided detection (CAD), on the next generation PowerLook Advanced Mammography Platform (AMP), for FujiFilm’s Aspire HD Full-Field Digital Mammography System.

 

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