August 10, 2011 – In the 3.0 Tesla (T) magnetic resonance (MR) marketplace, patient compliance often impacts image quality and patient throughput. As the only 3.0T MR system designed to improve patient compliance and comfort while offering advanced radiology capabilities, Toshiba America Medical Systems Inc.’s new Vantage Titan 3.0T open-bore MR has received U.S. Food and Drug Administration (FDA) clearance. The new system is the only 3.0T MR offering patient-friendly features such as noise reduction, a wide and open bore, feet-first imaging and Toshiba’s proprietary contrast-free techniques.
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