Toshiba Receives FDA clearance for Vantage Titan MR system | Toshiba Medical Systems Corporation
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Healthcare Company News Toshiba Medical Systems Corporation Toshiba Receives FDA clearance for Vantage Titan MR system

Toshiba Receives FDA clearance for Vantage Titan MR system

Company News - Toshiba Medical Systems Corporation
Toshiba America Medical Systems, Inc., announced FDA clearance for the new open-bore 1.5T Vantage Titan magnetic resonance (MR) system. Toshiba America Medical Systems, Inc., announced FDA clearance for the new open-bore 1.5T Vantage Titan magnetic resonance (MR) system. With this clearance, Toshiba is on schedule to make the system commercially available in the first quarter of 2008. The open-bore of the Vantage Titan is 18 per cent larger than other 1.5T systems on the market, featuring a large 71-centimeter patient aperture.

"Toshiba's Vantage Titan is now one of the most powerful MR units available with a 30/130 gradient platform," said Bob Giegerich, director, MR Business Unit, Toshiba. "It is a dramatic improvement over traditional open-bore 1.5T MR systems and offers the largest and widest bore available with a significant reduction in noise."

The Vantage Titan's large clinical field-of-view is unique for this bore size and produces high-quality images without compromising homogeneity or overall imaging performance. The system also features Toshiba's patented PianissimoTM noise reduction technology, which creates a better imaging experience for all patients.

The Vantage Titan MR system also takes advantage of Toshiba's proprietary, contrast-free MRA techniques - Fresh Blood Imaging (FBI), Contrast-free Improved Angiography (CIA), Time-Spatial Labeling Inversion Pulse (Time-SLIP) and Time-Slip Angiography (TSA). Contrast-free imaging is particularly important because gadolinium, the most common contrast agent used for magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) exams, has been directly linked to a sometimes fatal disease that occurs in patients with renal insufficiency, called Nephrogenic Systemic Fibrosis (NSF) or Nephrogenic Fibrosing Dermopathy (NFD).