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Thursday, May 24, 2012
News Making Money

GE Healthcare introduces in Mexico, Vscan, the pocket-sized ultrasound visualization tool

02/02/2012 04:18 (111 Day 22:49 minutes ago)

The FINANCIAL -- GE Healthcare introduced today in Mexico the pocket-sized, portable visualization tool, Vscan, a device that enables physicians to quickly look inside the body at the point of care.

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The ability to take a quick look inside the body using Vscan may help clinicians improve the quality of referral and triage of patients, enabling optimized care and possibly help reduce healthcare costs, according to General Electric Company.

 

The Vscan is a prescription device for ultrasound imaging, measurement and analysis in the clinical applications of abdominal; cardiac; urology, fetal/OB; pediatric; and thoracic/pleural motion and fluid detection, as well as for patient examination in primary care and in special care areas.

Until recently, for clinicians to obtain a quality ultrasound image of a patient, many patients had to move or be transported from one room to another to access a console ultrasound. Thanks to its compact size plus its black and white and color-coded image quality, today, Vscan provides access to outstanding image clarity at the physician’s fingertips.

Vscan is an intuitive tool; GE provides users with web based online education tools for both the product and basic clinical applications which include sections on imaging technique, anatomy and answers to frequently asked questions.

Designed for ease of use, the user interface and voice control enables clinicians to readily acquire an image and document findings. Included with the Vscan is a USB based docking station and gateway software with service tools and access to remote diagnostics that allow clinicians to share their information among their colleges. Battery life provides up to one hour of scanning without recharging, allowing on average the ability to scan up to 30 patients based on average of 2 minute scan.

Vscan has received 510(k) clearance in the U.S. from the Food and Drug Administration, the CE Mark from the European Union, and the Medical Device License from Health Canada. In Mexico the Federal Commission has approved it.

 

 

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