SwastiChemEx: US FDA approves Konica Minolta's AeroDR XE wireless digital

Friday 17 October 2014

US FDA approves Konica Minolta's AeroDR XE wireless digital

Konica Minolta Medical Imaging, a world class provider and market leader in medical diagnostic primary imaging, has received the US Food and Drug Administration (FDA) clearance for its new AeroDR XE wireless digital radiography solution.

Healthcare providers in the demanding ER/Trauma rooms and ICU/CCU units need simple, reliable, and robust primary imaging solutions that deliver the information they need to make important patient care decisions quickly and confidently.

To address the needs of these fast-paced, extreme environments, Konica Minolta offers the simple yet powerful AeroDR XE, the lightest DR panel available today. Designed to provide unparalleled reliability and high-capacity imaging in extreme "on the go" environments the robust and highly durable AeroDR XE is also ideal for teaching hospitals, portable use and at the bedside.

Built to endure the rigors of extreme imaging environments outside the radiology department, the AeroDR XE combines the industry's most robust wireless DR panel with a simple yet powerful software interface.  As a result, users benefit from the best weight-to-load ratio – up to 661 lbs – and the highest bend and liquid resistance on the market. Weighing only 5.7 lbs, the AeroDR XE is the lightest panel on the market and easiest to handle.

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