Konica Minolta Medical Imaging has received U.S. Food and Drug Administration (FDA) clearance for its AeroDR XE wireless digital radiography (DR) system.
With a weight of 5.7 lb, AeroDR XE is designed for use in extreme imaging environments such as emergency/trauma rooms and intensive care and critical care units, according to the vendor. It's also suitable for teaching hospitals, portable applications, and imaging at the bedside. AeroDR XE is resistant to bending and liquids and features a weight-to-load ratio up to 661 pounds.
"The AeroDR XE's rugged design and reliability provide peace of mind, keeping healthcare providers productive in the most challenging environments," said Guillermo Sander, Digital Radiography senior product manager, Konical Minolta Medical Imaging. "Plus, exceptionally quick access to images help boost clinical confidence, which is particularly important in critical care situations."
Konica Minolta said it has improved the detector's lithium ion capacitor, which now lasts a full shift or 300 images. The company has also incorporated new panel drop sensors and monitoring to provide ongoing data on panel handling. Technologists can also handle the panel using grip strips.
"The new AeroDR XE is the smart, financially responsible choice for facilities with extreme, portable imaging environments. It's simple, reliable and robust -- allowing for fast, hard-working imaging when and where it's needed," Sander noted.
Headquartered in Wayne, N.J., Konica Minolta Medical Imaging provides diagnostic primary imaging services and technologies to the medical industry. Its parent company, Konica Minolta Inc., is based in Tokyo, Japan, and employs more than 40,000 people. The company reported 2013 revenues of $9.4 billion.