CQ Medical's Iris AirShuttle™ Patient Transfer Platform Recognized at Women in Innovation Award Showcase

The Iris AirShuttle is an integral part of CQ Medical's Symphony® Imaging, Treatment & Transfer Solutions, which conveniently integrates the AirShuttle patient platform with the AirDrive™ system. This combination enables smooth and efficient patient transfers between imaging modalities and procedural platforms without the need for repositioning. Designed for use in CT, MR (up to 3 Tesla), and angiography, the Symphony solution ensures safe patient movement across various surfaces, including sheet-covered pads and mattresses, while minimizing the number of clinical staff required.

AVONDALE, Pa., 05/03/2025 (informazione.news - comunicati stampa - salute e benessere)

The is an integral part of , which conveniently integrates the patient platform with the system. This combination enables smooth and efficient patient transfers between imaging modalities and procedural platforms without the need for repositioning. Designed for use in CT, MR (up to 3 Tesla), and angiography, the solution ensures safe patient movement across various surfaces, including sheet-covered pads and mattresses, while minimizing the number of clinical staff required.

To learn how the Iris  can help workflow efficiency, safety, and patient care, visit CQMedical.com.

CQ Medical is the global leader in developing high-quality, innovative, patient-centric radiotherapy and cancer therapy solutions. With primary locations in Iowa and Pennsylvania and employees worldwide, the company has more than 80 years of combined experience bringing advanced hardware and consumables for patient immobilization and positioning, fiducial markers, couchtops, and patient care products to the market.

COPYRIGHT © 2025 CQ Medical. All rights reserved. CQ Medical is a trademark of Medtec LLC. Symphony is a registered trademark of Qfix Systems LLC. AirDrive, AirDrive Caddie, AirDrive Trolley, AirShuttle, and Iris AirShuttle are trademarks of Qfix Systems LLC.

This press release contains information about products that may or may not be available in particular countries. These products may not be licensed in accordance with Canadian law. Each country has specific laws and regulations governing the commercialization of medical devices and the communication of information regarding medical devices in printed and digital media. Products appearing in this press release or on our website may or may not have received approval, clearance, or marketing authorization by a governmental regulatory body in any particular country or may have received approval, clearance, or marketing authorization for different indications and restrictions in different countries or may be for investigational use only.

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