Gyrus ACMI DAC USA Elite System and USA Series Disposable Active Cord BX/12

Gyrus ACMI DAC USA Elite System and USA Series Disposable Active Cord BX/12

• Reference Number: DAC
• Box of 12

The Gyrus ACMI USA Elite System is a comprehensive urology/endoscopy system designed to support resection and visualization in cystoscopy, urethroscopy and similar procedures. This system includes the scope, telescopes, sheaths and compatible electrodes in the “USA Series” range, allowing the surgeon to choose the appropriate loop, knife or electrode for a given procedure (for example, 24 Fr or 26 Fr loops). The system is engineered to provide modularity and flexibility by matching the instrumentation and disposable accessories. With shipping dimensions of around 24″ × 12″ × 8″ and weight around 12 lb (in one listing), it is likely designed for portability or modular integration within urology suites. 

The USA Series Disposable Active Cord (DAC) is a single‐use active electrode cord, intended to connect the active electrode in the resectoscope or cautery instrument to the electrosurgical generator. It is described as “active, cautery, cysto, disposable” and packaged in a box of 12. Because it is designed for the Elite/USA system, it matches the interface and specifications required by the Gyrus ACMI system. Sterility, electrical safety, compatibility and single‐use design help maintain OR workflow, reduce cross‐contamination risk, and ensure performance consistency for each case. The disposable format allows hospitals to manage inventory of high‐use items without sterilization/reprocessing.

In a clinical setting, this combination allows a facility to standardize around the USA Elite platform, then use disposable cords and electrodes from the USA Series line—enabling cost‑control, predictable performance and simplified switching between patients. The disposable active cord helps streamline case turnover, and the modular electrodes (knives, loops) support a range of resection applications (enlarged prostate, bladder tumor, urethral strictures). Because the supplier spec sheets are limited, one must verify details such as active cord length, connector type, electrical load rating, insulation voltage, sterility (single‐use), and system compatibility (generator interface) before purchase and clinical use.