Artromot E2 Elbow CPM System

The Artromot E2 is engineered to accelerate and improve rehabilitation outcomes through controlled, passive motion. Its primary benefit is the restoration of a functional range of motion by gently guiding the elbow through programmed flexion and extension, which helps prevent the formation of scar tissue and joint stiffness. This movement also promotes crucial healing processes by reducing swelling and improving local circulation.

Furthermore, the system’s fully synchronized motors and support for physiologically authentic movement patterns ensure the therapy feels natural and reduces patient discomfort. The ability to extensively customize parameters like speed, range, and pause intervals allows clinicians to tailor a highly precise treatment protocol for each stage of recovery, from immediate post-op care to later-stage mobilization, all while minimizing strain on healing tissues.

The Artromot E2 Elbow CPM unit  is designed with practical usability as a priority. For clinicians, setup and programming are straightforward using the hand control unit, which stores individualized treatment data on a memory chip card for easy tracking and adjustments. The technical specifications, including a broad range of motion (-5° to 140°) and adjustable speed, provide the professional control necessary for effective prescription.

For patients using the unit at home, the interface is intentionally simplified for safety and ease. Key features like the Motor Control (On/Off), a clear timer, and a comfortable Warmup Mode (which initiates movement at 50% of the programmed range) make daily therapy sessions manageable. Its compact and relatively lightweight design (approx. 45 lbs) also facilitates transportation, supporting a seamless transition from clinic to home care without compromising therapeutic quality.

The Artromot E2 Elbow CPM unit is built to the highest medical device standards, ensuring patient safety and unit reliability. It has undergone rigorous third-party safety testing, certified to standards including CSA 601-0-M90 and UL 2601-1. These certifications confirm the unit meets stringent electrical and mechanical safety requirements for clinical use.

Operational safety features include the programmable Reverse-on-Load function, which causes the device to automatically reverse direction if it meets significant resistance, thereby protecting the patient from painful or harmful force. The robust construction using quality components ensures durability for long-term use across multiple patients. Together, these design and certification elements provide peace of mind that the therapy is delivered consistently and safely throughout the rehabilitation journey.