Cel Rehab

Cel Rehab specializes in proportional control interfaces tailored for individuals with complex mobility needs. Their devices, such as the Joy 250 Db9, PicoJoy variants (2g/f, 6g/f, and 10g/f), and the PuckJoy Db9, are designed to provide adjustable, precise input for mobility aids and assistive technologies. These products focus on enhancing accessibility for users whose requirements go beyond standard market solutions.

Cel Rehab is based in France. Their devices are classified as EU Class I medical devices, meaning they pose minimal risk and are subject to the EU’s regulatory requirements for such products. This classification aligns with the European Union’s medical device regulations, ensuring compliance with safety and performance standards.

Yes, Cel Rehab’s devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This listing ensures transparency and traceability, allowing healthcare professionals, regulators, and users to verify the device’s existence, classification, and compliance with EU medical device regulations. It also facilitates monitoring and reporting for post-market surveillance.

Cel Rehab’s devices are classified as EU Class I medical devices. This classification is determined by their intended purpose and risk level—these proportional control interfaces are designed for low-risk applications, such as enhancing mobility for users with specific accessibility needs. Class I devices typically require conformity assessment procedures, including manufacturer declarations of conformity, but they do not always require third-party involvement unless they incorporate measuring functions or are reusable surgical instruments.