Alix

Alix is a CE-marked Class I medical device developed by Beo Healthcare (France) in accordance with Regulation (EU) 2017/745 (MDR).

Alix is designed to support adapted physical activity, rehabilitation, reconditioning, and personalized exercise programs based on physiological data and user profiles. The application is intended to be used as part of structured physical activity pathways, including rehabilitation or reconditioning programs, under medical supervision or following the recommendations of a healthcare professional.

Alix provides personalized physical activity sessions based on user characteristics, progress, and data collected from compatible connected sensors. Sessions include warm-up phases, exercises, recovery, and rest periods, adapted to the user’s condition and objectives.

The application integrates a wide range of programs and exercises developed with input from healthcare and sports professionals. Alix guides users throughout their sessions and promotes regular, progressive, and personalized physical activity.

Some features of Alix require compatible connected devices or sensors (such as heart rate or activity sensors) in order to collect the physiological data necessary for personalization. Sensor compatibility depends on the device model, operating system, and manufacturer.

Alix does not function as a standalone medical measurement device and does not replace external medical equipment.

Permissions and data access

Alix may request access to certain data from Health Connect, including physical activity-related data, in order to assess daily activity levels and support users in reducing sedentary behavior. These data are used exclusively to personalize physical activity programs and improve user support.

The application may also request access to Bluetooth in order to connect to compatible sensors and retrieve health-related data in real time. Depending on the Android version and device configuration, access to location may be required solely to enable Bluetooth device discovery. Location data are not used for geolocation purposes.

Medical Device Information (EU)

Alix is a Class I medical device according to Regulation (EU) 2017/745 (MDR).
It is CE marked.
Manufacturer: Beo Healthcare, France.

Alix is not intended for emergency use and does not replace professional medical diagnosis or medical treatment. Users should always follow medical advice and consult a qualified healthcare professional for any medical decision.

Instructions for Use

The Instructions for Use (IFU) for the Alix medical device are available online at the following address:
https://projects.beohealthcare.com/alix/doc/D-DOC-07-IFU-patients-fr.pdf

This document is available in French only.