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In case of emergency…
To report a service outage or other platform emergency, contact firstname.lastname@example.org and your priority request will be routed accordingly.
the fine print
The Propeller System is a Class II medical device cleared by the FDA and CE Marked in Europe. The Propeller System includes the physical device ("sensors"), mobile and web applications, and associated back-end software (platform and API). Use or interpretation of the Propeller system or its corresponding data (including sensor data, software application data, or any other associated data) is subject to any applicable regulatory statues or legal requirements. Propeller Health retains no responsibility or liability for use or interpretation of the data outside of the intended use of the Propeller System. Please contact Propeller Health if you have any questions on this matter.
© 2020 Propeller Health.