Movesense Medical sensor specific additional Terms and Conditions

In order to comply with the medical regulations (European MDR 2017/745 et.al.), we need to make sure that you accept and understand these few additional medical sensor specific terms and conditions before we can deliver Movesense MD sensors or other Movesense medical products to you:

By purchasing Movesense MD sensors or other Movesense medical products you commit to:

• Provide us any and all safety or performance related feedback: medical@movesense.com
• Inform us as the Movesense medical product manufacturer of any clinical studies involving Movesense medical products: info@movesense.com

By purchasing Movesense medical products you understand that;

• The Movesense MD sensor, SKU number MS060222000, is certified as a class IIa medical device in conformity with the EU Medical Device Regulation MDR 2017/745.
• The Movesense MD is intended, by its manufacturer, to be used together with a host medical device or an application, such as the customer’s own device/application or the Movesense ECG Recorder application.
• You are responsible for making sure that the Movesense medical device(s) you purchase are used as intended and you will be responsible for the consequences of the use against the intended purpose of the device(s).
• In case you are using the Movesense MD sensors or other Movesense medical products in any clinical investigations, studies, or R&D projects involving user testing or similar, you are responsible for obtaining and maintaining the necessary permissions and authorizations, as required by the applicable local legislation.
• At this time the documentation is available in English language only, unless separately agreed in writing. You are responsible for any additional language translations that may be required in the target market where you intend to operate.

If you have any questions, please do not hesitate to contact us, we are happy to help!