Data collection for Post-Market Surveillance of Medical Devices

Your experience is essential for all!

We in Epitech Group SpA are proud of the quality of our products, however we are keen to do even better.
Our commitment is to constantly improve the performance and safety of our products to ensure user satisfaction.
If possible, please take a few moments to complete the following questionnaire* on our medical devices.

*This initiative is not aimed at promoting the sale of medical devices, rather at collecting information within the framework of the post-market surveillance system by Epitech Group SpA. The duty to conduct post-market surveillance activities is enshrined in Regulation (EU) 745/2017 on Medical Devices. The collected data will be used by Epitech Group SpA only for this purpose, they will not be communicated or provided to others and their processing will take place in full compliance with current privacy legislation.

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For further information or questions, please do not hesitate to contact us at, or through the net of our Italian Sales Representatives active in your area.

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EPITECH Group SpA unipersonale - Via Egadi, 7 - 20144 Milan Italy - VAT n° 03630550287