User Manual

This page provides access to the Instructions for Use related to DOCT’UP, a Class I medical device, in accordance with Regulation (EU) 2017/745 on medical devices (MDR).
It contains essential information for the safe and effective use of the device, intended for both patients and healthcare professionals.
The available documents are regularly updated to ensure access to information that complies with current regulatory requirements.
We encourage you to consult the most recent version before each use of the device.