At LABRHA, the safety of patients and healthcare professionals is our top priority.
If you wish to report :
- A complaint regarding one of our products
- An incident or malfunction
- An adverse event that occurred after using one of our medical devices
We invite you to share this information with us so that we can analyze the situation and continuously improve the quality of our products and your safety.
All reports are reviewed with the utmost care by our quality team.
How to submit your form?
1.
Download
the form
2.
Fill in
the information
3.
Send to
vigilance@labrha.com
Confidentiality of Information
The information provided will be treated confidentially by LABRHA as part of its post-market surveillance and medical device vigilance system, in accordance with applicable regulations.
This information may be used for safety analysis, the continuous improvement of our products, and, if necessary, to fulfill reporting obligations to the competent authorities.
Important Information
This form is intended for reporting product complaints or adverse events related to the use of a LABRHA medical device.
⚠️ This service does not replace medical advice.
In the event of a medical emergency, contact your healthcare provider or your country’s emergency services immediately.