Vigilance and risk reporting

In accordance with Regulation (EU) 2017/745, we ensure a vigilance system for monitoring the safety of medical devices. In case of adverse events or serious risks, please contact us at info@kaz-medical.com or the Public Agency for Medicinal Products and Medical Devices (JAZMP) at www.jazmp.si. The reporting procedure is described in the instructions for use of each device.

 

All personal information you provide will be treated confidentially and used solely for the purposes for which it was provided. If there is a need for further processing of your data for another purpose, we will contact you in advance and request your consent. In certain cases, legislation may require us to process or share your personal information. In such cases, we process your personal information based on the law, and such processing or sharing of personal information is mandatory.