Medical Devices / Incidents

If you experience a problem with the operation of our medical device, an adverse reaction, or other event that may affect the safety of the patient or user, please complete the form below. The information provided will be used solely to assess the safety of the medical device.

In accordance with Article 13 of the General Data Protection Regulation of April 27, 2016 (GDPR), we hereby inform you that the Controller of the personal data contained in the adverse reaction report is Curtis Health Caps S.A., with its registered office in Wysogotowo, ul. Batorowska 52, 62-081 Przeźmierowo.

Personal data will be processed for the purpose of monitoring incidents related to the use of medical devices in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009, and repealing Council Directives 90/385/EEC and 93/42/EEC, and the Act of 7 April 2022 on medical devices (Journal of Laws of 2022, item 974).

The data provided in the form will be stored for the period specified in Article 10 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017.