Postmarket surveillance

EXBIO Praha a.s. performs postmarket surveillance of IVD medical devices in accordance with the Regulation (EU) 2017/746 of the European Parliament and of the Council. The information obtained is necessary to provide evidence that our IVD medical devices consistently provide the required function, performance and safety within their intended purpose and in the context of a physiological or pathological state. An important part of proactive data collection is gathering valuable information from customers. For this purpose, we have created online questionnaires below, which can be completed very quickly.

We would kindly like to ask you to complete questionnaires only for IVD medical devices you use. By clicking on the links below you will be taken to the Google questionnaires. If you would like to be contacted regarding the information you have submitted, please leave your contact details in the questionnaire.