Questionnaire for Monitoring the Effects and Critical Issues of NegEnt Devices

In compliance with current regulations on the clinical monitoring of Medical Devices, we invite you to complete the Questionnaire for monitoring the effects and any critical issues related to NegEnt Devices.

The request to complete this questionnaire is part of our obligations as a manufacturer of CE Medical Devices. Your participation in the monitoring of the NegEnt Series products will provide an essential contribution to ensuring the safety and effectiveness of our products.