User Instructions
- In accordance with the new Medical Device Regulation (MDR), all Medical Device Manufacturers are required to collect and evaluate data related to the clinical safety and performance of their products on the market. For this reason, we thank you for your understanding and sensitivity on this matter and wish you continued success in your work.
- In the event of negative evaluations for the questions below, the explanatory information you provide in the comment section under the relevant question is extremely important for us to improve product safety and performance.
- If you have any opinions or comments you would like to share other than the questions below, we kindly ask you to state them in the relevant section at the end of the form.