CONAMCO S.A. DE C.V. dba Medental

Ensure that the conformity of devices is adequately monitored, technical documentation and the EU declaration of conformity are drawn up and kept up to date, and post-market surveillance obligations in accordance with Article 10(10) are met, as well as to ensure the notification of reportable serious incidents. Main Responsible Person for complying with the guidelines of the EU regulation 2017/745.

Management Representative for manufacturing site. Responsible for communication between senior management and regulatory bodies, European representative and other stakeholders. Second Person Responsible for complying with the guidelines of the EU regulation 2017/745.