Officers and regulatory representatives of Medina Bútor Kft.
NAGY András
- the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
- the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
- the post-market surveillance obligations are complied;
- the reporting obligations are fulfilled;
- in the case of investigational devices, the statement is issued;