Officers and regulatory representatives of DIOME DI FIORENZANO LUISA
DE INNOCENTIS Bruna
The compliance of the medical devices manufactured by this company is suitably checked and this should be done before the product is released.
The EU declaration and Eu technical documentation are managed and maintained whit the incorporation of all the necessary updates.
Authorization of the final product release
The PMS responsibilities are fulfilled consistently with the MDR
Reporting requirements to regulatory authorities are wll managed.