We update the data, in accordance with the requirements of regulatory authorities, on the platform for online registration of medical devices, medical devices and in vitro diagnostic.

We update the data concerning manufacturers, distributors, other agents of medical devices and devices.

We update the name or the address of the distributors in accordance with the provisions of Article 41, paragraph 1, subparagraph b) iii) of Decree-Law no. 145/2009 of 17 June.

We update the device data already recorded, such as manufacturer, representative, trade mark, model, designation, nomenclature GMDN, brief description, classification of DM, code of Notified Body, Reference manufacturer’s catalog price, NPDM Code.

We eliminated the registered devices. We discontinued devices.

We inform how to assign the code GMDN.

We update the data related with the identification of the entities related with the medical devices.