- Collects an information on economic operators and medical devices placed on the Latvian market;
- Collects, includes and stores an information which the Agency has an obligation or right to obtain and store in the electronic database of medical devices register LATMED;
- Ensures the issuance of the Certificates of Free Sale of medical devices;
- Ensures the authorization of the clinical investigations of medical devices and performance studies of in vitro diagnostic medical devices, and substantial modifications to clinical investigations and performance studies as well; supervises the conduct of clinical investigations and performance studies within the regulatory framework;
- Implements the functioning of the vigilance system of medical devices.