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Medical Devices Division

  • 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.