UDI system (Saudi- DI) aims to record and document the identifier codes for medical devices based on international standards. Device (DI) codes will help the users and stakeholders to recognize all information related to the device through registered UDI codes and labeled on the device package

The National Center For Medical Devices Reporting (NCMDR) is devoted to receive adverse events reports and feedback information about any medical devices malfunction from hospitals and healthcare facilities all around KSA, as well as, receiving product recalls from manufacturers and suppliers to insure that proper action had been conducted.

The Medical Device Marketing Authorisation (MDMA) system allows authorised representatives and local manufacturers to submit applications electronically for marketing authorisation that permits the relevant medical devices to be placed on the market of the KSA. For more information on how to register in the system Please

Medical Devices Importing License System "MDIL" is a Licensing system for the establishments involved in the importation of medical devices in Saudi Arabia. It is a web based system where all applications for importation of Medical IVD’s, Non-Medical IVD’s, Distillations, Chemicals and Gases shall be applied online. The Importing License shall be obtained prior to shipment.

​Finalize the importing, transporting and exporting of medical radioactive materials requests electronically easily and conveniently to serve the interests of health facilities, carriers and suppliers.