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Services of the General Authority for Food and Drugs

Unique Device Identifications (Saudi-DI)

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

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National Center For Medical Devices Reporting

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.

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Medical Devices Marketing Authorisation

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

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Medical Devices Importing License

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.

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Radioactive Material Registration System

​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.

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