Updates on the compliance timeframe for the requirements of medical devices unique device identification (Saudi -DI).

Reference to the published requirements for medical devices unique device identification (Saudi-DI) by Saudi Food & Drug Authority and after launching of UDI database (Saudi-DI), therefore, the timeframe to comply with the requirements has been updated as follows:

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For further inquiries regarding this announcement, please contact md.rs@sfda.gov.sa or call 19999.

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