EVENT
Unique Device Identification Requirements MDS-REQ XX
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Unique Device Identification (UDI) aims to register and document an ID for medical devices based on certified international standards to enable users who work closely with medical devices to identify their information through a unique code registered in the system along with an identification card for the product.
03/04/2022 - 17/04/2022
webmaster@sfda.gov.sa
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Last Modified Date: 12/04/2022 - 9:56 AM Saudi Arabia Time