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UDI system (Ramz) aims to document unique devices codes for medical devices based on accredited international standards, with the purpose to allow all stakeholders to identify medical devices information through the unique device identification code that is registered on the system.

Manufacturers and their authorized representatives are directly responsible to provide all data of unique device identification codes for their medical devices and modify them according to the compliance timeframe indicated by the Saudi FDA.

Speak to our experts to get your UDI registered before the deadline (1st September, 2024)

Points to remember before filling the form:-

• You MUST be an authorized representation with Bio-Standards.
• You MUST have a a valid MDMA registration
• UDI MUST be issued by the following agencies - GS1, HIBCC & ICCBBA
• ‍Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices

Incase of none of the above reach out to our customer care at info@bio-standards.com or fill in our Free consultation form.