UDI system (Ramz) aims to documenting unique devices codes for medical devices based on accredited international standards, in purpose to allow all stakeholders to identify medical devices information through the unique device identification code that is registered on the system.
Manufactures and their authorized representatives are directly responsible to provide all data of unique device identification codes for their medical devices and modify them.
Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices. Read