The Unique Device Identification (UDI) system for medical devices is an important measure to implement the Regulation on the Supervision and Administration of Medical Devices and effectively advance the State Council’s reform to control high-value medical consumables and deepening of the reform of medical and healthcare systems as well as an important means to innovate regulatory methods, increase regulatory efficiency, strengthen fine management throughout the lifecycle and promote high-quality development of the industry. In order to further achieve UDI demonstration and promotion, the National Medical Products Administration (“NMPA”) has selected the first batch of UDI demonstration units and required them to effectively play a leading and exemplary role. To further improve the demonstration and application effects, the China Association for Medical Devices Industry hereby shares and releases one of the “Experience Sharing and Training Videos from Unique Device Identification Implementation Demonstration Units”.
One of Experience Sharing and Training Videos from Unique Device Identification Implementation Demonstration Units
