Medical Polymer Products Branch Successfully Holds an Experience Sharing Meeting on the Implementation of Unique Device Identification (UDI)

  • 2022-05-05
According to the requirements of the Announcement on the Unique Device Identification for the Second Batch of Medical Devices officially released by the National Medical Products Administration on September 17, 2021, the Unique Device Identification (“UDI”) for the second batch of medical devices will be implemented from June 1, 2022. This means that from June 1, 2022, the medical devices produced by related medical device registrants should bear the unique device identifiers; before the marketing of these medical devices, registrants should upload the product identifiers and relevant data for their minimum sales units or higher-level packaging to the Unique Device Identifier Database according to the requirements of the relevant standards or specifications and ensure that the data is true, accurate, complete, and traceable.
In this regard, the Medical Polymer Products Branch (“Branch”) held an “Experience Sharing Meeting on the Implementation of Unique Device Identification (UDI)” on the afternoon of April 28 in its five DingTalk groups in the form of “online simultaneous broadcast”, where UDI project leaders from the Branch’s president unit WEGO Group and vice-president unit TUORen Group were invited to share their related implementation experience. The meeting was chaired by Ren Feifei, Deputy Secretary General of the Branch, and attracted nearly 2,000 viewers. The Branch hoped to help more member units to advance UDI compliance through the sharing meeting.

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