To facilitate the administration of medical device registration, in accordance with the Measures for the Registration and Filing of Medical Devices (Order No. 47 of the State Administration for Market Regulation), the National Medical Products Administration (NMPA) has revised the Catalog of Medical Devices Exempt from Clinical Evaluation (2023) (Announcement No. 33 of 2023) and formulated the Catalog of Medical Devices Exempt from Clinical Evaluation (2025). The updated catalog is hereby promulgated and shall come into effect as of the date of issuance.
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