Product Compliance
Test/Filing/Registration
In order to further standardize the management of artificial intelligence medical devices,The device audit center of the State Food and Drug Administration organized and formulated Guiding principles for registration and review of artificial intelligence medical devices ,It is hereby issued.
It is hereby notified.
enclosure Guiding principles for registration and review of artificial intelligence medical devices download
State Drug Administration
Medical device technical evaluation center
2022year3month7day
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