The notification on the implementation of medical devices and in vitro diagnostic reagent registration management practices related issues-SFDA No. 247 [2015]
Provinces, autonomous regions and municipalities Food and Drug Administration:
The newly revised "Medical Device Registration" (China Food and Drug Administration Order No. 4) and "in vitro diagnostic reagent registration management approach" (China Food and Drug Administration Order No. 5) was October 1, 2014 since implementation.
