Notice of CFDA on Relevant Matters Regarding the Implementation of Classification Catalogue for Medical Devices (2017 No. 143)

Updated: 2019/8/20

In order to implement the Regulations on Supervision and Administration of Medical Devices and Opinions of the State Council on the Reform of Review and Approval System for Drugs and Medical Devices (GF [2015] No. 44), China Food and Drug Administration promulgated Classification Catalogue for Medical Devices (hereinafter referred to as the new Classification Catalogue) on August 31, 2017, which will come into force as of August 1, 2018. For the implementation of the new Classification Catalogue, relevant issues are hereby announced as follows:

I. General Information of the New Classification Catalogue

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