I. What is the basis and main changes of the revision of Beijing Medical Device Administrative Punishment Discretion Benchmark?

Not long ago, the comprehensive Department of the NMPA released a message. The comprehensive Department of the NMPA publicly solicited Opinions on Strengthening the Hierarchical Supervision of the Production and Operation of Medical Devices (Exposure Draft).

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The implementation of medical device MAH in China is aiming at promoting the reform of medical device review and approval mechanism and enhancing the management of medical device whole life cycle.

In April 2022, NMPA approved 212 medical devices, including 35 Class III imported products, 20 Class II imported products, and 154 Class III domestic products.

The work of unique identification of medical devices has entered the last mile.

                                                                                    Top 10:

Large order for tens of millions of equipment purchases, only domestic equipment is purchased.

The Following content is selected from the medical device section of the statistical report：

Product type:

2978 new category ⅱ products were registered