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The Food and Drug Administration intends to tighten the right of approval of a class of medical devices

Southern News the reporter Ma Jianzhong reporter learned from reliable sources, the State Food and Drug Administration intends to use the right of approval of a class of medical automatic digital blood pressure monitor devices from the ground PUC reverted to the provincial bureau to strengthen the processing of checks.

Our country is currently registered product standards for the production of the first class of medical devices for review by the municipal districts drug supervision wrist blood pressure monitor and management departments. State Food and Drug Administration Health Department official said, when it is inevitable there will be deviations due to the implementation of the council is to consider a class of medical devices approval rights reverted to the provincial drug regulatory authorities. "Of course, the need to modify the regulations, may be implemented." The official also said that the current medical devices in China has reached 300 billion yuan in output value, however, the vast majority of this market share to foreign control.

Author: Hangzhou Hua'an Medical & Health Instruments Co., Ltd.
Keyword:wrist blood pressure monitor,automatic digital blood pressure monitor

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