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The state make further strengthens of the inspection of medical device industry

           In order to strengthen the quality supervision and management of medical equipment, to ensure the safety of medical equipment products use effectively, the state food and drug administration has asked enterprises to local food and drug supervision and administration authority in accordance with the regulations on the supervision and administration of medical devices and the food and drug supervision bureau general office work on further strengthening medical equipment of proper notice

medical apparatus and instruments

           Relevant dealing with medical device manufacturing enterprise does not conform to the stipulations of the standard products, does not conform to the stipulations of the standard project risk assessment, according to the severity of the medical equipment defect level of recall, is voluntarily recalling and public recall information. The food and drug administration department in the place where the enterprise is located shall supervise the recall of enterprises, and the recalled shall be ordered to be recalled. Provided is not in conformity with the standards of medical equipment products cause harm to human body or there is evidence that may endanger human body health, should be taken to suspend the production, import, management, use of emergency control measures. The relevant provincial food and drug supervision and administration departments should urge enterprises to find out the reasons as soon as possible, formulate rectification measures and fix them in place on time.

With regard to the national demand for medical devices, the relevant units must be taken seriously,Guangzhou Xiangli Instrument Co., LTD. is an expert in packaging materials testing instruments, and has cooperated with many well-known medical devices and equipments in China and abroad. With rich experience in research and development, it provides a guarantee for people's health.

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