Over the past two years,we received a number of public complaints or opinions on medical devices,from a reflection of the situation,the current medical device market,there are two more focused on the problem,

　 (1) reflected in some areas or parks set up medical devices experience of medical equipment sales, according to the provisions of the relevant state laws and regulations, the majority of medical equipment management to obtain a permit for the medical device business before sales, in addition to a class of products and a small portion of the second class medical device, currently in the city sales of for the old friends of instrument and equipment basically is must obtain a permit for the medical device business to sell products. Some enterprises set up some experience points free treatment and product promotion, such behavior even when they had no sales in accordance with requirements of the State Food and Drug Administration in 2006 No. 203 the to obtain a permit for the medical device business, therefore, members of the public in the face of market experience is should pay attention to several points: ask the enterprise to provide the venue medical equipment business license, and verify the medical devices business license whether by the Guangxi food and drug supervision and administration department approval. Two is to see whether the license is valid within the period or whether the scope of business covered by the sales of medical equipment. Three is to please people remember where in the non fixed place, such as parks, and medical equipment sales or free experience activity are unlicensed acts, people don't buy and in a timely manner to the US Food anddrug supervision and management departments to report.

　　 (2) there are complaints from the public some medical equipment after use did not reach the corresponding treatment effect, not as promotional products effective, this kind of product is mainly reflected in the elderly some rehabilitation instrument or equipment. This kind of products are mainly concentrated in of hypertension, cervical vertebra and lumbar vertebra therapy rehabilitation instrument or equipment, in accordance with the relevant provisions of the state, medical apparatus and instruments of all listed for sale must obtain medical device registration certificate, also product labels, brochures, packaging and labeling must and the certificate of registration of limited content consistent. Now reflected to the medical devices market is itself the product there is no after product registration or tying products no certificate of registration, such as some instrument with a charge, instrument although to obtain a registration certificate, but charge without management approval, this situation. There is the approval of the scope of treatment is only a range of products, but it is a propaganda. Therefore, the people in the purchase of medical equipment, first of all, as we have said before to obtain the "medical equipment business license" view, but also pay attention to the following points:

1,to see whether the product packaging has medical device registration certificate number.
2,obtain medical device product registration certificate and registration form, see if the registration certificate is valid.
3,see if the product is consistent with the product performance structure in the registration form.
4,see the specification or product publicity materials and the registration form of the product is consistent with the scope of application.
5,we can clearly tell you that any medical device can not be applied to the range of treatment can be applied to a variety of diseases.