Chinese medical equipment can be personal trading?

Chinese medical devices can not be bought and sold by individuals, engaged in medical equipment business activities, there should be with the scale and scope of operation of the business premises and storage conditions, as well as with the operation of the medical device quality management system and quality management institutions or personnel.

According to the "supervision and management of medical devices regulations" Article 29 engaged in medical device business activities, there should be with the scale and scope of business and storage conditions, as well as with the operation of medical devices and quality management system and quality management organizations or personnel.

Article 30 is engaged in the second class of medical devices, by the business enterprise to the municipal people's government where the municipal food and drug supervision and management department for the record and submit it to comply with the conditions of Article 29 of these Regulations.

Order 31 engaged in the third class of medical equipment business, the business enterprise shall be located in the municipal people's government food and drug supervision and management department to apply for a license and submit it to meet the conditions of the provisions of Article 29 of these Regulations.

The food and drug supervision and management department accepting applications for business license shall be accepted within 30 working days from the date of review, if necessary, the organization verification. To meet the prescribed conditions, permit and issue a medical device license; do not meet the prescribed conditions, not permit and explain the reasons in writing. Medical device license is valid for 5 years. The expiration of the validity of the need for continuation, in accordance with the provisions of the relevant administrative licensing law for continuation procedures.

Expanded information:

Medical equipment supervision and management regulations. p>"Supervision and Administration of Medical Devices Regulations" Article 47 Medical device manufacturers and operators, the use of units should be produced and operated or the use of medical devices to carry out adverse event monitoring; found that the medical device adverse events or suspected adverse events, shall be in accordance with the provisions of the State Council food and drug supervision and management department, to the medical device adverse event monitoring technical institutions report.

Any unit or individual found that the medical device adverse events or suspected adverse events, the right to food and drug supervision and management departments or medical device adverse event monitoring technical institutions to report.

Baidu Encyclopedia - Regulations for the Supervision and Administration of Medical Devices