Medical device agents need to be legally responsible for the safety of the product

1, product safety issues may arise in the production process, may also appear in the operation or use of the link.

2. Medical agents are legally responsible for the safety problems in the business process. Supervision and Administration of Medical Devices Regulations (State Council Decree No. 650), Article 29 provides that engaged in the operation of medical devices, there should be with the scale and scope of business operations and storage conditions, as well as with the operation of medical devices and quality management system and quality management organizations or personnel. Failure to meet the above conditions caused by the safety of medical devices, the agent is fully responsible.

3, for consumers, "Consumer Protection Law" and "Product Quality Law" provide that product quality problems caused by consumer losses, consumers have the right to choose the dealer or manufacturer to claim compensation; dealer compensation, if there is evidence to prove that is the responsibility of the producer, you can recover from the producer; manufacturer compensation, there is evidence to prove that the quality of the problems caused by the dealer, you can After the manufacturer's compensation, if there is evidence to prove that the quality problem is caused by the dealer, you can recover from the dealer.