Legal consequences of the person responsible for medical device quality

Legal analysis: If there is a quality problem with drugs or medical devices, if the medical institution fails to strictly implement the incoming inspection system, fails to verify the product conformity mark or fails to check the quality inspection report of medical devices, and the defective medical products are used on patients, causing damage consequences, the medical party shall bear the liability for damages at this time.

Legal basis: Article 43 of People's Republic of China (PRC) Product Quality Law. If a product is defective and causes personal injury or property loss to others, the victim may claim compensation from the producer or seller of the product.