How Do I Become a Medical Device Representative?
Medical devices refer to instruments, equipment, appliances, in vitro diagnostic reagents and calibrators, materials, and other similar or related items used directly or indirectly in the human body, including computer software required.
medical instruments
- Medical devices refer to instruments, equipment,
- The medical device industry involves multiple industries such as medicine, machinery, electronics, and plastics. It is a multi-disciplinary, knowledge-intensive, and capital-intensive high-tech industry. And high-tech
- The state implements classified management of medical devices according to the degree of risk.
- (Promulgated by Order No. 276 of the State Council of the People's Republic of China on January 4, 2000. Revised and adopted at the 39th Executive Meeting of the State Council on February 12, 2014. ] [2]
- On March 17, 2014, the State Food and Drug Administration held a press conference. From now on, the State Food and Drug Administration will launch a nationwide five-month medical device special action focused on medical treatment. Five acts of false registration and declaration of devices, illegal production, illegal operation, expanded publicity, and use of unlicensed products. The special action takes key products, key enterprises, and key case clues as breakthrough points, and through the combination of unannounced investigations, centralized investigations, and surprise inspections, it will severely crack down on illegal activities and further regulate market order.
- The State Food and Drug Administration requires that in the special actions, any violations of laws and regulations shall be dealt with promptly, rigorously, and severely, and punished in accordance with the upper limit stipulated by laws and regulations; if the circumstances are serious, the licenses of manufacturers and products will be revoked Documents; if a crime is suspected, they will all be transferred to public security organs for criminal responsibility according to law; for products with hidden safety hazards, all sales and use will be stopped, and companies will be ordered to recall and supervise destruction.
- Axillary anti-slip design (12 photos)