What are the banned words for medical device promotion in the country?

The first is the management of instructions.\x0d\Article 14 Medical device instructions and labels shall not contain the following content:\x0d\ "Cure", "radical cure", "immediate effect", "completely non-toxic and side effects" and other assertions or guarantees indicating efficacy; \x0d\ (2) Containing "the highest technology", "the most scientific", "the most advanced", " Absolute language and expressions such as "best"; \x0d\ (3) Explaining the cure rate or effectiveness; (4) Comparing the efficacy and safety with other companies' products; \x0d\ (5) Containing promising language such as "insurance company insurance" and "invalid refund"; \x0d\ (6) Using the name or image of any unit or individual to make certifications or recommendations; Statements that make people feel that they are already suffering from a certain disease, or that make people misunderstand that not using the medical device will cause a certain disease or worsen the condition, and other false, exaggerated, and misleading content; \x0d\ (8) Laws and regulations Other prohibited content. \x0d\Then comes the advertising:\x0d\Article 45: Medical device advertisements must be true and legal, and must not contain false, exaggerated, or misleading content. \x0d\ Medical device advertisements shall be reviewed and approved by the food and drug regulatory department of the people's government of the province, autonomous region, or municipality where the medical device manufacturer or imported medical device agent is located, and a medical device advertising approval document shall be obtained. Advertisement publishers who publish medical device advertisements must check the approval documents and their authenticity in advance; they are not allowed to publish medical device advertisements where the approval documents have not been obtained, the authenticity of the approval documents has not been verified, or the advertising content is inconsistent with the approval documents. The food and drug regulatory authorities of the people's governments of provinces, autonomous regions, and municipalities directly under the Central Government shall publish and promptly update the approved medical device advertising catalog and approved advertising content. \x0d\　The food and drug regulatory authorities of the people's governments at or above the provincial level have ordered the suspension of production, sale, import and use of medical devices, and shall not publish advertisements involving the medical devices during the suspension period. \x0d\ The review measures for medical device advertisements shall be formulated by the Food and Drug Administration Department of the State Council in conjunction with the Industry and Commerce Administration Department of the State Council.