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省、自治区、直辖市药品监督管理部门是医疗器械广告审查机关,负责本行政区域内医疗器械广告审查工作。县级以上工商行政管理部门是医疗器械广告监督管理机关。国家食品药品监督管理局对医疗器械广告审查机关的医疗器械广告审查工作进行指导和监督,对医疗器械广告审查机关违反本办法的行为,依法予以处理。医疗器械广告批准文号的申请人必须是具有合法资格的医疗器械生产企业或者医疗器械经营企业。医疗
The drug regulatory department of a province, autonomous region or municipality directly under the Central Government shall be the examination authority for the advertisement of medical devices and shall be responsible for the examination of advertisements for medical devices in its own administrative area. The administrative department for industry and commerce above the county level is the supervisory authority for the supervision of medical equipment. The State Food and Drug Administration shall supervise and supervise the examination of advertisements for medical devices of medical device advertisement examination organs, and handle the violation of these Measures by medical institution advertisement examination organs in accordance with the law. Applicants for medical device advertisement approval number must be legally qualified medical device manufacturers or medical device operators. Medical