依据《医疗器械监督管理条例》，第三类医疗器械是具备较高危，必须采用非常对策严控管理方法以确保其安全性、合理的医疗机械。例如普遍的注射器、注射针、静脉留置针、心脏支架、麻醉机、CT、磁共振等。
申请办理三类医疗器械许可证必须提前准备的原材料
（1）企业营业执照；
（2）公司章；
（3）房屋产权证明、租赁协议；
（4）法定代表人、主要负责人、品质管理员的身份、毕业证等证明材料；
（5）经营地平面设计图，仓库平面设计图。
申请办理三类医疗器械许可证的规定
（1）场所和仓库总面积规定：与经营地企业规模相一致。
（2）品质管理员规定：专科本科以上学历或是初级左右专业职称，另外理应具备3年左右医疗器械经营品质管理方面亲身经历。
（3）品质管理员技术专业规定：医疗机械有关技术专业，例如：医药学、药理学、生物技术、护理专业等。
nery with high risk, which must adopt extraordinary countermeasures and strict control management methods to ensure its safety and rationality. For example, common syringes, injection needles, intravenous indwelling needles, cardiac stents, anesthesia, machine, CT, magnetic resonance, etc. Raw materials that must be prepared in advance when applying for the Class III medical device license (1) Enterprise business license; (2) Company seal; (3) Property right certificate and lease agreement; (4) Identity of legal representative, principal person in charge, quality manager, graduation certificate and other certification materials; (5) Operation floor plan design drawing, warehouse floor plan design drawing. Provisions on applying for a class III medical device license (1) The total area of the place and warehouse provisions: consistent with the scale of the enterprise in the operating place. (2) Quality administrator regulations: college degree or above or junior professional title, in addition, should have about 3 years of personal experience in m
