开办第三类医疗器械经营企业，应当经省、自治区、直辖市人民政府药品监督管理部门审查批准，并发给《医疗器械经营许可证》。
依据《医疗器械经营监督管理办法》，开设三类医疗器械运营公司，食品类药品监督管理局单位将会对经营地开展当场审查。对不符合要求标准的，明确提出整顿规定或未予批准。根据《药品医疗器械飞行检查办法》，食品类药品监督管理局单位将会对医疗机械销货方式合理合法、工作人员在职人员在职、拿货检查、运送储存等层面开展不事先告之的监督管理。三类医疗器械的界定
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，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。
efinition of Class III medical devices According to theRegulations on the Supervision and Administration of MedicalDevices, the third type of medical devices is a medical machinerywith high risk, which must adopt extraordinary countermeasures andstrict control management methods to ensure its safety andrationality. For example, common syringes, injection needles,intravenous indwelling needles, cardiac stents, anesthesia,machine, CT, magnetic resonance, etc. Raw materials that must beprepared in advance when applying for the Class III medical devicelicense (1) Enterprise business license; (2) Company seal; (3)Property right certificate and lease agreement; (4) Identity oflegal representative, principal person in charge, quality manager,graduation certificate and other certification materials; (5)Business floor floor design drawing, warehouse floor designdrawing. Provisions on applying for a class III medical devicelicense (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 orjunior professional title, in addition, should have about 3 yearsof personal experience in medical device business qualitymanagement. (3) Technical professional regulations of qualityadministrators: related technical majors of medical machinery, suchas medicine, pharmac
