三类医疗器械经营许可证如何办理
1、三类医疗器械经营许可证办理方式如下：
（1）申请人提交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
2、法律依据：《医疗器械监督管理条例》第十四条
第一类医疗器械产品备案和申请第二类、第三类医疗器械产品注册，应当提交下列资料：
（一）产品风险分析资料；
（二）产品技术要求；
（三）产品检验报告；
（四）临床评价资料；（五）产品说明书以及标签样稿；(2)工商行政管理部门出具的企业名称预核准证明文件或《营业执照》复印件和校验原件；(3)企业质量管理负责人的身份证、学历或者职称证明复印件及个人简历；质量管理人员身份证、学历或者职称证明复印件；(4)经营场所、仓库的地理位置图、平面图（注明面积）、房屋产权证明或者租赁协议

department; (2) the relevant department accepts the application of the applicant; (3) investigate the actual site and review the product; (4) grant the Class III medical device license.2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices for the filing of Class I medical devices and the application for the registration of Class II and Class III medical devices, The following materials shall be submitted: (1) data on product risk analysis; (2) technical requirements of the product; (3) product inspection report; and (4) clinical evaluation data; (5) Product specification and label samples; (2) The copy of the pre-approval certificate of enterprise name or the business License issued by the administrative department for industry and commerce; (3) A copy of id card, educational background or professional title certificate of the person in charge of quality management of the enterprise and personal resume; Copy of the id card, educational background or professional title certificate of the quality management personnel; (4) Geographic locatio