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；
（六）与产品研制、生产有关的质量管理体系文件；
理或者不予核发《医疗器械经营企业许可证》，并给予警告。申请人在1年内不得申请《医疗器械经营企业许可证》。
申请人以欺骗、贿赂等不正当手
How to handle the equipment business license 1. The businesslicense of Class III medical devices is handled as follows: (1) Theapplicant shall submit the application materials to the relevantdepartments; (2) Relevant departments shall accept the applicationof the applicant; (3) Investigate the actual site and audit theproducts; (4) Grant the issuance of a class III medical devicelicense. 2. Legal basis: Article 14 of the Regulations on theSupervision and Administration of Medical Devices As for theregistration of Class II and III medical devices, the followingmaterials shall be submitted: (1) Product risk analysis data; (2)Technical requirements for the products; (3) Product inspectionreport; (4) Clinical evaluation data; (5) Product specification andlabel samples; (6) quality management system documents related toproduct development and production; The License of Medical DeviceOperating Enterprise shall not be issued and given a warning. Theapplicant shall not apply for the Medical Device BusinessEnterprise License again within one year. The applicant is the, byby cheating, bribery
