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；
（六）与产品研制、生产有关的质量管理体系文件；
（七）证明产品安全、有效所需的其他资料。
3、具有与经营产品相关的拥有中专以上学历的技术人员；
5、三类医疗器械经营许可证，需要直接去市级人民政府食品药品监督管理部门办理，在接受资料后
How to handle the business license of Class III medical device1. The business license of Class III medical devices is as follows:(1) the applicant submits the application materials to the relevantdepartments; (2) the relevant department accepts the application ofthe applicant; (3) investigate the actual site and review theproduct; (4) grant the issuance of the Class III medical devicelicense.2. Legal basis: Article 14 of the Regulations onSupervision and Administration of Medical Devices For the filing ofClass I medical devices and the application for the registration ofClass II and III medical devices, the following materials shall besubmitted: (1) product risk analysis data; (2) product technicalrequirements; (3) product inspection report; (4) clinicalevaluation data; (5) product instructions and label samples; (6)quality management system documents related to product developmentand production; (7) other materials required to prove the safetyand effectiveness of the product. 3. Technical personnel withtechnical secondary school education or above related to thebusiness products; 5. Business license of Class III medical devicesneeds to go directly to the food and drug supervision andadministration department of the municipal people's governmentafter receiving the materials
