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；办理三类医疗器械经营许可证的办理流程：
1、具有与经营范围相匹配的经营场所和仓库，并对其具体面积有具体要求；
2、具有国家认可的、与经营产品相关专门的在岗人员；
3、具有与经营产品相关的拥有中专以上学历的技术人员；
4、拥有与经营的医疗器械相适应的质量管理制度很多药品或者医疗器械的经销商，如果没有三类医疗器械经营许可证，很多产品就不能卖，比如说体外诊断试剂就属于三类医疗器械，只有有相关证书，才能
o handle the business license of third III medical devices is asfollows: (1) the applicant submits the application materials to therelevant departments; (2) the relevant departments accept theapplication of the applicant's application; (3) investigate theactual site and review the products; (4) grant the issuance of thethird III medical device license.2. Legal basis: Article 14 of theRegulations on the Supervision and Administration of MedicalDevices for the filing of Class I medical devices and theapplication for the registration of Class II and Class III medicaldevices, The following materials shall be submitted: (1) productrisk analysis data; (2) technical requirements of the product; (3)product inspection report; (4) clinical evaluation data; (5)product specification and label samples; 1. Having the businesspremises and warehouse matching with the business scope, And havespecific requirements for the specific area; 2, with the staterecognized, related to the management of products; 3, with atechnical secondary school education; 4, with the management ofmedical devices with the quality management system of the dealersof many drugs or medical devices, Without the operating license, Alot of products can't be sold, In vitro diagnostic reagents, forexample, fal
