（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；
6、公司章程、股东会决议等；
7、财务人员身份证和上岗证；1、经营企业提交的《医疗器械经营企业许可证申请表》应有法定

 departments shall accept the application; (3) investigate the actual site and review the products; (4) grant the issuance of the third III medical device license.2. Legal basis: Article 14 of the Regulations on Supervision and Administration of Medical Devices for medical devices and application for the registration of Class II and III medical devices, the following data shall be submitted: (1) product risk analysis data; (2) technical requirements of the product; (3) product inspection report; (4) clinical evaluation data; (5) the product description; product description and label samples; the resolution of shareholders; 7. ID card and working certificate of financial personnel; 1. the Application form for Medical Device Operating Enterprise License submitted by the operating enterprise shall be statutory