）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。

7.制证、发证。

办理三类医疗器械经营许可证的条件如下：

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

plicant; (3) Investigate the actual site and audit the products; (4) Grant the issuance of a class III medical device license. 2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices As for the registration of Class II and III medical devices, the following materials shall be submitted: (1) Product risk analysis data; (2) Technical requirements for the products; (3) Product inspection report; (4) Clinical evaluation data; (5) Product specification and label samples; (6) quality management system documents related to product development and production; (7) other materials required to prove the safety and effectiveness of the product. 7. Making certificates and issuing certificates. The conditions for the third III medical device business license are as follows: 1. Have a business site and warehouse matching the business scope, and have specific requirements for its specific area; 2. State-recognized professional personnel related to business products; 3. Technical personnel with technical secondary school education or above related to business products; 4, with the operation of medical devices