一、办理医疗器械三类经营许可证需要哪些材料？

1.法定代表人、企业负责人、质量负责人、售后服务人员等人员的身份证明、学历或者职称证明原件照片或复印件

2.组织机构与部门设置说明

3.经营范围、经营方式说明

4.经营场所、库房地址的地理位置图、平面图、房屋产权证明文件或者租赁协议（附房屋产权证明文件）复印件

5.经营设备、设备目录

6.经营质量管理制度、工作程序等文件目录

7.计算机信息管理系统基本情况介绍和功能说明

8.经办人授权证明

9.材料真实性声明

二、办理医疗器械三类经营许可证的流程是什么？

1. 提交申请

2. 窗口受理

3. 审核材料

4. 老师下户现场检查

5. 审批通过

6. 领取医疗器械三许可证

sentative, enterprise person in charge, person in charge of quality, after-sales service personnel, etc 2. Description of organizational structure and department setting up 3. Description of business scope and business mode 4. Copy of the geographical location map, floor plan, house property right certificate document or lease agreement (attached with the house property right certificate document) of the business site and warehouse address 5. Operating equipment and equipment catalogue 6. Catalogue of operation quality management system, working procedures and other documents 7. Basic information introduction and function description of the computer information management system 8. Authorization certificate of the agent 9. Declaration of authenticity of materials 2. What is the process of handling the third business license of medica