北京平谷区时间医疗器械三类经营许可证，医疗器械二类备案办理提供办公地址优质服务

In Beijing, the application for a Class III medical device license requires the following steps: 1. Prepare application materials: In accordance with the Regulations on Supervision and Administration of Medical Devices and relevant provisions, prepare relevant application materials, including the business license of enterprise legal person, product quality management system documents, product registration certificate, product technical documents, product operation manual, production license, etc. 2. Self-inspection preparation: conduct self-inspection of the internal

首先，我们必须清楚办理医疗器械三类经营许可证需要哪些资料；

1、公司执照正副本

2、公章

3、办公和库房房本复印件

4、人员（主要是质量管理人和主管检验师）

其中 质量管理人：要求大专毕业满三年

主管检验师：要求本科毕业满三年 检验学相关专业