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软件安全可靠

办理三种医疗器械经营许可证准备必要的处理资料:
(1)《医疗器械经营许可证申请表》； 
(2)资格证书； 
(3)营业执照或企业名称预先核准证书复印件； 
(4)质量管理人员证书； 
(5)售后服务人员资格证书。 

1.需要办理许可证的企业经营者携带上述材料到当地市级人民政府食品监督管理部门申请营业执照； 
2.管理部门受理资料，30个工作日内审核，必要时组织审核； 
3.符合条件的，管理部门发行医疗器械经验许可证，不符合条件的，管理部门不予许可，书面说明理由。 

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