朝阳姚家园北京医疗器械三类经营许可证，医疗器械二类备案提供人员库房专业快捷包下证。

二、第三类医疗器械经营许可证办理流程：

1、经营企业经办人携带上述资料前往监督管理部门申请经营许可；

2、工作人员受理资料，并于30个工作日内进行审查，必要时组织核查；

3、对符合规定条件的，准予许可并发给医疗器械经营许可证；对不符合规定条件的，不予许可并书面说明理由。

三、第三类医疗器械经营许可证办理所需材料:

1、企业名称与经营范围，注册资本及股东出资比例，股东等sfz明；

2、医疗器械产品注册证书、供应商营业执照、许可证及授权书；

3、质量管理文件等；

4、2个或以上医学专业或相关专业人员证书、sfz明与简历；

5、符合医疗器械经营要求的办公场地及仓库证明；

6、公司章程、股东会决议等；

7、财务人员sfz和上岗证；

8、其它相关材料。

l Devices: 1. The operator of the operating enterprise shallbring the above information to the supervision and administrationdepartment to apply for the business license; 2. The staff shallaccept the materials, and review them within 30 working days, andorganize the verification if necessary; 3. Grant license andmedical device operation license for those who meet the prescribedconditions, and give reasons in writing. 3. Materials required forhandling the business license of Class III medical devices: 1, theenterprise name and business scope, the registered capital and theproportion of shareholder contribution, shareholders and other sfzMing; 2. Medical device product registration certificate, supplierbusiness license, license and authorization letter; 3. Qualitymanagement documents, etc.; 4,2 or more medical professional orrelated professional certificates,