西城阜成门北京医疗器械三类经营许可证，医疗器械二类备案提供进销存软件人员专业快捷包下证。

7）经营质量管理制度、工作程序等文件目录;

8）办理医疗器械经营许可证企业已安装的计算机信息管理系统基本情况介绍和功能说明,

9）凡申请企业申报材料时,办理人员不是法定代表人或企业负责人本人,企业应当提交《授权委托书》 (原件1份)

10）申报材料真实性的自我保证声明,包括申请材料目录和企业对材料作出如有虚假承担法律责任的承诺(原件1份).

三、现场提交成功后约去现场勘察，现场需提交材料

1）岗位职责

2）工作程序

3）公司制度

4）供应商档案

5）培训记录

6）新法律法规

7）员工档案等

现场核查成功后一周内就可以拿证了。

我公司主要经营代办北京医疗器械公司注册|代办北京三类医疗器械公司注册|代办北京二类医疗器械备案凭证|代办北京食品经营许可证|代办北京医疗器械网络备案|代办北京辐射安全许可等资质专项审批服务

三类医疗器械指的是植入人体，用于支持、维持生命，对人体具有潜在危险，对其安全性、有效性必须严格控制的医疗器械。现行制度规范下，经营三类医疗器械的经营主体需要按程序办理三类医疗器械经营许可证。

dling person is not the legal representative or the person incharge of the enterprise himself, and the enterprise shall submitthe power of attorney (1 original) 10) self-guarantee statement ofthe authenticity of the application materials, including thecatalogue of the application materials and the enterprise'scommitment to bear the legal liability if there is any falsematerial (1 original). 3. after successful site submission, go tothe site for investigation, and submit materials on site 1) jobresponsibilities 2) working procedures 3) company system 4)supplier files 5) training records 6) new laws and regulations 7)employee files, etc you can get the certificate within a week afterthe successful on-site verification. my company main business agentbeijing medical e company registration | agent beijingthree types of medical e company registration | agentbeijing class medical e for the record certificate |beijing food business license | beijing medical e networkfor the record | beijing radiation safety license