朝阳十八里店北京办理医疗器械三类经营许可证没有库房怎么办包下证快捷

器械经营许可证办理方式如下：
（1）申请人提交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
2、法律依据：《医疗器械监督管理条例》第十四条
第一类医疗器械产品备案和申请第二类、第三类医疗器械产品注册，应当提交下列资料：
（一）产品风险分析资料；
（二）产品技术要求；
（三）产品检验报告；
（四）临床评价资料；
（五）产品说明书以及标签样稿；医疗器械二类备案流程： 1、准备执照副本，

（六）具有与经营的医疗器械相适应的质量管理制度。

其次，经营企业要知晓办理三类医疗器械经营许可证需要准备哪些资料。

(1)提交医疗器械经营企业许可证申请表，法定代表人签字或加盖企业公章；

(2)工商行政管理部门出具的企业名称预核准证明文件或《营业执照》复印件和校验原件；

(3)企业质量管理负责人的身份证、学历或者职称证明复印件及个人简历；质量管理人员的身份证、学历或者职称证明

a; (2) product technical requirements; (3) product inspection report; (4) clinical evaluation data; (5) product description and label samples; the filing process of medical devices: 1. Prepare a copy of the license, (6) It shall have a quality management system suitable for the medical devices in operation. Secondly, the operating enterprise should know what information it needs to prepare for the business license of three types of medical equipment. (1) Submit the application form for the license of the medical device operating enterprise, signed by the legal representative or affix the official seal of the enterprise; (2) The copy of the pre-approval certificate of enterprise name or the business License issued by the administrative department for industry and commerce; (3) The copy of the id card, educational background or professional title certificate and personal resume of the quality management manager of the enterprise; the id card, educational background or professional title certificate of the quality management personnel