朝阳高碑店北京办理医疗器械三类经营许可证没有库房怎么办包过包下证快捷

器械经营许可证如何办理
1、三类医疗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，
3.数据正式受理；
4.有关部门的行政审查；
5.现场评价；

of device 1. Class III medical device business license is handled as follows: (1) the applicant submits the application materials to the relevant departments; (2) the relevant departments accept the application of the applicant; (3) investigate the actual site and review the product; (4) grant the issuance of Class III medical device license.2. Legal basis: Article 14 of the Regulations on Supervision and Administration of Medical Devices and the registration of Class II and III medical devices shall submit the following materials: (1) product risk analysis data; (2) the product technical re; (ii) product inspection report; (4) clinical evaluation data; (4) clinical evaluation data; (5) product specification and label samples; filing process of medical devices: 1. copy of license; 3. Official acceptance of data; 4. administrative review of relevant departments; 5. On-