海淀温泉北京医疗器械三类经营许可证提供人员库房专业快捷包下证

（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；
关资质全部带上，还需要带上质量人员的相关资料。（二）具有与经营规模和经营范围相适应的相对独立的经营场所；

（三）具有与经营规模和经营范围相适应的储存条件，包括具有符合医疗器械产品特性要求的储存设施、设备；

（四）应当建立健全产品

se.2. Legal basis: Article 14 of the Regulations on Supervision and Administration of Medical Devices for the filing of Class I medical devices and the application for the registration of Class II and III medical devices, the following data shall be submitted: (1) product risk analysis data; (2) product technical requirements; (3) product inspection report; (4) clinical evaluation data; (5) product instructions and label samples; all qualifications, and relevant data of quality personnel.(2) having a relatively independent business site commensurate with the scale and scope of operation; (3) It shall have storage conditions commensurate with the scale and scope of business, including storage facilities and equipment that meet the requirements of the characteristics of the medical device products; (4) The products shall be established and improved