西城南礼士路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

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；
（六）与产品研制、生产有关的质量管理体系文件；1、经营企业提交的《医疗
7.制证、发证。
办理三类医疗器械经营许可证的条件如下：
1、具有与经营范围相匹配的经营场所和仓库，并对其具体面积有具体要求；
2、具有国家认可的、与经营产品相关专门的在岗人员；
3、具有与经营产

istration of Class II and Class III medical devices, thefollowing materials shall be submitted: (1) product risk analysisdata; (2) product technical requirements; (3) product inspectionreport; (4); (4) clinical evaluation data; (5) productspecification and label samples; (6) quality management systemdocuments related to product development and production; 1. Medical7. Certificate preparation and certification submitted by theoperating enterprise. The conditions for applying for the businesslicense of Class III medical devices are as follows: 1. Havingbusiness sites and warehouses matching the business scope, andspecific requirements for their specific area; 2. State-recognizedspecialized personnel related to business products; 3. Having andbusiness products