丰台长辛店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

（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；
5.现场评价；
6.有关部门的行政决定；
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

accept the application of the applicant's application; (3) investigate the actual site and review the products; (4) grant the issuance of a class III medical device license.2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices, the applicant shall submit the following materials: (1) product risk analysis data; (2) product technical requirements; (3) product inspection report; (3) product evaluation report; (4) clinical evaluation data; product specification and label samples; 5. On-site evaluation; 6. administrative decisions of relevant departments; 7. Certificate making and issuance. The conditions for applying for the business license of Class III medical devices are as follows: 1. Having a business site and warehouse matching the business scope, and having specific requirements for its specific area; 2. Having the