朝阳南磨房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

（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；
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、与经营产品相关专门的在岗人

al device license.2. Legal basis: Article 14 of the Regulations on Supervision and Administration of Medical Devices for filing of Class I medical devices and application for registration of Class II and Class III medical devices, the following materials shall be submitted: (1) product risk analysis data; (2) product technical requirements; (2) product technical requirements; (3) product inspection report; (4) clinical evaluation data; (5) product instructions; and label samples; filing process of medical devices: 1. Preparation of license copies; 3. Official acceptance of data; 4. Administrative review of relevant departments; 5. On-site evaluation; 6. Administrative decisions of relevant departments; 7. Certificate preparation and issuance. The conditions for applying for the business license of Class III medical devices are as follows: 1. Having business premises and warehouses matching the business scope, and having specific requirements for their specific area; 2. Having nationally recognized professional employees related to the business products