朝阳红庙北京医疗器械三类经营许可证二三类专业快捷包拿证

）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；

（七）证明产品安全、有效所需的其他资料。

4、2个或以上医学专业或相关专业人员证书、sfz明与简历；

5、符合医疗器械经营要求的办公场地及仓库证明；

6、公司章程、股东会决议等；

7、财务人员sfz和上岗证；

 investigate the actual site and audit the products; (4)Grant the issuance of a class III medical device license. 2. Legalbasis: Article 14 of the Regulations on the Supervision andAdministration of Medical Devices As for the registration of ClassII and III medical devices, the following materials shall besubmitted: (1) Product risk analysis data; (2) Technicalrequirements for the products; (3) Product inspection report; (4)Clinical evaluation data; (5) Product specification and labelsamples; (6) quality management system documents related to productdevelopment and production; (7) other materials required to provethe safety and effectiveness of the product. 4,2 or more medicalprofessional or related professional certificates, sfz Ming andresume; 5. Office space and warehouse certificate that meet thebusiness requirements of medical equipment; 6. Articles ofassociation, resolutions of shareholders' meeting, etc.; 7,financial personnel sfz and work certificate;