大兴兴丰大街北京医疗器械三类经营许可证二三类专业快捷包拿证

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；
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；

8、其它相关材料。

ucts; (4) grant the issuance of a class iii medical devicelicense.2. legal basis: article 14 of the regulations onsupervision and administration of medical devices for the filing ofclass i medical devices and the application for the registration ofclass ii and iii medical devices, the following materials shall besubmitted: (1) product risk analysis data; (2) product technicalre; (3) product inspection report; (4) clinicalevaluation data; (5) product instructions; product description andlabel samples; (6) management system documents related toproduct development and production; 5. office space and warehousecertificates that meet the business re of medicaldevices; 6. articles of association, resolutions of shareholders'meeting, etc.; 7, financial personnel sfz and work certificate; 8.other related materials.