东城东直门北京医疗器械三类经营许可证二三类专业快捷包拿证

（1）申请人提交申请资料到相关部门；
（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pplicantshall submit the application materials to the relevant departments;(2) the relevant departments shall accept the application of theapplicant; (3) investigate the actual site and review the products;(4) grant the issuance of the third III medical device license.2.Legal basis: Article 14 of the Regulations on Supervision andAdministration of Medical Devices for the filing of Class I medicaldevices and the application for the registration of Class II andClass III medical devices, the following materials shall besubmitted: (1) product risk analysis data; (2) product technicalrequirements; (ii) product technical requirements; (3) productinspection report; (4) clinical evaluation data; (5) productdescription and label samples; 7. The enterprise shall establishquality management files or forms of medical devices according toits actual conditions. 8. The self-guarantee statement of theauthenticity of the application materials shall be signed by thelegal representative and affixed with the official seal of theenterprise.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；7、企业应根据自身实际建立医疗器械质量管理档案或表格。

8、申请材料真实性的自我保证声明应由法定代表人签字并加盖企业公章，如无公章，则须有法定代表