房山燕山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

1、三类医疗器械经营许可证办理方式如下：
（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。
产品检验报告应当符合国务院药品监督管理部门的要求，可以是医疗器械注册申请人、备案人的自检报告，也

pplication materials to the relevant departments; (2) therelevant departments accept the application of the applicant; (3)investigate the actual site and review the products; (4) grant theissuance of the Class III medical device license.2. Legal basis:Article 14 of the Regulations on Supervision and Administration ofMedical Devices For the filing of Class I medical devices and theapplication for the registration of Class II and III medicaldevices, the following materials shall be submitted: (1) productrisk analysis data; (2) product technical requirements; (3) productinspection report; (4) clinical evaluation data; (5) productinstructions and label samples; (6) quality management systemdocuments related to product development and production; (7) othermaterials required to prove the safety and effectiveness of theproduct. The product inspection report shall meet the requirementsof the drug regulatory department under The State Council, and maybe the self-inspection report of the medical device registrationapplicant and the record holder