朝阳三元桥北京医疗器械三类经营许可证二三类专业快捷包拿证

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。

4、2个或以上医学专业或相关专业人员证书、身份证明与简历；

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、财务人员身份

s III medical devices is handled as follows: (1) The applicantshall submit the application materials to the relevant departments;(2) Relevant departments shall accept the application of theapplicant; (3) Investigate the actual site and audit the products;(4) Grant the issuance of a class III medical device license. 2.Legal basis: Article 14 of the Regulations on the Supervision andAdministration of Medical Devices As for the registration of ClassII and III, the following materials shall be submitted: (1) Productrisk analysis data; (2) Technical requirements for the products;(3) Product inspection report; (4) Clinical evaluation data; (5)Product specification and label samples; (6) quality managementsystem documents related to product development and production; (7)other materials required to prove the safety and effectiveness ofthe product. 4,2 or more certificates, identification certificateand resume of medical professionals or related professionals; 5.Office space and warehouse certificate that meet the businessrequirements of medical equipment; 6. Articles of association,resolutions of shareholders' meeting, etc.; 7. Identity offinancial personnel