顺义杨镇裕龙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

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；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，则须有法定代表人本人签字或签章。9、凡申请材料需提交复印件的，申请人（单位）须在复印件上注明“此复印件与原件相符”字样或者文字说明，注明日期，加盖单位公章；个人申请的须签字或签章。10、申请材料应完整

se of class medical devices are as follows: (1) the applicantsubmits the application materials to the relevant departments; (2)the relevant departments accept the application of the applicant;(3) investigate the actual site and review the products; (4) grantthe issuance of the third class medical device license.2. Legalbasis: Article 14 of the Regulations on the Supervision andAdministration of Medical Devices for filing and registration ofClass II and III medical devices, the following data shall besubmitted: (1) product risk analysis data; (2) product technicalrequirements; (3) product inspection report; (4) clinicalevaluation data; (5) product description and labels; productdescription and label samples; 8. Self-assurance statement of theauthenticity of the application materials shall be signed by thelegal representative and affixed with the official seal of theenterprise, if no official seal, with the signature or signature ofthe legal representative.9. If the application materials need to besubmitted, the applicant (unit) shall indicate the words "thecopy