朝阳柳芳北京医疗器械三类经营许可证可全包代办专业快捷包下证

（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；
6.有关部门的行政决定；
7.制证、发证。
办理三类医疗器械经营许可证的条件如下：
1、具有

partments shall accept the application of the applicant'sapplication; (3) investigate the actual site and review theproducts; (4) grant the issuance of the third iii medical devicelicense.2. legal basis: article 14 of the regulations onsupervision and administration of medical devices for filing ofclass i medical devices and application for registration of classii and class iii medical devices, the following materials shall besubmitted: (1) product risk analysis data; (2) product technicalre; (3) product inspection report; (4) clinicalevaluation data; 6. administrative decisions of relevantdepartments; 7. certificate preparation and certification. theconditions for applying for the business license of class ii