朝阳甜水园北京医疗器械三类经营许可证，医疗器械二类备案提供人员库房专业快捷包下证

（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；
（五）产品说明书以及标签样稿；4、工商行政管理部门出具的《企业名称预先核准通知书》或《工商营业执照》的复印件应与原件相同，复印件确认留存，原件退回；5、房产证明、房屋租赁证明（出租方要提供产权证明）应有效；6、企业负责人、质量管理人的简历、学历证明或职称证明应有效；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、

partments shall accept the application of the applicant; (3)investigate the actual site and review the products; (4) grant theissuance of the third iii medical device license.2. legal basis:article 14 of the regulations on the supervision and administrationof medical devices for the filing of class i medical devices andthe application for the registration of class ii and class iiimedical devices, the following materials shall be submitted: (1)product risk analysis data; (2) technical re of theproduct; (3) product inspection report; (4) clinical evaluationdata; (5) product specification and label samples; 4, the copy ofthe "enterprise name pre-approval notice" or "industrial andcommercial business license" issued by the industrial andcommercial administrative department should be the same as theoriginal, copy of confirmation and retention, the original copy isreturned; 5. the property certificate and house lease certificate(the lessor shall provide the property right certificate)shall