门头沟东辛房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

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；
二、三类医疗器械许可证注册需要什么材料：1、经营企业提交的《医疗器械经营企业许可证申请表》应有法定代表人签字或加盖企业公章；2、《医疗器械经营企业许可证申请表》所填写项目应填写齐全、准确；3、法定代表人的身份证明、学历职称证明、任命文件应有效；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，5、房产证明、房屋租赁证明（出租方

cle 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 requirements for product;(3) product inspection report; (4) clinical evaluation data; (5)product description and label samples; what materials are requiredfor registration of Class III medical device license: 1.Application Form for License of Medical Device Operating Enterprisesubmitted by the operating enterprise shall be signed by the legalrepresentative or affixed with the official seal of the enterprise;2. The items filled in the Application Form for License of MedicalDevice Business Enterprises should be complete and accurate; 3. Theidentity certificate, academic title certificate and appointmentdocuments of the legal representative shall be valid; 4, the copyof the "enterprise name and 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, 5, real estatecertificate, house lease certificate (the lessor