海淀西三旗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

（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；4、工商行政管理部门出具的《企业名称预先核准通知书》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10、申请材料应完整、清晰、签字，并逐份加盖公章，所有申请表格电脑打字填写，使用A4纸打印，复印使用A4纸，按照申请材料目录顺序装订成册。申请人隐瞒有关情况或者提供虚假材

suance of a class 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)data on product risk analysis; (2) technical requirements of theproduct; (3) product inspection report; and (4) clinical evaluationdata; 4. Notice of Pre-approval of Enterprise Name issued by theadministrative department for industry and commerce The applicant(unit) shall indicate on the copy "this copy corresponds to theoriginal" or the written description, date, With the official sealof the unit; The application materials shall be complete, clear andsigned, And affix the official seal to each copy, All applicationforms are filled out by computer-based typing, Printed using A4paper, Copying using A4 paper, Bind a book in the order ofappli