（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；
（六）与产品研制、生产有关的质量管理体系文件；
6、公司章程、股东会决议等；
7、财务人员身份证和上岗证；
8、其它相关材料。医疗器械二类备案流程：1、准备执照副本，公章，实际经营地址房本复印件，租房合同2、需
the application of the applicant; (3) investigate theactual site and review the product; (4) grant the issuance of theclass III medical device license.2. Legal basis: Article 14 of theRegulations on Supervision and Administration of Medical Devicesfor the filing of Class I medical devices and application for theregistration of Class II and Class III medical devices, thefollowing data shall be submitted: (1) product risk analysis data;(2) product technical requirements; (3) product inspection report;(4) clinical evaluation data; (5) product description and labelsamples; (6) quality management system documents related to productdevelopment and production; 6. Articles of association, resolutionof shareholders meeting, etc.; 7. ID card of financial personneland working certificate; 8. Other related materials. Medicalequipment class II filing process: 1, prepare the license copy,official seal, a copy of the actual business address r
