（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；申请人隐瞒有关情况或者提供虚假材料的，省、自治区、
3.数据正式受理；
4.有关部
ant's application; (3) investigate the actual site and reviewthe product; (4) grant the issuance of a class III medical devicelicense.2. Legal basis: Article 14 of the Regulations on theSupervision and Administration of Medical Devices for the filing ofClass I medical devices and the application for the registration ofClass II and Class III medical devices, the following materialsshall be submitted: (1) product risk analysis data; (2) producttechnical requirements; (2) product technical requirements; (3)product inspection report; (4) clinical evaluation data; if theapplicant conceals relevant information or provides falsematerials, province, autonomous region and 3. Data formalacceptance; 4. Relevant departments
