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；办理三类医疗器械经营许可证的办理流程：
3、具有与经营产品相关的拥有中专以上学历的技术人员；4、拥有与经营的医疗器械相适应的
ccept the application of the applicant; (3) investigate theactual site and review the products; (4) grant the issuance of theclass III medical device license.2. Legal basis: Article 14 of theRegulations on the Supervision and Administration of MedicalDevices For the filing of Class I medical devices and for theregistration of Class II and Class III medical devices, thefollowing materials shall be submitted: (1) the product riskanalysis data; (2) the product technical re; productinspection report; (3) the procedures for handling the businesslicense of Class III medical devices: 3; the technical personnelwith a technical secondary school degree or above; 4 and theoperating medical devices
