（1）申请人提交申请资料到相关部门；
（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；
（七）证明产品安全、有效所需的其他资料。
产品检验报告应当符合国务院药品监督管理部门的要求，可以是医疗器械注册申请人、备案人的自检报告，也可以是委托有资质的医疗器械检验机构出具的检验报告。
符合本条例第二十四条规定的免于进行临床评价情形的，可以免于提交临床评价资料。
cation materials to the relevant departments; (2) the relevantdepartments shall accept the application of the applicant; (3)investigate the actual site and review the products; (4) grant theissuance of the third III medical device license.2. Legal basis:Article 14 of the Regulations on Supervision and Administration ofMedical Devices for the filing of Class I medical devices andapplication for the registration of Class II and III medicaldevices shall submit the following materials: (1) product riskanalysis data; (2) technical requirements (3) product; (3) productinspection report; (4) clinical evaluation data; (5) productinstructions and label samples; (6) quality management systemdocuments related to product development and production; (7) othermaterials required to prove the safety and effectiveness of theproduct. The product inspection report shall meet the requirementsof the drug regulatory department under The State Council, and maybe the self-inspection report of the medical device registrationapplicant or record holder, or the inspection report issued by aqualified medical device inspection institution. Those who areexempted from the clinical evalua
