（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；1、经营企业提交的《医疗器械经营企业许可证申请表》应有法定代表人签字或加盖企业公章；2、《医疗器械经营企业许可证申请表》所填写项目应填写齐全、准确；3、法定代表人的身份证明、学历职称证明、任命文件应有效；4、工商行政管理部门出具的《企业名称预先核准通知书》或《工商营业执照》的复印件应与原件相同，复印件确认留存，原件退回；5、房产证明、房屋租赁证明（出租方要提供产权证明）应有效；6、企业负责人、质量管理人的简历

accept the application of the applicant's application; (3) investigate the actual site and review the products; (4) grant the issuance of the class III medical device license.2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices for the filing of Class I medical devices and the application for the registration of Class II and Class III medical devices, The following materials shall be submitted: (1) product risk analysis data; (2) technical requirements of the product; (3) product inspection report; (4) clinical evaluation data; (5) product specification and label samples; (6) quality management system documents related to product development and production; 1. The Application Form for Medical Device Business Enterprise License submitted by the operating enterprise shall be signed by the legal representative or affixed with the official seal of the enterprise; 2. The items filled in the Application Form for License of Medical Device Business Enterprises should be complete and accurate; 3. The identity certificate, academic title certificate and appointment documents of the legal representative shall be valid; 4, the copy of the "enterprise name pre-approval notice" or "industrial and commercial business license" issued by the industrial and commercial administrative department should be the same as the original, Copy of confirmation