（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；
二、三类医疗器械许可证注册需要什么材料
7、财务人员身份证和上岗证；
8、其它相关材料。对申请材料的要求：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

ce license.2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices for Class 1, the following materials shall be submitted: (1) product risk analysis data; (2) the product technical requirements; (3) product inspection report; (3) clinical evaluation data; (4) clinical evaluation data; (5) the product specification and label sample; 7. ID card and work certificate of financial personnel; 8, other related materials. Requirements for application materials: 1. The Application Form for Medical Device Enterprise License submitted by the operating enterprise shall be signed by the legal representative or stamped with the official seal of the enterprise; 2, the items filled in the Application Form shall be complete and accurate; 3, the identification certificate of the legal representative, academic title certificate and appointment document shall be valid; 4