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。
9、凡申请材料需提交复印件的，申请人（单位）须在复印件上注明“此复印件与原件相符”字样或者文字说明，注明日期，加盖单位公章；个人申请的须签字或签章。
10、申请材料应完整、清晰、签字，并逐份加盖公章，所有申请表格电脑打字填写，使用A4纸打印，复印使用A4纸
3) Investigate the actual site and audit the products; (4) Grantthe issuance of a class III medical device license. 2. Legal basis:Article 14 of the Regulations on the Supervision and Administrationof Medical Devices As for the registration of Class II and IIImedical devices, the following materials shall be submitted: (1)Product risk analysis data; (2) Technical requirements for theproducts; (3) Product inspection report; (4) Clinical evaluationdata; (5) Product specification and label samples; (6) qualitymanagement system documents related to product development andproduction; (7) other materials required to prove the safety andeffectiveness of the product. 9. If the application materials needto be submitted, the applicant (unit) shall indicate the words "thecopy conforms to the original" or the copy, indicate the date andstamp the official seal of the unit; the individual applicationshall be signed or signed. 10. The application materials should becomplete, clear and signed, and stamped with the official seal percopy. All the application forms should be filled in by computertyping, printed with A4 paper, an
