（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
医疗器械经营许可证。
医疗企业经营许可证一共有三类，其中办理一类医疗器械许可证可以直接办理，经营二类产品是需要
ministration of Medical Devices for the filing of Class Imedical devices and application for the registration of Class IIand III medical devices, the following materials shall besubmitted: (1) product risk analysis data; (2) product technicalrequirements; (3) product technical requirements; (3) productinspection report; (5); (5) clinical evaluation data; productspecification and label samples; (6) quality management systemdocuments related to product development and production; 1.Business license of medical and medical devices submitted by theoperating enterprise. There are three kinds of medical enterprisebusiness licenses, among which the first class medical devicelicense
