（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；办理三类医疗器械经营许可证的办理流程：
1.向食品药品监督管理局提交医疗器械经营许可证申请材料；
2.食品药品监督管理局数据形式审查；
3.数据正式受理；
4.有关部门的行政审查；
5.现场评价；
6.有关部门的行政决定；
7.制证、发证。
办理三类医疗器械经营许可证的条件如下：
1、具有与经营范围相匹配的经营场所和仓库，并对其具体面积有具体要求；
2、具有国家认可的、与经营产品相关专门的在岗人员；
hall be submitted: (1) product risk analysis materials; (2) technical requirements for the product and (3) product inspection report; Procedures for handling the business license of Class III medical devices: 1. Submit application materials for medical device business license to the Food and Drug Administration; 2. Examination of data form of the Food and Drug Administration; 3. Official acceptance of data; 4. Administrative examination of relevant departments; 5. On-site evaluation; 6. Administrative decisions of relevant departments; 7. License making and issuance. The conditions for applying for the business license of Class III medical devices are as follows: 1. Having the business site and warehouse matching the business scope, and having specific requirements for its specific area; 2. Having special personnel recognized by the state and related to the business products;
