8、其它相道关材料。
二、办理三回类医疗器械许可证的要求：
1、场地要求：必须是办公性质，使用面积要少达到45平方米;
2、人员要求：需要有3名相关人员(公司负责人、质量负责人、质量检查人员)的备案并且持有证书;
3、产品要求：必须要有合乎业务范围的产品信息，并出具证书;
4、其他相关法律法规要求。
三、办理三类医疗器械许可证的流程：
1、申请人提交申请资料到相关部门;
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。
以上就是对三类医疗器械经营许可证办理的相关介绍，办理的程序可能较为繁琐。
uct information in accordance with the business scope, and issuea certificate; 4. Other relevant laws and regulations andrequirements. 3. Procedures for obtaining the Class III MedicalDevice License: 1. The applicant shall submit the applicationmaterials to the relevant departments; 2. Relevant departmentsshall accept the application of the applicant; 3. Investigate theactual site and audit the products; 4. Grant the issuance of aclass III medical device license. The above is the relevantintroduction of the three types of medical device business licenseprocessing, the procedures may be more cumbersome.
