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。
. 2. Requirements for three-of medical device license: 1, siterequirements: must be office nature, the use area should be lessthan 45 square meters; 2. Personnel requirements: 3 relevantpersonnel (company responsible person, quality responsible person,quality inspection personnel) need to record and hold thecertificate; 3, product requirements: must have the productinformation in accordance with the business scope, and issue acertificate; 4. Other relevant laws and regulation requirements. 3.Procedures for obtaining the Class III Medical Device License: 1.The applicant shall submit the application materials to therelevant departments; 2. Relevant departments shall accept theapplication of the applicant; 3. Investigate the actual site andaudit the products; 4. Grant the issuance of a class III medicaldevice license. The above is the relevant introduction of the threetypes of medical device business license processing, the
