申请三类医疗器械所需材料清单：

（一）营业执照、组织机构代码证复印件；
（二）申请企业持有的所生产医疗器械的注册证及产品技术要求复印件；
（三）法定代表人、企业负责人身份证明复印件；
（四）生产、质量和技术负责人的身份、学历、职称证明复印件；
（五）生产管理、质量检验岗位从业人员学历、职称一览表；
（六）生产场地的证明文件，有特殊生产环境要求的还应当提交设施、环境的证明文件复印件；
（七）主要生产设备和检验设备目录；
（八）质量手册和程序文件；
（九）工艺流程图；
（十）经办人授权证明；
（十一）其他证明资料。

Where there are errors in the application materials that can be corrected on the spot, The applicant shall be allowed to make corrections on the spot; if the application materials are incomplete or do not conform to the statutory form, Should inform the applicant on the spot or within five days of all the contents to be corrected, Failure to inform you after the time limit, It shall be accepted from the date of receipt of the application materials; The matters to apply for fall within the scope of the functions and powers of the administrative organ, The application materials are complete and in line with the legal form, Or where the applicant submits all the supplementary and corrected application materials as required by the respective administrative organ, The application for administrative license shall be accepted.