办理三类医疗器械许可证要求:
1.地址要求:普通类:办公面积不少于100平，仓库面积不少于60平;
2.一次性无菌:办公面积不少于60平，仓库面积不少于80;
3.体外诊断试剂:办公面积不少于60平，仓库面积不少于100平，冷藏室面积不少于20立方
4.人员要求:医学相关专业毕业满三年办理三类医疗器械许可证的注意事项:
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.
