5、一定有其销售三类医疗器械产品的注册证,有这个证,才能确定这个三类医疗器械是合格正规的,后续申请三类医疗器械许可证,,递交材料,这个产品注册证就是主要的材料之一。
1、经营企业提交的《医疗器械经营企业许可证申请表》应有法定代表人签字或加盖企业公章；
2、《医疗器械经营企业许可证申请表》所填写项目应填写齐全、准确；
3、法定代表人的身份证明、学历职称证明、任命文件应有效；
4、工商行政管理部门出具的《企业名称预先核准通知书》或《工商营业执照》的复印件应与原件相同，复印件确认留存，原件退回；
5、房产证明、房屋租赁证明（出租方要提供产权证明）应有效；
6、企业负责人、质量管理人的简历、学历证明或职称证明应有效
Where there are errors in the applicationmaterials that can be corrected on the spot, The applicant shall beallowed to make corrections on the spot; if the applicationmaterials are incomplete or do not conform to the statutory form,Should inform the applicant on the spot or within five days of allthe contents to be corrected, Failure to inform you after the timelimit, It shall be accepted from the date of receipt of theapplication materials; The matters to apply for fall within thescope of the functions and powers of the administrative organ, Theapplication materials are complete and in line with the legal form,Or where the applicant submits all the supplementary and correctedapplication materials as required by the respective administrativeorgan, The application for administrative license shall beaccepted.
