1.《 医疗器械经营许可申请表》(原件1份)
2.《营业执照》复印件(交验原件);(复印件1份)
3.法定代表人、企业负责人、质量负责人的身份证明(查验原件)、学历或者职称证明复印件(对于统一采购渠道,采取连锁经营的非法人零售企业,提供连锁企业总部质量负责人身份证明、学历或者职称证明复印件);(交验原件)(复印件共3份)
4.企业基本情况(原件1份)。(内容包含:组织机构与部门设置说明、经营场所、库房的地理位置图、平面图(注明面积)、库房的产权证明及使用权证明复印件、(委托贮存的,应提交经营场所地理位置图、平面图(注明面积)和与被委托方签署的书面协议复印件、被委托方的《医疗器械经营许可证》复印件)
5.企业设施设备情况(原件1份)。(内容包含:经营设施、设备目录、经营质量管理制度、工作程序等文件目录、计算机信息管理系统基本情况介绍和功能说明)(原件1份)
ality certificate, head of the degree or title copy); (submitthe original) (copy of 3 copies) 4. Basic information of theenterprise (1 original copy).(Contains: organization and departmentset instructions, premises, warehouse location map, plan (indicatearea), warehouse of property certificate and the right certificatecopy, (entrust storage, should be submitted to the site locationmap, plan (indicate area) and the written agreement signed with theprincipal party, the principal copy of the medical device businesslicense) 5. Enterprise facilities and equipment information (1original copy).(Contents include: business facilities, equipmentcatalogue, business quality management system, working proceduresand other documents catalogue, basic information introductionof