服务项目Service Items
High Tech Enterprise
National high-tech enterprise certification
Shenzhen High tech Enterprise Certification
Cultivation and storage of high-tech enterprises
ISO certification
ISO9001 quality management system
ISO14001 environmental management system
ISO45001/OHSAS18001 Occupational Health and Safety Management
ISO13485 Medical Device Management System
IATF16949/TS16949 Quality Management in the Automotive Industry
ISO20001 Information Technology Service Management
ISO22001 Food Safety Management System
ISO27001 Information Security Management System
SA8000 Social Responsibility Standard
GB/T23001 Integrated Management System
GB/T50430 Quality Management of Engineering Construction Enterprises
GB/T27922 Service Evaluation System
ROHS Raw Material Hazardous Substance Testing
QC080000 Hazardous Substance Detection
government funding
Shenzhen Municipal Government Project Funding
District level government funding
Private and small and medium-sized enterprise funding
Double Soft Enterprise Evaluation
Research and development funding
Intellectual Property Standardization
Intellectual Property Standardization Certification
Integrated Management System of Informatization
Product Certification
Qualification agency
National Industrial Production License Agency
Food Production License Agency
Construction industry qualification agency
Contract abiding and trustworthy enterprise
Medical Device Qualification Agency
Factory inspection coaching
Jesse Penny Factory Inspection
做二类医疗器械产品没有“医疗器械备案”可不行,教你办理备案
二类医疗器械经营备案是什么?生活中常见的那些物品属于二类医疗器械呢?
如果你的企业经营口罩、眼镜、计生用品等都需要办理第二类医疗器械备案凭证,另外入驻淘宝、京东等商城也都是需要提供第二类医疗器械备案凭证的。
今天小尼就来给大家分享下办理二类医疗器械经营备案凭证的材料
1.《 第二类医疗器械经营备案表》
2.营业执照复印件(交验原件);
3.法定代表人、企业负责人、质量负责人的身份证明、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)
4.组织机构与部门设置说明;
5.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《第二类医疗器械经营备案凭证》复印件)
6.经营设施、设备目录;
7.经营质量管理制度、工作程序等文件目录;
8.申报材料真实性自我保证声明,并对材料作出如有虚假承担法律责任的承诺。