一、三类医疗器知械许可证注册所需材料
1、企业名称与经营范围，注册资本及股东出资比例，股东等身份证明;
2、医疗器械产品注册证书、供应商营业执照、许可证及授权书;
3、质量管理文件等;
4、2个或以上医学專业或相关專业人员证书、身份证明与简历;
5、符合医疗器械经营要求的办公场地及仓库证明;
6、公司章程、股东会决议等;
7、财务人员身份证和上岗证;
8、其它相道关材料。
ipment license 1. Enterprise name and business scope, registeredcapital and the proportion of shareholder contribution,shareholders and other identity certificates; 2. Medical deviceproduct registration certificate, supplier business license,license and authorization letter; 3. Quality management documents,etc.; 4,2 or more certificates, identification certificate andresume of medical professionals or related professionals; 5. Officespace and warehouse certificate that meet the business requirementsof medical equipment; 6. Articles of association, resolutions ofshareholders
