注册办理所需料
(有效期四年,有效期满前6个月应申请重新注册)
1、境外医疗器械注册申请表
Application form for registration of import medical device
2、医疗器械生产企业资格证明
Legal Qualification certification for medical device manufacturing enterprise.
3、申报者的营业执照副本和生产企业授予的代理注册的委托书
A Copy of applicant’s business license and proxy for registration entrusted by the
Manufacturing enterprise
4、境外政府医疗器械主管部门批准或认可的该产品作为医疗器械进入该国(地区)市场的证明文件
proving that the product can enter a certain country (or region) as medical
Device approved or by the medical device competent of overseas
5、适用的产品标准(及说明)
Applicable product standard and instructions
6、医疗器械说明书
Specification for medical device
7、医疗器械检测机构出具的产品注册检测报告(适用于第二类、第三类医疗器械)
Test report on product registration given by medical device inspection institutions(applicable to II and III medical device)
8、医疗器械临床试验资料
Medical device clinical trials report.
9、生产企业出具的产品质量保证书
Product Quality Guarantee issued by the manufacturer certifying that the quality of the product to be registered for sale in China is exactly the same as that of the product marketed in the country (region) of origin.
10、生产企业在中国指定代理人的委托书、代理人的承诺书及营业执照或者机构登记证明
Proxy of assigned agent of the manufacturer enterprise in china, written of the agent and business license or registration certificate of the agent
11、在中国指定售后服务机构的委托书、被委托机构的承诺书及资格证明文件
Letter of Authorization for designated after-sales service agency in China and Letter of Promisa and business license of the authorized agency. 上海食品报关,上海服饰报关,上海干果报关,上海坚果报关,上海酒类报关,上海日用品报关,上海化妆品报关,上海化工品报关 ,上海电子报关,上海机械报关,上海工艺品报关,上海家具报关,上海报关公司,上海快递清关,上海机场报关,上海个人物品报关,上海邮寄报关,上海进口代理报关,上海空运进口报关,上海海关报关,上海进口报关,浦东机场报关,上海自贸区报关