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俄罗斯测试认证集团/海关联盟EAC认证中心

Центр сертификации EAC Таможенного союза ?ООО ТЕСТ СЕРТ 

上海经合工业设备检测有限公司    俄语区域产品认证专家

021-36411223      eac@cu-tr.org   WeChat:18621862553
乌兹别克斯坦医疗器械认证-medical Uzbekistan regsitration
来源: | 作者:pmt1ac5e9 | 发布时间 :2018-11-08 | 4177 次浏览: | 分享到:
乌兹别克斯坦医疗器械认证,medical Uzbekistan regsitration,re-registration of if imported to Uzbekistan “Регистрация ИМН и МТ в Узбекистане”

乌兹别克斯坦医疗器械认证,medical  Uzbekistan regsitration,re-registration of if imported to Uzbekistan “Регистрация ИМН и МТ в Узбекистане”

List of documents required for registration

Medical devices and equipments in Uzbekistan

 

1) Content.申请表

2) When registration through the representative — power of attorney.授权书

3) General information about the medical device or medical equipment, and its manufacturer.制造商介绍

4) Copy of the Registration Certificate of the medical device or medical equipment in the country of origin, as well as in other countries (if available). 企业法人营业执照,ISO13485工厂体系证书,中华人民共和国医疗器械企业生产许可证和中华人民共和国医疗器械注册证,中华人民共和国医疗器械产品出口销售证明书

5) Normative document that includes the order and methods of testing a medical device or medical equipment, an international, interstate or national product standard. 规范性文件:包括测试医疗设备或医疗设备的顺序和方法或国家产品标准。

6) Passport, operation manual of medical equipment, instruction for use of a medical device in Russian (for medical device - also in the state language). 产品技术护照,医疗设备操作手册,医疗器械使用说明(医疗器械中文英文和俄文语言)。

7) Technical description of medical equipment. 医疗设备的技术描述和声明(包括详细注册)

8) Protocols of laboratory tests, technical tests, technical tests of medical measuring instruments,preclinical and clinical studies. 实验室试验报告:技术测试,功能性试验、毒理分析试验,生物相容性试验,临床试验报告

9) Compliance information of the conditions of production of medical devices and medical equipment with the requirements of international standards (if any).ISO13485 CE证书/CE一致性声明;其他FDA或其他国家的注册证证书和测试报告。

10) Information about absence of infectious agents in products for ?in vitro? diagnosis, prepared from biological materials. 生物相容性报告,从生物材料制备的用于“体外”诊断的产品中不存在感染因子的信息。

11) Information on stability during storage of medical devices. 医疗器械储存期间的稳定性信息。

12) Illustrated promotional materials, brochures, catalogs, photo with size not less than 13 x 18 cm.宣传彩页,小册子,目录,尺寸不小于13 x 18厘米的每个型号照片。

13) Colored graphic models of primary and secondary packaging (for medical devices).包装的照片内包装,外包装。

14) Additional information about a quality, efficiency and safety of medical equipment, medical devices. 有关医疗设备的质量、效率和安全性的其他信息。

 

如果你有上述证书上的任何一种证书,费用是  30万+同一个系列增加每个型号10万 (包括乌兹别克斯坦证书费用和我们服务费用),认证时间是4个月内。快速简化程序,乌兹别克斯坦注册



sending List of required documents for Registration in Uzbekistan.

Official cost depends on many factors, if possible send Product specification which will be registered, and i will revert with Prices.

Usually registration time is 6 months.



We offer the services of registration:

·         Medical supplies and drug

·         Medical equipment

·         Food supplements and substances (API)

·         Veterinary products

·         Cosmetics and perfumery

 

 

Health care equipment and medical devices produced in Kazakhstan are eligible for state registration and re-registration of if imported to Uzbekistan taking into account their classification depending on degree of potential risk in medical applications, including the following:

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