欧盟授权代表（European Authorized Representative，EU Representative，欧代，EC REP,EU REP）简介

参考文件

MEDDEV 2.5/10

GUIDELINE FOR AUTHORISED REPRESENTATIVES

欧盟CE认证和欧盟授权代表（欧代地址）的区别是什么?

欧盟授权代表(European Authorized Representative )是指由位于欧洲经济区EEA(包括EU与EFTA)境外的制造商明确指定的一个自然人或法人。该自然人或法人可代表EEA境外的制造商履行欧盟相关的指令和法律对该制造商所要求的特定的职责。

为了更好地保护欧盟的消费者和环境，欧盟的法律要求，为了实现产品的可追溯性，制造商投放到欧盟市场的加贴了CE标志的产品必须标有制造商的名称和联络地址；如果制造商来自欧洲经济区EEA(包括EU与EFTA)以外的国家，其产品必须同时标有制造商和制造商的欧盟授权代表的名称和联络地址。

EU DECLARATION OF CONFORMITY

1.No … (unique identification of the product)

2.Name and address of the manufacturer or his authorised representative:

3.This declaration of conformity is issued under the sole responsibility of the manufacturer (or installer):

4.Object of the declaration (identification of product allowing traceability. It may include a colour image of sufficient clarity to enable the identification of the product, where appropriate.)

5.The object of the declaration described in point 4 is in conformity with the relevant Union harmonisation legislation:

6.References to the relevant harmonised standards used, or references to the specifications in relation to which conformity is declared:

7.Where applicable: the notified body ... (name, number)… performed … (description of intervention)… and issued the certificate:

8.Additional information:

Signed for and on behalf of:

(place and date of issue)

(name, function)(signature)