Leveraging the EU CE Mark for independent 3rd party end-product certifications - Facts and Myths

James L. Bender, Brunno P. Covolan
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Abstract

Many companies erroneously conflate the familiar European CE mark to be equivalent to North American safety certification recognized component approvals. For purposes of this publication, “North America” only includes the United States and Canada. Although a CE marked component or subassembly cannot solely be used to support such recognized component certifications, it can offer value to both product developers and independent certification laboratories to optimize component selection. A common situation occurs when a product developer desires end-product Listing certification based on a critical component/subassembly level CE mark for North American compliance. Even if the CE mark is provided against a harmonized standard, this may not be acceptable to 3rd party safety certification laboratories in absence of a more formal recognized component evaluation. This paper will provide an overview of the importance of CE mark product safety compliance claim and benefits of supplemental certification approvals.
利用欧盟CE标志进行独立的第三方最终产品认证-事实和神话
许多公司错误地将我们熟悉的欧洲CE标志与北美安全认证认可的部件批准相混淆。就本出版物而言,“北美”仅包括美国和加拿大。虽然CE标志的组件或组件不能单独用于支持此类认可的组件认证,但它可以为产品开发人员和独立认证实验室提供价值,以优化组件选择。当产品开发人员希望获得基于关键组件/子组件级别CE标志的最终产品清单认证以满足北美合规性时,会出现一种常见情况。即使CE标志是根据协调标准提供的,在缺乏更正式的认可组件评估的情况下,第三方安全认证实验室也可能无法接受。本文将概述CE标志产品安全符合性声明的重要性和补充认证批准的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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