The European medical device EMC specifications

R. Anderson
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引用次数: 1

Abstract

Medical device EMC compliance became mandatory for sales in the European Union on January 1, 1996. This paper reviews current requirements, provides examples of experiences and issues associated with compliance and provides insight on the development of a revision to the EMC standard for medical devices.
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欧洲医疗器械EMC规范
1996年1月1日,医疗设备EMC合规成为欧盟销售的强制性要求。本文回顾了当前的要求,提供了与合规性相关的经验和问题示例,并对医疗设备EMC标准修订的开发提供了见解。
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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