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I.S. EN 60601- 1:2006&A1:2013&AC:2014&A12:2014現(xiàn)行

MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE

出版:National Standards Authority of Ireland

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基本信息
標(biāo)準(zhǔn)編號(hào): I.S. EN 60601- 1:2006&A1:2013&AC:2014&A12:2014
標(biāo)準(zhǔn)類別:Standard
出版單位:National Standards Authority of Ireland
標(biāo)準(zhǔn)頁(yè)數(shù):0
標(biāo)準(zhǔn)簡(jiǎn)介

Renumber the note as Note 1. Delete the fourth paragraph. Replace the fifth paragraph with: The IEC 60601 series does not apply to: – in vitro diagnostic equipment that does not fall within the definition of ME EQUIPMENT, which is covered by the IEC 61010 series [61]; – implantable parts of active implantable medical devices covered by the ISO 14708 series [69]; or – medical gas pipeline systems covered by ISO 7396-1 [68].

本標(biāo)準(zhǔn)替代的舊標(biāo)準(zhǔn)

I.S. EN 60601-1-4:1998

I.S. EN 60601-1-1:2001

I.S. EN 60601-1:1991