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DS EN 60601-2-23:2000被替代

Medical Electrical Equipment - Part 2-23: Particular Requirements For The Safety, Including Essential Performance, Of Transcutaneous Partial Pressure Monitoring Equipment

出版：Danish Standards

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基本信息
標(biāo)準(zhǔn)編號(hào)： DS EN 60601-2-23:2000
發(fā)布時(shí)間：2001/3/7 0:00:00
標(biāo)準(zhǔn)類別：Standard
出版單位：Danish Standards
標(biāo)準(zhǔn)頁(yè)數(shù)：44
標(biāo)準(zhǔn)簡(jiǎn)介

Defines requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment hereinafter referred to as EQUIPMENT, whether this EQUIPMENT is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.

替代本標(biāo)準(zhǔn)的新標(biāo)準(zhǔn)

DS EN 60601-2-23:2015

等同采用的國(guó)際標(biāo)準(zhǔn)

EN 60601-2-23:2015 - Identical