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SN EN 60601-2-23:2000現(xiàn)行

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

出版：Swiss Standards

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基本信息
標(biāo)準(zhǔn)編號(hào)： SN EN 60601-2-23:2000
發(fā)布時(shí)間：2000/3/1 0:00:00
標(biāo)準(zhǔn)類別：Standard
出版單位：Swiss Standards
標(biāo)準(zhǔn)頁(yè)數(shù)：0
標(biāo)準(zhǔn)簡(jiǎn)介

Defines particular requirements for the safety, including essential performance of transcutaneous partial pressure monitoring equipment as specified. Applicable to transcutaneous monitors for use with adults, children and neonates, including the use of these devices in foetal monitoring during birth. Not applicable to haemoglobin saturation oximeters or to devices applied to body surfaces other than skin (eg. conjunctiva, mucosa)

等同采用的國(guó)際標(biāo)準(zhǔn)

DIN EN 60601-2-23 (2000-11) - Identical

BS EN 60601-2-23:2000 - Identical

SS EN 60601-2-23 Ed. 2 (2000) - Identical

UNE EN 60601-2-23:2001 - Identical

I.S. EN 60601-2-23:2004 - Identical

IEC 60601-2-23 Ed. 2.0 - Identical

NF EN 60601-2-23:2000 - Identical

NF EN 60601-2-23:2016 - Identical

EN 60601-2-23:2015 - Identical

DIN EN 60601-2-23:2016 - Identical

SS EN 60601-2-23 Ed. 3 (2015) - Identical

BS EN 60601-2-23:2015 - Identical

BS EN 60601-2-23 : 2015 - Identical

BS EN 60601-2-23 : 2015 - Identical

I.S. EN 60601-2-23:2015 - Identical