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NF EN 60601-2-23:2000被替代

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

出版：Association Francaise de Normalisation

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基本信息

標(biāo)準(zhǔn)編號： NF EN 60601-2-23:2000

發(fā)布時間：2000/1/1 0:00:00

標(biāo)準(zhǔn)類別：Standard

出版單位：Association Francaise de Normalisation

標(biāo)準(zhǔn)頁數(shù)：32

標(biāo)準(zhǔn)簡介

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)

標(biāo)準(zhǔn)備注

Indice de classement: C74-386PR. Supersedes NFC 74 386. (03/2000) PR NF EN 60601-2-23 May 2009. (05/2009)

本標(biāo)準(zhǔn)替代的舊標(biāo)準(zhǔn)

NFC 74 386:1989

替代本標(biāo)準(zhǔn)的新標(biāo)準(zhǔn)

NF EN 60601-2-23:2016

等同采用的國際標(biāo)準(zhǔn)

BS EN 60601-2-23:2015 - Identical

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

EN 60601-2-23:2015 - Identical

SN EN 60601-2-23:2000 - Identical

BS EN 60601-2-23:2000 - Identical