UNE EN 60601-2-23:2001现行
Medical Electrical Equipment - Part 2-23: Particular Requirements For The Safety, Including Essential Performance, Of Transcutaneous Partial Pressure Monitoring Equipment
出版：Asociacion Espanola de Normalizacion
专家解读视频
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)
BS EN 60601-2-23 : 2015 - Identical
BS EN 60601-2-23 : 2015 - Identical
I.S. EN 60601-2-23:2015 - Identical
BS EN 60601-2-23:2015 - Identical
SS EN 60601-2-23 Ed. 3 (2015) - Identical
DIN EN 60601-2-23:2016 - Identical
EN 60601-2-23:2015 - Identical
NF EN 60601-2-23:2016 - Identical
SN EN 60601-2-23:2000 - Identical
BS EN 60601-2-23:2000 - Identical
NF EN 60601-2-23:2000 - Identical
IEC 60601-2-23 Ed. 2.0 - Identical
I.S. EN 60601-2-23:2004 - Identical
SS EN 60601-2-23 Ed. 2 (2000) - Identical
DIN EN 60601-2-23 (2000-11) - Identical
