DIN EN 60601-2-23 (2000-11)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：German Institute for Standardisation (Deutsches Institut für Normung)
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)
Supersedes DIN EN 60601-3-1 & DIN IEC 62D-235-CDV. (11/2001)
IEC 60601-2-23 Ed. 2.0 - Identical
NF EN 60601-2-23:2000 - Identical
BS EN 60601-2-23:2015 - Identical
SS EN 60601-2-23 Ed. 3 (2015) - Identical
VDE 0750-223:1993 - Identical
EN 60601-2-23:2015 - Identical
VDE 0750-2-23:2000 - Identical
NF EN 60601-2-23:2016 - Identical
SN EN 60601-2-23:2000 - Identical
BS EN 60601-2-23:2000 - Identical
I.S. EN 60601-2-23:2004 - Identical
UNE EN 60601-2-23:2001 - Identical
SS EN 60601-2-23 Ed. 2 (2000) - Identical
