IEC 60601-2-23 Ed. 2.0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：International Electrotechnical Committee
專家解讀視頻
Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.
NEN EN IEC 60601-2-23:2000 - Identical
SS EN 60601-2-23 Ed. 2 (2000) - Identical
AS/NZS 3200.2.23:2001 - Identical
PN EN 60601-2-23:2006 - Identical
CSA C22.2.601.2.23:1998 - Identical
CSA C22.2.60601.2.23:2002 (R2011) - Identical
I.S. EN 60601-2-23:2004 - Identical
NF EN 60601-2-23:2000 - Identical
OVE/ONORM EN 60601-2-23:2001 - Identical
VDE 0750-2-23:2000 - Identical
DIN EN 60601-2-23 (2000-11) - Identical
BS 5724-2.123:1996 - Identical
BS EN 60601-2-23:2000 - Identical
SN EN 60601-2-23:2000 - Identical
CEI EN 60601-2-23 Ed. 2 (2001) - Identical
UNE EN 60601-2-23:2001 - Identical
