Ревидиран
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.
ПОВУЧЕН
IEC 60601-2-23:1993 ED1
ПОВУЧЕН
IEC 60601-2-23:1999 ED2
99.60
Повлачење ступило на снагу
25. 2. 2011.
ОБЈАВЉЕН
IEC 60601-2-23:2011 ED3