Revised
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.
WITHDRAWN
IEC 60601-2-23:1993 ED1
WITHDRAWN
IEC 60601-2-23:1999 ED2
99.60
Withdrawal effective
25 shk 2011
PUBLISHED
IEC 60601-2-23:2011 ED3