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.
Legislation related to this standard
WITHDRAWN
EN 60601-2-23:1997
WITHDRAWN
EN 60601-2-23:2000
99.60
Withdrawal effective
Sep 15, 2018
PUBLISHED
EN 60601-2-23:2015