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.
NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.
WITHDRAWN
SRPS IEC 60601-2-23:1999
WITHDRAWN
SRPS EN 60601-2-23:2009
95.99
Withdrawal of Standard
Dec 17, 2018
PUBLISHED
SRPS EN 60601-2-23:2017