Specifies requirements for the safety of multifunction patient monitoring equipment. Multifunction patient monitoring equipment is defined as a modular or pre-configured device including more than one physiological monitoring unit designed to collect information from a single patient and process it for monitoring purposes and to generate alarms.
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WITHDRAWN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 EN 60601-2-49:2009
95.99
Withdrawal of Standard
Dec 17, 2018
WITHDRAWN
SRPS EN 60601-2-49:2017