Dräger Babylog 8000 plus Instructions For Use Manual page 110

Technical Data
EMC Declaration
Electromagnetic environment
The medical device is intended for use in an electromagnetic
environment as specified below. The user must ensure its use
in such an environment.
Emissions
Radio frequency emissions
(CISPR 11)
Harmonic emissions
(IEC 61000-3-2)
Voltage fluctuations/flicker emis-
sions (IEC 61000-3-3)
110
Compliance according to Electromagnetic environment
Group 1
Class A
Not applicable
Not applicable
The medical device uses RF energy only
for its internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby elec-
tronic equipment.
The medical device is suitable for use in
all establishments other than domestic
establishments and those directly con-
nected to the public low-voltage power
supply network that supplies buildings
used for domestic purposes.