Introduction
2002938-002E Cardiolab® II Plus Amplifier Manual 1-15
It is the user’s responsibility to report the need for service to GE
Medical Systems - Information Technologies or to one of their
authorized agents.
Failure on the part of the responsible individual, hospital, or
institution using this equipment to implement a satisfactory
maintenance schedule may cause undue equipment failure and
possible health hazards.
Regular maintenance, irrespective of usage, is essential to ensure
that the CardioLab II Plus Amplifier will always be functional when
required
Equipment Identification
Every GE Medical Systems - Information Technologies device has a
unique serial number for identification. The serial number appears on
the back of the CardioLab II Plus Amplifier.
New Identification Tags
Identification Tags
Item Name
A Name of Device
B Manufacturer
XXXXXXXXXXXXXX
XXXXXXXXXXXXXXXXXX
XXXXXXXXX
XX
XXXXXXXXXXX
XXXXXXXXXXXXX
AA5 XX XX XXXX X X
A
B
C
D
E
F
G
H
I