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Innova 2100-IQ, 3100/3100-IQ, 4100/4100-IQ Cardiovascular Imaging System Pre-Installation Manual
GE Healthcare
2 Recommended Power Distribution System
ANY SAFETY LABELS AFFIXED ON THE PDB AND ON THE EMI FILTER
ENCLOSURE WOULD HAVE TO FULFILL THE LEGAL REQUIREMENT OF THE
COUNTRY CONCERNING THE LANGUAGE TO BE USED FOR INFORMATION FOR
SAFETY ON PROFESSIONAL EQUIPMENT.
To prevent risk of cable overheating or fire.
Local regulations concerning cable tightening inside the PDB must be respected.
The drawing hereafter is a guide to illustrate all functions included inside the
main disconnect room device.
It should be compliant with the specific country rules.
NOTE:
According to the country, the PDB/MDP can be ordered from GEHC.
One configuration 480 V, 60 Hz is certified to UL 508 and CSA C22.2 N 14: North America.
Second configuration (380/400/415 V, 50/60 Hz) is certified to EN 60439-1 and is CE marked
(not certified for Japan and China). Please check your country local regulations for the
applicable configuration or refer to your local GE representative.
2.1 Main functions
Lock–out/Tag–out by S1 (Europe) or CB1 handle (US),
Main disconnect device by DMD1 (Europe) or CB1 handle (US),
Low voltage created by TR1 applied on remote, L1 and L2,
Separated injection circuit by TR2/CPT2 and BR,
L is mandatory for French standards,
Protect the Room Emergency Off (AU1, AU2) from accidental activation
MANDATORY FOR FLUORO UPS OPTION THE PDB FRONT PANEL MUST WARN
THE OPERATOR WITH AN ELECTRICAL HAZARD LABEL.
L1 is mandatory in several countries. By the same L1 circuit one or many other(s)
light indicator(s) have to be mounted inside the examination room and have to be
visible from anywhere by operators.
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Direction 5314528-2-1EN, Revision 1
2 Recommended Power Distribution System
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