9
2.6.
Transportation
Disconnect all cables from the monitor when transporting.
When you transport this LCD display, hold the base sections of the display stand firmly in both
hands. If you drop the monitor, you may be injured or the monitor may be damaged.
When you transport this monitor for repair or shipment, use the original cardboard box and packing
materials.
Be always sure that the monitor is stable and safe during the transport.
(for more detail see the Mounting Instruction chapter)
The enclosure has to be checked upon collision damage; refer to qualified service personnel.
To prevent damage which may result in fire or shock hazard, do not expose this appliance to rain
or excessive moisture
2.7.
Replacement of the backlight
Specially designed fluorescent tubes are installed as the lighting apparatus for this monitor. If the
screen becomes dark, unstable, or does not come on, consult your Customer service for replacing
the fluorescent tube
2.8.
Serviceability
There are
no user serviceable parts within the 56” LCD monitor. Attempting to open or disassemble
the monitor may expose the user to hazardous voltages, risk of excessive temperatures, fire or
explosion from enclosed energy sources, or impairment of function.
This product is intended to be installed in a medical system only by trained system integrator. In
the medical systems where the life of the patient or the success of a clinical intervention depend
from the image displayed by this 56" monitor, an adequate backup solution has to be provided at
medical system level.
This monitor can be repaired only by trained service personnel (contact your local dealer to get
assistance).
FIMI will make available on request circuit diagrams, component part lists, description, calibration
instruction, or other information that will assist Service Personnel to repair the monitor.
2.9.
Biological Hazard and Returns
The structure and the specifications of this device as well as the materials used for manufacturing
makes it easy to wipe and clean and therefore suitable to be used for various applications in
hospitals and other medical environments, where procedures for frequent cleaning are specified.
However, normal use shall exclude biological contaminated environments, to prevent spreading of
infections.
Therefore use of this device in such environments is at the exclusive risk of Customer.
In case this device is used where potential biological contamination cannot be excluded, Customer
shall implement the decontamination process as defined in the latest edition of the ANSI/AAMI
ST35 standard on each single failed Product that is returned for servicing, repair, reworking or
failure investigation to Seller (or to the Authorized Service Provider). At least one adhesive yellow
label shall be attached on the top site of the package of returned Product and accompanied by a
declaration statement proving the Product has been successfully decontaminated.
Returned Products that are not provided with such external decontamination label, and/or
whenever such declaration is missing, can be rejected by Seller (or by the Authorized Service
Provider) and shipped back at Customer expenses.
