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To reduce the risk of electric shock, Do not remove the back cover.
No-user serviceable parts inside, Refer to qualied service Personnel.
Safety Precautions
Attention, Consult accompanying documents
Dangerous Voltage, Risk of electric shock
FCC Information
FCC
(U.S.Federal Communications Commission)
This equipment has been tested and found
to comply with the limits for a Class A digital
device, pursuant to part 15 of the FCC Rules.
These limits are designed to provide reasonable
protection against harmful interference in a
residential installation. This equipment
generates, uses, and can radiate radio frequency
energy, and if not installed and used in
accordance with the instructions, may cause
harmful interference to radio communications.
However, there is no guarantee that interference
will not occur in a particular installation. If this
equipment does cause unacceptable inter-
ference to radio or television reception, which
can be determined by turning the equipment off
and on, the user is encouraged to try to correct
the interference by one or more of the following
measures:
- Reorient or relocate the receiving antenna.
- Increase the separation between the
equipment and receiver.
- Connect the equipment into an outlet on a
circuit different from that to which the receiver
is connected.
- Consult your dealer or an experienced
radio/TV technician for help.
FCC Warning:
To assure continued FCC compliance, the
user must use a grounded power supply cord
and the provided shielded video interface cable
with bonded ferrite cores. Also, any unauthorized
changes or modications to this monitor would
void the user's authority to operate this device.
The Responsible Party located
within United States
U.S.ELECTRONICS, INC.
Tel:1-888-926-2605
CE Certication
This device complies with the
requirements of the MDD directive
93/42/EEC "Medical Device
Directive".
Warning
- This apparatus must be earthed because of
Class I equipment.
- This apparatus is no patient contact equipment.
- When using at 240 V in United States,
supply must be from center-tapped, 240 V,
single phase circuit.
- Please consult with the dealer from whom you
purchased it about waste disposal.
- This equipment shall not to be used around the
patient vicinity, which is the space with surfaces
likely to be contacted by the patient or an
attendant who can touch the patient.
This encloses a space within the room 1.83 m
(6 feet) beyond the perimeter of the bed in its
intended location, and extending vertically 2.29
m (7-1/ 2 feet) above the oor.
Equipment Classication
- Type of protection against electric shock:
Class II equipment
- Protection against harmful ingress of water :
Ordinary Equipment (IPX0)-No protection.
- Not suitable for use in the presence of a ammable
anesthetics or oxygen.
- Mode of operation: Continuous operation