Safety Precautions
Attention, Consult accompanying documents
Dangerous Voltage, Risk of electric shock
To reduce the risk of electric shock, Do not remove the back cover.
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 modifications to this monitor would void the user's authority to operate this device.
CE Certification
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
-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
Equipment Classification
-Type of protection against electric shock: Class II equipment
-Protection against harmful ingress of water : Ordinary Equipment
-Not suitable for use in the presence of a flammable anesthetics or oxygen.
-Mode of operation: Continuous operation
The Responsible Party located within United States
U.S.ELECTRONICS, INC.
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