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Warnings and Cautions
1
This symbol alerts the user that important information regarding the installation and / or operation of this
equipment follows. Information preceded by this symbol should be read carefully in order to avoid
damaging the equipment.
This symbol warns user that un-insulated voltage within the unit may have sufficient magnitude to cause
electrical shock. Therefore, it is dangerous to make contact with any part inside the unit. To reduce the risk
of electric shock, DO NOT remove cover (or back). There are no user serviceable parts inside. Refer servicing
to qualified service personnel.
This symbol cautions the user that important information regarding the operation and / or maintenance of
this equipment has been included. Information preceded by this symbol should be read carefully to avoid
damage to the equipment.
This symbol denotes the manufacturer.
This symbol denotes the manufacturer's European Community representative.
To prevent fire or shock hazards, do not expose this unit to rain or moisture. Also, do not use this unit's polarized plug
with an extension cord receptacle or other outlets unless the prongs can be fully inserted. The product is designed to
meet the medical safety requirements for a patient vicinity device.
This product is a Class I medical device. No modifications are allowed.
This equipment/system is intended for use by healthcare professionals only.
Safety Compliance:
This product is T.U.V. approved WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANICAL
HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1/CAN/CSA C22.2 NO. 60601-1 and ANSI/AAMI
ES60601-1.
Safety Compliance:
This product meets the requirements of EN-60601-1 so as to conform to the Medical Device Directive
93/42/EEC and 2007/47/EC (general safety information).
WARNING:
CLASS I LASER PRODUCT. DO NOT STARE INTO LASER BEAM
This product complies to the above standards only when used with the supplied medical grade power supply.
Power supply:
Ault and SL Power Electronic Corp Model: MENB1030A1200C02 12VDC
Disconnect the power supply from the AC mains. The power supply is the only recognized disconnect device.
The MEDICAL EQUIPMENT should be positioned so that its disconnect device is readily accessible.
The product should be powered from a center tapped circuit when used in the US at voltages over 120 volts.
Product is intended for continuous operation.
This product is energized from an external electrical power source for class 1 equipment. It is the responsibility of the
installer to test the product's earth ground to verify that it complies with the hospital, local and national impedance
requirements.
Recycling:
Follow local governing ordinances and recycling plans regarding the recycling or disposal of this
equipment .
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