NDS EndoVue Plus 15", User Manual

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Warnings and Cautions
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.
A ground post, located on the back of the product, may be used for the purpose of grounding the unit’s chassis. Any
such ground must be installed in accordance with applicable electrical codes. The ground post is shown on the
mechanical drawing found on page 2.
Recycling:
Follow local governing ordinances and recycling plans regarding the recycling or disposal of this equipment.
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 suf fi cient 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 quali fi ed 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 fi re 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 modi
fi cations are allowed.
This equipment/system is intended for use by healthcare professionals only.
This monitor complies to the above standards only when used with the supplied medical grade power supply.
Power Cord: Use a hospital grade power cord with the correct plug for your power source.
Disconnect the power cord from the AC mains. The power cord 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.
Model 15” and 19” EndoVue LED
Power Supply Bridge Power JMW190KB2400F05
AC Input 100 to 240 Volts at 50 to 60 Hz.
DC Output 24 volts at 3.75 amps
Safety Compliance:
This product is T.U.V. approved with respect to electric shock, fi re and mechanical hazards only in
accordance with CAN/CSA C22.2 No. 60601-1 and ANSI/AAMI ES60601-1.
Safety Compliance:
This product meets the requirements of EN60601-1 so as to conform to the Medical Device Directive
93/42/EEC and 2007/47/EC (general safety information).