
1
ii
Recycling:
Follow local governing ordinances and recycling plans regarding the recycling or disposal of this
equipment.
Safety Compliance:
This device 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).
Safety Compliance:
This device is T.U.V. approved with respect to electric shock, fire and mechanical hazards
only in accordance with CAN/CSA C22.2 No. 60601-1 and ANSI/AAMI ES60601-1.
FCC Identification:
UEZ-WT-P42-13, UEZ-WR-P42-11
Industry Canada: 9203A-90T2072, 9203A-90T2071
Radio Approval:
This device meets the requirements of EN 302 065 V1.2.1 and conforms to Radio and
Telecommunications Terminal Equipment (R&TTE) Directive 1999/5/EC.
TBD
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 II medical device. No modifications are allowed.
This equipment/system is intended for use by healthcare professionals only.
This product complies to the above standards
only
when used with an NDS 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 device should be powered from a center tapped circuit when used in the US at voltages over 120
volts. This product is intended for continuous operation.
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