NDS ZEROWIRE G2 User Manual - page 6
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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:
UK2-SII-SK63102, UK2-SII-SK63101
Industry Canada:
6705A-SIISK63102, 6705A-SIISK63101
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.
0984
Warnings and Cautions
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 according to M.D.D. in Europe. No modifications are allowed.
This product is a Class II medical device in the United States and Canada. No modifications are allowed.
This equipment/system is intended for use by healthcare professionals only.
Federal law restricts this device to sale by or on the order of a medical practitioner.
These are the European countries that accept CE marked devices: Belgium, Bulgaria, Croatia, Cyprus, Germany,
Hungary, Iceland, Macedonia, Montenegro, Norway, Romania, Slovakia, Spain, Switzerland and United Kingdom.
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.
Model
ZeroWire G2
Power Supply
Ault MW172KB2400B02 or GlobTek GTM91120-3024-T3A
AC Input
100 to 240 Volts at 50 to 60 Hz.
DC Output
Ault 24 volts at 0.75 amps / GlobTek 24 volts at 1.25 amps