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Warnings and Cautions
WARNING:
CLASS I LASER PRODUCT. DO NOT STARE INTO LASER BEAM
Safety Compliance:
This product meets the requirements of EN-60601-1 so as to conform to the Medical Device Direc ve
93/42/EEC and 2007/47/EC (general safety informa on).
Safety Compliance:
This product 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.
This symbol alerts the user that important informa on regarding the installa on and / or opera on of this
equipment follows. Informa on 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 cau ons the user that important informa on regarding the opera on and / or maintenance of this
equipment has been included. Informa on 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 representa ve.
To prevent fire or shock hazards, do not expose this unit to rain or moisture. Also, do not use the polarized plug on this unit
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 pa ent vicinity device.
This product is a Class I medical device. No modifica ons are allowed.
This equipment/system is intended for use by healthcare professionals only.
This product is energized from an external electrical power source for class 1 equipment. It is the responsibility
of the installer to test the earth ground on the unit to verify that it complies with the hospital, local and na onal
impedance requirements.
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
Op onal power supply: GTM91120-3024-T3A, 24VDC
Disconnect the power supply from the AC mains. The power supply is the only recognized disconnect device.
The MEDICAL EQUIPMENT should be posi oned 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 con nuous opera on.
Recycling:
Follow local governing ordinances and recycling plans regarding the recycling or disposal of this
equipment .
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