Safety Information; Warnings And Cautions - NDS EndoVue 19" User Manual

Safety Information

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 the user that un-insulated voltage within the unit may have sufficient magnitude to
cause electrical shock. 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).
NOTE: 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.
EndoVue series monitors are designed to display high quality video and graphic images for use in a medical
environment. They are designed to accept all standard video and graphic signals, and most special timings from
medical equipment. Built-in video controllers convert and format incoming signals of various signal types to
match the resolution of the LCD panel. The user can make adjustments to video parameters using the front
keypad of the monitor with the On Screen Display (OSD) interface to optimize the viewing experience for
different applications.
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.
Warning: To avoid risk of electric shock, this equipment must be only connected to a supply mains with
protective earth.
The installation shall only be carried out by NDS authorized and trained personnel.
This device is only intended to be used in professional healthcare environment.
This equipment/system is intended for use by healthcare professionals only.
This product is a Class I medical device. No modifications are allowed.
Monitors are intended for continuous operation.
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.
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 and EMI Compliance
GB9254, GB4943.1 and GB17625.1
S&E
Safety Information | iii