Bedienungsanleitung Ag neovo DR-17P (Seite 9 von 46) (Englisch)

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PRECAUTIONS

Notice for the LCD Display

In order to maintain the stable luminous performance, it is recommended to use low brightness setting.

Due to the lifespan of the lamp, it is normal that the brightness quality of the LCD display may decrease

with time.

When static images are displayed for long periods of time, the image may cause an imprint on the LCD

display. This is called image retention or burn-in.

To prevent image retention, do any of the following:

• Set the LCD display to turn off after a few minutes of being idle.

• Use a screen saver that has moving graphics or a blank white image.

• Switch desktop backgrounds regularly.

• Adjust the LCD display to low brightness settings.

• Turn off the LCD display when the system is not in use.

Things to do when the LCD display shows image retention:

• Turn off the LCD display for extended periods of time. It can be several hours or several days.

• Use a screen saver and run it for extended periods of time.

• Use a black and white image and run it for extended periods of time.

When the LCD display is moved from one room to another or there is a sudden change from low to high

ambient temperature, dew condensation may form on or inside the glass surface. When this happens, do

not turn on the LCD display until the dew disappears.

Due to humid weather conditions, it is normal for mist to form inside the glass surface of the LCD display.

The mist will disappear after a few days or as soon as the weather stabilizes.

There are millions of micro transistors inside the LCD display. It is normal for a few transistors to be

damaged and to produce spots. This is acceptable and is not considered a failure.

The intended use of the DR-17P is to serve as a LCD monitor for integration with the hospital system. It is

designed for general purpose for hospital environment. For displaying and viewing of images for reference.

The use of this device does not require any direct contact with patients.

Accessory equipment connected to the analog and digital interfaces must be in compliance with the

respective nationally harmonized IEC standards (i.e. IEC 60950 for data processing equipment, IEC 60065

for video equipment, IEC 61010-1 for laboratory equipment, and IEC 60601-1 for medical equipment.)

Furthermore all congurations shall comply with the system standard IEC 60601-1-1. Everybody who

connects additional equipment to the signal input part or signal output part congures a medical system,

and is therefore, responsible that the system complies with the requirements of the system standard

IEC 60601-1-1. The unit is for exclusive interconnection with IEC 60601-1 certied equipment in the patient

environment and IEC 60XXX certied equipment outside of the patient environment. If in doubt, consult the

technical services department or your local representative.

Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle

marked “Hospital Only” or “Hospital Grade”.

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