Description

Intended use

This instrument has been designed to be used with Olympus endoscopes, light

source, video system center, camera control units and endoscopic ultrasound

centers for endoscopic diagnosis and video observation.

Do not use this instrument for any purpose other than its intended use.

Instruction manual

This instruction manual contains essential information on using this instrument

safely and effectively. Before use, thoroughly review this manual and the

manuals of all equipment that will be used during the procedure and use the

equipment as instructed.

Keep this and all related instruction manuals in a safe, accessible location. If you

have any questions or comments about any information in this manual, please

contact Olympus.

• Terms used in this manual

Video system center:

The video system center is a device that converts signals from a

videoscope or video converter into monitor images.

Camera control unit:

The camera control unit is a device that converts signals from a fiberscope

or rigid endoscope into monitor images.

Ultrasound center:

The ultrasound center converts the ultrasonic signals from an ultrasonic

endoscope or probe into monitor images.

Light source:

The light source provides light and electrical signals to the endoscope.

Wall mains socket outlet:

An electrical outlet that has a terminal used exclusively for grounding.

Aspect ratio:

It is a unit that expresses a rate of a screen side and a vertical length.

The aspect ratio of 4:3 is used usually for SDTV.

The aspect ratio of 16:9 is used usually for HDTV.

VESA mounting standards:

These are the standards to be applied when mounting an LCD panel on a

monitor mount or stand. These standards were defined by the Video

Electronics Standards Association (VESA), a US-based organization

concerned with computer display devices.

Mobile workstation:

The mobile workstation is a special trolley on which this monitor is placed.

PIP (Picture in Picture)

The sub display is put in the main display.

POP (Picture out Picture)

The sub display by the side of the main display.

Instrument compatibility

Refer to the “System chart” in the Appendix to confirm that this instrument is

compatible with the ancillary equipment being used. Using incompatible

equipment can result in patient or operator injury and/or equipment damage. It

may also impair the functionality of the instrument.

This instrument complies with medical electrical equipment edition 2

(IEC 60601-1-2: 2007). However when connecting with an instrument that

complies with medical electrical equipment edition 1 (IEC 60601-1-2: 1993), the

whole system complies with edition 1. (See, “EMC information” on page 94 for

EMC compliance level.)