CLV-180 Instruction Manual

INSTRUCTIONS
EVIS EXERA II XENON LIGHT SOURCE
OLYMPUS CLV-180
USA: CAUTION: Federal law restricts this device to sale by or on the order of a physician.
Contents
Contents
Labels and Symbols .....................................................................
Important Information Please Read Before Use....................
Intended use ............................................................................................
Instruction manual ....................................................................................
User qualifications.....................................................................................
Instrument compatibility ...........................................................................
Repair and modification ...........................................................................
Signal words..............................................................................................
Dangers, warnings and cautions...............................................................
Cardiac applications..................................................................................
12
Summary of the functions of the instrument .............................
13
Chapter 1
Checking the Package Contents............................
15
Chapter 2
Nomenclature and Functions .................................
16
2.1
Front panel......................................................................................
16
2.2
Rear and side panels ......................................................................
22
Inspection ................................................................
24
3.1
Inspection work flow........................................................................
25
3.2
Checking the lamp ignition mode....................................................
27
3.3
Inspection of the power supply .......................................................
27
3.4
Checking the lamp hour indicator ...................................................
30
3.5
Inspection of the examination light..................................................
31
3.6
Inspection of brightness adjustment ...............................................
33
3.7
Inspection of the high intensity mode..............................................
37
3.8
Inspection of air and water feeding .................................................
39
3.9
Inspection of transillumination function ...........................................
41
3.10 Inspection of the NBI observation function .....................................
43
3.11 After inspection ...............................................................................
44
Chapter 3
EVIS EXERA II XENON LIGHT SOURCE CLV-180
Contents
Chapter 4
Operation..................................................................
45
4.1
Operation flow .................................................................................
48
4.2
Connection of an endoscope ..........................................................
50
4.3
Turning the light source ON and igniting the examination lamp......
53
4.4
Brightness adjustment ....................................................................
55
4.5
Adjusting air/water pressure............................................................
58
4.6
Using the transillumination function ................................................
59
4.7
Using the high intensity mode .........................................................
60
4.8
Using the NBI observation mode ....................................................
61
4.9
Extinguishing the examination lamp................................................
63
4.10 Turning the light source OFF ..........................................................
63
Chapter 5
Lamp and Fuse Replacement .................................
64
5.1
Replacement of the examination (xenon) lamp...............................
64
5.2
Fuse replacement ...........................................................................
72
Care, Storage and Disposal ....................................
74
6.1
Care ................................................................................................
74
6.2
Storage ...........................................................................................
75
6.3
Disposal ..........................................................................................
75
Installation and Connection....................................
76
7.1
Installation work flow .......................................................................
77
7.2
Installation of equipment .................................................................
78
7.3
Selecting the lamp ignition mode ....................................................
81
7.4
Installation of the water container ...................................................
83
7.5
Connection of the video system center ...........................................
84
7.6
Connection to the AC mains power supply .....................................
85
Troubleshooting ......................................................
87
8.1
Troubleshooting guide ....................................................................
87
8.2
Returning the light source for repair................................................
93
Appendix........................................................................................
95
System chart ............................................................................................
95
Transportation, storage and operating environments ...............................
98
Specifications ............................................................................................
99
EMC information........................................................................................
101
Chapter 6
Chapter 7
Chapter 8
ii
Labels and Symbols
Labels and Symbols

Safety-related labels and symbols are attached to the light source at the
locations shown below. If labels or symbols are missing or illegible, contact
Olympus.
Rear side
Electrical rating
Caution that only the
exclusive cable can be
connected.
The product name, rated voltage and

frequency are shown.
EVIS EXERA II XENON LIGHT SOURCE
MODEL OLYMPUS CLV-180
INPUT 100-120V
50/60Hz 500VA
CSA/UL marking
Fuse rating
Potential equalization
terminal
FUSES
T8AH250V
Serial number plate
Manufacturer name
Cautions that the inside is
extremely hot immediately
after the lamp is
extinguished.
Caution on lamp
replacement.
Labels and Symbols
Back cover of this instruction manual

Manufacturer
Authorized representative in the European Community
Important Information Please Read Before Use
Important Information Please Read

Before Use
Intended use
This light source has been designed to be used with Olympus endoscopes,
video system center, and other ancillary equipment for endoscopic diagnosis,
treatment and video observation.
Do not use this light source for any purpose other than its intended use.
Instruction manual
This instruction manual contains essential information on using this light source
safely and effectively. Before use, thoroughly review this manual and the
manuals of all equipment which 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

EVIS EXERA II video system center:
The EVIS EXERA II video system center is a device that converts signals
from a videoscope or camera head into monitor images.
Camera head:
The camera head is a device that converts endoscopic images from a
fiberscope or a rigidscope into monitor images.
Automatic brightness control:
The automatic brightness control automatically adjusts the intensity of the
light emitted from the light source so that the endoscopic image will be
maintained at constant brightness even if the distance between the distal
end of the endoscopes insertion tube and the subject changes.
Mobile workstation:
The mobile workstation is a special trolley on which this light source is
placed and used for endoscopic diagnosis and treatment.
Wall mains outlet:
The wall mains outlet is a wall AC mains power outlet socket with a
terminal used exclusively for grounding.
Isolation transformer:
The isolation transformer is a safety device that is used to isolate noninsulated equipment with potentially high leakage currents to decrease the
possibility of electric shock.
Transillumination function:
With this function, the distal end of the endoscope emits more intense
examination light, which transmits through the body wall tissue of the
patient and enables the operator to confirm the position of the distal end
from outside the patients body, provided that the operating room
illumination is low. This function is available only with EVIS videoscopes
and a few fiberscopes.
High intensity mode:
This mode emits brighter illumination light than usual. It is available only
with the endoscopes and light guide cables compatible with this mode.
Special light observation:
This is an observation using specific filtered light (e.g. NBI).
NBI (Narrow Band Imaging) observation:
NBI observation mode utilizes an optical filter, which filters the white light
spectrum, changing it from a broad band to a narrow band. The filter sets
the narrow bands to specific wavelengths within the green and blue
spectrum that are within the visible light spectrum.
User qualifications
If there is an official standard on user qualifications to perform endoscopy and
endoscopic treatment that is defined by the medical administration or other
official institutions, such as academic societies on endoscopy, follow that
standard. If there is no official qualification standard, the operator of this
instrument must be a physician approved by the medical safety manager of the
hospital or person in charge of the department (department of internal medicine,
etc.).
The physician should be capable of safely performing the planned endoscopy
and endoscopic treatment following guidelines set by the academic societies on
endoscopy, etc., and considering the difficulty of endoscopy and endoscopic
treatment. This manual does not explain or discuss endoscopic procedures.
Instrument compatibility
Refer to the System chart in the Appendix to confirm that this light source is
compatible with the ancillary equipment being used. Using incompatible
equipment can result in patient injury or equipment damage and makes it
impossible to obtain the expected functionality.
This instrument complies with the EMC standard for medical electrical
equipment; edition 2 (IEC 60601-1-2: 2001). However, when connecting to an
instrument that complies with the EMC standard for medical electrical
equipment; edition 1 (IEC 60601-1-2: 1993), the whole system complies with
edition 1.
Repair and modification

This light source does not contain any user-serviceable parts. Do not
disassemble, modify or attempt to repair it; patient or user injury and/or
equipment damage can result.
Some problems that appear to be malfunctions may be correctable by referring
to Chapter 8, Troubleshooting. If the problem cannot be resolved using the
information in Chapter 8, contact Olympus.
Signal words
The following signal words are used throughout this manual:
Indicates an imminently hazardous situation which, if not

avoided, will result in death or serious injury.
Indicates a potentially hazardous situation which, if not

avoided, could result in death or serious injury.
Indicates a potentially hazardous situation which, if not

avoided, may result in minor or moderate injury. It may also
be used to alert against unsafe practices or potential
equipment damage.
Indicates additional helpful information.
Dangers, warnings and cautions

Follow the dangers, warnings and cautions given below when handling this light
source. This information is to be supplemented by the dangers, warnings and
cautions given in each chapter.
Strictly observe the following precautions. Failure to do so

may place the patient and medical personnel in danger of an
electric shock.
When the light source is used to examine a patient, do not
allow metal parts of the endoscope or its accessories to
touch metal parts of other system components. Such
contact may cause unintended current flow to the patient.
Keep fluids away from all electrical equipment. If fluids are
spilled on or into the unit, stop operation of the light
source immediately and contact Olympus.
Do not prepare, inspect or use this light source with wet
hands.
Never install and operate the light source in locations where:

The concentration of oxygen is high.
Oxidizing agents (such as nitrous oxide (N2O)) are
present in the atmosphere.
Flammable anesthetics are present in the atmosphere.
Otherwise, explosion or fire may result because this light
source is not explosion-proof.
In case of instrument failure or malfunction, always keep

another light source in the room ready for use.
Never insert anything into the ventilation grills of the light

source. It can cause an electric shock and/or fire.
Although the illumination light emitted from the endoscopes

distal end is required for endoscopic observation and
treatment, it may also cause alteration of living tissues such
as protein denaturation of liver tissue and perforation of the
intestines through inappropriate use.
Observe the following warnings on the illumination.
Always set the minimum required brightness. The
brightness of the image on a video monitor may differ
from the actual brightness at the distal end of an
endoscope. Especially in combination with endoscopes
using an electrical shutter function, pay attention to the
brightness level setting of this instrument. When this
instrument is used with a video system center compatible
with automatic brightness control function, be sure to use
this function. The automatic brightness control can keep
the illumination at a proper level. Refer to the instruction
manual of the video system center for details.
Do not continue observation in the proximity to tissue or
keep the distal end of the endoscope in contact with living
tissue for a long time. It may cause patient burns.
When discontinuing the use of the endoscope, be sure to
turn this instrument OFF or extinguish the examination
lamp by pushing the lamp button.
Do not look directly into the distal end of the endoscope, the
distal end of the light guide cable or the output socket of the
light source while the light source is ON. The intense light
causes eye injury.
Do not touch the distal end of the light guide connector of the
endoscope, the distal end of the light guide cable or the
output socket of the light source immediately after removing it
from this instrument because they are extremely hot.
Operator or patient injury can result.
Xenon light sources produce significant heat due to the high

intensity light required for endoscopic procedures. If the
disconnected end of the light guide cable or the distal end of
an endoscope touches operating room drapes or other
flammable materials, fire can result.
Observe the following warnings:
Never place the unattached end of an illuminated light
guide cable on an operating room drape or other
flammable material.
Never allow the distal end of an illuminated endoscope to
come in contact with operating room drapes or other
flammable material.
Be sure to turn OFF the light source or extinguish the
examination lamp whenever the light source is not used.
This product may interfere with other medical electronic

equipment used in combination with it. Before use, refer to
the Appendix to confirm the compatibility of this instrument
with all equipment to be used.
Do not use this product in any place where it may be subject

to strong electromagnetic radiation (for example, in the
vicinity of a microwave therapeutic device, MRI, wireless set,
short-wave therapeutic device, cellular/portable phone, etc.).
This may impair the performance of the product.
If the endoscopic image dims during use, blood, mucus or

debris may adhere to the light guide on the distal end of the
endoscope. Carefully withdraw the endoscope from the
patient and remove the blood or mucus in order to obtain
optimum illumination and to ensure the safety of the
examination. If you continue to use the endoscope in such a
condition, the distal end temperature may rise and cause
mucosal burns. It may also cause patient and/or operator
injury.
Do not rely on the special light observation method alone for

primary detection of lesions or for a decision regarding any
potential diagnostic or therapeutic intervention.
For reasons described below, do not rely on the NBI imaging

modality alone for primary detection of lesions or to make a
decision regarding any potential diagnostic or therapeutic
intervention.
It has not been demonstrated to increase the yield or
sensitivity of finding any specific mucosal lesion including
colonic polyps or Barretts esophagus.
10
Do not use a pointed or hard object to press the buttons on

the front panel. This may damage the buttons.
Avoid applying excessive force to the connectors, as this

may damage the instrument.
Do not leave the examination lamp ON when an endoscope

is connected to the light source. The examination light
reaches the maximum intensity and the endoscopes distal
end becomes hot. In addition, smoke may also be produced
if the debris attached to the distal end is heated.
Avoid using this instrument in a dusty environment, as this

may damage the instrument.
Be sure that this instrument is not used adjacent to or

stacked with other equipment (other than the components of
this instrument or system) to avoid electromagnetic
interference.
Electromagnetic interference may occur to this instrument

when it is placed near equipment marked with the following
symbol or other portable and mobile RF communications
equipment such as cellular phones. If radio interference
occurs, mitigation measures may be necessary, such as
reorienting or relocating this instrument or shielding the
location.
If the emergency lamp, instead of the examination lamp,

lights up frequently when pressing the Lamp button to light
the examination lamp, this instrument may have already
malfunctioned.
Return the instrument for repair, following 8.2, Returning the
light source for repair on page 93.
As defined by the international safety standard (IEC 606011), medical electrical equipment is classified into the
following types: TYPE CF applied part (the instrument can
safely be applied to any part of the body, including the heart),
and TYPE B/BF applied part (the instrument can safely be
applied to any organ except the heart). The part of the body
that an endoscope or electrosurgical accessory can safely be
applied to depends on the classification of the equipment to
which the instruments are connected. Before beginning the
procedure, check the current leakage classification type of
each instrument to be used for the procedure. Classification
types are clearly specified in the instruments' instruction
manuals.
Symbol
Classification
TYPE CF applied part
TYPE BF applied part
TYPE B applied part
11
Cardiac applications
Use only the devices listed in the System chart in the

Appendix for endoscopic observation or treatment of the
heart or areas near the heart. Other combinations of
equipment may cause ventricular fibrillation or seriously
affect the cardiac function of the patient.
For cardiac applications, never support the endoscope with a

metal surgical arm which is not electrically isolated from the
ground. If not isolated, the endoscope will be connected to
the ground through the surgical arm and bed, and will
conduct unexpected leakage current which may seriously
affect the cardiac function of the patient.
The use of medical devices not specifically designed for

cardiac applications may cause ventricular fibrillation or
seriously affect the cardiac function of the patient. As
specified by the international standard IEC 60601-1, any
applied part used for observation or treatment of the heart or
areas near the heart must meet TYPE CF applied part
requirements for low electrical leakage current. When using
endoscopes for endoscopic cardiac applications, the applied
part requirements include all devices directly connected to
the endoscope, such as the light guide cable, camera head
and telescope holder. Each of these devices must
individually meet the TYPE CF applied part requirements
for leakage current limits if they are to be used for cardiac
applications.
The OLYMPUS light guide cables and camera heads listed in

the System chart in the Appendix (TYPE CF applied part)
which are suitable for cardiac applications bear a
12
mark.
Summary of the functions of the instrument
Summary of the functions of the

instrument
Some of the functions described below may be unavailable or restricted
depending on the ancillary equipment used with this instrument. Refer to the
instruction manuals for the light source and the required ancillary equipment for
details.
Illuminating the operation

The light of the examination lamp built into this instrument is provided to the
endoscope.
Section 4.3, Turning the light source ON and igniting the examination lamp
on page 53
Adjusting the examination light

When this instrument is used in combination with the EVIS EXERA II video
system center and a videoscope, the examination light intensity is adjusted
automatically.
When this instrument is used in combination with a fiberscope, the examination
light intensity has to be adjusted manually.
Section 4.4, Brightness adjustment on page 55
NBI observation
NBI observation is possible.
Section 4.8, Using the NBI observation mode on page 61
Selecting the high intensity mode

Brighter examination light is available by using an endoscope and light guide
that are compatible with high intensity mode operation.
Section 4.7, Using the high intensity mode on page 60
Air and water feed

This instrument incorporates an air pump and exclusive water feed tank for use
in feeding air and water from the nozzle at the endoscopes distal end to the
body cavity and adjusting the air/water flow.
Section 4.5, Adjusting air/water pressure on page 58
13
Summary of the functions of the instrument
Transillumination function
The endoscopes distal end emits the intense light. The light transmits through
the patients body wall so the operator can confirm the position of the distal end
from outside the patients body provided that the operating room illumination is
low.
Section 4.6, Using the transillumination function on page 59
Monitoring the operating hours of examination lamp

The lamp hour indicator on the front panel of this instrument displays the total
accumulated operating hours of the examination lamp to indicate the time for
replacement.
Section 3.4, Checking the lamp hour indicator on page 30
Automatic switching to emergency lamp

If the examination lamp does not light or blows in the middle of an examination
making endoscopic observation impossible, the light source switches
automatically to the emergency light. The emergency light provides enough
brightness for withdrawing the endoscope from the patients body.
Section 3.3, Inspection of the power supply on page 27 and Section 3.5,
Inspection of the examination light on page 31
14
Chapter 1 Checking the Package Contents
Chapter 1 Checking the Package

Contents
Match all items in the package with the components shown below. Inspect each
item for damage. If the light source is damaged, a component is missing or you
have any questions, do not use the light source; immediately contact Olympus.
EVIS EXERA II xenon light source

(CLV-180)
Light source cable

(MAJ-1411)
Power cord
Foot holder
(MAJ-1205, 4 pcs.)
Spare fuse
(MAJ-1412, 2 pcs.)
Instruction manual
15
Chapter 2 Nomenclature and Functions

2.1
Front panel
2. Power indicator
3. Output socket
1. Power switch
Control panel
Refer to the next page.
1. Power switch
Press to turn the light source ON or OFF.
2. Power indicator
Lights up when the light source is ON.
3. Output socket
This socket provides light and air to the endoscope.
16
Control panel (buttons)
1. Transillumination button
3. Filter mode button
2. High intensity mode button
4. Air feed button
5. Airflow regulator button
6. Brightness adjustment
buttons
8. Lamp button
7. Auto/manual (AUTO/MAN.)
brightness button
9. Reset button
17
1. Transillumination button
When this buttonis pressed, light emitted from the endoscopes distal end
becomes brighter for 7 seconds, then returns automatically to its original
brightness level.
2. High intensity mode button
Press to switch between the high intensity mode and normal intensity mode
when using an endoscope compatible with the high intensity mode.
3. Filter mode button
Pressing this button activates the NBI observation function.
4. Air feed button
Pressing this button starts or stops air feeding from the endoscopes distal
end.
5. Airflow regulator button
This button is used to control the air pressure being fed from the endoscope.
6. Brightness adjustment buttons
These buttons are pressed to adjust the brightness level.
7. Auto/manual (AUTO/MAN.) brightness button
This button is pressed to select automatic or manual brightness control.
8. Lamp button
This button is pressed to turn ON or OFF the examination (xenon) lamp.
Section 4.3, Turning the light source ON and igniting the examination
lamp on page 53
Section 4.9, Extinguishing the examination lamp on page 63
9. Reset button
After replacing the examination (xenon) lamp, the lamp hour indicator is
reset by pressing this button for at least 3 seconds.
Lamp hour indicator reset on page 71
18
Control panel (indicators)
1. Transillumination indicator
3. Air feed ON/OFF indicator
2. High intensity
mode indicator
4. Special light observation mode indicators
5. Airflow regulator indicator
6. Emergency lamp
indicator
7. Brightness level indicator
8. Auto/manual (AUTO/MAN.)
indicator
10. Lamp hour indicator
9. Lamp ON/OFF indicator
19
1. Transillumination indicator
This indicator lights when the transillumination function is activated.
2. High intensity mode indicator
This indicator lights when high intensity mode is selected.
3. Air feed ON/OFF indicator
These indicators display whether the air feeding function is activated (ON)
or not (OFF).
4. Special light observation mode indicators
This indicator lights in green to indicate that the light source can perform the
special light observation and turns white when the special light observation
mode is active.
NBI shows the NBI observation. The OP.1 and OP.2 indicators are
reserved for future system expansion.
5. Airflow regulator indicator
These indicators display the current airflow pressure level setting (L (low),
M (medium) or H (high)).
6. Emergency lamp indicator
This indicator lights when the emergency lamp (halogen) is in use, and
blinks when the emergency lamp (halogen) is disconnected or not mounted.
Section 3.3, Inspection of the power supply on page 27
Section 3.5, Inspection of the examination light on page 31
7. Brightness level indicator
These indicators display the current brightness level.
8. Auto/manual (AUTO/MAN.) indicator
This indicator displays the brightness adjustment setting (AUTO or
MAN.).
9. Lamp ON/OFF indicator
These indicators display whether the examination lamp (xenon lamp) lights
(ON) or not (OFF).
Section 4.3, Turning the light source ON and igniting the examination
lamp on page 53
Section 4.9, Extinguishing the examination lamp on page 63
20
10. Lamp hour indicator

This indicator displays the total working hours of the examination (xenon)
lamp.
21
2.2
Rear and side panels

5. Lamp ignition mode switch
6. Foot switch terminal

4. CV terminal
7. Water container holder
3. System terminal
2. Fuse box
1. AC power inlet
8. Potential equalization
terminal
Ventilation grills
Rear foot
Rear panel
Lamp chamber
9. Lamp cover
Knobs
Left side
22
1. AC power inlet
Connect the provided power cord to supply the AC power via this inlet.
2. Fuse box
The fuses protect the light source from electrical surges.
Section 5.2, Fuse replacement on page 72
3. System terminal
The terminal is the receptacle for the communication cable (MAJ-202) for
use with the endoscopic surgical system.
4. CV terminal
This terminal is the receptacle for the light source cable to connect the light
source to the EVIS EXERA II video system center.
Section 7.5, Connection of the video system center on page 84
5. Lamp ignition mode switch
This selector is set to automatic or manual ignition of the examination lamp.
When the automatic ignition is selected, turning ON the light source lights
the examination lamp simultaneously. When the manual ignition is selected,
pushing the lamp button on the control panel lights the examination lamp.
Section 7.3, Selecting the lamp ignition mode on page 81
6. Foot switch terminal
(Unavailable)
7. Water container holder
This holder is used for the installation of the water container.
Section 7.4, Installation of the water container on page 83
8. Potential equalization terminal
This terminal is connected to a potential equalization terminal of the other
equipment connected to this instrument. The electric potential of the
equipment are made equal.
9. Lamp cover
This cover has to be removed to replace the examination lamp.
Removing the lamp on page 66
23
Chapter 3 Inspection
Review Chapter 7, Installation and Connection thoroughly,

and prepare the instruments properly before inspection. If the
equipment is not properly prepared before each use,
equipment damage, patient and operator injury and/or fire
can occur.
Before each procedure, inspect this light source as instructed

below. Inspect other equipment to be used with this light
source as instructed in their respective instruction manuals.
Should any irregularity be observed, do not use the light
source and see Chapter 8, Troubleshooting. If the
irregularity is still observed after consulting Chapter 8,
contact Olympus. Damage or irregularity may cause electric
shock, burns and/or fire.
Do not leave the examination lamp ON before and/or after

inspection. The distal end temperature of the endoscope may
rise and cause patient and/or operator injury.
Inspect the light source and other equipment to be used with the light source.
Refer to the respective instruction manuals for each piece of equipment.
24
3.1
Inspection work flow

Please see the inspection work flow in Figure 3.1 below. Follow each step of the
work flow for inspection of the light source before use.
1. Check the lamp ignition mode.

Section 3.2, Checking the lamp ignition mode on page 27
2. Confirm that the light source is turned ON normally.

Section 3.3, Inspection of the power supply on page 27
3. Check the total accumulated operating hours of the examination lamp.

4. Confirm that the examination lamp turns ON/OFF normally.

Section 3.5, Inspection of the examination light on page 31
5. Confirm that the brightness of the examination light is adjustable.

Section 3.6, Inspection of brightness adjustment on page 33
6. Inspect the necessary functions (available with the connected endoscope).

High intensity mode
Section 3.7, Inspection of the high intensity mode on page 37
Air/water feeding
Section 3.8, Inspection of air and water feeding on page 39
Transillumination
Section 3.9, Inspection of transillumination function on page 41
NBI observation
Section 3.10, Inspection of the NBI observation function on page 43
continued on next page
25
7. After inspection
Section 3.11, After inspection on page 44
Turn the examination lamp OFF if the light source will not be used immediately.
Figure 3.1
26
3.2
Checking the lamp ignition mode

Check the lamp ignition mode set, manual ignition or auto ignition (refer to
Section 7.3, Selecting the lamp ignition mode on page 81).
The factory default setting is the manual ignition.
3.3
Inspection of the power supply

If the auto ignition is set, turning ON the light source ignites
the examination lamp automatically. Do not look directly into
the distal end of the endoscope or the output socket of the
light source when they are emitting light. Eye injury may
result.
1.
Confirm that the ventilation grills on the bottom and rear panels of the light
source are not covered with dust or other materials.
2.
Confirm that the lamp cover is closed firmly.
For safety reasons, a lamp cover that is not firmly closed will
prevent the light source from being turned ON.
3.
Press the power switch of the light source with no endoscope connected.
The power indicator lights up (see Figure 3.2).
Power indicator
Control panel
Power switch
Figure 3.2
4.
Confirm that the indicators on the control panel light up normally. If the
indicators on the control panel blink, the light source is not working properly.
Contact Olympus.
27
5.
Press again the power switch to turn the light source OFF.
6.
Connect an endoscope to the light source.
Refer to Section 4.2, Connection of an endoscope on

page 50 for connecting an endoscope.
7.
Press the power switch of the light source. The power indicator lights up
(see Figure 3.3).
Power indicator
Power switch
Figure 3.3
8.
Confirm that air is exhausted by holding your hand in front of the ventilation
grills on the rear panel.
If the exhaust does not emit air, do not use the light source
and contact Olympus.
If the power fails to come ON

If the power fails to come ON, turn the light source OFF. Then, confirm that the
power cord is connected firmly and that the lamp cover is firmly closed. Then,
turn the light source ON again. If the power fails to come ON, replace the fuses
with new ones as described in Section 5.2, Fuse replacement on page 72. If
the power still fails to come ON, contact Olympus.
28
If the emergency lamp indicator lights up

If the emergency lamp indicator lights up, turn the light source OFF and then ON
again and try to ignite the examination lamp again. If the emergency lamp
indicator still lights up, replace the examination lamp with a new one as
described in Section 5.1, Replacement of the examination (xenon) lamp on
page 64. If the emergency lamp indicator still lights up, contact Olympus.
If the emergency lamp, instead of the examination lamp,

lights up frequently when pressing the Lamp button to light
the examination lamp, this instrument may have already
malfunctioned.
Return the instrument for repair, following 8.2, Returning the
light source for repair on page 93.
Pressing the lamp button when the examination lamp is OFF

or turning the light source ON when the auto ignition is active
automatically tries to ignite the examination lamp for
5 seconds. If ignition fails, the light source automatically
switches to the emergency lamp and the emergency lamp
indicator lights up.
If the emergency lamp indicator blinks

If the emergency lamp indicator blinks, the installed emergency lamp is not
working properly. Contact Olympus.
If the indicators on the control panel blink

If the indicators on the control panel blink, the light source is not working
properly. Contact Olympus.
29
3.4
Checking the lamp hour indicator

Check the lamp hour indicator.
When the 500 h indicator on the lamp hour indicator lights up or when the lamp
light intensity has lessened from when the lamp was new even if the indicator
does not light up, replace the examination lamp with a new one as described in
Section 5.1, Replacement of the examination (xenon) lamp on page 64 (see
Figure 3.4).
The lamp hour indicator displays the total working hours of

the examination (xenon) lamp (e.g. 500 h means
500 hours).
Lamp hour indicator
500 h
Figure 3.4
30
3.5
Inspection of the examination light

Do not look directly into the distal end of the endoscope or
the output socket of the light source when they are emitting
light. Eye injury may result.
1.
Press the lamp button if the examination lamp is OFF and confirm that the
lamp ON indicator lights up (see Figure 3.5).
Lamp ON/OFF indicator
ON lights.
Lamp button
Figure 3.5
2.
Confirm that the examination light is emitted from the distal end of the
endoscope (see Figure 3.6).
Distal end of endoscope
Examination light
Figure 3.6
3.
Press and hold the lamp button for one second. The lamp ON/OFF indicator
is turned OFF.
4.
Confirm that the examination light is not emitted from the distal end of the
endoscope.
31
If the emergency lamp indicator lights up

If the emergency lamp indicator lights up, turn the light source OFF and then ON
again and try to ignite the examination lamp again. If the emergency lamp
indicator still lights up, replace the examination lamp with a new one as
described in Section 5.1, Replacement of the examination (xenon) lamp on
page 64.
Pressing the lamp button when the examination lamp is OFF

or turning the light source ON when the auto ignition is active
automatically tries to ignite the examination lamp for
5 seconds. If ignition fails, the light source automatically
switches to the emergency lamp and the emergency lamp
indicator lights up.
32
3.6
Inspection of brightness adjustment

When using a fiberscope or a rigidscope without camera
head, set the AUTO/MAN. brightness button to MAN..
Setting to AUTO does not enable the automatic brightness
adjustment, and the brightness may not be adequate.
Selecting automatic or manual brightness control

Press the AUTO/MAN. brightness button and confirm that the auto/manual
modes are switched between AUTO and MAN. with a short beep.
Confirm that the AUTO indicator lights when the auto adjustment mode is
selected and the MAN. indicator lights when the manual adjustment mode is
selected (see Figure 3.7).
AUTO/MAN. indicators
AUTO/MAN. brightness button
Figure 3.7
Automatic brightness adjustment

When disconnecting the camera head from the endoscope
without turning the lamp OFF, make sure that the brightness
adjustment mode selector button is set to MAN. and that
the light intensity adjustment button is set to the minimum
examination light intensity. If the camera head is
disconnected while the brightness adjustment mode selector
button is set to AUTO, the intense light may cause eye
injury.
Before inspection, connect the videoscope to the video system center, or
connect the fiberscope or rigidscope with the camera head to the video system
center.
33
1.
Press the AUTO/MAN. brightness button and select AUTO.
Turning OFF the video system center does not enable the
automatic brightness adjustment. If this function is not
activated, the brightness may be insufficient..
2.
Point the distal end of the endoscope at a suitable object and vary the
distance between 5 and 60 mm (see Figure 3.8). Confirm that the light being
emitted from the distal end varies with the distance.
5 - 60 mm
Figure 3.8
3.
Hold the distal end of the endoscope at a distance between 30 and 40 mm

to the object and press the brightness adjustment buttons (
or
).
Confirm the following (see Figure 3.9):
Each time either of the brightness adjustment buttons is pressed, a

beep is heard and the brightness level increases or decreases
accordingly. The present brightness level is indicated and the indicator
moves one level up or down.
When either of the brightness adjustment buttons is pressed

continuously, successive beeps are heard and one of the brightness
level indicator moves continuously.
Each time either of the brightness adjustment buttons is pressed, the

brightness of the endoscopic image increases or decreases.
The brightness indication is interlocked with the brightness

level indication of the video system center connected. When
the brightness adjustment buttons on the video system
center are pressed, the brightness indication on the light
source changes accordingly.
34
AUTO lights.
Brightness level indicator
Brightness adjustment buttons
Figure 3.9
Manual brightness adjustment

When the light source is combined with a fiberscope or a rigidscope, perform the
following inspection.
When using manual brightness adjustment, always set the

brightness to the minimum level necessary to complete the
examination. If the light is too bright, eye injury or burns can
result.
When switching the normal intensity mode to high intensity

mode, be sure to set the brightness level to or below 0.
Otherwise, the brightness will exceed the necessary level. It
may result in operator and/or patient injury.
1.
Press the AUTO/MAN. brightness button and select MAN..
2.
Press the brightness adjustment buttons (
or
) and confirm the
following (see Figure 3.10):
Each time either of the brightness adjustment buttons is pressed, a

beep is heard and the brightness level increases or decreases
accordingly. The present brightness level is indicated and the indicator
moves one level up or down.
When either of the brightness adjustment buttons is pressed down

continuously, successive beeps are heard and one of the brightness
level indicator moves continuously.
The brightness of the light emitted from the distal end of the endoscope
increases or decreases.
35

level indication of the video system center connected. When
the brightness adjustment buttons on the video system
center are pressed, the brightness indication on the light
source changes accordingly.
MAN. lights.
Figure 3.10
36
3.7
Inspection of the high intensity mode

The high intensity mode is not available when no endoscope
is connected to the light source. The function is available only
when a compatible endoscope is connected.
1.
Press the AUTO/MAN. brightness button and confirm that the MAN.
indicator lights (see Figure 3.11).
2.
Press the brightness control buttons to set the brightness level to 0.
3.
Connect an endoscope compatible with high intensity mode to the output

socket on the light source.
4.
Press the intensity mode button to change the normal mode to high intensity
mode (see Figure 3.11).
5.
Confirm that the high intensity mode indicator lights and the light emitted
from the endoscopes distal end increases compared to the normal mode.
6.
Press the intensity mode button to switch to the normal intensity mode.
7.
Confirm that the high intensity mode indicator goes out and the light emitted
from the endoscopes distal end decreases compared to the high intensity
mode.
8.
Press the intensity mode button again and confirm that the high intensity
mode is restored.
9.
Disconnect the endoscope. Confirm that the high intensity mode indicator
still lights.
10.
Turn the light source OFF and turn it ON again. Confirm that the high
intensity mode indicator lights.
11.
Connect the endoscope compatible with the high intensity mode to the
output socket on the light source again. Confirm that the high intensity mode
indicator still lights.
12.
Press the AUTO/MAN. brightness button and confirm that the AUTO
indicator lights.
37
Intensity mode
button
High intensity
mode indicator
Brightness level
indicator
AUTO/MAN.
brightness button
MAN. lights.
Brightness
adjustment buttons
Figure 3.11
The following endoscopes and light guide cables are

compatible with the high intensity mode:
Light guide cable
A3290, A3291, A3292, A3293, A3294, A3295, A3296,
A3297, A3298
Fiberscope
CHF TYPE CB30L/S,
URF TYPE P3
Videoscope
LTF TYPE V3/VP,
A50001A, A50003A, A50021A, A50023A,
WA50A series, WA50L series
38
This instrument includes a memory function for the intensity

mode, which stores the intensity setting being used when the
light source is turned OFF. Therefore, the user may start the
next operation with the same setting used when the light
source was turned OFF. The default setting of this function is
normal intensity.
3.8
Inspection of air and water feeding

The air and water feeding function is not available when no
endoscope is connected to the light source. The function is
available only when a compatible fiberscope or videoscope is
connected.
When using a water container to feed water from the endoscope, inspect the air
and water feeding functions as follows:
1.
Confirm that the airflow ON indicator lights. If OFF lights, press the
airflow button and confirm that a short beep is heard and the indicator lights
up.
2.
Then press the airflow regulator button repeatedly and confirm that the
indication of the airflow regulator indicator is switched in the cycle of L
(low), M (medium) and H (high) (see Figure 3.12).
Airflow ON/OFF
indicator
Airflow button
Airflow regulator indicator
Airflow regulator button
Figure 3.12
3.
When the light source is turned OFF, the airflow regulator

setting is automatically stored and recalled when the light
source is turned ON again.
The factory setting of the airflow level is H (high).
Set the airflow level to H, immerse the distal end of the connected
endoscope in sterile water and operate the endoscopes insufflation function
following the instructions given in the endoscopes instruction manual.
39
4.
Block the hole of the air/water valve so that air bubbles are emitted. Press
the airflow button and confirm that the bubbles from the air/water nozzle
stop (see Figure 3.13).
Air/water valve
Sterile water
Figure 3.13
5.
Block the hole of the air/water valve so that air bubbles are emitted. Press
the airflow regulator button and confirm that the lighting airflow regulator
indicator changes to the indicator for the higher level (except that the L
level indicator lights after the H level indicator), and that the amount of
bubbles from the air/water nozzle vary corresponding to the airflow level
setting (see Figure 3.13).
6.
Remove the distal end of the endoscope from the sterile water and operate
the endoscopes water feeding function following the instructions given in
the endoscopes instruction manual. Confirm that the amount of water
emitted from the air/water nozzle varies corresponding to the airflow level
setting (see Figure 3.13).
40
3.9
Inspection of transillumination function

Do not use the transillumination function while looking
through the eyepiece of a fiberscope. Otherwise, the
maximum light intensity may injure your eyes.
The transillumination function is not available when no

connected.
1.
Press the transillumination button (see Figure 3.14).

Transillumination indicator
Blinks.
Transillumination button
Figure 3.14
41
2.
Confirm that:
A beep is heard.
The transillumination indicator on the front panel blinks.
Brightness is set to maximum for manual brightness control (see Figure

3.15).
After 7 seconds, the light returns to its original brightness.
Distal end of
endoscope
Figure 3.15
Pressing the transillumination button while the

transillumination function is active cancels the function and
returns to the original setting. Also, pressing any lighted
button on the control panel cancels the transillumination
function and the function returns to the original setting.
The following endoscopes are compatible with the

transillumination function:
EVIS series videoscope
OES 10/20/30/40 series
OES E/E3 series
42
3.10 Inspection of the NBI observation function

The conditions that must be present for NBI observation are as follows:
1.
The video system center is connected to the light source.
An NBI compatible endoscope is connected to the light source and the

video system center.
The video system center is ON.
Confirm that the filter mode button lights and the NBI indicator lights in
green (see Figure 3.16).
2.
Press the filter mode button. The color of the NBI indicator turns white and
the color of the examination light emitted from the endoscope distal end is
changed.
Filter mode button
NBI indicator
Figure 3.16
43
3.11 After inspection

After the inspection described on the previous pages, press the lamp button for
one second to turn the examination lamp OFF if the light source will not be used
immediately (see Figure 3.17).
If the light source will not be used for a while, turn the light source OFF (refer to
Section 4.10, Turning the light source OFF on page 63).
Lamp button
Figure 3.17
44
Chapter 4 Operation
Chapter 4 Operation
This chapter explains the work flow of endoscopic observation using the light
source.
The operator of this instrument must be a physician or medical personnel under
the supervision of a physician and must have received sufficient training in
clinical endoscopic technique. This manual, therefore, does not explain or
discuss clinical endoscopic procedures. It only describes basic operation and
precautions related to the operation of this instrument.
Be sure to wear protective equipment such as eye wear, face

mask, moisture-resistant clothing and chemical-resistant
gloves that fit properly and are long enough so that your skin
is not exposed. Otherwise, dangerous chemicals and/or
potentially infectious material such as blood and/or mucus of
the patient may cause an infection.
Should any irregularity be observed, do not use the light

source. Damage or irregularity may cause electric shock,
burns and/or fire.
Anytime you observe an abnormality in a light source

function, stop the examination immediately and take action
according to the following procedures. Using a defective light
source may cause patient and/or operator injury.
After withdrawing the endoscope from the patient, refer to the
instructions in Chapter 8, Troubleshooting. If the problem
cannot be resolved by the remedial action as described in
Chapter 8, do not use this light source and immediately
contact Olympus.
If the image on the monitor becomes completely white or
black when the automatic brightness adjustment is
selected, the automatic brightness adjustment may be
malfunctioning. In this case, set the AUTO/MAN.
brightness button to MAN. and adjust the brightness
manually. Withdraw the endoscope from the patient
slowly as described in the endoscopes instruction
manual.
45
Chapter 4 Operation
If the examination lamp fails and the emergency lamp

lights, withdraw the endoscope from the patient slowly as
described in the endoscopes instruction manual.
If any other abnormality occurs or is suspected, stop
using the equipment and immediately withdraw the
endoscope from the patient slowly as described in the
endoscopes instruction manual.
46
Turn the light source OFF or extinguish the examination lamp

while not using the light source. Leaving the examination
lamp ON will cause the distal end of the endoscope to
become hot and could cause operator and/or patient burns.
Use only Olympus high-frequency electrosurgical equipment

with this unit. Non-Olympus equipment can cause instability
of the automatic brightness adjustment.
Before using high-frequency electrosurgical equipment,

make sure that the noise does not affect the observation and
surgical procedures. If high-frequency electrosurgical
equipment is used without such confirmation, patient injury
may result.
When using spray-type medical agents such as lubricant,

anesthetic, or alcohol, use them away from the light source
so that the medical agents do not contact the light source.
Medical agents might enter the light source through the
ventilation grills and may cause equipment damage.
Do not use a humidifier near the light source as dew

condensation possibly might occur and it may cause
equipment failure.
If the endoscopic image seems to be dark in the special light

observation, change to the normal observation. Otherwise,
the examination might not be performed safely.
Chapter 4 Operation
Set the brightness of the examination light to the minimum

necessary to perform the procedure safely. If the endoscope
is used for a prolonged period at or near maximum light
intensity, vapor like smoke may be observed in the
endoscopic image. This is caused by the evaporation of
organic material (remaining blood, moisture of stool and so
on) due to heat generated by the light guide near the light
guide lens. If this vapor continues to interfere with the
examination, remove the endoscope, wipe the distal end of
the endoscope with a lint-free cloth moistened with 70% ethyl
or isopropyl alcohol, reinsert the endoscope and continue the
examination.
47
Chapter 4 Operation
4.1
Operation flow
Please see the operation work flow in Figure 4.1 below. Follow each step of the
work flow for using the light source.
1. Connect an endoscope.
Section 4.2, Connection of an endoscope on page 50
2. Inspect the light source and the ancillary equipment.

Chapter 3, Inspection on page 24
3. Turn the light source ON and ignite the examination lamp.

Section 4.3, Turning the light source ON and igniting the examination lamp on page 53
4. Operate the light source (available with the connected endoscope).

Adjusting the examination light
Air and water feeding
Transillumination
High intensity mode
NBI observation
5. After examination, extinguish the examination lamp or turn the light source OFF.
Section 4.9, Extinguishing the examination lamp on page 63 or Section 4.10, Turning the light source
OFF on page 63
6. Disconnect the endoscope.
continued on next page
48
Chapter 4 Operation
7. Reprocess and store the instrument and ancillary equipment as appropriate after use.
Section 6.1, Care on page 74
Figure 4.1
49
Chapter 4 Operation
4.2
Connection of an endoscope
Do not look directly into the distal end of the endoscope, the
distal end of the light guide cable or the output socket of the
light source while the light source is ON. The intense light
may injure your eyes.
Do not touch the distal end of the light guide connector of the
endoscope, the distal end of the light guide cable or the
output socket of the light source immediately after removing it
from this instrument because they are extremely hot.
Operator or patient injury can result.
Xenon light sources produce significant heat due to the high

intensity light required for endoscopic procedures. If the
disconnected end of the light guide cable or the distal end of
an endoscope touches operating room drapes or other
flammable materials, fire can result.
Observe the following warnings:
Never place the unattached end of an illuminated light
guide cable on an operating room drape or other
flammable material.
Never allow the distal end of an illuminated endoscope to
come in contact with operating room drapes or other
flammable material.
Be sure to turn OFF the light source or extinguish the
examination lamp whenever the light source is not used.
50
Before connecting the endoscope connector to the light

source, make sure that it is completely dry. Otherwise,
electric shock or equipment damage can result.
Chapter 4 Operation
Connection of a rigidscope
Connect equipment in the order described below. If
connections are made in the wrong order, the light emitted
from the distal end of the light guide cable may pose the
following risks:
Operator and/or patient injury.
It may ignite flammable material such as an operating
room drape, which can cause a fire.
1.
Connect the light guide cable to the rigidscope.
2.
Insert the light guide connector into the output socket on the front panel of
the light source until it stops (see Figure 4.2).
Figure 4.2
51
Chapter 4 Operation
Connection of a flexible endoscope

Insert the endoscope connector or light guide connector into the output socket
on the front panel of the light source until it stops (see Figure 4.3).
The connector design varies depending on the endoscope model.
Figure 4.3
52
Chapter 4 Operation
4.3
Turning the light source ON and igniting the

examination lamp
When turning ON the light source, never allow the distal end
of an endoscope or a light guide cable to come in contact
with the patient, operating room drapes, and/or other
flammable material. Patient injury and/or fire can result.
Be careful and avoid accidentally pressing the power switch

or lamp button. Otherwise, the endoscopic image may
suddenly darken.
1.
Confirm that the endoscope connector is connected to the output socket of

the light source.
2.
Press the power switch of this instrument to turn it ON (see Figure 4.4).
If the automatic ignition is selected, the examination lamp is turned ON. If
the manual ignition is selected, pressing the lamp button turns the
examination lamp ON. Confirm that the lamp ON indicator lights up (see
Figure 4.5).

Output socket
Power switch
Figure 4.4
53
Chapter 4 Operation
Lamp ON/OFF indicator

ON lights.
Figure 4.5
54
Chapter 4 Operation
4.4
Brightness adjustment
When using a fiberscope or a rigidscope without camera
head, set the AUTO/MAN. brightness button to MAN..
Setting to AUTO does not enable the automatic brightness
adjustment, and the brightness may not be adequate.
When switching from the normal intensity mode to high

intensity mode, be sure to set the brightness level to or below
0. Otherwise, the brightness will exceed the necessary level.
It may result in operator and/or patient injury.
Automatic brightness adjustment

When disconnecting the camera head from the endoscope
without turning the lamp OFF, make sure that the brightness
adjustment mode selector button is set to MAN. and that
the light intensity adjustment button is set to the minimum
examination light intensity. If the camera head is
disconnected while the brightness adjustment mode selector
button is set to AUTO, the intense light may injure your
eyes.
Turn the video system center ON to enable the automatic

brightness adjustment function of the light source. If the video
system center is OFF, the automatic brightness adjustment is
not enabled and the brightness may not be adequate.
55
Chapter 4 Operation
1.
Press the AUTO/MAN. brightness button to select the automatic brightness

adjustment (see Figure 4.6).
AUTO lights.

Figure 4.6
2.
Press either of the brightness adjustment buttons (
or
) to set the
brightness to a level suitable for observation. The standard setting is 0.

level indication of the connected video system center (CV180). When the brightness adjustment buttons on the video
system center are pressed, the brightness indication on the
light source varies in an interlocked operation.
Depending on the endoscopic system being used and the

part being observed, the standard setting may be too bright
or too dark. In this case, adjust the brightness as needed.
This can also be done during observation, if necessary.
Pressing either of the brightness adjustment buttons (
) once moves the level one step; pressing the button
continuously moves the level continuously.
56
or
Chapter 4 Operation
Manual brightness adjustment
1.
Always adjust the brightness to the minimum level required

for observation. Do not allow the endoscope to come in
contact with a mucous membrane for a long period of time.
Use of higher brightness than required may cause eye injury
or burns to the tissue.

Press the AUTO/MAN. brightness button to select manual brightness

adjustment (see Figure 4.7).
MAN. lights.

Figure 4.7
2.
Press either of the brightness adjustment buttons (
or
) to set the
brightness to a level suitable for observation.
Pressing either of the brightness adjustment buttons (
or
) once increases or decreases the level one step;
pressing the button continuously increases or decreases the

level continuously.
57
Chapter 4 Operation
4.5
Adjusting air/water pressure

1.
Confirm that the airflow ON indicator lights. If not, press the airflow button
(see Figure 4.8).
Airflow ON/OFF indicator
Airflow regulator indicator
ON lights.
Airflow button
Airflow regulator button
Figure 4.8
2.
Press the airflow regulator button to select the L (Low), M (Medium) or

H (High) airflow level.
3.
The standard air pressure is H (High).
The air and water feeding function is not available when no

connected.
Change the air pressure according to the examination technique or the

patients condition.
4.
Feed water or air as described in the endoscopes instruction manual.
5.
Pressing the airflow button stops air feeding from the light source.
The airflow level setting is automatically stored in memory

when the light source is turned OFF or the airflow button is
pressed to stop the airflow. The airflow level is set to the
saved level when the light source is turned ON again.
58
Chapter 4 Operation
4.6
Using the transillumination function
Do not use the transillumination function unless absolutely

necessary. Otherwise, eye injury or burns can result.

The transillumination function is not available when no

connected.
Refer to Section 3.9, Inspection of transillumination function
on page 41 for the compatible endoscopes.
1.
Press the transillumination button. The transillumination indicator blinks and

the examination light is set automatically to the maximum intensity (see
Figure 4.9).
Transillumination indicator
Blinks.
Transillumination button
Figure 4.9
2.
After about 7 seconds, the transillumination indicator is extinguished and

the examination light returns to the original intensity setting. To end the
transillumination before the end of the 7 second period, press the
transillumination button again or press any lighted button on the control
panel.
When transillumination is returned to normal observation, it

may be difficult to confirm the position of the endoscope
inside the patients body depending on the position of
observation.
59
Chapter 4 Operation
4.7
Using the high intensity mode

The high intensity mode is not available when no endoscope
is connected to the light source. The function is available only
when a compatible endoscope is connected.
Refer to Section 3.7, Inspection of the high intensity mode
on page 37 for the compatible endoscopes.
1.
Press the intensity mode button. The high intensity mode indicator lights
and the intensity of the examination light becomes automatically high (see
Figure 4.10).
Intensity mode button
High intensity mode indicator
Figure 4.10
2.
60
To engage the normal mode, press the intensity mode button again.
Chapter 4 Operation
4.8
Using the NBI observation mode
If the endoscopic image seems to be dark in the NBI

observation, change to the normal observation. Otherwise,
an improper image may be obtained.
Do not rely on the special light observation method alone for

primary detection of lesions or for a decision regarding any
potential diagnostic or therapeutic intervention.
The conditions that must be present for NBI observation are as follows:
The video system center is connected to the light source.
An NBI compatible endoscope is connected to the light source and the

video system center.
The video system center is ON.
All mucosal areas are to be viewed using traditional white light.

NBl imaging should not be used as a substitute for a thorough traditional
examination of the mucosa.
1.
Confirm that the filter mode button lights and the NBI indicator lights in
green (see Figure 4.11).
Filter mode button
NBI indicator
Green
Figure 4.11
2.
In Figure 4.11, normal observation is active.
61
Chapter 4 Operation
3.
Press the filter mode button. The color of the NBI indicator turns white (see
Figure 4.12).
Filter mode button
NBI indicator
White
Figure 4.12
4.
In Figure 4.12, NBI observation is active.
5.
To return to the normal observation, press the filter mode button again. The
color of the NBI indicator turns green.
62
An endoscopes scope switch set by the video system center

enables the function as well.
The NBI indicator lights in conjunction with the indicator of

the video system center.
Chapter 4 Operation
4.9
Extinguishing the examination lamp

To extinguish the examination lamp, press and hold the lamp button for one
second (see Figure 4.13), or turn the light source OFF (refer to Section 4.10,
Turning the light source OFF on page 63).
Lamp button
Figure 4.13
4.10 Turning the light source OFF

1.
Press the power switch to turn the light source OFF. The power indicator is
extinguished (see Figure 4.14).
Power indicator
Power switch
Figure 4.14
2.
If the light source is not to be used for an extended period of time,

disconnect the power cord.
63
Chapter 5 Lamp and Fuse Replacement

5.1
Replacement of the examination (xenon) lamp

Always use the examination lamp designated below. To order new examination
lamp, contact Olympus.
Xenon short-arc lamp
64
MD-631
Never install a lamp that has not been approved by Olympus.

The use of a non-approved lamp can cause damage to the
light source and ancillary equipment, malfunction or fire.
Turn the light source OFF and remove the power cord from
the wall mains outlet before replacing the lamp with a new
one. Otherwise, electric shock may result.
Do not touch anything inside the lamp chamber. The lamp

chamber is extremely hot immediately after the lamp is
turned OFF.
When replacing the lamp, do not leave any objects (such as

a cloth) inside the lamp chamber. Fire and/or equipment
damage can result.
Do not apply shock, excessive force or scratches to the lamp.

It could break the glass and/or shorten the lamp life due to
the high internal pressure of the lamp.
Store the hexagon wrench securely on the back side of the

lamp cover. If the wrench falls inside the light source, turn
OFF the light source immediately, disconnect the power cord
and contact Olympus. If the light source is used while the
wrench is left inside the light source, equipment damage
and/or electric shock can result.
When disposing of the used lamp, make sure to cut the

projection part of the electrode on the + side of the
examination lamp by using a nipper and discharge the
internal gas (see Figure 5.1). Otherwise, the glass could
break due to the high internal pressure of the lamp.
When cutting the projection part of the electrode on the +

side of the examination lamp, wear appropriate protection
equipment at all times and be sure to cover the lamp with a
cloth. Otherwise, the projection could burst and scatter in all
direction, possibly causing injury. The protective equipment
may include eye wear, face mask and gloves.
Projection part
Pin
Examination lamp
Figure 5.1
Do not touch the glass surface of the lamp, filter or reflector.

Natural skin moisture from your fingers can cause cracks and
damage the light source.
Handle the lamp carefully. Otherwise, the lamp may be

damaged, resulting in equipment failure.
Some examination lamps are provided with a mesh on the

glass surface side (see Figure 5.2). This mesh is installed to
protect the end surface of the endoscopes light guide from
thermal damage and should not be removed.
Mesh
Examination lamp
Figure 5.2
65
Be sure to reset the lamp hour indicator as described in

Lamp hour indicator reset on page 71 after replacing.
Otherwise, the incorrect total working hours of the
examination lamp will be indicated.
Removing the lamp

1.
When the examination lamp is ON, press and hold the lamp button for about
one second to extinguish it.
2.
Wait a few seconds to allow the light source to cool the lamp chamber
sufficiently.
While the light source is ON and the examination lamp is

extinguished, a fan built into the light source cools the lamp
chamber.
3.
Turn the light source OFF and disconnect the power cord.
4.
Turn the knobs of the lamp cover and remove the lamp cover.
5.
Confirm that the inside of the lamp chamber is not too hot.
If the lamp chamber is extremely hot, attach the lamp cover, connect the
power cord, turn the light source ON and then repeat steps 1. through 5.
above.
6.
Remove the hexagon wrench from the rear of the lamp cover (see Figure
5.3).
Lamp cover
Hexagon wrench
Knobs
Knob (B)
Figure 5.3
66
7.
Turn knob (A) counterclockwise by 90 to loosen it.
8.
Turn knob (B) counterclockwise by 90 to loosen it.
Knob (A)
9.
Holding the knobs or projections of the heat sinks, remove the examination
lamp with heat sinks (A) and (B) attached (see Figure 5.4).
Heat sink (B)
Heat sink (A)
Insertion groove
Knob (B)
Knob (A)
Figure 5.4
10.
Using the hexagon wrench, loosen the three bolts on heat sink (B) (on the
+ side of the examination lamp or heat sink (B)) and remove heat sink (B)
from the examination lamp (see Figure 5.5).
Heat sink (B)

Bolts
Back of heat sink (B)
Examination
lamp
Clamp
Heat sink (A)

Front of heat sink (A)
Figure 5.5
11.
Remove the clamp of heat sink (A) and pull out the examination lamp.
67
When replacing the examination lamp, use a clean lint-free

cloth to wipe off residual heat compound from the heat sink. If
the heat compound is not wiped off completely, the lamps
heat efficiency will be impaired and the examination lamp life
will be shortened significantly.
12.
Using a clean lint-free cloth, wipe off any residual heat compound from the
heat sink.
13.
Proceed with Inserting the lamp below.
Inserting the lamp

1.
2.
Hold the new examination lamp without touching the glass surface.
Do not apply the heat compound to the glass surface and the
ceramic part of the examination lamp. If any compound gets
on the glass surface, wipe it off with a clean lint-free cloth.
Apply enough heat compound. If not enough heat compound

is applied, the heat can cause lamp ignition failures.
Using your finger, apply the heat compound, provided with the new
examination lamp thickly and evenly on the + side electrode of the
examination lamp (see the shaded sections in Figure 5.6).
Examination lamp
Ceramic part
Pin
Heat compound
Figure 5.6
When inserting the examination lamp into the heat sink, align
their pin positions and tighten the bolts firmly. If the bolts are
not tightened firmly, poor heat radiation may result in
equipment damage, examination lamp ignition failure and a
considerable drop in the life of the examination lamp.
68
3.
Insert the + side electrode of the examination lamp (see Figure 5.6) into
heat sink (B) and tighten the three bolts firmly with the hexagon wrench.
4.
Using your finger, apply the heat compound thickly and evenly on the outer
periphery of the side electrode of the examination lamp (see the other
shaded section in Figure 5.6).
5.
Insert the side electrode of the examination lamp (see Figure 5.6) into
heat sink (A) until it stops.
Be sure to tighten the heat sink clamp firmly. Otherwise, poor

heat radiation may result in equipment damage, examination
lamp ignition failure and a considerable drop in the life of the
examination lamp.
6.
Place heat sink (A) and heat sink (B) so that their undersides are flat, close
the heat sink clamp firmly.
7.
Insert the combination of heat sink (A) and (B) into the lamp chamber along
the insertion grooves (see Figure 5.7).
If the heat sinks are not installed properly, their overheating

may result in equipment damage or drop in the examination
light brightness.
Heat sink (A)
Insertion groove
Lamp chamber
Heat sink (B)
Knob (B)
Knob (A)
Figure 5.7
8.
Turn the knob (B) clockwise by 90 from the horizontal position until it stops,
while pushing the knob.
9.
Turn the knob (A) clockwise by 90 from the horizontal position until it stops,
while pushing the knob.
69
10.
Confirm that the heat sinks are attached firmly by pulling the knobs (A) and
(B).
11.
Store the hexagon wrench back on the rear of the lamp cover (see Figure
5.8).
12.
Turn the knobs of the lamp cover and close the lamp cover securely.
Hexagon wrench
Lamp cover
Knobs
Knob (B)
Figure 5.8
13.
70
Proceed with Lamp hour indicator reset below.
Knob (A)
Lamp hour indicator reset

Do not reset the lamp hour indicator unless the examination
lamp is being exchanged. If the indicator is reset, it will show
an incorrect total of working hours.
1.
Connect the power cord and press the power switch to ON. If the
examination lamp turns ON because automatic ignition was selected, press
the lamp button for one second to turn it OFF.
2.
Press and hold the reset button for at least 3 seconds to reset the lamp hour
indicator. Confirm that the lamp hour indicator shows 0. After that, turn the
light source OFF immediately (see Figure 5.9).
The reset button is not active while the examination lamp

lights. To reset the lamp hour indicator, press the button after
pressing the power switch to ON but before pressing the
lamp button.
Reset button
Lamp hour indicator
Figure 5.9
3.
Inspect the light source as described in Chapter 3, Inspection before use.
71
5.2
Fuse replacement
Always use the fuses designated below. To order new fuses, please contact
Olympus.
Spare fuses
1.
MAJ-1412
Never use a fuse other than the fuse model designated by

Olympus. Otherwise, malfunction or failure of the light source
may cause a fire or electric shock hazard.
Be sure to turn the light source OFF and unplug the power
cord before removing the fuse box from the light source.
Otherwise, fire or electric shock may result.
If the power fails to come on after replacing the fuses, unplug

the power cord immediately from the AC mains power inlet
and then contact Olympus. Otherwise, electric shock may
result.
Turn the light source OFF and disconnect the power cord from the wall
mains outlet.
2.
Pull the fuse box straight out, squeezing the tabs projected on both sides of
the fuse box using a pair of tweezers (see Figure 5.10).
Tabs
Figure 5.10
72
3.
Replace both fuses (see Figure 5.11).
Fuse box
Fuse
Figure 5.11
Insert the fuse box into this instrument until it clicks into
position. If the fuse box is inserted incompletely, the power
may fail to come ON or the power failure may occur during
operation.
4.
Insert the fuse box into the light source until it clicks into position.
5.
Plug the power cord and turn the light source ON and confirm the power
output.
73
Chapter 6 Care, Storage and Disposal

6.1
Care
After wiping with a piece of moistened gauze, dry the light

source thoroughly before using it again. If it is used while still
wet, there is the risk of an electric shock.
When cleaning the light source, always wear appropriate

personal protection equipment. Blood, mucus and other
potentially infectious material adhering to the light source
could pose an infection control risk.
Do not apply spray-type medical agents such as rubbing

alcohol directly to the light source. Medical agents might
enter the light source through the ventilation grills and may
cause equipment damage.
Do not clean the output socket, other connectors or the AC

power inlet. Cleaning them can deform or corrode the
contacts, causing damage to the light source.
Do not autoclave or gas sterilize the light source. These

methods will damage it.
Do not wipe the external surface with hard or abrasive wiping

material. The surface will be scratched.
If the light source is soiled, perform the following cleaning procedure immediately
after use. If cleaning is delayed, residual organic debris will begin to solidify, and
it may be difficult to effectively clean the light source. The light source should
also be cleaned routinely.
1.
2.
Should the equipment become soiled with blood or other potentially

infectious materials, first wipe off all gross debris using a neutral detergent,
then wipe with a lint-free cloth moistened with a surface disinfectant.
3.
Wipe the surface of the light source using a soft, lint-free cloth moistened
with 70% ethyl or isopropyl alcohol to remove dust, dirt, etc.
4.
74
Dry the light source with a clean, lint-free cloth.
6.2
Storage
Do not store the light source in a location exposed to direct
sunlight, X-rays, radio activity or strong electromagnetic
radiation (e.g. near microwave medical treatment equipment,
short-wave medical treatment equipment, MRI equipment,
radio or mobile phones). Damage to the light source may
result.
1.
2.
Disconnect all ancillary equipment connected to the light source.
3.
Store the equipment at room temperature in the horizontal position in a

clean, dry and stable location.
6.3
Disposal
Before disposing of the examination lamp, discharge the internal gas with
reference to Section 5.1, Replacement of the examination (xenon) lamp on
page 64. Then follow all applicable national and local laws and guidelines.
When disposing of this instrument or any of its components (such as fuses),
follow all applicable national and local laws and guidelines.
75
Chapter 7 Installation and Connection

Review this chapter thoroughly, and prepare the instruments
properly before use. If the equipment is not properly prepared
before each use, equipment damage, patient and operator
injury and/or fire can occur.
Turn OFF all system components before connecting them.

Otherwise, equipment damage or malfunction can result.
Use appropriate cables only. Otherwise, equipment damage
or malfunction can result.
Properly and securely connect all cables. Otherwise,

equipment damage or malfunction can result.
The cables should not be sharply bent, pulled, twisted or

crushed. Cable damage can result.
Never apply excessive force to connectors. This could

damage the connectors.
Use this instrument only under the conditions described in

Transportation, storage and operating environments and
Specifications in the Appendix. Otherwise, improper
performance, compromised safety and/or equipment damage
may result.
Prepare the light source and compatible equipment (shown in the System chart
in the Appendix) before each use. Referring to the instruction manuals of each
system component, install and connect the equipment according to the
procedure described in this chapter.
76
7.1
Installation work flow

Please see the installation work flow in Figure 7.1 below. Follow each step of the
work flow before using the light source.
1. Install the light source and the ancillary equipment on the mobile workstation or another stable
location.
Section 7.2, Installation of equipment on page 78
2. Select the lamp ignition mode.

Section 7.3, Selecting the lamp ignition mode on page 81
3. Install the water container.

Section 7.4, Installation of the water container on page 83
Not necessary if the air/water feeding is not used.
4. Connect the light source to the video system center.

Section 7.5, Connection of the video system center on page 84
Not necessary if the video system center is not used.
5. Connect the light source to the power source.

Section 7.6, Connection to the AC mains power supply on page 85
Figure 7.1
77
7.2
78
Installation of equipment
Do not place any equipment other than the EVIS EXERA II

video system center on the top of the light source. Otherwise,
Keep the ventilation grills of the light source clear. The

ventilation grills are located on the bottom and rear panels.
Blockage can cause overheating and equipment damage.
Clean and vacuum dust the ventilation grills using a vacuum

cleaner. Otherwise, the light source may break down and
gets damaged from over heating.
Place the light source on a stable, level surface using the foot
holders (MAJ-1205). Otherwise, the light source may topple
down or drop, and user or patient injury may occur, or
If a trolley other than the mobile workstation (WM-NP1 or

WM-WP1) is used, confirm that the trolley can withstand the
weight of the equipment installed on it.
Do not install the light source near a source of strong

magnetic wave (microwave treatment device, short wave
treatment device, MRI, radio equipment, etc.). Otherwise, the
video system center may malfunction.
Installation on the mobile workstation (WM-NP1, WM-WP1)

1.
Place the mobile workstation on a level surface. Lock the caster brakes as
shown in Figure 7.2.
Push to lock.
Push to release.
Caster brakes
Figure 7.2
2.
Install the shelf of the mobile workstation as described in the mobile

workstations instruction manual.
3.
Align the two front feet of the light source with the anti-slip projections on the
mobile shelf of the mobile workstation (see Figure 7.3).
4.
Peel the paper from the bottom of the two provided foot holders. Place the
foot holders to the two corresponding positions on the rear and attach them
lightly (see Figure 7.3).
Foot holder
Video system center
CLV-180
Anti-slip projections
Figure 7.3
5.
Remove the light source from the mobile workstation and attach the foot
holders firmly.
6.
Place the light source on the mobile shelf so that the rear feet fit into the foot
holders.
79
Installation in another location

1.
Place the pattern sheet provided with the foot holders on the installation
location. Peel the paper from the bottom of the foot holders and lightly attach
the foot holders against the sheet (see Figure 7.4).
Pattern sheet
Foot holder
Peel off
To front
Figure 7.4
2.
Place the light source on the pattern sheet and check that the feet fit into the
the foot holders.
3.
Remove the light source from the pattern sheet.
4.
Remove the pattern sheet and attach the foot holders firmly.
5.
Place the light source so that the feet of the light source fit into the foot
holders.
80
7.3
Selecting the lamp ignition mode

Either manual or auto ignition mode is selectable to ignite the examination lamp.
Manual ignition
The mode ignites the examination lamp by pushing the lamp button after
turning the light source ON.
Auto ignition
The mode ignites the examination lamp by turning the light source ON
simultaneously.
Select the lamp ignition mode as follows:
Manual ignition (MAN.)

Set the lamp ignition mode switch on the rear panel to MAN. (see Figure 7.5).
Lamp ignition mode switch
CLV-180
Figure 7.5
81
Automatic ignition (AUTO)

Set the lamp ignition mode switch on the rear panel to AUTO (see Figure 7.6).
Lamp ignition mode switch
CLV-180
Figure 7.6
82
7.4
Installation of the water container

When using an endoscope used for water feeding via the light source, prepare
the water container as shown in the System chart in the Appendix. Install the
water container in the water container holder on the left side of the light source
(see Figure 7.7).
Figure 7.7
83
7.5
Connection of the video system center

Compatible video system center
EVIS EXERA II video system center CV-180
For connecting the video system center (CV-180) to the light source, use the
cable listed below.
Part No.
Part name
note
MAJ-1411
Light source cable
CV-180
LIGHT SOURCE
MAJ-1411
CV terminal
CLV-180
Figure 7.8
84
7.6
Connection to the AC mains power supply
Be sure to connect the power plug of the power cord directly

to a grounded wall mains outlet. If the light source is not
grounded properly, it can cause an electric shock and/or fire.
Do not connect the power plug to the 2-pole power circuit

with a 3-pole to 2-pole adapter. It can prevent proper
grounding and cause an electric shock.
Always keep the power plug dry. A wet power plug may
cause electric shocks.
Confirm that the hospital-grade wall mains outlet to which this

instrument is connected has adequate electrical capacity that
is larger than the total power consumption of all connected
equipment. If the capacity is insufficient, fire can result or the
circuit breaker may trip and turn OFF this instrument and all
other equipment connected to the same power circuit.
Do not bend, pull or twist the power cord. Equipment damage

including separation of the power plug and disconnection of
the cord wire as well as fire or electric shock can result.
Be sure to connect the power plug securely to prevent

erroneous unplugging during use. Otherwise, the equipment
will not function.
Do not extend a single wall mains outlet into multiple outlets

for connecting the power cords of both the electrosurgical
unit and light source. Otherwise, malfunction of the
equipment may result.
The plug of the power cord that follows the equipment may
vary from this drawing, as in each country the
commercialized cable is in accordance to the local applicable
norm.
85
1.
Confirm that the light source is OFF.
2.
Connect the power cord to the AC power inlet of the light source and to the
wall mains outlet (see Figure 7.9).
Wall mains outlet
Figure 7.9
86
Chapter 8 Troubleshooting
If the light source is visibly damaged, does not function as expected or is found
to have irregularities during the inspection described in Chapter 3, Inspection
and Chapter 7, Installation and Connection, or the use described in Chapter 4,
Operation, do not use the light source and contact Olympus. Some problems
that appear to be malfunctions may be correctable by referring to Section 8.1,
Troubleshooting guide. If the problem cannot be resolved by the described
remedial action, stop using the light source and contact Olympus
Never use the light source if an abnormality is suspected.

Damage or irregularity in the instrument may compromise
patient or user safety and may result in more severe
equipment damage.
8.1
Troubleshooting guide
The following table shows the possible causes of and countermeasures against
troubles that may occur due to equipment setting errors or deterioration of
consumable.
Troubles or failures other than those listed in the following table need repair. As
repair performed by persons who are not qualified by Olympus could cause
patient or user injury and/or equipment damage, be sure to contact Olympus for
repair.
If an abnormality is suspected, turn the light source OFF

once and turn it ON again. If the abnormality cannot be
solved, turn the light source OFF and disconnect the power
cord to stop the flow of electricity completely.
87
Irregularity
description
Solution
The endoscope
cannot be
connected to the
light source.
The endoscope is not compatible with

this light source.
Connect an endoscope
that is listed in the
System chart in the
Appendix.
The power fails to

come ON.
The power cord is not connected.
Connect to a wall mains

outlet as described in
Section 7.6 on page 85.
The power switch is not turned ON.
Turn the power switch

ON.
The lamp cover is not closed.
Close the lamp cover

firmly.
The fuses have blown.
Replace both fuses with

new ones as described
in Section 5.2 on
page 72.
The examination lamp has not been

ignited yet.
Press the lamp button.
The examination lamp is not installed.
Install an examination
lamp as described in
The examination lamp is not installed

correctly.
Reinstall the
examination lamp as
described in Section 5.1
on page 64.
The examination lamp is broken.
Replace the
examination lamp with a
new one as described in
The examination
lamp does not
ignite
automatically
when the light
source is turned
ON.
The manual ignition mode is selected to

ignite the examination lamp.
Set the lamp ignition

mode switch on the rear
panel to AUTO.
The examination
lamp ignites
automatically
when the light
source is turned
ON.
The auto ignition mode is selected to

ignite the examination lamp.
Set the lamp ignition

mode switch on the rear
panel to MAN..
The examination
lamp does not
ignite.
88
Possible cause
Irregularity
description
Possible cause
Solution
The examination The lamp button is pressed only for a

lamp does not
short time.
turn OFF even
when the lamp
button is pressed.
Press and hold the lamp

button for one second or
more.
The examination
lamp does not
ignite, and the
emergency lamp
indicator lights.
The examination lamp is not installed.
Install an examination
lamp as described in
The examination lamp is not installed

correctly.
Reinstall the
examination lamp as
on page 64.
The examination lamp is broken.
Replace the
The examination
lamp does not
ignite, and a beep
is heard.
The temperature of the light source is

too high.
Turn the light source

OFF and confirm that
the ventilation grills are
not covered. Allow the
light source to cool
down, then turn it ON
again.
The emergency
lamp, instead of
This instrument may have already

malfunctioned.
Return the instrument

for repair, following 8.2,
the examination
lamp, lights up
frequently.
The lamp hour
indicator cannot
be reset.
Returning the light

source for repair on
page 93.
The examination lamp is lit.
Extinguish the
examination lamp, and
press and hold the reset
button for 3 seconds.
The reset button is pressed only for a

short time.
Press and hold the reset

button for three seconds
or more.
No light is emitted
The examination lamp has not been
Press the lamp button.
from the
endoscope.
ignited yet.
The endoscope is not connected to the
output socket.
Connect the endoscope

to the output socket
securely as described in
The lamp button was accidentally

pressed.
Press the lamp button

again.
89
Irregularity
description
Possible cause
Solution
The brightness
level does not
change even
when the
brightness
adjustment
buttons are
pressed.
The level is set to the minimum or

maximum.
Adjust the brightness to

an optimum level as
on page 55 or turn the
light source OFF then
ON again.
The field of view

and the image
are too dark or
too bright.
The examination lamp is old.
Replace the
The emergency lamp is active.
Replace the

output socket.

The brightness level is unsuitable.
Adjust the brightness to

a suitable level as
on page 55.
90
Transillumination is activated.
Wait for auto return to
(The transillumination indicator blinks.)
the original level (in

about 7 seconds) or
press the
transillumination button
again.
The video system center and/or light

source cable is connected improperly.
Connect the video

system center and light
sure cable properly.
The video system center is OFF.
Turn the video system

center ON.
NBI mode is set. (The filter mode button

lights.)
Press the filter mode

button to return to the
normal observation
mode.
Irregularity
description
The field of view
and image color
are poor.
The air/water
feeding function
does not operate.
The
transillumination
function cannot
be activated.
The high intensity

mode cannot be
set.
Possible cause
Solution
The emergency lamp is active.
Replace the
A filter mode is set. (The filter mode

indicator illuminates white.)
Press the filter mode

button to return to the
normal observation
mode.
The air/water feeding function is not

being operated.
Operate the air/water

feeding function as
on page 58.

output socket.

The light guide is connected to the

output socket.
Connect the light guide

to an endoscope with air
feed capability.

output socket.

A light guide is connected to the output

socket. Or an incompatible endoscope is
connected to the output socket.

with the
transillumination
function compatibility as
on page 41.
An endoscope or light guide with high

intensity mode compatibility is not
connected to the output socket.
Connect an endoscope
or light guide cable with
high intensity mode
compatibility as
on page 37.
91
Irregularity
description
NBI observation
is not enabled.
92
Possible cause
Solution
An endoscope incompatible with NBI is

connected.
Connect an NBI
compatible endoscope.
The video system center is OFF.
Turn the video system

center ON.
NBI mode is not selected.
Select the NBI mode

and confirm that the
color of the NBI
indicator is changed
from green to white.
8.2
Returning the light source for repair

Olympus is not liable for any injury or damage which occurs
as a result of repairs attempted by non-Olympus personnel.
When returning the light source for repair, contact Olympus. With the light
source, include a description of the malfunction or damage and the name and
telephone number of the individual at your location who is most familiar with the
problem. Include a repair purchase order.
If an accessory of the instrument (e.g., examination lamp,

spare fuse, foot holder, power cord, light source cable) needs
to be replaced, contact Olympus to purchase a replacement.
93
94
Appendix
Appendix
System chart
The recommended combinations of equipment and accessories that can be
used with this light source are listed below. New products released after the
introduction of this light source may also be compatible for use in combination
with this light source. For further details, contact Olympus.
If combinations of equipment other than those shown below

are used, the full responsibility is assumed by the medical
treatment facility.
95
Appendix
Videoscope
(EVIS 100/130/140/160/1801 series)
Ultrasonic videoscope
Water container
(See page 98.)
Videoscope cable EXERA II

(MAJ-1430)
Fiberscope
Video adapter
(A10-T1/T2)
Camera head
(OTV-S7H-N/1N/1D/NA/1NA,
OTV-S7H-D-6M)
Fiberscope
Video adapter
Camera head
(OTV-S7H-NA-10E/12E/10Q/12Q,
OTV-S7H-1NA-10E/12E/12Q,
OTV-S7H-FA-E/Q, OTV-S7H-1FA-E,
OTV-SP1H-NA-12E/12Q, OTV-SP1H-N-12E/12Q)
Rigidscope
Camera head
(OTV-S7H-1D-F08E/L08E)
Light guide cable
Light guide cable
Camera head
(OTV-S7H-VA)
Rigid videoscope
(A500A series, WA50A/L series)
Flexible videoscope
(ENF-V/VT/V21/VQ1,
CYF-V/VA/V21/VA21, HYF-V, LTFV3/VP. LF-V)
96
Appendix
The OLYMPUS EVIS EXERA II video system can be configured for

cardiac applications only when TYPE CF applied part (camera heads
and light guide cables) bearing the
symbol are used.
High-definition LCD monitor

(OEV181H, OEV191H)
LCD monitor
(OEV191)
Color video monitor
(OEV203, OEV143)
EVIS EXERA II video system center

(CV-180)
Mobile workstation
(WM-NP1, WM-WP1)
Light source cable

(MAJ-1411)
Keyboard
(MAJ-1428)
The followings are compatible with NBI:

GIF-H180, CF-H180AL/I, GIF-Q180, CF-Q180AL/I,
PCF-Q180AL/I, GIF-N180, BF-Q180, BF-P180,
BF-1T180, ENF-V2/VQ, CYF-V2, CYF-VA2
EVIS EXERA II
xenon light source
(CLV-180)
97
Appendix
Water container
BF endoscopes do not use the water container.
Water container
Endoscope
MAJ-901
MAJ-902
MH-884
MH-970
MD-431
MA-995
EVIS EXERA II 180 series
EVIS EXERA 160 series,

Ultrasonic videoscope 160
series
EVIS 140 series,

series
EVIS 100, 130 series,

series
OES 40 series
OES 10, 20, 30, E, E3 series
: applicable, : not applicable
Transportation, storage and operating environments

Transportation and
storage environment
Ambient temperature 25 to +70C

(13 to + 158F)
Relative humidity
Operating
environment
98
10 - 90%
Ambient temperature 10 - 40C

(50 - 104F)
Relative humidity
30 - 85% (without condensation)
Atmospheric
pressure
700 - 1060 hPa

(0.7 - 1.1 kgf/cm2)
(10.2 - 15.4 psia)
Appendix
Specifications
Item
Power supply
Size
Illumination
Automatic
brightness control
Air feeding
Water feeding
Specification
Voltage
100 - 120 V AC
Voltage fluctuation
Within 10%
Frequency
50/60 Hz
Frequency
fluctuation
Within 1 Hz
Consumption
electric power
500 VA
Fuse rating
8 A, 250 V
Fuse size
5 20 mm
Dimensions
383 (W) 162 (H) 536 (D) mm

(maximum)
Weight
15.4 kg
Examination lamp
Xenon short-arc lamp (ozone-free)

300 W
Average lamp life
Approximately 500 hours of

continuous use (With intermittent
use, the lamp life may vary slightly.)
Ignition method
Switching regulator
Brightness
adjustment
Light-path diaphragm control
Intensity mode
Normal or high intensity
Cooling
Forced-air cooling
Color conversion
Possible using special-purpose

filter.
Emergency lamp
Halogen lamp (within mirror) 12 V

35 W
Average emergency
lamp life
Approximately 500 hours
Automatic
brightness control
method
Servo-diaphragm method
Automatic exposure
17 steps
Pump
Diaphragm type pump
Pressure switching
4-level available
(OFF, low, medium, high)
Method
Air pressurization or detachable

water container
99
Appendix
Item
Indicators on front
panel
Specification
Emergency lamp
It reports absence of emergency

lamp, disconnection and use of
emergency lamp.
NBI
It lights in green under the normal

observation and lights in white
under the NBI observation.
OP.1
It lights if a special filter is installed

into the light source.
OP.2
It lights if a special filter is installed

into the light source.
Setting memory
Classification
(medical electrical
equipment)
EMC
Settings (except filter setting) are

stored even when the light source is
OFF.
Type of protection
against electric
shock
Class I
Degree of
protection against
electric shock of
applied part
Depend on applied part

See also applied part (Camera head
or videoscope).
Degree of
protection against
explosion
This instrument should be kept

away from flammable gases.
Applied standards;
IEC 60601-1-2: 2001
This instrument complies with the

standards listed in the left column.
CISPR 11 of emission:
Group 1, Class B
This instrument complies with the
EMC standard for medical electrical
equipment; edition 2 (IEC 60601-12: 2001). However, when
connecting to an instrument that
complies with the EMC standard for
medical electrical equipment;
edition 1 (IEC 60601-1-2: 1993), the
whole system complies with edition
1.
Year of manufacture
7612345
The last digit of the year of
manufacture is the second digit of
the serial number.
100
Appendix
EMC information
This model is intended for use in the electromagnetic environments specified
below. The user and the medical staff should ensure that it is used only in these
environments.
Magnetic emission compliance information and

recommended electromagnetic environments
Emission standard
RF emissions
Compliance
Guidance
Group 1
This instrument uses RF (Radio Frequency) energy only for its

internal function. Therefore, its RF emissions are very low and are not
likely to cause any interference in nearby electronic equipment.
Class B
This instrument's RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
Harmonic emissions
IEC 61000-3-2
Class A
This instrument's harmonic emissions are low and are not likely to
cause any problem in the typical commercial power supply connected
to this instrument.
Voltage
fluctuations/flicker
emissions
IEC 61000-3-3
Complies
This instrument stabilizes own radio variability and has no affect such
as flicker of a lighting apparatus.
CISPR 11
RF emissions
CISPR 11
Main terminal
conducted emissions
CISPR 11
101
Appendix
Electromagnetic immunity compliance information and

recommended electromagnetic environments
Immunity test
IEC 60601-1-2
test level
Electrostatic
discharge (ESD)
Contact:
2, 4, 6 kV
IEC 61000-4-2
Air:
2, 4, 8 kV
Electrical fast
transient/burst
2 kV
for power supply lines
IEC 61000-4-4
1 kV
for input/output lines
Surge
Differential mode:
0.5, 1 kV
IEC 61000-4-5
Compliance level
Guidance
Same as left
Floors should by be made of wood, concrete,

or ceramic tile that hardly produces static. If
floors are covered with synthetic material that
tends to produce static, the relative humidity
should be at least 30%.
Same as left
Mains power quality should be that of a typical

commercial (original condition feeding the
facilities) or hospital environment.
Same as left

commercial or hospital environment.
Same as left

commercial or hospital environment. If the
user of this instrument required continued
operation during power mains interruptions, it
is recommended that this instrument be
powered from an uninterruptible power supply
or a battery.
Same as left
It is recommended to use this instrument by

maintaining enough distance from any
equipment that operates with high current.
Common mode:
0.5, 1, 2 kV
Voltage dips,
short interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
< 5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
< 5% UT
(>95% dip in UT)
for 5 seconds
Power frequency
(50/60 Hz)
magnetic field
3 A/m
IEC 61000-4-8
UT is the a.c. mains power supply prior to application of the

test level.
102
Appendix
Cautions and recommended electromagnetic environment

regarding portable and mobile RF communications
equipment such as a cellular phones
Immunity test
IEC 60601-1-2
test level
Conducted RF
3 Vrms
IEC 61000-4-6
(150 kHz - 80 MHz)
Compliance
level
3 V (V1)
Guidance
Formula for recommended separation distance
(V1=3 according to the compliance level)
3.5
d = -------V1
Radiated RF
IEC 61000-4-3
3 V/m (E1)
3 V/m
(80 MHz - 2.5 GHz)
Formula for recommended separation distance

(E1=3 according to the compliance level)
3.5
d = -------E1
80 MHz to 800 MHz
7
d = -----E1
800 MHz to 2.5 GHz
Where P is the maximum output power rating of the

transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
This instrument complies with the requirements of

IEC 60601-1-2: 2001. However, under electromagnetic
environment that exceeds its noise level, electromagnetic
interference may occur on this instrument.
Electromagnetic interference may occur on this instrument

near a high-frequency electrosurgical equipment and/or other
equipment marked with the following symbol:
103
Appendix
Recommended separation distance between portable and

mobile RF communications equipment and this instrument
Rated maximum output

power of transmitter
P (W)
Separation distance according to frequency of transmitter (m)

(Calculated as V1=3 and E1=3)
150 kHz - 80 MHz
80 MHz - 800 MHz
800 MHz - 2.5 GHz
d = 1.2 P
d = 1.2 P
d = 2.3 P
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
The guidance may not apply in some situations.

Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
Portable and mobile RF communications equipment such as
cellular phones should be used no closer to any part of this
instrument, including cables than the recommended
separation distance calculated from the equation applicable
to the frequency of the transmitter.
104
2006 OLYMPUS MEDICAL SYSTEMS CORP. All rights reserved.

No part of this publication may be reproduced or distributed without the
express written permission of OLYMPUS MEDICAL SYSTEMS CORP.
OLYMPUS is a registered trademark of OLYMPUS CORPORATION.
Trademarks, product names, logos, or trade names used in this
document are generally registered trademarks or trademarks of each
company.
Manufactured by
2951 Ishikawa-cho, Hachioji-shi, Tokyo 192-8507, Japan
Fax: (042)646-2429 Telephone: (042)642-2111
Distributed by
3500 Corporate Parkway, P.O. Box 610, Center Valley, PA
18034-0610, U.S.A.
Fax: (484)896-7128 Telephone: (484)896-5000
5301 Blue Lagoon Drive, Suite 290 Miami, FL 33126-2097, U.S.A.

Fax: (305)261-4421 Telephone: (305)266-2332
(Premises/Goods delivery) Wendenstrasse 14-18, 20097 Hamburg, Germany

(Letters) Postfach 10 49 08, 20034 Hamburg, Germany
Fax: (040)23773-4656 Telephone: (040)23773-0
KeyMed House, Stock Road, Southend-on-Sea, Essex SS2 5QH, United Kingdom
Fax: (01702)465677 Telephone: (01702)616333
117071, Moscow, Malaya Kaluzhskaya 19, bld. 1, fl.2, Russia

Fax: (095)958-2277 Telephone: (095)958-2245
A8F, Ping An International Financial Center, No. 1-3, Xinyuan South Road,
Chaoyang District, Beijing, 100027 P.R.C.
Fax: (86)10-5976-1299 Telephone: (86)10-5819-9000
Olympus-Tower, 114-9 Samseong-Dong, Gangnam-Gu, Seoul 135-090 Korea

Fax: (02)6255-3494 Telephone: (02)6255-3210
491B, River Valley Road #12-01/04, Valley Point Office Tower, Singapore 248373
Fax: 6834-2438 Telephone: 6834-0010
31 Gilby Road, Mount Waverley, VIC., 3149, Australia

Fax: (03)9543-1350 Telephone: (03)9265-5400
GT0862 12
Printed in Japan 20110615 *0000

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What are the main components and functions of the device?

What are the main components and functions of the device?

What are the steps for inspecting the device?

What are the steps for inspecting the device?

INSTRUCTIONS

EVIS EXERA II XENON LIGHT SOURCE

Important Information Please Read Before Use....................

Intended use ............................................................................................

Instruction manual ....................................................................................

Instrument compatibility ...........................................................................

Repair and modification ...........................................................................

Dangers, warnings and cautions...............................................................

Summary of the functions of the instrument .............................

Checking the Package Contents............................

Nomenclature and Functions .................................

Rear and side panels ......................................................................

Inspection work flow........................................................................

Checking the lamp ignition mode....................................................

Inspection of the power supply .......................................................

Checking the lamp hour indicator ...................................................

Inspection of the examination light..................................................

Inspection of brightness adjustment ...............................................

Inspection of the high intensity mode..............................................

Inspection of air and water feeding .................................................

Inspection of transillumination function ...........................................

3.10 Inspection of the NBI observation function .....................................

3.11 After inspection ...............................................................................

EVIS EXERA II XENON LIGHT SOURCE CLV-180

Operation flow .................................................................................

Connection of an endoscope ..........................................................

Turning the light source ON and igniting the examination lamp......

Brightness adjustment ....................................................................

Adjusting air/water pressure............................................................

Using the transillumination function ................................................

Using the high intensity mode .........................................................

Using the NBI observation mode ....................................................

Extinguishing the examination lamp................................................

4.10 Turning the light source OFF ..........................................................

Lamp and Fuse Replacement .................................

Replacement of the examination (xenon) lamp...............................

Fuse replacement ...........................................................................

Care, Storage and Disposal ....................................

Installation and Connection....................................

Installation work flow .......................................................................

Installation of equipment .................................................................

Selecting the lamp ignition mode ....................................................

Installation of the water container ...................................................

Connection of the video system center ...........................................

Connection to the AC mains power supply .....................................

Troubleshooting guide ....................................................................

Returning the light source for repair................................................

System chart ............................................................................................

Transportation, storage and operating environments ...............................

EVIS EXERA II XENON LIGHT SOURCE CLV-180

Labels and Symbols

Labels and Symbols

The product name, rated voltage and

Serial number plate

EVIS EXERA II XENON LIGHT SOURCE CLV-180

Labels and Symbols