Professional Documents
Culture Documents
CLV-190
ISSUE 1
2012/04
CLV-190
CONTENTS
Chapter 1: Introduction.......................................................................... 1-1
Chapter 2: Product Outline.................................................................... 2-1
1 Product Overview ............................................................................................................... 2-1
2 Features............................................................................................................................... 2-2
3 Restrictions ......................................................................................................................... 2-3
4 Specifications ..................................................................................................................... 2-4
CONTENTS 1 ISSUE 1
CLV-190
Chapter 1: Introduction
Introduction
Repair and maintenance of this product requires highly specialized knowledge and techniques. We
recommend that you contact an Olympus service center in your area if a problem develops with the
product.
If repairs or modifications are made by personnel not authorized by Olympus, the warranty is void, and
Olympus shall not be liable for damage that occurs to or as a result of use of the modified product.
The information contained in this manual is subject to change at any time without notice. Later editions of
this manual will contain revised and updated material.
Applicable Unit
Copyright
© 2012 Olympus Medical Systems Corp. All rights reserved.
Unauthorized reproduction or distribution in part or in whole is prohibited.
Trademarks
OLYMPUS is a registered trademark of Olympus Corporation.
The company names, product names, and proprietary technical terms in this document are the
trademarks or registered trademarks of their respective owners.
1 Product Overview
(1) Intended use
The light source is intended to be used with Olympus endoscopes, video system centers, and
other ancillary equipment for endoscopic diagnosis, treatment and video observation. Do not
use the light source for any purpose other than its intended use.
2 Features
(1) Light source exclusively for CV-190/OTV-S190.
(2) Mechanical discriminant mechanism on the scope socket allows for automatic adjustment
of maximum allowable light intensity suitable for the scope connected. 3 types of connectors
may be discriminated: GI system endoscope connector, SP high intensity compatible LG
connector and SP high intensity incompatible LG connector.
(3) When a videoscope with air-feeding conduit and fiberscope are connected to the endoscope
connector, scope end injection light intensity equivalent to the EXERA II system with CLV-180
can be achieved.
(4) Electrical contacts on the endoscope connector allow for mechanical and electrical connection
with 190 endoscopes by just one action (one-touch connector).
(5) When halogen incompatible endoscope and light guide for RF connector (endoscope connector
and light guide connector without air-feeding conduit) are connected, the maximum allowable
illuminance (white light) equivalent to the injection light intensity of the CLV-180 can be achieved
on the LG incident end face.
(6) When high intensity compatible scope and light guide for RF connector are used, the high
intensity mode is available to realize lighter illuminating radiation. The maximum allowable
illuminance (white light) on the LG incident end face, which is equivalent to the CLV-180
normal mode or twice the injection light intensity in the normal mode, can be obtained.
In addition, the intensity equivalent to or twice as light as the normal mode can be selected
by the intensity mode switch for the high intensity mode.
(7) Optical filter available for NBI (Narrow Band Imaging) special observation is installed. When
an NBI compatible endoscope is connected, NBI special observation can be performed.
(8) Optical filter available for PDD special observation can be installed. In addition, optical filter
for other special observation (exclusive use with PDD) can be installed as necessary.
(9) Following examination lamp ignition modes can be selected:
a) The examination lamp ignites automatically when the power switch is turned ON
(auto ignition mode).
b) Pressing the lamp switch after turning ON the power switch will ignite the examination
lamp (manual ignition mode).
*The factory default setting is the manual ignition mode.
(10) The examination lamp can be turned ON/OFF by pressing and holding the "Lamp" button
(for about one second).
(11) Heat discharge direction is rear (rear heat discharge).
(12) When ignition fails despite pressing the lamp button, the light source automatically switches
to the emergency lamp. When ignition fails or the lamp goes out, brightness required for
endoscope withdrawal is obtained as an emergency response. Lighting of this emergency
lamp is indicated on the panel.
(13) 17-staged level adjustment is available for both automatic brightness adjustment and manual
brightness adjustment.
(14) Air-feeding can be stopped, or adjusted to three stages (high, medium and low).
(15) Self-check for emergency lamp breaking is performed and indicated on the panel, if any.
(16) Transillumination function is available from the transillumination button (only for endoscope
with air-feeding conduit on the endoscope connector).
(17) The panel setting is backed up and applied when the power is reactivated. However, the
filter button setting is not backed up and the normal filter (infrared cut + heat absorption)
is applied upon power reactivation.
(18) Ethanol for disinfection (70% ethyl or isopropyl alcohol) or neutral detergent can be used
for bed bath of exterior parts and the control panel.
3 Restrictions
(1) Applicable video system center
CV-190, OTV-S190
(2) Use this product under the supervision of a physician within a medical facility.
(3) Direct use on the heart is prohibited (However, it is allowed to use for the heart in
combination with equipment with TYPE CF applied part).
(4) The exterior must be grounded for safety's sake.
(5) Use in flammable atmosphere is prohibited.
(6) Combined use of this device and following electrical devices is prohibited:
a) Devices that are intended for electrical treatment of patients and whose safety in
combined use is not confirmed
b) Other devices whose safety with regard to electrical leakage current is not confirmed
(7) Power
a) Voltage : AC 100 to 240 V
b) Input power : 600 VA
c) Frequency : 50/60 Hz
d) Voltage fluctuation : Within ±10%
e) Frequency fluctuation : Within ±1 Hz
(8) Environment
1) Operating environment
Ambient temperature 10~40°C
Relative humidity 30 to 85% (non condensation)
Atmospheric pressure 700 to 1060 hPa
2) Transportation and storage environment
Ambient temperature -25~+75°C
Relative humidity 10~90%
Atmospheric pressure 700 to 1060 hPa
4 Specifications
4-1 Scope of application
(1) Videoscope
EVIS 100, 130, 140, 150, 170 series
EVIS EXERA 145, 160 series
EVIS EXERA II 165, 180 series
EVIS EXERA III 190 series
VISERA videoscope series
(2) EUS videoscope
EUS 130, 140, 160, 180 series
(3) Fiberscope
OES 10, 20, 30, 40, 60 series
E, E2, E3 series
(4) High intensity compatible light guide
A3290, A3291, A3293, A3294, A3295, A3296, A3297, A3298
(5) Rigid endoscope
Products other than rigid endoscope that can be connected with high intensity compatible
light guide are not applicable.
(6) High intensity fiberscope
CHF-CB30L, CHF-CB30S, URF-P3/P5, LF-TP/DP/GP, CYF-5A, ENF-GP
(7) High intensity compatible videoscope
TF-V, LTF-V2, LTF-V3, LTF-VP, LTF-VP-S, LTF-VH, LTF-VP2, LTF-VH2, PEF-V2, ENF-NH,
LTF-VP2/VH2, PEF-V2, ENF-VH, ENF-V3, CYF-VH, URF-V2, A4804A, A4805A, A50000A,
A50001A, A50010A, A50011A, A50020A, A50021A, A50023A, WA50****series
(8) Water container
MH-884, MA-995, MD-431, MH-970, MAJ-901, MAJ-902
4-2-9 Display method for front panel in the special observation mode
Observation mode How to display front panel
In NBI special observation mode Filter mode changeover button, observation mode
ON/STBY display ON and special light observation
changeover display NBI dot LED are ON
In OP. mode Filter mode changeover button, observation mode
ON/STBY display STBY and special OP. dot LED are ON
4-4 Connection
4-4-1 Endoscope, light guide and electrical contacts
One-touch connection
4-6 Panel
4-6-1 Saving the setting value
(1) The setting value before power shut down is saved in the event of power shut down.
Manual/automatic brightness adjustment setting
Intensity adjustment level
High intensity mode setting
Indication of absence/presence of the special observation system
Lamp life meter (Pressing and holding the counter reset switch when the power is turned
ON and the examination lamp is OFF will reset this meter)
Air feeding setting
4-7 Safety
4-7-1 Light shielding
(1) During endoscope withdrawal, light emitted from the endoscope connector is shielded by
the screen fitted to the endoscope socket.
4-7-2 Cleaning
(1) Ethanol for disinfection (70% ethyl or isopropyl alcohol), neutral detergent, or sterile water
can be used for bed bath of exterior parts.
4-7-3 Warning
(1) When the internal temperature exceeds the specified temperature, the temperature switch
is turned OFF to block power supply to the lamp for safety's sake. In this case, the device
detects that the temperature switch has gone OFF and generates warning beep.
4-8 Others
4-8-1 Usage restrictions
Ambient temperature 10~40°C
Humidity 30~84%
Atmospheric pressure 700 to 1060 hPa
Operating atmosphere Use in flammable atmosphere prohibited
Format of protection against
electric shock Class I, protection level: TYPE BF applied part
Rated voltage AC 100 V (national specifications)
AC 100 – AC 240 V (other areas)
Frequency 50/60 Hz
Power fluctuation ±10% or less
Frequency fluctuation ±1 Hz or less
Power consumption 600 VA
4-8-3 Others
Weight About 18 kg
Profile Maximum profile: 390 (W) x 551 (D) x 162 (H) (mm)
Basic dimensions: 370 (W) x 476 (D) x 150 (H) (mm)
Power cord 3-pole cord with hospital grade plug (national, North America)
3P inlet, 3-pole cord plug not included (regions other than the above)
Chapter 3: Specifications
Refer to the “Specifications” of Instruction Manual.
Chapter 6: Inspection
Refer to the “Inspection” of Instruction Manual.
Inspection
Serial nomber: Month & Year /
Day 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Inspector
6-2
Day 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
Inspector
ISSUE 1
CLV-190
1 Check procedures
1-1 Electrical safety test
1-1-1 Standard
Conduct the following leakage current inspections. Each value should not exceed the listed values.
Leakage current Under normal Under single failure
conditions (NC) conditions (SFC)
Patient leakage DC 10 50
current AC 100 500
Enclosure leakage
100 300/500*
current
Earth leakage current 500 1000
300: UL region, 500: other than UL region (μA)
CLV-190
clip connection
Enclosure screw
Inlet earth
2 Check card
Date of inspection
Product
SN
Inspected by
Checked by
Chapter 9 : Troubleshooting
Refer to the “Troubleshooting” of Instruction Manual.
Engineering 2
Service Engineering Department
Service Division