OLYMPUS
OLYMPUS Video and Image Management Systems
CV-190 Plus EVIS EXERA III Video System Center Instructions March 2021
Instructions
426 Pages
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Page 1
INSTRUCTIONS
EVIS EXERA III VIDEO SYSTEM CENTER
Labels and Symbols
1
Important Information - Please Read Before Use
3
Summary of Equipment Functions
13
Chapter 1
Checking the Package Contents
17
Chapter 2
Nomenclature and Functions
19
Chapter 3
Installation and Connection
37
Chapter 4
Function setup
101
Chapter 5
Inspection
195
Chapter 6
Operation
217
Chapter 7
Function
235
Chapter 8
Reprocessing, Storage, Disposal, and Transportation
335
Troubleshooting
347
OLYMPUS CV-190 PLUS
Chapter 9
Appendix
367
Contents
Contents Labels and Symbols ... 1 Important Information - Please Read Before Use ... 3 Intended use/Intended purpose ... 3 Contraindications ... 3 Clinical benefit ... 3 Applicability of endoscopy and endoscopic treatment ... 4 Instruction manual ... 4 User qualifications ... 7 Instrument compatibility ... 7 Repair and modification ... 7 Signal words ... 8 Precautions ... 8 Security ... 12
Summary of Equipment Functions ... 13 Displaying the endoscopic images on the monitor ... 13 Optical-digital observations ... 13 Adjusting the endoscopic images ... 14 Recording images ... 14 Entering patient data ... 14 Customizing the operations ... 15 Operation of ancillary equipment ... 15
Chapter 1 Checking the Package Contents ... 17 1.1
Checking the package contents ... 17
Chapter 2 Nomenclature and Functions ... 19 2.1
Symbols and descriptions ... 19
2.2
Front panel ... 22
2.3
Rear panel ... 24
2.4
Keyboard ... 26
2.5
Side panels ... 32
2.6
Videoscope cable EXERA II (MAJ-1430) ... 33
2.7
Monitor ... 34 Endoscopic image screen ... 34 Setting display (e.g.) ... 36
Chapter 3 Installation and Connection ... 37 3.1
Precautions for installation and connection ... 37
3.2
Installation workflow ... 39
3.3
Installation of the equipment ... 40 Installation on the mobile workstation (WM-NP2, WM-DP2, WM-NP1, WM-WP1) ... 41 CV-190 PLUS INSTRUCTION MANUAL
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Installation in another location ... 42
3.4
Fitting of accessories ... 43 Scope cable holder (MAJ-1466) ... 43 White cap set (MAJ-941) ... 44
3.5
Connection to the AC mains power supply ... 46 When the mobile workstation (WM-NP2, WM-DP2, WM-NP1, WM-WP1) is used ... 47 When a mobile workstation other than the WM-NP2, WM-DP2, WM-NP1, WM-WP1 is used or when no mobile workstation is used ... 48
3.6
Connection of the light source ... 50 Compatible light sources ... 50 CLV-190 ... 50 CLV-180, CLE-165 ... 52
3.7
Connection of the monitor ... 54 Compatible monitors ... 54 OEV262H ... 54 OEV261H ... 56 OEV191H ... 58 OEV181H ... 62 OEV191 ... 64
3.8
Connection of the keyboard ... 66
3.9
Connection of the video recorder (DVR) ... 67 Compatible video recorders ... 67 IMH-20 ... 67 IMH-10 ... 69 Other DVRs ... 71
3.10 Connection of the video printer ... 74 Compatible video printers ... 74
3.11 Connection of endoscope position detecting unit ... 76 Compatible endoscope position detecting units ... 76 UPD-3 ... 76 UPD ... 78
3.12 Connection of the ultrasound center ... 80 Compatible ultrasound centers ... 80 EU-ME2 Series ... 80 EU-ME1 ... 82 EU-M60, EU-MA ... 84 EU-C60 ... 86
3.13 Connection of the foot switch ... 87 3.14 Connection of the flushing pump ... 88 Compatible flushing pumps ... 88
3.15 Connection of the server ... 90 3.16 Installation of the CV interface converter (MAJ-1916) ... 90 3.17 Connection of equipment having the LINK-IN and LINK-OUT terminals ... 94 CLV-190 ... 94
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CLV-180, CLE-165 ... 96
3.18 Connection of the Endoscopic CO2 regulation unit ... 98
Chapter 4 Function setup ... 101 4.1
Setup list ... 101
4.2
Basic operation of the system setup ... 102 Displaying the system setup screen ... 102 Editing the system setup ... 104 Saving the system setup to the portable memory ... 106 Loading the system setup from the portable memory ... 107
4.3
System setup (system) ... 108 “Date/comment” tab ... 109 “Operation” tab ... 111 “Record setting” tab ... 112 “Printer” tab ... 114 “Output format” tab ... 116 “PIP/NR” tab ... 118 “Release time H” tab ... 119 “Release time S” tab ... 120
4.4
System setup (connection setting) ... 121 “Peripheral (1)” tab ... 122 “Peripheral (2)” tab ... 127
4.5
Basic operation of the user settings ... 130 Displaying the user settings screen ... 130 Editing and newly registering user settings ... 132 Deleting the user settings ... 135 Saving the user settings to the portable memory ... 137 Loading the user settings from the portable memory ... 140
4.6
User settings (basic setup) ... 144 “Release 1” tab ... 145 “Release 2” tab ... 146 “PIP/POP” tab ... 147 “Enhancement” tab ... 149 “Color/Bright” tab ... 151 “Observation 1” tab ... 153 “Observation 2” tab ... 155 “PLUS” tab ... 157
4.7
User settings (switch presets) ... 158 “Scope switch” tab ... 158 “Front panel” tab ... 159 “Keyboard” tab ... 160 “Foot switch” tab ... 161 Setting value of custom switch function ... 161
4.8
User settings (OSD customization) ... 165 “OSD” tab ... 165 “Custom disp 1” tab ... 168 CV-190 PLUS INSTRUCTION MANUAL
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“Custom disp 2” tab ... 169 “Custom disp 3” tab ... 170
4.9
User settings (UPD) ... 171 “Model” tab ... 171 “View” tab ... 173 “Screen” tab ... 175
4.10 User settings (Color tone) ... 176 4.11 Security settings for administrators ... 177 Basic operation of the security settings ... 177 “Account” tab ... 180 “User” tab ... 181 “Target menu” tab ... 182 “Admin” tab ... 183
4.12 Secure user registration ... 184 Displaying the user ID ... 184 Editing and newly registering user IDs ... 187 Deleting a user ID ... 189 Saving a user ID to the portable memory ... 190 Loading the user ID from the portable memory ... 191
4.13 Password ... 192
Chapter 5 Inspection ... 195 5.1
Precautions of workflow ... 195
5.2
Inspection workflow ... 196
5.3
Connection of an endoscope ... 197 EVIS 190 series videoscope ... 198 EVIS Videoscope except for EVIS 190 series and ultrasound videoscope ... 199 170 Series videoscope ... 200 Fiberscope and camera head ... 201
5.4
Inspection of the power supply ... 203
5.5
Monitor display inspection ... 204
5.6
Inspection of the monitor display ... 204
5.7
Inspection of the endoscopic image ... 205
5.8
Inspection of the automatic brightness adjustment function ... 207
5.9
Inspection of the freeze function ... 208
5.10 Inspection of the release function ... 209 5.11 Inspection of the PIP/POP function ... 210 5.12 Inspection of the orientation function ... 210 5.13 Inspection of the custom switches ... 210 5.14 Inspection of the optical-digital observation function ... 211 Confirming the available observation mode ... 211 Inspection of NBI observation ... 212
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5.15 Inspection of the endoscopic CO2 regulation unit (UCR) ... 213 5.16 After inspection ... 215
Chapter 6 Operation ... 217 6.1
Precautions for operation ... 217
6.2
Operation workflow ... 220
6.3
Turning the video system center ON ... 221
6.4
White balance adjustment ... 222
6.5
Recall of user settings ... 225
6.6
Patient data ... 228 Entering patient data ... 229 Editing and deleting patient data ... 230
6.7
Observation and recording of the endoscopic image ... 231
6.8
Termination of the examination ... 232
Chapter 7 Function ... 235 7.1
Basic operation of the menu list ... 235
7.2
Logging in ... 237
7.3
Brightness adjustment ... 238 Iris mode ... 238 Brightness ... 239 Exposure ... 241 Iris area ... 243 Electronic shutter ... 244 Automatic gain control (AGC) ... 245
7.4
Image enhancement ... 246 Image enhancement ... 246 Contrast mode ... 248 Noise reduction ... 249
7.5
Color tone adjustment ... 249 Color tone level adjustment ... 249
7.6
Zooming the image ... 251 Electronic zoom function ... 251
7.7
Changing the endoscopic image screen ... 252 Freeze ... 252 Two screens display (PIP and POP displays) ... 253 Image size ... 258 Focus ... 259
7.8
Changing the displayed text information ... 260 Clearing characters from the screen ... 260 Cursor ... 262 Displaying the endoscope information window ... 262 Displaying the custom switch information window ... 264 CV-190 PLUS INSTRUCTION MANUAL
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Arrow pointer ... 265 Stopwatch ... 267 Displaying the hardware information ... 268
7.9
Changing the observation mode ... 269 Changing the observation mode (“WLI”, “NBI”) ... 269 Confirm the available optical-digital observation ... 269 NBI observation ... 270 NBI color mode ... 271
7.10 Recording the frozen image (releasing) ... 272 7.11 Recording and playing back the frozen image (portable memory or internal buffer) 273 Inserting the portable memory into the portable memory port ... 275 Removing the portable memory from the portable memory port ... 276 Formatting the portable memory ... 277 Checking the portable memory ... 278 Remaining capacity indicator of the memory ... 279 Recording the frozen image to the memory ... 280 Basic operation on thumbnail screen ... 281 Operation on the image screen (playback and printing) ... 285 Generating, printing, and storing the annotation images ... 288 Deleting the data including a folder ... 290 Transferring the unsent images ... 291 Image files and folders ... 293 Playing back the images using the personal computer ... 299
7.12 Remotely controlling the video recorder ... 301 7.13 Remotely controlling the video printer ... 304 Setting the number of sheets to be printed and the number of images on the print sheet 308 Printer lock ... 310
7.14 Recording on the image filing system ... 311 7.15 Remotely controlling the monitor ... 312 Image source of the monitor ... 312 FLIP function ... 313
7.16 Remotely controlling the UPD-3 ... 314 7.17 Presetting, calling, saving, and loading patient data ... 315 Displaying the “Select patient” screen ... 315 Newly registering and editing patient data ... 316 Deleting patient data ... 318 Calling patient data ... 320 Saving patient data to the portable memory ... 321 Loading patient data from the portable memory ... 324
7.18 Other functions ... 327 Assigning functions to the custom switches ... 327 Locking the keyboard ... 328 Reset ... 329 Displaying the color bar and the 50% white screen ... 330 Selecting the mode of character input from the keyboard ... 331
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Confirming and editing data of the endoscope ... 332 System reset ... 334
Chapter 8 Reprocessing, Storage, Disposal, and Transportation . 335 8.1
Reprocessing ... 335 Surface disinfectant cleaner ... 337
8.2
Signs of degradation from reprocessing and maximum number of reprocessing 338 Preparing equipment for reprocessing ... 340 Reprocessing the video system center and accessories ... 341
8.3
Storage ... 344
8.4
Disposal ... 344
8.5
Transportation ... 345
Chapter 9 Troubleshooting ... 347 9.1
Troubleshooting ... 347
9.2
Troubleshooting guide ... 348
9.3
Returning the video system center for repair ... 366
Appendix ... 367 Combination equipment ... 367 System chart ... 367
Specifications ... 370 Transportation, storage, and operation Environment ... 370 Specifications ... 371
Default settings list ... 376 System setup ... 376 User settings ... 378 Security settings for administrators ... 381
Multilingual typing by the keyboard ... 382 Security ... 384 Security level ... 384 Initial value of the password ... 384
EMC information ... 385 License information of Open Source Software ... 391 GNU GPL ... 391
End User License Agreement of Open Source Software modules ... 392 GNU GENERAL PUBLIC LICENSE Version 2 with Exception ... 392 GCC RUNTIME LIBRARY EXCEPTION Version 3.1, 31 March 2009 ... 393 Others ... 394 newlib ... 395 libgloss ... 407
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Index ... 411
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Labels and Symbols
Labels and Symbols Safety-related labels and symbols are attached on the locations shown below. If labels or symbols are missing or illegible, contact Olympus.
Rear panel Electric rating The product name, rated voltage, and frequency are shown.
Blue
Indicates to see the instruction manual for the cable to be connected.
MEDICAL DEVICE EVIS EXERA III VIDEO SYSTEM CENTER MODEL OLYMPUS CV-190 PLUS POWER INPUT 100–240V 50/60Hz 150VA CE marking
Manufacturer Potential equalization terminal Crossed-out wheeled bin’ symbol Authorized representative in the European Community
Date of manufacturer
Serial number
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Labels and Symbols
Front panel CAUTION Dry the video connector before insertion. ATTENTION Vaillez séchez le connecteur vidéo avant de l’insérer.
UDI label The UDI label is required by some countries’ regulations regarding the identification of a medical device also known as Unique Device Identification (UDI).
Back cover of this instruction manual Symbol
Description Manufacturer
Authorized representative in the European Community
Importer (into European Union)
Translation
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CV-190 PLUS INSTRUCTION MANUAL
Important Information - Please Read Before Use
Important Information - Please Read Before Use
Intended use/Intended purpose This video system center is intended to be used with OLYMPUS camera heads, endoscopes, light sources, monitors, EndoTherapy accessories, and other ancillary equipment for endoscopic diagnosis, treatment, and video observation.
Contraindications 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. Other combinations of equipment may cause ventricular fibrillation or seriously affect the cardiac function of the patient.
Clinical benefit Provides clear image of location, shape, and structure of the lesions leading to high rates of diagnostic yield.
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Important Information - Please Read Before Use
Applicability of endoscopy and endoscopic treatment If there is an official standard on the applicability of endoscopy and endoscopic treatment that is defined by the healthcare facility administration or other official institutions such as academic societies on endoscopy, follow that standard. Before starting endoscopy and endoscopic treatment, thoroughly evaluate its properties, purposes, effects, and possible risk (their natures, extent, and probability). Perform endoscopy and endoscopic treatment only when its potential benefits are greater than its risks. Fully explain to the patient the potential benefits and risks of the endoscopy and endoscopic treatment as well as any examination/treatment methods that can be performed in its place, and perform the endoscopy and endoscopic treatment only after obtaining the consent of the patient. Even after starting the endoscopy and endoscopic treatment, continue to evaluate the potential benefits and risks, and immediately stop the endoscopy/treatment and take proper measures if the risks to the patient become greater than the potential benefits.
Instruction manual This instruction manual contains essential information on using the video system center safely and effectively. Before use, thoroughly review this manual and the manuals for all equipment that will be used during the procedure and use the equipment as instructed. Keep this and all related instruction manuals in a safe, accessible location. If you have any questions or comments about any information in this manual, contact Olympus.
Terms used in this manual Light source: The light source provides light and electrical signals to the endoscope. It also provides electrical signals to the video system center.
Camera head: The camera head is a device that converts endoscopic images from a fiberscope into monitor images.
Video printer: The video printer is a device that prints the frozen video image.
Video recorder: The video recorder is a device that records the video.
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Important Information - Please Read Before Use
Wall mains outlet: The wall mains outlet is a wall AC mains power outlet socket having the exclusive terminal for grounding.
Isolation transformer: The isolation transformer is a safety device that is used to isolate the noninsulated equipment with potentially high leakage currents to decrease the possibility of an electric shock.
Automatic brightness adjustment: The automatic brightness adjustment 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 endoscope’s insertion tube and the subject changes.
Image sensor (CCD): The image sensor (CCD) is a device that converts light into electrical signals.
Electronic shutter: The electronic shutter function changes the exposure time of the image sensor so that the brightness of an image is maintained on the monitor.
Iris: The iris function is used to electrically measure the brightness of an endoscopic image to obtain a control signal for the purpose of automatic light adjustment.
Color adjustment: Color adjustment adjusts the color balance and the chroma on the monitor.
Freeze: The freeze function creates a stationary view of the moving image.
Release: The release function is used to capture and record an endoscopic image.
Edge enhancement: Edge enhancement is an image processing technique that electronically sharpens the edges of an image.
Structure enhancement: Structure enhancement is an image processing technique that electronically emphasizes the detailed patterns and edges of an image to increase sharpness.
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Important Information - Please Read Before Use
AGC (automatic gain control): The AGC is used to increase the brightness of an endoscopic image electrically when the brightness of the image is dark because the distance between the endoscope’s distal end and the object is too long.
PIP (Picture in Picture): PIP function displays the image of the endoscopic live image and the image of an external device on the monitor simultaneously, where one image is embedded into the other image.
POP (Picture out Picture): POP function displays the image of the endoscopic live image and the image of an external device side by side on the monitor simultaneously.
Annotation: A recorded frozen image is displayed with comments and a title. Up to 4 images can be displayed on the monitor at once.
Portable memory: A digital medium for storage of images, etc.
Wash out: Wash out is the inability to see details in the endoscopic image due to excessive brightness.
SDTV: Standard Definition Television. It is the format used in standard video systems.
HDTV: High Definition Television. This is a format for high resolution video transmission featuring higher definition than the standard SDTV format.
Normal light observation (WLI = White Light Imaging): This is observation using white light.
Optical-digital observation: This is observation using filtered light.
NBI (Narrow Band Imaging) observation: This is optical-digital observation using narrowband light.
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Important Information - Please Read Before Use
Custom switch: The custom switch is a general term for the buttons, keys, and switches to which functions can be assigned: “CUSTOM” button 1 and 2 on the front panel, “CUSTOM” key A, B, C, and D on the keyboard, remote switch 1, 2, 3, 4, and 5 on the endoscope and remote switch 1, 2, 3, and 4 on the foot switch.
Internal buffer: This is buffer space to store the frozen images, patient data, and user settings data.
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 healthcare facility or person in charge of the department (department of internal medicine, etc.). The physician should be qualified to operate and perform safely 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 “ System chart” on page 367 to confirm that the video system center 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 4 (IEC 60601-1-2: 2014), edition 3 (IEC 60601-1-2: 2007), and edition 2 (IEC 60601-1-2: 2001). However, when connected with 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 The video system center does not contain any user-serviceable parts. Do not disassemble, modify, or attempt to repair it; patient or operator injury, equipment damage and/or the impossibility to obtain the expected functionality can result. Some problems that appear to be malfunctions may be correctable by referring to Chapter 9, “Troubleshooting”. If the problem cannot be resolved using the information in Chapter 9, contact Olympus. This instrument is to be repaired by Olympus technicians only. Olympus is not liable for any injury or damage that occurs as a result of repairs attempted by non-Olympus personnel.
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Important Information - Please Read Before Use
Signal words The following signal words are used throughout this manual:
WARNING
Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
CAUTION
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.
NOTE
Indicates additional helpful information.
Precautions Follow the warnings and cautions given below when handling the video system center. This information is to be supplemented by the warnings and cautions given in each chapter.
WARNING • Do not use this instrument for any purpose other than its “ Intended use/Intended purpose” on page 3. • Strictly observe the following precautions. Failure to do so may place the patient and medical personnel in danger of an electric shock. − When the video system center 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 video system center immediately and contact Olympus. − Do not prepare, inspect, or use the video system center with wet hands. • Never install and operate the video system center in locations where: − The concentration of oxygen is high; − Oxidizing agents (such as nitrous oxide (N2O)) are present in the atmosphere; − Flammable gases are present in the atmosphere; − Flammable liquids are near. Otherwise, explosion or a fire may result because the video system center is not explosion-proof. • In case of video system center failure or malfunction, always keep another video system center in the room ready for use.
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Important Information - Please Read Before Use
WARNING • Never insert anything into the ventilation grills of the video system center. It can cause an electric shock and/or a fire. • Although the illumination light emitted from the endoscope’s 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 biological tissue and perforation of the intestines by inappropriate use. Observe the following warnings on the illumination. − Always set the minimum required brightness. The brightness of the image on a monitor may differ from the actual brightness at the distal end of an endoscope. Especially in combination with endoscopes using an electronic shutter function, pay attention to the brightness setting of the light source. When the video system center is used with a light source compatible with automatic brightness control function, be sure to use this function. The automatic brightness control function can keep the illumination light adjusted properly. Refer to the instruction manual for the light source for details. − Do not continue observation in 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 the light source OFF. • 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 the video system center with all equipment to be used. • Do not use the video system center in any place where it may be subject to strong electromagnetic radiation (for example, in the vicinity of a microwave therapeutic equipment, MRI, wireless set, short-wave therapeutic equipment, cellular/portable phone, etc.). This may impair the performance of the video system center. • If the endoscopic image dims during use, blood, mucus or debris may have adhered to the light guide on the distal end of the endoscope. Carefully withdraw the endoscope from the patient and remove the blood or mucus 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 optical-digital observation method alone for primary detection of lesions or for a decision regarding any potential diagnostic or therapeutic intervention.
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Important Information - Please Read Before Use
WARNING • For reasons described below, do not rely on the NBI observation 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 lesions including colonic polyps or Barrett’s esophagus. • To display endoscopic images, connect the output terminal of the video system center directly to the monitor. Do not make the connection via any ancillary equipment. Images may disappear during observation depending on the condition of the ancillary equipment. • The SDI signal is transmitted by daisy-chaining (chaining in a row) several devices. If one of the devices is turned OFF, the SDI signal is not transmitted to the rest of them.
CAUTION • Do not use a pointed or hard object to press the buttons on the front panel and/or keyboard. This may damage the buttons. • Do not touch the electrical contacts inside the video system center’s connectors. • Do not allow a foreign object to penetrate the inside of the portable memory port or video connector socket. The video system center may be damaged. • Do not simultaneously touch any of the exposed electrical contact pins and the patient. It may pose a risk of an electric shock to the patient and/or user. • Do not apply excessive force to the video system center and/or other instruments connected. Otherwise, damage and/or malfunction can occur. • Do not connect or disconnect the endoscope, videoscope cable, or camera head while the video system center is turned ON. Connecting or disconnecting the endoscope while the video system center is ON may destroy the CCD. Turn the video system center OFF before connecting or disconnecting the endoscope. • Be sure that the video system center is not used adjacent to or stacked with other equipment (other than the components of the video system center or system) to avoid electromagnetic interference.
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Important Information - Please Read Before Use
CAUTION • Electromagnetic interference may occur to the video system center 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 the video system center or shielding the location.
NOTE • As defined by the international safety standard (IEC 60601-1), 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
• In case any serious incident happens to User or Patient while operating the device, the incident should be reported to Olympus and the competent authority of the respective member state or country.
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