BARCO AMM190WTDSW LCD Color Display User Manual
Advan Int'l Corp. LCD Color Display Users Manual
BARCO >
Users Manual
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| Document ID | 1451105 |
| Application ID | o8t2+AMGBKaX/L8KqJd9dA== |
| Document Description | Users Manual |
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| Document Type | User Manual |
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| Filesize | 188.19kB (2352386 bits) |
| Date Submitted | 2011-04-20 00:00:00 |
| Date Available | 2011-04-20 00:00:00 |
| Creation Date | 2011-04-04 14:28:18 |
| Producing Software | Adobe PDF Library 9.0 |
| Document Lastmod | 2011-04-19 12:43:02 |
| Document Title | Users Manual |
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WiSe™ 19" HDTV Surgical Display 0240030990 Contents Warnings and Cautions Warnings Cautions About Your Device Intended Use Indications Contraindications Package Content Device Features 10 Setup 10 Connections 12 Basic Video Setup 13 Operation 13 On-Screen Display (OSD) 19 Troubleshooting 21 Periodic Maintenance 21 Cleaning 22 Disposal 23 Technical Specifications 27 Symbols Warnings and Cautions Please read this manual and follow its instructions carefully. The words warning, caution, and note carry special meanings and should be carefully reviewed: Warning The personal safety of the patient may be involved. Disregarding this information could result in personal injury. Caution Special service procedures or precautions must be followed to avoid damaging the device. Note Special information to make maintenance easier or important information more clear. An exclamation mark within a triangle is intended to alert the user to the presence of important operating and maintenance instructions in this manual. A lightning bolt within a triangle is intended to warn of the presence of hazardous voltage. Refer all service to authorized personnel. The WiSe 19" HDTV Surgical Display has been tested under the UL 60601-1 standard and is UL listed for medical application. The warranty is void if any of the following warnings or cautions are disregarded. Warnings To avoid potential serious injury to the user and the patient and/or damage to this device, please note the following warnings: • Read this manual thoroughly and be familiar with its contents prior to using this device. • Federal law (United States of America) restricts this device to sale by, or on the order of, a physician. • Carefully unpack the device and check if any damage occurred during shipment. • This device is non-sterile and therefore should not be placed in the sterile field. • Do not place the device or any other heavy object on the power cord. Damage to the cable can cause fire or electric shock. • To avoid electric shock, avoid removing the bezel. • This device should not be used adjacent to or stacked with other devices. If adjacent or stacked use is necessary, the device should be observed to verify normal operation in the configuration in which it will be used. • Test this device prior to a surgical procedure. This device was fully tested at the factory before shipment. • Do not attempt internal repairs or adjustments not specifically detailed in this manual. Ensure that readjustments, modifications, and/or repairs are carried out by persons authorized by Stryker Endoscopy. • Do not put any liquid or solid object into the panel. If this occurs, unplug the device and have it checked by qualified personnel before operating it any further. • Use appropriate caution to prevent contact with fluids if the device is being used with a power supply in patient environments. • The use of cables and/or other accessories with this device, other than those specified, may result in increased emissions or decreased immunity of this device. Cautions • Connect the device to an AC adapter connected to a hospital grade power cord ensuring the power cord is plugged into a grounded power outlet to achieve grounding reliability. • Do not sterilize the device, as the delicate electronics cannot withstand this procedure. • Use only the proprietary surgical display power supply for the display. Completely secure the connection between the DC power cord and the extension cord. • Never operate the device immediately after transportation from a cold location to a warm location. • To connect to an international power supply, use an attachment plug appropriate for the power outlet, as outlined in the "Technical Specifications" section of this manual. • Unplug the device if it is not to be used for an extended period of time. To disconnect the cord, unscrew the plug first, then pull the cord out by the plug. Never pull the cord itself. • Do not expose the device to moisture or apply liquid cleaners directly to the screen. Spray the cleaning solution into a soft cloth and clean gently. For further detail, refer to the "Periodic Maintenance" section of this manual. • Allow adequate air circulation to prevent internal heat buildup. Do not place the device on surfaces (rugs, blankets, etc.) or near materials (curtains, draperies) that may block the ventilation slots. The device is cooled by natural convection and has no fan. • Do not touch the patient with signal input or output connectors. Equipment with SIP/SOP connectors should either comply with IEC 60601-1 and/or IEC 60601-1-1 harmonized national standards or the combination should be evaluated for safety. • To ensure electromagnetic compatibility, refer to the “Electromagnetic Compatibility” section of this manual. The WiSe 19" HDTV Surgical Display (0240030990) must be installed and operated according to the EMC information provided in this manual. • Pay close attention to the cleaning instructions in this manual. A deviation may cause damage. • Do not install the device near sunlight, excessive dust, mechanical vibration, or shock. • Do not operate with the glass device screen facing downward. • Handle the device with care. Do not strike or scratch the screen. • Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the device. Note: This device has been tested and found to comply with the limit for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This device generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. There is no guarantee that interference will not occur in a particular installation, which can be determined by turning the device off and on. The user is encouraged to try to correct the interference by one or more of the following measures: • Reorient or relocate the receiving device. • Increase the separation distance between the device. • Connect the device to an outlet on a circuit different from that to which the other device(s) are connected. • Consult the manufacturer or field service technician for help. About Your Device The WiSe 19" HDTV Surgical Display (display) is a wide screen LCD surgical display that can support a maximum resolution of 1080p. The display supports various video inputs, including digital RGB, analog RGB, serial digital interface (SDI), component video (YPbPr/RGB), S-video, C-video, and wireless RGB. The display features an optional WiSe HDTV Transmitter, which allows it to receive a high-definition video signal over a radio-frequency link (USA and Canada only). Intended Use The WiSe 19" HDTV Surgical Display is intended for video display during surgical procedures. Indications This device is indicated for the following surgical procedures: • • • • • • • • • • • • • General surgery General laparoscopy Nasopharynogoscopy Ear endoscopy Sinusocopy Plastic surgery wherever a laparoscope/endoscope/ arthroscope is indicated for use Laparoscopic cholecystectomy Laparoscopic hernia repair Laparoscopic appendectomy Laparoscopic pelvic lymph node dissection Laparoscopically assisted hysterectomy Laparoscopic & thorascopic anterior spinal fusion Anterior cruciate ligament reconstruction • • • • • • • • • • • • • Knee arthroscopy Shoulder arthroscopy Small joint arthroscopy Decompression fixation Wedge resection Flexible endoscopy Urology Gynecology Lung biopsy pleural biopsy Dorsal sympathectomy Pleurodesis Internal mammary artery dissection for coronary artery bypass grafting where endoscopic visualization is indicated and examination of the evacuated cardiac chamber during performance of valve replacement The indicated users of this device are as follows: • • • • General surgeons Gynecologists Cardiac surgeons Thoracic surgeons • • • • Plastic surgeons Orthopedic surgeons ENT surgeons Urologists The display is a non-sterile, reusable device not intended for use in the sterile field. The display is intended for use by qualified physicians having complete knowledge of these surgical procedures. Contraindications There are no known contraindications for this device. Package Content Package Content Part Number 1. WiSe 19" HDTV Surgical Display 240-030-990 2. (4) M4 × 10 mm VESA screws 3. Hospital-grade AC power cord (USA and Canada only) 4. WiSe 19'' Surgical Power Supply 5. Cable Cover – – 240-030-992 – Optional Accessories Part Number WiSe HDTV Transmitter (USA and Canada only) 240-030-971 15-ft. (5 pin) DC extension cable 240-030-951 75-ft. (5 pin) DC extension cable 240-030-952 WiSe 19" Display Cover 240-030-991 Hospital-grade AC power cord (USA and Canada only) 105-033-001 Device Features Front panel Operate the display using the rotary control located on the front panel. A list of the display controls and their functions is provided below. 1. Display Screen Shows video image. 2. Power switch (soft) Powers the display ON and OFF. 3. Power LED Indicates current status. Shines green if the display is powered on or is in screen saver mode; blinks red if the display is in standby mode; blinks amber if over voltage. 4. Token slot Token insertion site used to establish a wireless connection with the transmitter (optional for USA and Canada only). 5. Token LED Provides feedback when linking the display and transmitter (optional for USA and Canada only). 6. Rotary control Accesses the on-screen display and navigates through its functions. Rear panel 1. VESA mounting holes (75 mm) Provide access points for mounting the display. 2. VESA mounting holes (100 mm) Provide access points for mounting the display. 3. Connector labels Indicate the types of video connectors. 4. Power connector Connects to the 13V DC power supply. 5. Power switch (hard) Powers the input DC power ON and OFF. 6. Cable-management Velcro Straps Organize cables (3 straps included). 7. Cable-management cover Covers cables. Cable Cover Installing the Cable Cover 1. Align the left and right hinges of the cable cover onto the bottom rear of the display. 2. Snap on the top section of the cable cover to the aligning clips. 3. With your fingers, turn the thumbscrews clockwise to tighten and lock the cable cover onto the display. Uninstalling the Cable Cover 1. With your fingers, turn the thumbscrews counter clockwise to loosen. 2. Once the thumbscrews are completely loosened, pinch the left and right clips and pull the cable cover towards you. 3. Remove the cable cover off the left and right hinges. Setup Stryker Endoscopy considers instructional training, or inservice, an integral part of this device. Your local Stryker Endoscopy sales representative will perform at least one inservice at your convenience to help set up your device and instruct you and your staff on its operation and maintenance. To schedule an inservice, contact your local Stryker Endoscopy representative after your device has arrived. Connections Connection Ports Video input signals are connected to the rear of the display, as illustrated below: 10 10 11 12 13 14 1. Power 13V 8. G/Y 2. Non-Functional 9. B/Pb 3. DVI 10. H-sync 4. VGA 11. V-sync 5. S-Video 12. HD/SD SDI IN 6. C-Video/SOG 13. HD/SD SDI OUT 7. R/Pr 14. RS232 Connecting the WiSe 19" Surgical Display Power Supply 1. Connect the power supply to the 13V input on the display. 2. Connect the power cord to the power supply. 3. Connect the AC power, using the supplied hospital-grade power cord. 4. (Optional, not shown) Connect an extension cord between the power supply and display. 5. Install cable cover. 11 Basic Video Setup WiSe 19" HDTV Surgical Display SDC Camera 1. Ensure the cable cover has been removed. 2. Route the video output 1 from the camera to the SDC. 3. Route the video output 1 from the SDC to input on the DVI input on the display. 4. Reinstall the cable cover. 12 Operation Operate the display using the rotary control located on the front panel. A list of the display controls and their functions is provided below. On-Screen Display (OSD) Accessing the On-Screen Display To access the OSD, use the Rotary Control as outlined below: • Turn Right/Left — With the on-screen display menu activated, turning increases/decreases the value of the selected parameter. With the on-screen display deactivated, turning activates the video source selection menu. • Push — Accesses/selects on-screen display menu. • Push and Hold — Exits on-screen display menu. Operating On-Screen Display The device OSD helps navigate through various device menus. 1. Press the Rotary Control to activate the OSD menu. 2. Rotate the Rotary Control to move up or down through the menu. The parameter will be highlighted when selected. 3. Press the Rotary Control to enter the next level OSD. 4. Rotate the Rotary Control to increase or decrease the value of the selected parameter, or to make a selection on different options. 5. To exit the OSD menu screen from the second — or third — level OSD menu, select the Exit option. To completely exit the OSD, press and hold the Rotary Control. If no keys are pressed, the OSD will automatically exit after the factory-set predetermined time (the time is customizable). 6. While the OSD menu is deactivated, rotate the Rotary Control to activate the input signal selection menu. The current input signal will be indicated by a dot. Rotate the Rotary Control to select the preferred input signal. Input Selection List • • • • Digital RGB Analog RGB S-Video Component (Y/Pb/Pr) • HD/SD-SDI • SOG • RGBS • C-Video • Wireless RGB • Exit 13 OSD Menus Speciality Menu Item Description Color Temperature* Chooses between color temperatures for Standard, Arth, Lap, PACS, or Norm Range — Red Red balance -128 – 127 Green Green balance -128 – 127 Blue Blue balance -128 – 127 Gamma Gamma value 0.1 – 2.5, S0, S1, S2 Menu Item Description Range Brightness Increases or decreases the brightness 0 – 100 Contrast Increases or decreases the contrast 0 – 100 Phase** Increases or decreases the Phase level 0 – 100 Chroma** Increases or decreases the Chroma level 0 – 100 Image Sharpness Sets image sharpness 1 – 10 Video Sharpness** Increases or decreases the video sharpness 0 – 100 Setting 14 Color Temperature RGB adjustment is available only for Standard, Arth, and Lap settings. PACS and Norm adjustments are only avaliable under SOG input. ** Only available under SDI-, S-, or C-video input. Image Effect Menu Item Description Scale Mode Chooses scale mode between Fill All, V-Fill, H-Fill, One-To-One, or Fill-Aspect Freeze Frame Enables or disables freeze frame PIP Enables PIP (picture in picture) function POP Enables POP (picture on picture) function PBP Enables PBP (picture by picture) function Advanced Menu Item Description Key Lock Sets to key lock mode Auto Source Select Adjusts Auto Source Select between on and off DPMS Chooses DPMS (display power OFF, 30, 60, 90, management signaling) or 120min OSD Control Controls OSD Menu Position, Background, and Time out Restore Factory Settings Sets to factory default Screen Control*** Controls and adjusts Horizontal, Vertical, Frequency, and Phase *** Only available under analog inputs under certain respective inputs. Wireless Module (for the USA and Canada only) Status Description RX MAC: XXXXXXXX Receiver RX SW: vXX.XX.XX TX MAC: XXXXXXXX Transmitter TX SW: vXX.XX.XX SIGNAL: Excellent, Good, Poor REGIONLAL SETTING: XXXXXXXX CHANNEL XXXX MHz 15 Information Menu Item Description User Name Entry Enters custom user name display for boot-up display Serial Number Displays device serial number Runtime Displays current device total run time Input Format Displays current input format Note: Actual on-screen display values may vary with updated versions of the firmware and user settings. 16 Linking Transmitter to Auxiliary Display (for USA and Canada Only) Temporary Linking Caution Equipment that employs RF communications may affect the normal function of the transmitter. When choosing a location for the transmitter, consult the “Electromagnetic Compatibility” section of this manual to ensure proper function. The transmitter functions in the 4.9 – 5.9 GHz spectrum. As necessary, remove or reconfigure other wireless devices from the environment, such as cordless phones and 802.11a/n routers to make channels available for the transmitter and display. To link the display to the transmitter and thereby enable wireless communication, any blue WiSe HDTV Transmitter token will suffice. 1. Power on the transmitter and auxiliary display. The token LED shines amber as the units perform startup functions. 2. Insert the token into the token slot on the transmitter. The token LED continues to shine amber as it writes the data. 3. When the token LED turns green, remove the token from the transmitter. 4. Within 2 minutes, insert the token into the token slot on the auxiliary display. An audible tone will sound from the transmitter and the token LED will change from amber to green when the display and transmitter have been linked. 17 5. Remove the token from the token slot on the auxiliary display. 6. By repeating steps 4 and 5, as many as two additional auxiliary displays may be linked. All linking must be done within two minutes. 7. Store the token in the transmitter token slot when not in use. Note: If multiple transmitters are within 100 feet of each other, for example, in adjacent operating rooms, link each transmitter to its respective display(s) one set at a time. Wait 15 seconds before linking the next transmitter/display set. Permanent Linking Please contact your Stryker rep in order to permanently link the display(s) with a specific transmitter, as deemed appropriate. A permanent link may be desirable in certain cases. Once the display(s)/transmitter set has been permanently linked, the set will automatically link when powered on. Display(s)/transmitter sets that have been set to permanent link mode should be kept in the same operating room. To return the display(s)/transmitter set to default linking mode please follow the instructions below using a blue WiSe Linking Token. 1. Power on the display(s) and transmitter. 2. Insert the blue token into the transmitter and remove it when the token LED turns green. 3. Insert the blue token into each display, one at a time, and remove the token when the token LED turns green. 4. Power off all devices. 5. Power on all devices. Now the system can be linked as described in the default linking mode procedure. 18 Troubleshooting Before returning your display for service, consult the troubleshooting list below: Display Problem No picture Current Status Remedy Power LED on Using the OSD Menu, adjust the brightness and contrast to maximum, or reset them to their default settings. Power LED off Ensure the power switch at the front and rear of the display are set to ON. Check if the AC power cord is properly connected to the AC adapter and outlet. Power LED blinking Check if the video signal cable is properly connected at the back of the display. Check if power of the video signal source system is ON. Abnormal picture OSD Menu error message Oversized, undersized, or missing display; or center shift. Using the Screen Control Menu, adjust the Phase, Frequency, Horizontal, and settings in order to correct the display image. “Video format not supported” Ensure that an acceptable video source is connected. Refer to the "Technical Specifications" section of this manual for a list of acceptable video formats. Wait a few seconds after initial sync of video signals, or power cycle the display. 19 Optional Transmitter (for the USA and Canada Only) Problem 20 Current Status Remedy Wireless link not established within 2 minutes (with optional WiSe HDTV transmitter). “Wireless RGB No Signal” Cycle the hard power switch at the rear of the display. Cycle the hard power switch at the front of the transmitter. Wireless link established with some but not all displays (with optional WiSe HDTV transmitter). “Wireless RGB No Signal” Cycle the hard power switch on the affected display only. Re-insert the token into the display. Transmitter token LED blinks amber No channels available for WiSe System Remove or reconfigure other wireless devices from the environment, such as cordless phones and 802.11 a/n routers, to make channels available for the display and transmitter. Periodic Maintenance Caution Do not expose the display to moisture or apply liquid cleaners directly to the display screen. Spray the cleaning solution into a soft cloth and clean the screen gently. Cleaning 1. Disconnect the display from the power supply before cleaning. 2. Clean the plastic areas of the display with a dry, soft cloth, or a soft cloth lightly moistened with mild detergent solution. Do not use any type of solvent, such as alcohol or benzine, which might damage the finish. Recommended cleaning agents for bezel cleaning based on testing include: • Cidex (2.4% glutaraldehyde solution) • 0.5% Chlorhexidine in 70% isopropyl alcohol 3. Clean the display screen with a dry, soft cloth, or soft cloth lightly moistened with warm water. Other acceptable cleaning agents are listed below: • 70% isopropyl alcohol • Cidex (2.4% glutaraldehyde solution) • 0.5% Chlorhexidine in 70% isopropyl alcohol 4. Dry thoroughly with a soft towel or gauze surgical sponge. Before using a cleaning agent not listed, ensure that the respective agent is validated in order to assure durability of the cleanability of the device. To validate the agent, a cleaning process repeated 104 times needs to be conducted with the respective cleaning agent. This cleaning process includes using the prospective cleaning agent, moistening a cloth or sponge, and wiping the front and sides of the console. A visual check incorporating the following is used to ensure compatibility: • The device should still function appropriately • The device finish should not discolor or scratch • The device finish should not dissolve or rub off • The device labeling should still be legible These validation steps need to be performed in order to validate any and all cleaning agents outside of those listed. 21 Disposal This product contains electrical waste or electronic equipment. It must not be disposed of as unsorted municipal waste and must be collected separately in accordance with applicable national or institutional related policies relating to obsolete electronic equipment. Dispose of any system accessories according to normal institutional practice relating to potentially contaminated items. 22 Technical Specifications Display LCD Display Panel 18.95" (481.33 mm) Diagonal (a-Si TFT active matrix LCD) Synchronization 2.5 – 5.0 Vpp separated sync Pixel Pitch 0.2835 (H) × 0.2835 (V) mm Response Time < 5 ms Typ Viewing Angle Right/Left 80 (Typ) Up 75 (Typ), Down 85 (Typ) Display Colors 16.7 million colors Native Resolution 1440 (H) lines × 900 (V) lines Input Signal 1 DVI, 1 VGA, 1 HD/SD-SDI, 1 C-Video/SOG, 1 S-Video, 1 Component (Y/G, Pb/B, Pr/R, H, VS), 1 Wireless Maximum Pixel Clock 160 MHz Electrical Power Adapter Power Consumption Current 100 – 240 VAC; 13 VDC 90 W (max) Direct Current/Voltage Rating Please ensure the respective power cord complies with applicable local regulations and standards. 110V +/- 10V power outlets Select a power supply cord that is UL Listed and C.S.A Certified, type SJT or SVT, 3 – conductor, 18AWG, terminated in a molded on hospital grade plug cap rated 110V +/- 10V, 15A, with a minimum length of six feet. 220V +/- 20V power outlets Select a power supply cord that is internationally harmonized and marked “”, 3 – conductor, 0.75 mm^2 minimum wire, rated 220V +/- 20V, 10A with a PVC insulated jacket. The cord must have a molded on plug cap rated 220V +/-20V, 10A. The cord and plug cap must be suitable for medical use. Dimensions Dimensions (W × H × D) 462.3 × 340.8 × 106.7 mm 18.2 × 13.4 × 4.2 in Weight (approximate) 5.8 kg; 12.79 lbs. VESA Mounting Interface VESA 100 × 100 mm VESA 75 × 75 mm Operating Conditions Operating Temperature Relative Humidity Electrical Input Rating 41 – 104°F (5 – 40°C) 30 – 95% 13V DC 6.92A 23 Transport & Storage Conditions Storage -0.4 – 140°F (-18 – 60°C) Relative Humidity Range 10 – 85% Classification and Approvals Class I Equipment Medical equipment with respect to electric shock, fire, and mechanical hazards only in accordance with UL 60601-1 and CAN/CSA C22.2 No. 601.1. IPX1 Water Ingress Protection Continuous Operation Compliance Medical Safety Standards IEC 60601-1:1988 + A1:1991 + A2:1995 CAN/CSA C22.2 No 601.1-M90 UL 60601-1:2003 AS/NZS 3200.1.0:1998 CSA 22.2.601.1.1:2002 Medical EMC Standard IEC 60601-1-2:2007 FCC Regulations FCC Part 15 Class B FCC Identifier: QVXAMM190WTDSW IC Regulations IC: 7680A-AMN12100 (WiSe 19" and 26" HDTV Surgical Display) Note: Please contact your local Stryker Endoscopy sales representative for information on changes and new products. Electromagnetic Compatibility Like other electrical medical equipment, the WiSe™ 19" HDTV Surgical Display requires special precautions to ensure electromagnetic compatibility with other electrical medical devices. To ensure electromagnetic compatibility (EMC), the display must be installed and operated according to the EMC information provided in this manual. The display has been designed and tested to comply with IEC 60601-1-2:2001 requirements for EMC with other devices. Warning Caution 24 When this device is connected with other electrical equipment, leakage currents may be additive. To minimize total leakage current per patient, ensure that all systems are installed according to the requirements of IEC 60601-1-1. Portable and mobile RF communications equipment may affect the normal function of the display. Do not use cables or accessories other than those provided with the display, as this may result in increased electromagnetic emissions or decreased immunity to such emissions. If the display is used adjacent to or stacked with other equipment, observe and verify normal operation of the display in the configuration in which it will be used prior to using it in a surgical procedure. Consult the tables below for guidance in placing the display. Guidance and Manufacturer’s Declaration: Electromagnetic Emissions The WiSe™ 19" HDTV Surgical Display is intended for use in the electromagnetic environment specified below. The customer or the user of the WiSe™ 19" HDTV Surgical Display should ensure it is used in such an environment. Emissions test Compliance Electromagnetic Environment - guidance RF emissions CISPR 11 Group 1 The WiSe™ 19" HDTV Surgical Display uses RF 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. RF emissions CISPR 11 Class B Harmonic emissions IEC61000-3-2 Class D Voltage Fluctuations/ flicker emissions IEC61000-3-3 Complies The WiSe™ 19" HDTV Surgical Display is suitable for use in all establishments other than domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes, provided the following warning is heeded: Warning: This system is intended for use by health care professionals only. This system may cause radio interference or may disrupt the operation of nearby equipment. It may be necessary to take mitigation measures, such as reorienting or relocating the system or shielding the location. Guidance and Manufacturer’s Declaration — Electromagnetic Immunity The WiSe™ 19" HDTV Surgical Display is intended for use in the electromagnetic environment specified below. The customer or the user of the WiSe™ 19" HDTV Surgical Display should ensure that it is used in such an environment. Electromagnetic Environment-Guidance Immunity Test IEC 60601 Test Level Compliance Level Electrostatic Discharge (ESD) IEC61000-4-2 6kV contact 8kV air 6kV contact 8kV air Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. Electrical fast transient/burst IEC61000-4-4 2kV for power supply lines 1kV for input/output lines 2kV line to ground 1kV line to line Mains power quality should be that of a typical commercial or hospital environment. Surge IEC61000-4-5 1kV differential mode 2kV common mode 1kV differential mode 2kV common mode Mains power quality should be that of a typical commercial or hospital environment Voltage dips, short interruptions and voltage variations on power supply input lines • <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 sec. • <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 sec Mains power quality should be that of a typical commercial or hospital environment. If the user of the transmitter requires continued operation during power mains interruptions, it is recommended that the Wireless Transmitter be powered from an uninterruptible power supply or a battery. 3.0 A/m 3.0 A/m Power-frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. IEC61000-4-11 Power frequency (50/60Hz) magnetic field IEC 61000-4-8 Note: Ut is the AC mains voltage prior to application of the test level. 25 Guidance and Manufacturer’s Declaration: Electromagnetic Immunity The WiSe™ 19" HDTV Surgical Display is intended for use in the electromagnetic environment specified below. The customer or the user of the WiSe™ 19" HDTV Surgical Display should ensure that it is used in such an environment. Immunity Test IEC 60601 Test level Compliance Level Electromagnetic Environment - Guidance Portable and mobile RF communications equipment should be used no closer to any part of the WiSe 19" HDTV Surgical Display, including its cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended Separation Distance: Conducted RF IEC 61000-4-6 3 Vrms 150 kHz to 80 MHz 3V d = 1.17√P Radiated RF IEC 61000-4-3 3 V/m 80MHz to 2.5 GHz 3 V/m d = 1.17√P 80 MHz to 800 MHz d = 2.33√P 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). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey (a), should be less than the compliance level in each frequency range(b). Interference may occur in the vicinity of equipment marked with the following symbol: NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. (a) Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast, cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the WiSe™ 19" HDTV Surgical Display is used exceeds the applicable RF compliance level above, the display and transmitter should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the WiSe™ 19" HDTV Surgical Display. (b) Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the WiSe™ 19" HDTV Surgical Display The WiSe™ 19" HDTV Surgical Display is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of the WiSe™ 19" HDTV Surgical Display can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the WiSe™ 19" HDTV Surgical Display as recommended below, according to the maximum output power of the communications equipment. Separation distance (m) according to frequency of transmitter Rated maximum output power (W) of transmitter 150 kHz to 80 MHz d = 1.17√P 80 kHz to 800 MHz d = 1.17√P 800 kHz to 2.5 GHz d = 1.17√P 0.01 0.12 0.12 0.23 0.1 0.37 0.37 0.74 1.17 1.17 2.33 10 3.70 3.70 7.37 100 11.70 11.70 23.30 For transmitters rated at a maximum output power not listed above, the recommended separation distance (d) in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. 26 Symbols The following symbols appear on the product, its labeling, or the product packaging. Each symbol carries a special definition, as defined below: Direct Current For Indoor Use Only Do Not Get Device Wet DC Power Control Switch Maximum Stacking This Side Up Wireless Transmission Fragile Tested to comply with FCC Class B standards IC IPX1 Degrees of protection against the ingress of water Operating Humidity Ratings Operating Temperature Ratings Medical Equipment is in accordance with UL 60601-1 and CAN/CSA C22.2 No. 601.1 in regards to electric shock, fire hazards, and mechanical hazards. This symbol indicates that this product is compliant to applicable standards and is suitable for the Australian market. Industrial Canada MADE IN KOREA Made in Korea No Servicable Parts Refer to Instructions Japan PSE Mark Denan UL Functional Safety Recognized Component Efficiency Level This product contains waste electrical or electronic equipment. It must not be disposed of as unsorted municipal waste and must be collected separately. 27 Stryker Endoscopy 5900 Optical Court San Jose, CA 95138 USA 1-408-754-2000, 1-800-624-4422 www.stryker.com European Representative: Regulatory Manager, Stryker France ZAC Satolas Green Pusignan Av. De Satolas Green 69881 MEYZIEU Cedex, France Stryker Corporation or its divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: WiSe and the Stryker logo. All other trademarks are trademarks of their respective owners or holders. P16023 A 2011/04
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