BARCO AMM261WTDS 26 Inch LCD Monitor User Manual P22286A Book indb
Advan Int'l Corp. 26 Inch LCD Monitor P22286A Book indb
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User manual
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| Document ID | 1926743 |
| Application ID | 3aueg2eVk8biWb6w/6c1Bw== |
| Document Description | User manual |
| Short Term Confidential | No |
| Permanent Confidential | No |
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| Document Type | User Manual |
| Display Format | Adobe Acrobat PDF - pdf |
| Filesize | 147.29kB (1841137 bits) |
| Date Submitted | 2013-03-28 00:00:00 |
| Date Available | 2013-03-28 00:00:00 |
| Creation Date | 2013-02-15 16:33:21 |
| Producing Software | Acrobat Distiller 10.1.4 (Windows) |
| Document Lastmod | 2013-03-25 12:58:31 |
| Document Title | P22286A_Book.indb |
| Document Creator | PScript5.dll Version 5.2.2 |
| Document Author: | SPerkins |
VisionPro 26” LED Display 0240-031-020 Table of Contents Warnings and Cautions ............................................................................................1 About Your Device .....................................................................................................3 Intended Use ........................................................................................................................3 Indications .............................................................................................................................3 Contraindications................................................................................................................3 Package Contents ...............................................................................................................4 Device Features....................................................................................................................5 Setup ............................................................................................................................9 Connections ..........................................................................................................................9 Basic Video Setup ............................................................................................................. 11 Operation ................................................................................................................. 12 On-Screen Display (OSD) ............................................................................................... 12 OSD Menus ......................................................................................................................... 14 Troubleshooting ............................................................................................................... 16 Cleaning and Maintenance................................................................................... 17 Technical Specifications ........................................................................................ 18 Symbols and Definitions ....................................................................................... 22 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: Indicates measures to avoid potential serious injury to the user and the patient and/or damage to this device. Caution: Indicates risks to the equipment. Failure to follow cautions may result in product damage. Note: Provides special information to clarify instructions or present additional useful information. Warnings To avoid potential serious injury to the user and the patient and/or damage to this device, please note the following warnings: 1. Read this manual thoroughly and be familiar with its contents prior to using this device. 2. Federal law (United States of America) restricts this device to sale by, or on the order of, a physician. 3. Carefully unpack the device and check if any damage occurred during shipment. 4. This device is non-sterile and therefore should not be placed in the sterile field. 5. Do not place the device or any other heavy object on the power cord. Damage to the cable can cause fire or electric shock. 6. To avoid electric shock, avoid removing the bezel. 7. 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. 8. Test this device prior to a surgical procedure. This device was fully tested at the factory before shipment. 9. 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. 10. 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. 11. Use appropriate caution to prevent contact with fluids if the device is being used with a power supply in patient environments. 12. 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 1. 2. 3. 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. 4. 5. 6. 7. 8. 9. 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 cations" section of this manual. Unplug the device if it is not to be used for an extended period of time. To disconnect the rst, 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 "Cleaning and 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/ national standards or the combination should be evaluated for safety. 10. To ensure electromagnetic compatibility, refer to the “Electromagnetic Compatibility” section 11. Pay close attention to the cleaning instructions in this manual. A deviation may cause damage. 12. Do not install the device near sunlight, excessive dust, mechanical vibration, or shock. cult to disconnect the power cord from the supply mains. 14. Do not operate with the glass device screen facing downward. 15. Handle the device with care. Do not strike or scratch the screen. cations not expressly approved by the party responsible for compliance could void the user’s authority to operate the device. The warranty is void if any of these warnings or cautions are disregarded. This product contains electrical waste or electronic equipment. It must not be disposed of as unsorted municipal waste and must be collected separately. For a Class B digital device or peripheral, the instructions furnished the user shall include the following or similar statement, placed in a prominent location in the text of the manual: NOTE: This equipment has been tested and found to comply with the limits 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 equipment 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. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment 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 antenna. —Increase the separation between the equipment and receiver. —Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. —Consult the dealer or an experienced radio/TV technician for help. (c) The provisions of paragraphs (a) and (b) of this section do not apply to digital devices exempted from the technical standards under the provisions of § 15.103. (d) For systems incorporating several digital devices, the statement shown in paragraph (a) or (b) of this section needs to be contained only in the instruction manual for the main control unit. (e) In cases where the manual is provided only in a form other than paper, such as on a computer disk or over the Internet, the information required by this section may be included in the manual in that alternative form, provided the user can reasonably be expected to have the capability to access information in that form. About Your Device VisionPro 26” LED Display REF: 0240-031-020 The VisionPro 26” LED Display is a wide screen LED surgical display that can support a maximum resolution of WUXGA (1920x1200). The display supports various video inputs, including digital RGB, analog RGB, serial digital interface (SDI), component video (YPbPr/RGBS), S-video, and C-video. Intended Use The VisionPro 26” LED Display is intended for video display during surgical procedures. Indications This device is indicated for the following surgical procedures: • Arthroscopy (orthopedic surgery) • Laparoscopy (general and gynecological surgery) • Thorascopy • Endoscopy (general, gastroenterological and ENT) • ENT • Gynecology • General surgery 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 Contents Reference Part Number Package Contents 0240-031-020 VisionPro 26” LED Display – (4) M4 × 16 mm VESA screws – Hospital-grade AC power cord 0240-031-004 Medical Power Supply – Cable Cover Part Number Optional Accessories 0240-031-002 VisionPro 26” Display Cover 0240-030-951 15-ft. (5 pin) DC extension cable 0240-030-952 75-ft. (5 pin) DC extension cable 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. 2. 3. 4. Auxilliary device status indicator Display Screen Power switch (soft) Power LED 5. 6. 7. 8. 9. PIP Bright Specialty Input Rotary control LED shines red to indicate an active connection to a connected device. Shows video image. Powers the display ON and OFF. Indicates current status. Shines green if the display is powered on or is in screen saver mode; blinks red if the display is in sleep mode; blinks amber if over or under voltage. Accesses the Picture in Picture adjustment menu. Accesses the Brightness adjustment menu Accesses the Specialty adjustment menu Accesses the Input selection menu Accesses the on-screen display and navigates through its functions. Rear panel 12 11 10 1. Accessory mount 2. 3. 4. 5. VESA mounting holes Power switch (hard) Power connector Handles 6. 7. 8. Cable cover hinges Velcro straps Cable cover thumbscrews 9. 10. 11. 12. Cable cover Cable cover clips Cable wrap Locking feature Provides an access point for mounting optional accessories. Provide access points for mounting the display. Powers the input DC power ON and OFF. Connects to the 24V DC power supply. Aid in display positioning. Caution: The handles are not intended to bear the entire weight of the display Attach the bottom of the cable cover to the display. Straps aid in cable management. Attach the cable cover to the display, and are tightened or loosened using fingers. Covers and conceals cables. Attach the top of the cable cover to the display. Provides a location for wrapping cables. A locking mechanism or cable may be routed here for security purposes. 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. Removing the Cable Cover 1. With your fingers, turn the thumbscrews counterclockwise 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 from the left and right hinges. Display Handles Caution: The handles are intended to aid in positioning the display, not for transporting the display. The handles should not bear the full weight of the display. Removing or Reinstalling the Display Handles To Remove: 1. Using a 3mm hex key, loosen the two M4 x 30mm screws and gently pull the handle away from the display. To Reinstall: 1. Align the handle with the screw holes on the rear of the display. 2. Using a 3mm hex key, install the two M4 x 30mm screws to attach the handle. 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: 1. 2. 3. 4. 5. 6. 7. DVI 3G/HD/SD SDI-in 3G/HD/SD SDI-out VGA S-Video C-Video/SOG R/Pr 8. 9. 10. 11. 12. G/Y B/Pb H-sync V-sync RS232 10 11 12 Connecting the Power Supply 1. 2. 3. 4. 5. 10 Connect the power supply to the 24V input on the display. Connect the AC power cord to the power supply*. Connect the AC power, using the supplied hospital-grade power cord. (Optional, not shown) Connect an extension cord between the power supply and display. Install cable cover. * Power supply Model Number: BPM150S24F11 Manufacturer: Bridgepower Corp. Basic Video Setup 1. 2. Route the video output 1 from the camera to the SDC DVI input. Route the video output 1 from the SDC DVI output to the DVI input on the display. 11 Operation Operate the display using the rotary control and the four buttons 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 use the four front-panel buttons: Note: Use the Rotary Control to navigate the menus once they are activated. 1. 2. 3. 4. PIP: Activates Picture Mode (Picture in Picture, Picture by Picture, Picture on Picture) Bright: Activates the Brightness adjustment menu. Specialty: Activates the Specialty adjustment menu. Input: Activates the Input selection menu. To use the Rotary Control: • Push — Accesses/selects on-screen display menu. • Turn Right/Left — With the on-screen display menu activated, turning increases/decreases the value of the selected parameter. • Push and Hold — Exits on-screen display menu. 12 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). 13 OSD Menus Speciality Menu Item Description Range Color Temperature* Chooses between color temperatures for Lap A, Lap B, Standard, Arthro, PACS, NORM, ENT, GYN. — 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 Color Temperature RGB adjustment is available only for Standard, Arth, and Lap settings. PACS and Norm adjustments are only avaliable under SOG input. Brightness Settings 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 ** 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 Settings Menu Item Description Key Lock Key lock on: Disables all key functions Press and hold the rotary knob to turn off key lock. 14 Menu Item Description Auto Source Select Scans inputs until an active video source is detected. Sleep Timer On: The display enters sleep mode if no active video source is detected. Off : The display will not enter sleep mode. Timer: Set the time until the display enters sleep mode: 30, 60, 90, or 120 minutes. OSD Control Controls OSD (On Screen Display) Menu Position, Background, and Timeout Restore Factory Settings Sets to factory default Screen Control VGA S-Video, C-Video, SOG, RGBs, Component • • • • Horizontal Vertical Phase Frequency • • Horizontal Vertical 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. 15 Troubleshooting Before returning your display for service, consult the troubleshooting list below: Problem Current Status Remedy No picture 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. Check that the power supply is fully connected and functioning properly. Power LED blinking Abnormal picture Oversized, undersized, or missing video; or center shift. Red Display is in sleep mode. Press any key to wake the display. Amber The power supply may be over or under voltage. Using the Screen Control Menu, adjust the Phase, Frequency, Horizontal, and Vertical settings in order to correct the display image. Adjust settings in Scale Mode For VGA input only: push and hold the rotary control for 1-2 seconds to re-sync the video feed. Wait a few seconds after initial sync of video signals, or power cycle the display. OSD error message 16 “Out of Range” Ensure that an acceptable video source is connected. Refer to the “Technical Specifications” section of this manual for a list of acceptable video formats. Cleaning and Maintenance Warning To avoid electric shock and potentially fatal injury, unplug the display from the electrical outlet before cleaning. Caution • • • • Do not spray cleaning liquid directly onto the display as product damage may result. Spray on the cloth before wiping the unit. Do not immerse the display in any liquid as product damage will result. Do not use corrosive cleaning solutions to clean the display as product damage may result. Do not sterilize the display as product damage may result. Cleaning Should the unit need cleaning: 1. If the display cover is in place, remove the cover prior to cleaning. 2. Apply standard disinfectant or mild detergent to a dry sterile cloth. 3. Wipe the unit. 4. Take extra care when cleaning the screen. Excess liquid or drips that enter the bottom of the screen may result in product damage. 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. 17 cations Display (a-Si TFT active matrix LCD) Viewing Angle Electrical Power Adapter Power Consumption (approximate) Right/Left/Up/Down 89 Degrees Input: 100 – 240 VAC; 50 – 60 Hz; 2.5 A Output: 24V DC; 6.25A (150W Max) Model Number: BPM150S24F11 35 - 65 Watts 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 ed, type SJT or SVT, 3 – conductor, 18AWG, terminated in a molded on hospital grade plug cap rated 220V +/- 20V power outlets Select a power supply cord that is internationally harmonized and marked “”, 3 – conductor, 0.75 be suitable for medical use. Dimensions Dimensions (W × H × D) VESA Mounting Interface Operating Conditions Temperature Range Relative Humidity Range Transport & Storage Conditions 18 41 – 104°F (5 – 40°C) 30 – 95% Temperature Range Relative Humidity Range -0.4 – 140°F (-18 – 60°C) 15 – 90% cation and Approvals Class I Equipment re, and mechanical hazards only in IP23 Water Ingress Protection Continuous Operation Compliance FCC Regulations FCC Part 15 Class B er: QVXAMM261WTDS Note: Please contact your local Stryker Endoscopy sales representative for information on changes and new products. Electromagnetic Compatibility Like other electrical medical equipment, the VisionPro 26” LED Display requires special precautions to ensure electromagnetic compatibility with other electrical medical devices. according to the EMC information provided in this manual. The display has been designed and tested to comply with IEC 60601-1-2 requirements for EMC with other devices. Warning Caution 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. ect 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, guration 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 user of the display should ensure it is used in such an environment. ed below. The customer or the Emissions test Compliance Electromagnetic Environment - guidance RF emissions CISPR 11 Group 1 The VisionPro 26” LED 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. 19 RF emissions CISPR 11 Class B Harmonic emissions IEC61000-3-2 Class D Voltage Fluctuations/ flicker emissions IEC61000-3-3 Complies The VisionPro 26” LED 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 VisionPro 26” LED Display is intended for use in the electromagnetic environment specified below. The customer or the user of the display should ensure that it is used in such an environment. Immunity Test IEC 60601 Test Level Compliance Level Electrostatic Discharge (ESD) ± 6kV contact ± 6kV contact ± 8kV air ± 8kV air Electrical fast transient/burst ± 2kV for power supply lines ± 2kV line to ground IEC61000-4-4 ± 1kV for input/output lines ± 1kV line to line Surge ± 1kV differential mode ± 1kV differential mode IEC61000-4-5 ± 2kV common mode ± 2kV common mode Voltage dips, short interruptions and voltage variations on power supply input lines • <5% UT (>95% dip in Ut) for 0.5 cycle • <5% UT (>95% dip in Ut) for 0.5 cycle • 40% UT (60% dip in Ut) for 5 cycles • 40% UT (60% dip in Ut) for 5 cycles • 70% UT (30% dip in Ut) for 25 cycles • 70% UT (30% dip in Ut) for 25 cycles IEC61000-4-11 • <5% UT (>95% dip in Ut) for 5 sec. • <5% UT (>95% dip in Ut) for 5 sec Power frequency (50/60Hz) magnetic field 3.0 A/m 3.0 A/m IEC61000-4-2 IEC 61000-4-8 Note: UT is the AC mains voltage prior to application of the test level. 20 Electromagnetic Environment-Guidance Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. Mains power quality should be that of a typical commercial or hospital environment. Mains power quality should be that of a typical commercial or hospital environment 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. Power-frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. Guidance and Manufacturer’s Declaration: Electromagnetic Immunity The VisionPro 26” LED Display is intended for use in the electromagnetic environment specified below. The customer or the user of the 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 theVisionPro 26” LED 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 3 Vrms IEC 61000-4-6 150 kHz to 80 MHz Radiated RF 3 V/m IEC 61000-4-3 80MHz to 2.5 GHz 3V d = 1.17√P 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 VisionPro 26” LED 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 VisionPro 26” LED 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 VisionPro 26” LED Display The VisionPro 26” LED Display is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of the VisionPro 26” LED Display can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the VisionPro 26” LED 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 80 kHz to 800 MHz d = 1.17√P 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. 21 nitions The following symbols appear on the product, its labeling, or the product packaging. Each ned below: EC REP Consult Instructions for Use Attention: See Instructions for Use Serial Number Direct Current Authorized European Representative Catalog number QTY Made in Korea Quantity Country of Origin Date of Manufacture Legal manufacturer Tested to comply with FCC Class B standards Federal law restricts this device to sale by or on the order of a physician Complies with the requirements of directive 93/42/EEC IP23 Degrees of protection against the ingress of water Medical Equipment is in accordance with UL 60601-1 and CAN/CSA C22.2 No. 601 in regards to electric shock, fire hazards, and mechanical hazards. This product contains electrical waste or electronic equipment. It must not be disposed of as unsorted municipal waste and must be collected separately. 22 23 Produced for: 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 P22286A 2013/02
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