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EndoVue® Plus 24” Instructions for Use ENGLISH...
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Information in this document has been carefully checked for accuracy; however, no guarantee is given to the correctness of the contents. This document is subject to change without notice. NDS provides this information as reference only. Reference to products from other vendors does not imply any recommendation or endorsement.
ISO and UL/EN/IEC 60601-1 safety standards. The installation shall only be carried out by NDS authorized and trained personnel. This device is only intended to be used in professional healthcare environment.
Power Supply For Customers in North America EndoVue series monitors comply to the above standards only when used with the supplied hospital grade power supply. Note: This power supply is a part of the medical device. Model BridgePower BM060S24F AC Input 100 - 240 Volts, 50 to 60 Hz DC Output 24 Volts, 2.7 Amps For Customers in China This power supply is to be used with this monitor.
VESA Compliant Display Mounting EndoVue series displays are compliant with the VESA Mounting Interface Standard, with MIS hole mount patterns configured to size and weight of the display, suitable for stand, wall, or armature mounting. The MIS-D 100 x 100 mm interface is shown below. 100 mm M4 X 0.7 Thread...
Enclosure Assembly and Cleaning Cable Cover Installation 1. Connect power, control, and video cables before installing the cable cover. 2. Align the cable cover to the cable well recess on the back of the display. 3. Slide the cable cover forward into the recess, with cables positioned under the cut-out. 4.
Display User Interface EndoVue series monitors are designed to display high quality video and graphic images for use in a medical environment. They are designed to accept all standard video and graphic signals, and most special timings from medical equipment. Built-in video controllers convert and format incoming signals of various signal types to match the resolution of the LCD panel.
SmartSync™/Alternative Modes (VGA/RGBS, YPbPr only) NDS proprietary SmartSync technology examines incoming signals to automatically display the video image in its proper format. Alternative Modes are used to manually distinguish between modes whose timing characteristics are very close.
Video Format (Composite, 3G-SDI, S-Video only) Auto: Examines incoming signals to automatically display the video image in NTSC or PAL format. NTSC/PAL: Press the buttons to manually select. Color Menu Gamma To select a gamma setting, press the buttons.. 1.8, 2.0, 2.2, 2.4 or 2.6: Preset gamma values Video: Linear gamma Look Up Table (LUT) PACS: DICOM gamma LUT...
Operating Hours Displays in hours and minutes the accumulated time the monitor has been in use. Version number of the display firmware. Defaults Menu Factory Defaults To return all changed parameter settings to factory preset values, press the button. The “Restoring Factory Defaults” message displays while processing.
This symbol appears below the open, or off, side of the display On/Off switch. Optional 5 VDC Fiber Power Cable J1 Pinout J2 Pinout 5 VDC OUT NDS 35X0100 5 VDC FIBER Connector Center (1) Shield (2) +5 VDC Return...
Cable Bend Radius We recommend that the bend radius of metallic cables be no less than 63 mm (2.5 inches) or 7 times the diameter of the cable whichever is greater. The bend radius of Fiber Optic cables should be no less than 10 times the diameter of the cable.
Specifications Specifications Specifications are subject to change without notice. Contact factory for current specifications. EndoVue Plus 24" Viewing Area (Diagonal) 24.1 in. (612 mm) Typical Luminance (cd/m Native Resolution 1920 x 1200 Aspect Ratio 16:10 Pixel Pitch (mm) 0.270 Viewing Angle (Horizontal & Vertical) 178°...
Supported Resolutions DVI Supported Resolutions Signal Parameter Supported Range Active Resolution (Horizontal x Vertical) 640 x 480 min to 1920 x 1200 max Refresh Rate (Vertical Frequency) 23.98 Hz up to 85 HZ Pixel Clock (Pixel Frequency) 25 MHz up to 165 MHz The DVI-D input can automatically detect any valid digital DVI signal within the resolution, vertical refresh, and pixel clock ranges specified in the table above.
1920 1080p 29.97 1920 1080p 1920 1080p 1920 1080p 59.94 1920 1080p EndoVue Parts List by Region EndoVue Plus 24" 90K0086 North America and Japan 90K0087 China 90K0088 Europe EndoVue Accessory 26B0102 EndoVue Display Stand - 24" Specifications | 11...
Troubleshooting Image Size is Large for the Screen (VGA, RGBS, YPbPr analog inputs only) If the image does not appear to be the correct format, then SmartSync must be run. To run SmartSync, press the MENU button. In the Picture Menu, press the SCROLL button to highlight SmartSync and press the button.
Electromagnetic Compatibility Tables All medical electronic devices must conform to the requirements of IEC 60601-1-2. Precautions, adherences to the Electromagnetic Compatibility (EMC) guideline information provided in this manual and verification of all medical devices in simultaneous operation are required to ensure the electromagnetic compatibility and co- existence of all other medical devices prior to a surgical procedure.
Electromagnetic Emissions Guidance and manufacturer’s declaration; electromagnetic emissions The product is intended for use in the electromagnetic environment specified below. The customer or the user of the product should assure that it is used in such an environment. Emissions Compliance Electromagnetic environment-- guidance RF emissions Group 1...
Recommended Separation Distances Recommended separation distances between portable and mobile RF communications equipment and the product The product is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the product can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the product as recommended below, according to the maximum output power of the communications equipment.
Terms and Conditions Declarations of Conformity FCC and Council Directives of European Standards This device complies with Part 15 of FCC rules and 2017/745 Medical Device Regulation of European Union. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesirable results.
NDS neither assumes nor authorizes any person to assume for it any other liabilities in conjunction with and/or related to the sale and/or use of its products. To ensure proper use, handling and care of NDS products, customers should consult the product specific literature, instruction manual, and/or labeling included with the product or otherwise available.
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Global Headquarters www.ndssi.com NDS Surgical Imaging, LLC 100 Paramount Drive, Suite 101 Sarasota, FL 34232 +1 (888) 982-4469 info@ndssi.com Europe Novanta Europe GmbH Werk 4 92442 Wackersdorf Germany Tel: +49 9431 7984-0 info.novanta-europe@novanta.com Asia Pacific Novanta Japan East Square Omori...
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