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Related Manuals for NDS ExpandOR
Summary of Contents for NDS ExpandOR
- Page 1 ExpandOR™ Medical-Grade Video Streaming System USER MANUAL E N G L I S H...
- Page 3 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.
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Page 5: Table Of Contents
About This Manual ------------------------------------------------------------- 1 Overview -------------------------------------------------------------------------- 1 Installation and Setup --------------------------------------------------------- 1 Intended Use and Contraindications -------------------------------------- 2 Specifications -------------------------------------------------------------------- 2 Section 3 ExpandOR Connections ------------------------------------------------------- 3 Cable Bend Radius -------------------------------------------------------------- 3 Section 4 Transmit --------------------------------------------------------------------------- 4 Section 5 Receive ----------------------------------------------------------------------------- 5... -
Page 6: Warnings And Cautions
This product meets the requirements of EN60601-1 so as to conform to the Medical Device Directive 93/42/EEC and 2007/47/EC (general safety information). This product complies to the above standards only when used with the supplied medical grade power supply. Model ExpandOR GlobTek GTM91120-3024-T3A Power Supply AC Input 100 to 240 Volts at 50 to 60 Hz, 1.0A... -
Page 7: Declarations Of Conformity
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. -
Page 9: About This Manual
Installation and Setup The ExpandOR is designed to be easy to install and set up by a hospital’s IT Department, and be made ready for doctors and nurses to operate it. After initial setup by the IT Department, a doctor or a nurse in the operating room can easily: •... -
Page 10: Intended Use And Contraindications
Intended Use and Contraindications Intended Use: This device is intended for use in a medical environment to deliver high quality video and graphic images. Contraindications: This device may not be used in the presence of flammable anesthetics mixture with air, oxygen or nitrous oxide. -
Page 11: Expandor Connections
Cable Bend Radius NDS recommends that the bend radius of metallic cables be no less than 2.5 inches (63 mm) or 7 times the diameter of the cable whichever is greater. Sharper bends may damage the cable and/or degrade... -
Page 12: Transmit
Transmit ExpandOR allows streaming a surgical video of a patient in the OR/procedure room to one or multiple hospital destinations. The steps required to transmit from the ExpandOR in the operating room to a single ExpandOR within the hospital are shown below. Confirm with your IT department that the ExpandOR’s parameters are set appropriately for your specific use prior to operation. -
Page 13: Receive
Receive ExpandOR can receive streaming surgical video of a patient in the operating room/ procedure room from an- other ExpandOR in the hospital. This section explains how to accomplish this task. The steps required to receive surgical video from another ExpandOR within the hospital are shown below. Pri- or to operating the unit, please confirm with your IT department and verify that the unit’s parameters are set... -
Page 14: Simultaneous Transmit/Receive
If you want to record the video stream and/or capture images, verify with your IT department that the ExpandOR is setup for video streaming and/or capturing images. If it is, then proceed as shown below. Start recording video by pressing the RECORD VIDEO button, as shown below, until the LED below it turns on. Stop recording video by pressing the RECORD VIDEO button until the RECORD VIDEO LED turns off. -
Page 15: Transmitting To Multiple Locations
The ExpandOR is capable of simultaneously transmitting (broadcasting) to multiple locations. The IT department can set it up if required. When the ExpandOR has been configured for broadcasting, press the TRANSMIT button, shown below, to begin broadcasting to destinations defined in the ExpandOR configuration. -
Page 16: Privacy Feature
Privacy Feature The purpose of the Privacy Mode is to prevent transmission of sensitive parts of a surgical video stream. When privacy is enabled, the receiving end will see the screen shown below and audio will be muted. Privacy is enabled or disabled by pressing the PRIVACY button on the front panel. When Privacy Mode is on, the LED below the PRIVACY button will be on. -
Page 17: Record And Capture Features
Record Video Feature 1. A USB drive must be installed in the USB connector on the back of the ExpandOR before using this feature. USB drives must be USB 2.0 or better, capable of a minimum write speed of 5 MB/sec Video recording starts when the RECORD VIDEO button, shown below, is pressed. -
Page 18: Configuration Options
Configuration Options The ExpandOR can transmit to and receive from an ExpandOR or can transmit to a computer. Signal capabilities of an ExpandOR are constrained by the device with which it is communicating. The table below each device shows direction parameters for device combinations. -
Page 19: Cleaning Instructions
Ethanol 80 % by volume Unacceptable solvents: MEK (Methyl Ethyl Ketone) Toluene Acetone Note: The acceptable cleaning and disinfecting materials listed above have been tested on NDS products and, when used as directed, do not harm the product’s finish and or its plastic components. -
Page 20: Electromagnetic Compatibility Tables
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. - Page 21 Electromagnetic Emissions Emissions Compliance Electromagnetic environment-- guidance RF emissions Group 1 The product 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 CISPR 11 electronic equipment.
- Page 22 Electromagnetic Immunity 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. Immunity Test Immunity Test Electrostatic discharge (ESD) IEC 61000-4-2 ±2, ±4, ±6, ±8kV contract discharge...
- Page 23 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.
- Page 25 Tokyo 140-0013 Japan +81 3 5753 2466 info@ndssi.com Oriental Media Center Suite 2302, Tower C No.4, Guang Hua Road Chao Yang District Beijing, 100026 China +86 10 8559 7859 info@ndssi.com NDS Quality System ISO 13485 FDA Registration #2954921 60A0530 Rev D...