User Manual for the CARESTREAM Focus 43C Detector Publication No.
All rights reserved. No part of this manual may be reproduced or copied in any form by any means—graphic, electronic, or mechanical, including photocopying, typing, or information retrieval systems—without written permission.
Notices and Conventions The information herein is based on the experience and knowledge relating to the subject matter gained by Carestream Health, Inc. prior to publication. No patent license is granted by this information. Carestream Health reserves the right to change this information without notice, and makes no warranty, express or implied, with respect to this information.
Notices and Conventions CAUTION: Federal law restricts this device to sale by or on the order of a physician. CAUTION: If you witness or become aware of a potential safety issue with this equipment, take the appropriate safety measures and report this to your Carestream Service representative immediately.
Notices and Conventions Disclaimer • • • • • Carestream shall not be liable to the purchaser of this product or third parties for any damage, loss, or injury incurred by the purchaser or third parties as a result of fire, earthquake, any accident, misuse, or abuse of the product.
Notices and Conventions -vi AJ4311 | 2020-02-10
Contents Notices and Conventions Disclaimer.......................................................................................................................................... -v 1 Safety and Regulatory Information Symbols............................................................................................................................................1-1 Cautions..................................................................................................................................
Contents Set the Connection Mode............................................................................................................ A-IX Wireless Client Mode.............................................................................................................. A-IX Wireless AP Mode.................................................................................................................... A-X Shortcuts...................................................................................
1 Safety and Regulatory Information Symbols Symbols and Conventions WARNING: This is used to identify conditions under which improper use of the product may cause death or serious personal injury. This is used to indicate a prohibited operation. This is used to indicate an action that must be performed. Labels and Markings on the Equipment This indicates that the product has passed CE certification and is followed by the CE number.
Safety and Regulatory Information This is used to identify the manufacturer’s series number, which is after, below, or adjacent to the symbol. The series number usually consists of 19 digits as shown in the following example: 1A2A3A4 B1B2 C1C2 L M1M2 D1D2 Y1Y2 X1X2X3X4 • • • • • • • • 1A2A3A4 - Product code B1B2 - Derived classes C1C2 - Version L - Production site M1M2 - Month D1D2 - Day Y1Y2 - Year X1X2X3X4 - Numerical order This indicates the name and address of the manufacturer.
Safety and Regulatory Information This indicates storage temperature limits. This indicates the product radiates a wireless signal. Package symbol: Fragile Package symbol: Keep away from sunlight. Package symbol: Keep dry. This indicates the humidity limits. Keep the product upright. Do not roll the transportation packaging. This indicates the stacking limit number. FDP is allowed to withstand 100 kg on its surface. Rx only IP AJ4311 | 2020-02-10 Device is for prescription use only.
Safety and Regulatory Information Cautions Environment for Installation and Use WARNING: Do not use or store the product near flammable chemicals such as alcohol, thinner, benzene, etc. Environment for Installation and Use Chemicals that are spilled or evaporated may result in fire or electric shock through contact with electric parts inside the product. Also, some disinfectants are flammable. Be sure to take care when using them.
Safety and Regulatory Information CAUTION: Do not allow cables to become tangled to avoid a malfunction of the product. Do not get your feet caught by a cable to avoid tripping and injury. Installation and Environment of Use CAUTION: Non-medical equipment such as battery chargers and access point and infrared register tools cannot be used in the vicinity of a patient.
Safety and Regulatory Information WARNING: Do not operate the product with a power supply other than the one indicated on the rating label to avoid fire or electric shock. WARNING: Do not handle the product with wet hands to avoid electric shock that could result in death or serious injury. Power Supply WARNING: Do not place heavy object on cables and cords. Co not pull, bend, bundle, or step on them to prevent damage to the sheath. Do not alter them.
Safety and Regulatory Information WARNING: Securely insert the power cord into the AC outlet to avoid a contact failure. If a contact failure occurs or if metal objects come in contact with the exposed metal prongs of the plug, fire or electric shock may result. Power Supply WARNING: Be sure to turn off the power before connecting or disconnecting the cords to avoid an electric shock that could result in death or serious injury. WARNING: Be sure to hold the plug or connector to disconnect the cord.
Safety and Regulatory Information Handling WARNING: No modification is allowed. Never disassemble or modify the product to avoid fire or electric shock. The product incorporates parts that may be hazardous or cause electric shock Touching them may cause death or serious injury. Handling WARNING: Do not place an object on top of the product. The object may fall and cause an injury. Metal objects such as needles or clips that fall into the product or spilled liquid may result in fire or electric shock.
Safety and Regulatory Information CAUTION: Do not spill liquid or chemicals onto the equipment. Do not allow an injured patient’s blood or body fluids contact with the equipment. Doing so may result in fire or electric shock. Handling In such a situation, protect the equipment with a disposable cover as necessary. CAUTION: For safety Turn OFF the power and remove the plug for all equipment when not used. CAUTION: Handle the product carefully. Do not submerge the product in water.
Safety and Regulatory Information CAUTION: Do not place excessive weight on the panel to avoid damage to the internal image sensor and an incorrect image. Patients stand on the product temporarily, and the intended weight can be 135 kg.
Safety and Regulatory Information CAUTION: Be sure to use the product on a flat surface to prevent the product from bending and doing damage to the internal image sensor. Be sure to securely hold the product while using it in an upright positions to prevent the product from tipping or flipping over, resulting in injury to the user or patient damage to the inner device. Handling Keep the same pressure on the product when acquiring an image to avoid an incorrect image.
Safety and Regulatory Information CAUTION: • • • Handling • • • • • • • • • • • • • Do not use the product close to fire or in high temperature. Do not invert the positive and negative poles. Do not allow the product to make contact with metal to avoid a short circuit. Do not insert sharp objects into the battery. Do not strike the battery. Do not stand on the battery. Do not use the battery outside of the guidelines. Do not dispose of the battery or change the inner structure.
Safety and Regulatory Information Maintenance and Inspection WARNING: • • • Maintenance and Inspection Turn off the power of the product and disconnect the power cord of the adapter before cleaning. Never use alcohol, ether, and other flammable cleaning agent for safety. Never use methanol, benzene, and acid to avoid corrosion on the equipment. Do not place the product in liquid. WARNING: Make sure that the surface and connectors are dry before turning on the product to avoid fire or electric shock.
Safety and Regulatory Information Medical Equipment Classification Type of protection against electrical shock External electrical power source equipment Class I Equipment (medical approved adapter) Internal electrical power source equipment (battery) Degree of protection against electrical shock Type-B applied part Degree of protection against ingress of water IPX1 Mode of operation Continuous operation Flammable anesthetics Not suitable for use in the presence of a flammable anesthetic mixture w
Safety and Regulatory Information Standards ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes IEC 60601-1:2005/AMD1:2012 Medical electrical equipment — Part 1: General requirements for basic safety and essential performance IEC 60601-1-2:2014/EN60601-1-2:2015 Medical electrical equipment — Part 1-2: General requirements for basic safety and essential performance — Collateral standard: Electromagnetic disturbances v Requirements and tests IEC 60601-2-54
Safety and Regulatory Information CAN/CSA-C22.2 No.
Safety and Regulatory Information Emissions and Immunity Compliance to the IEC60601-1-2 Standard Electromagnetic Emissions Emissions Test RF emissions Compliance CISPR 11 Group 1, Class B Harmonic distortion IEC 61000-3-2 Class A Voltage fluctuations and flicker IEC 61000-3-3 Compliance Electromagnetic Environment The Focus 43C Detector uses RF energy only for its internal function.
Safety and Regulatory Information Proximity Fields From RF Wireless Communications Equipment Test Levels Test Frequency (MHz) Band (MHz) 385 380–390 Pulse modulation 18 Hz, 27 V/m 450 430–470 FM, ±5kHz deviation, 1 kHz sine, 28 V/m 704–787 Pulse modulation 217 Hz, 9 V/m 800-–960 Pulse modulation 18 Hz, 28 V/m 1700–1990 Pulse modulation 217 Hz, 28 V/m 2400–2570 Pulse modulation 217 Hz, 28 V/m 5100–5800 Pulse modulation 217 Hz, 9 V/m Professional healthcare facility environment 710 745 78
Safety and Regulatory Information Test Levels Emissions Test EMC Standard Professional healthcare facility environment Surges IEC 61000-4-5 ±0.5 kV, ±1kV IEC 61000-4-5 ±0.5 kV, ±1kV, ±2 kV IEC 61000-4-6 3 V, 0.15 MHz–80MHz Line-to-line Surges Line-to-ground Conducted disturbances induced by RF fields 6 V in ISM bands between 0.15 MHz and 80 MHz 80 % AM at 1 kHz Voltage dips Voltage dips 0 % UT; 0.
Safety and Regulatory Information Test Levels Emissions Test EMC Standard Professional healthcare facility environment Conducted disturbances induced by RF fields IEC 61000-4-6 3 V, 0.15 MHz–80 MHz 6 V in ISM bands between 0.15 MHz and 80 MHz 80 % AM at 1 kHz Reference Cables Provided Against EMC Recommended Cable Length Shielded or Unshielded Number Cable Classification AC Power Cable 3m Unshielded 1 pcs AC Power DC Power Cable 3.
Safety and Regulatory Information Radio Frequency Compliance Country Item FCC Code CFR47 Part15B (2018) ANSI C63.4(2014) FCC CFR47 Part 15C (2018)Radio Frequency Devices ANSI C63.10(2013) KDB 558074 D01 15.247 Meas Guidance v05r02 FCC CFR47 Part 15E (2018) Unlicensed National information infrastructure devices ANSI C63.10(2013) U.S.A KDB 789033 D02 General UNII Test Procedures New Rules v02r01 KDB 662911 D01 Multiple Transmitter Output v02r01 248227 D01 802.
Safety and Regulatory Information Country Item ETSI EN 300 328 V2.1.1 ETSI EN 301 893 V2.1.1 ETSI EN 300 440 V2.1.1 ETSI EN 301 489-3 V2.1.1 Draft ETSI EN 301 489-1 V2.2.1 Draft ETSI EN 301 489-17 V3.2.0 European Union EN 55032: 2015 EN 55035: 2017 EN 61000-3-2: 2014 EN 61000-3-3: 2013 EN 50566: 2017 EN 62209-2: 2010 EN 62479: 2010 FCC Compliance • • The panel has been tested to comply with limits for a Class B digital device, pursuant to part 15 of FCC Rules.
Safety and Regulatory Information Correction and Calibration Template Generation Correction and calibration should be performed after installation and every six months. The new correction and calibration should be performed after any major change on the system settings and hardware configuration.
Safety and Regulatory Information Battery Safety Standards Standards Description CAN/CSA E62133:13 1st Ed. Rev. Secondary cells and batteries containing alkaline or other nonacid electrolytes — Safety requirements for portable sealed secondary cells, and for batteries made from them, for use in portable applications First Edition UL 62133, 1st Ed. Rev.
Safety and Regulatory Information Intended Use and Essential Performance Intended Use These devices are indicated for digital imaging solutions designed to provide general radiographic diagnosis for human anatomy including both adult and pediatric patients. They are intended to replace film/screen systems in all general-purpose diagnostic procedures. This device is not intended for mammography or dental applications.
Safety and Regulatory Information Exposure to ionizing radiation is of particular concern in pediatric patients because: 1. For certain organs and tumor types, younger patients are more radio sensitive than adults (the cancer risk per unit dose of ionizing radiation is higher for younger patients); 2. Use of equipment and exposure settings designed for adults of average size can result in excessive and unnecessary radiation exposure of smaller patients; 3.
Safety and Regulatory Information Body Parts Patient Size kVp mAs SID Grid Very Low Birth Weight 50 1 1m no Low Birth Weight 55 1 1m no Newborn 65 1 1m no Infant 70 1.6 1m no Child 70 1.6 1m no Preadolescent 90 2 1m yes Adolescent 90 2 1m yes Adult Small 110 1.8 1.8m yes Adult Medium 110 2.8 1.8m yes Adult Large 120 4 1.8m yes Very Low Birth Weight 50 1 1m no Low Birth Weight 55 1 1m no Newborn 57 1 1m no Infant 57 1.
Safety and Regulatory Information Adult Extremities List kVp mAs SID Grid Femur - AP 70 16 1 yes Femur - Lateral 70 10 1 yes Hand - PA 53 1.8 1 no Hand - oblique 53 1.8 1 no Humerus - AP 75 7.1 1 yes Humerus - Lateral 70 3.2 1 yes Knee - AP 65 10 1 yes Knee - Lateral 65 10 1 yes Wrist - PA 55 1.8 1 no Wrist - Lateral 55 1.
2 Overview The Focus 43C Detector is a cassette-size, wireless x-ray flat panel detector based on amorphous silicon thin-film transistor technologies. It is developed to provide the highest quality of radiographic images with an active matrix of 3072×3072 with 139 um pixel pitch. The detector supports wireless communication between the panel and the workstation and is powered by an internal battery. Scope This manual contains information about the Focus 43C.
Overview Components and Specifications Product Components Component Description Detector Item 2-2 Description Notes B DC jack For optional power input A Ethernet port For service C Detector indicator Detector indicator of control panel D Power button Power button of control panel E Mode button Mode switch AJ4311 | 2020-02-10
Overview Item Description Notes F Power indicator The other Power indicator G Handle Optional Battery Item Description A Battery label B Battery interface C Pilot pin D Indicator Notes 8 pin battery connector Installation direction indicator Battery Charger AJ4311 | 2020-02-10 2-3
Overview Item Description Notes A Battery Interface A 8 pin battery connector B Battery Interface B Not used C Battery Interface C Not used D Indicator The indicator definition is as follow E The limit ball plug / F Hand Pull Position / G AC Jack 220V (ac) input Battery Charger Indicator Item 2-4 Name A Power Indicator B Charging Indicator C Charge Full Indicator AJ4311 | 2020-02-10
Overview X Indicator Operating Status All off No power input A indicator on • • A indicator on Battery insertion self test AC power input Multiple batteries inserted B and C alternately blink 2 times A and B indicator on Battery charging A and C indicator on Battery capacity full, charging stops A indicator on Battery is not charging properly B and C alternately blinking Two or more batteries charging cannot be charged at the same time.
Overview Product Specifications Detector Item 2-6 Specifications Model Focus 43C Image Sensor a-Si (amorphous silicon) TFT Pixel Size 139 µm Active Array 3072 x 3072 Active Area (H x V) 427.0 x 427.0 mm (16.8 x 16.8 in.) Gray Scales 16 bit Spatial Resolution 3.6 Lp/mm Cycle Time Min. 8.5 sec. Power Consumption Max. 20 W Dimension (L × W × H) 460.0 x 460.0 x 15.0 mm (18.1 x 18.1 x 0.6 in.) Weight (with one battery) 4.68 kg (10.32 lb) Image Transfer Wireless: IEEE802.
Overview Item Data Transmission Rate (Wireless) Specifications 802.11b: Max. 11 Mbps 802.11a/g: Max. 54 Mbps 802.11n: Max. 300 Mbps (MIMO 2 x 2) 802.11ac: Max. 867 Mbps(MIMO 2 x 2) Battery Item Specifications Model Battery-KV Rated capacity Typ. 4180 mAh @ Discharge 0.2C Nominal voltage 10.8 V Charge voltage 12.6 ± 0.
Overview Item Operating temperature Specifications Charge 0–60 °C (32–140 °F) Discharge 0–60 °C (32–140 °F) Storage temperature ≤3 month -20 °- +45 ° (-4–113 °F) ≤6 month -20°- +35 ° (-4–95 °F) Relative humidity 5 %~95 % Dimension (L × W × H) 210.0 x 115 x 7.5 mm (8.3 x 4.5 x 0.30in.) Weight 0.28 kg (0.
Overview Power Supply Item Specifications DC Power (Optional) 24V (dc), 0.8A Battery Package 10.8V (dc), 1.78A CAUTION: The charging cable can only be used in areas not are accessible to the patient, such as in the Bucky. The product must be used with the approved adapter and CB certificate number SG PSB-MD-00191. Wireless Communication Item Specifications Wireless Standard IEEE 802.11 a/b/g/n/ac Frequency Range 2.412~2.472 GHz: ch1~ch13 5.18~5.24 GHz: ch36~ch48 5.745~5.
Overview Item Specifications Security WPA, WPA-PSK, WPA2, WPA2-PSK, WEP 64 bit & 128 bit Antenna 2 dual band inner antenna Mechanical Outlines Use Environment Operating Temperature Temperature Change Humidity Atmospheric Pressure Pressure Change 5–35 °C < 1k/min 10 %–90 % RH 700–1060 hPa <10 kp/min (1 kp=1.0197E-5Pa) < 1k/min 5 %–95 % RH 700–1060 hPa <10 kp/min (1 kp=1.
Overview Temperature Temperature Change Humidity Atmospheric Pressure Pressure Change Focus 43 detectors shall operate at a specified altitude of not more than 3000.0 m (9842.5 ft). The environment specific is only for the detector. IT Network Purpose for IT-network Transmission of image data and command/status communication between the detector and the workstation. Required Features Wireless communication follows IEEE 802.11a/b/g/n/ac protocol. It works on 2.4 GHz and 5 GHz.
Overview Item Data Transmission Rate Specifications 802.11b: Max. 11 Mbps 802.11a/g: Max. 54 Mbps 802.11n: Max. 300 Mbps (MIMO 2x2) 802.11ac: Max. 867 Mbps (MIMO 2x2) Modulation 802.11b: CCK, DQPSK, DBPSK 802.11a/g/n: 64 QAM, 16 QAM, QPSK, BPSK 802.11ac: 256 QAM, 64 QAM, 16 QAM, QPSK, BPSK Security WPA, WPA-PSK, WPA2, WPA2-PSK, WEP 64 bit, and 128 bit Intended Information Flow The detector sends the acquired image data to the workstation. The workstation sends the user's commands to the detector.
Overview Service Information Product Lifespan The estimated product lifetime is up to 7 years under appropriate regular inspection and maintenance (battery 5 years). Regular Inspection and Maintenance In order to ensure the safety of patients and operator, and to maintain the performance and reliability of the panel, be sure to perform regular inspections at least once a year. If necessary, clean the panel, make adjustments, or replace consumables such as fuses etc.
Overview Disposal CAUTION: Do not dispose of this product with your residential or commercial waste. Improper handling of this type of waste could have a negative impact on health and on the environment. Some countries or regions, such as the European Union, have set up systems to collect and recycle electrical or electronic waste. Contact your local authorities for information about dropping off waste products for recycling.
3 Installation Panel Installation Install the Detector Battery The detector can be powered by the battery package or DC power. The detector will be activated as soon as power is supplied and will power off as soon as power is removed.
Installation 1. Make sure that the connectors for the battery and battery compartment are aligned. 2. Slide the battery into the battery compartment. Note: Make sure the battery level is >10 % of full capacity. 3. Slide the two battery lock levers toward the center of the detector.. Power on the Detector On the control panel, the power button is used to power the detector on and off.
Installation To power on the detector, press and hold the power button for 4 seconds. The detector must either have a battery installed with >10 % charge or have the DC power connected. To power off the detector, press and hold the power button for 4 seconds. To reset the detector, press and hold the power button for 8 seconds. Power Indicator After booting up, the user can check the status LED indicator.
Installation Operating Status Power Indicator Lighting Status Operating Battery Capacity DC Input Green Fast Blinking Power OFF ≥95 % and <100 % Yes OFF Power OFF =100 % Yes Link Indicator Power Indicator Lighting Status Description Off • • Green On Wired connection is built Blue On • • Blue Blinking Client mode, no connection is built Green and Blue Blinking Initialization Shut down Wired connection broken and wireless connection not ready Client mode, wireless connection is buil
Installation Power Indicator Lighting Status Description Green On Exposure enable Green Blinking Image transmission Orange On Error Orange Blinking Safety mode Mode Indicator Power Indicator Lighting Status Description Off • • Green On AP mode, wireless AP is ready (Not used) Blue On Client mode, wireless client is ready Blue and Green Blinking Initialization AJ4311 | 2020-02-10 Shut down Wired connection is built 3-5
Installation Button Function Power Action Mode Note FPD Status Power ON Short hold No action Hold for 4 seconds Hold for more than 7 seconds. Forced restart Long hold No action Press 3 times No action Release the power button when the power indicator is ON. Power OFF Exit the battery from ship mode Enter safety mode Forced restart Enter/exit sleep mode Power OFF Restore default configuration 3-6 Short hold Power ON Long hold Release after two short presses (interval < 1second).
Installation Power Action Mode Note FPD Status 1. Hold the Mode button hold for 7 seconds. 2. Release the Mode button after Mode indicator starts blinking, and then press again in 5 seconds. Wireless ConnectionMode Switch Power ON No action Long hold and then short click The mode starts switching. 3. Press the Mode button to switch modes. The Mode indicator blinks at the corresponding color. 4. Wait at intended mode, the Mode indicator will switch color after several seconds.
Installation Install the Detector Battery Charger 1. Remove the battery from the battery charger. 2. Insert battery into battery charger in the orientation shown below. 3. Press the battery down into the battery compartment.
Installation Detector Battery Lock and Activation To ensure the safety of the battery during transportation or storage, the battery can be set to ship mode where it is locked and will not provide any voltage output. Enter Ship Mode Method Steps Factory configuration Web write in 1. Connect the adapter to the detector and power it on. 2. Connect the other end of the adapter to the PC. 3. Insert the battery into the detector. 4. Open a web browser and enter the following address: http://10.0.1.
Installation Method Charger 3-10 Steps 1. Power on the charger. 2. Insert the battery into the charger for 3 to 5 seconds to exit ship mode.
4 Operation Notes for Using Do the following to ensure that the detector functions correctly. Before Exposure Inspect the detector daily and confirm it is working properly. Check that there is no condensation on the any of the surfaces of the detector. Condensation can be caused by the sudden heating of the room in cold areas. If this occurs, wait until the condensation evaporates before performing an exposure or problems may occur with the quality of captured images.
Operation CAUTION: Do not spray disinfectants or detergents directly onto the detector. To prevent damage to the surface of the detector, wipe with a cloth slightly dampened with a neutral detergent. Do not use solvents such as benzene and acid. It is recommended to use a waterproof non-woven cover as the isolated layer between the detector and a patient who is bleeding. Applied Part The front and back of the detector is an application part.
Operation Detector Position To prevent abnormal light lines, place the detector behind the patient in the orientation shown below.
Operation 4-4 AJ4311 | 2020-02-10
Appendix (For Service Personnel Only) Software and Settings Main Interface Button Function Home Home page, shows the list of the detectors Acquire Acquire images, free for use after connecting the detector SDK Configure UI for SDK, free for use after connecting the detector Detector Configure UI for detector, free for use after connecting the detector Calibrate Calibrate UI, for generation and management of the calibration template Local File Image management, free for use at any time Connect
Appendix (For Service Personnel Only) Tab Description Remaining power of the battery, shown as a percentage Progress Bar If the progress bar • • Is green while taking an x-ray, the image quality is acceptable Is not green while taking an x-ray, the image quality will be degraded General Settings Parameter II Description Can be Modified Product No. Type number of the detector No Sub Product No. Sub-type of the detector No Serial No.
Appendix (For Service Personnel Only) Parameter Description Can be Modified Integrate Time Should not be modified; keep the original value Yes Src Port Port number for detector No Src IP IP address for detector No Src MAC MAC address for detector Yes Dest Port Port number for PC No Dest IP IP address for detector No Self Clear Enable Related to Prep CapMode, the value should be configured as On if Prep CapMode is configured as PrepCapMode_ClearAcq.
Appendix (For Service Personnel Only) Parameter Description Can be Modified Ftp Upload Host IP FTP upload server IP; keep the same as Host IP Yes Ftp Upload Host Port FTP upload server Port; keep the same as Host Port Yes Network Settings Button Description Add Add the information of SSID and the AP Key Del Delete the information of SSID and the AP Key Up Move up the AP information Down Move down the AP information Select Select the AP Read Config Read the parameters of the AP informa
Appendix (For Service Personnel Only) Operating Modes Software Mode Block Diagram Software mode is the basic way to acquire an x-ray image. The workstation is a host device installed with iDetector and SDK. Installation describes how to establish connections between the panel and workstation. In software mode, the workstation does not control the x-ray generator. Users decide when to take x-rays. Work Flow 1. Workstation receives prep request and sends clear command to the panel. 2.
Appendix (For Service Personnel Only) Inner2 Mode Block Diagram The workstation is a host PC device installed with iDetector and SDK. Installation describes how to establish connections between the panel and workstation. In inner2 mode, the workstation does not control the x-ray generator. Users decide when to take x-rays. Work Flow 1. Workstation receives prep request. 2. X-ray generator is ready to take x-rays and starts releasing the x-ray. 3.
Appendix (For Service Personnel Only) mode, the user does not interact with the workstation. After taking x-rays, images immediately appear on the screen. Work Flow 1. X-ray generator is ready to take x-rays and starts releasing the x-ray. 2. Workstation receives Exposure Prohibited from the panel. 3. Panel starts uploading a Pre-dark image and a Light image to the workstation for preview. If hardware offset is selected, panel first performs an offset and then uploads the preview image. 4.
Appendix (For Service Personnel Only) Software Installation Do the following if the iDetector application is not working: 1. Install MICROSOFT .NET Framework 4.5. 2. Install vcredist_x86_2013 (or vcredist_x64_vs2013). Important: The iDetector application should not be used for a hospital terminal.
Appendix (For Service Personnel Only) Set the Connection Mode The detector supports the following two connection modes and should be configured per site requirements. Wireless Client Mode 1. Connect one end of the Gigabit Ethernet cable to the workstation. 2. Connect another end to the LAN port of external wireless AP. 3. From the workstation, open the Control Panel and then the Network and Sharing Center. 4. In the Connections: field, click on Local Network. 5. Open the IPV4 settings. 6.
Appendix (For Service Personnel Only) 15. Select: • • • • Detector Wifi Read Config Client 16. Select Add and enter the SSID and Password. Select Apply. 17. Choose SSID and select the one with a check mark. Select Write Config to save the parameters. 18. Turn on the wireless router. a. Make sure there is a wired connection between the outer, work station, and IP 10.0.1.251. b. Select Read Wifi Status to check wireless transmission status, numerical value occurred means the link is up and available.
Appendix (For Service Personnel Only) The detector will connect to the wireless AP the next time it is powered on. 10. Configure the external wireless card. a. Open the local wireless signal list. b. Select the SSID that belongs to the detectors. Enter the password and select OK. c. Open the wireless card configuration. d. Open the IPV4 setting and set the following values:. • • IP setting—IP address: 10.0.1.251 Network mask setting—Subnet mask: 255.255.255.0 e. Open SDK and select the detector. f.
Appendix (For Service Personnel Only) Shortcuts Shortcut Result Double-click the window using the left mouse button. The image is centered and displayed at the maximum size. Double-click the window using the right mouse button. The window level and width are adjusted to WL: 32767/WW: 65535. Drag the left mouse button to move the displayed image. Drag the right mouse button horizontally to adjust the window width, and drag the right mouse button vertically to adjust the window level.
Appendix (For Service Personnel Only) Establish a Connection with the Detector 1. Open SDK, select the detector, and select Connect. 2. Confirm that the values for IP address and Port are the same as the values in config.ini. Note: The value for Cfg_HostPort should be the default of 28000. Note: When the connection is changed to a different network card, the user must reconnect the detector using a different IP address. The rule of Multi-Share control is based on the IP address.
Appendix (For Service Personnel Only) Configure the Detector 1. From the iDetector menu, select the Acquire tab. 2. Acquire the module related setting, such as loading correction and calibration template, acquiring images. 3. See the SDK module-related settings, such as IP address. 4. See the Detector module related settings, such as trigger module, wireless signal. 5. Calibrate the module related setting, such as making correction and calibration template.
Appendix (For Service Personnel Only) Correction and Calibration Template Generation Correction and calibration should be performed after installation and every six months. The new correction and calibration should be performed after any major change on the system settings and hardware configuration. Pre-offset Template Generation If panel is configured to do Pre-offset correction, Pre-offset Template is necessary. 1. Select Calibrate. 2. Select Start Generate Templates. 3. Select Create Offset. 4.
Appendix (For Service Personnel Only) 1. On the Defect Calibration page, start the exposure. Eight images need to be captured. 2. Select Start. 3. Select PREP and start the exposure. 4. When completed, select Acquire to get the light image. 5. If the value meets the expected value, select Accept, and then acquire the other seven images. If the value does not meet the expected value, do not select Acquire. Adjust the exposure dose, then select PREP to acquire the light image again. 6.
Appendix (For Service Personnel Only) Image Check and Upload OPEN provides two features for image check and uploading: Local Image Check and Panel Image Upload. Local Image Check is used to check images saved in the workstation. Panel Image Upload is used to upload images stored in the panel. Local Image Check 1. From the Local File tab, select Load File. Choose the specified file. 2. Choose the images stored in the workstation. The screen will display the images.
Appendix (For Service Personnel Only) Defect Template Check and Modification The iDetector software provides the ability to check the defect template. If the template has updates, the user can add and delete pixels or defective lines by modifying the opened defect template. Defect Template Check 1. From the Local File page, select Load File. 2. Select the specified defect template, and select Open. The defect template will be displayed. Defect Template Modification 1. Open the specified defect template.
Appendix (For Service Personnel Only) Correction and Calibration Management Correction and Calibration Template Synchronization The detector supports correction and calibration template storage. Templates in the detector can be uploaded to a workstation, and templates in a workstation can be downloaded to a detector. 1. After generating the offset, gain, and defect templates, select the templates and select Download to FPD. 2. Select Download. 3. Select Read Status. 4.
Appendix (For Service Personnel Only) Update the Firmware The Internet can be used to upgrade the detector firmware. This procedure applies to MCU, FPGA, and ARM. 1. Connect the panel to a PC. 2. Open a browser, type detector IP in the search bar, and then press Enter. 3. Enter the following and select login. • • User name: admin Password: admin 4. Click on the three squares located on the left side of the screen. 5. Select Upgrade and then Browse. 6.
Publication History AJ4311 | 2020-02-10 Version Date A 2020-02-10 Changes Initial release I
Carestream Health, Inc. 150 Verona Street Rochester, NY, USA 14608 © Carestream Health, Inc., 2020 Made in China for Carestream Health, Inc. CARESTREAM is a trademark of Carestream Health. Pub. No. AJ4311 Rev A.
FCC Regulations: Contains module’s FCC ID：2ACHK-01070189 This device complies with part 15 of the FCC Rules. 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 undesired operation. 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.
the maximum value. This is because the device is designed to operate at multiple power levels so as to use only the power required to reach the network. In general, the closer you are to a wireless Base station antenna, the lower the power output. The exposure standard for wireless devices employing a unit of measurement is known as the Specific Absorption Rate, or SAR. The SAR limit recommended by the ICNIRP used by the general public is 2.
methods and procedures specified in IEEE 1528 and IEC 62209. This equipment should be installed and operated with minimum distance of 0 cm between the radiator and your body. This device and its antenna(s) must not be co-located or operating in conjunction with any other antenna or transmitter. Cet appareil est conforme aux Normes RSS d'Industy Canada.
l'exposition aux radiofréquences lorsqu'il est testé en contact direct avec le corps. Pour cet appareil, la valeur SAR la plus élevée pour une utilisation près du corps est de 0.042 W/kg. Bien qu'il puisse exister des différences entre les niveaux de SAR selon les dispositifs et les emplacements où ils sont utilisés, tous répondent aux exigences Gouvernementales. La valeur SAR déclarée conforme est une distance de 0 mm entre l'unité et le corps humain.
