Safety Information .................................................................................................................................... 7
Battery Pack and Battery Charger Safety Information ......................................................................... 9
General Hazards ...................................................................................................................................... 11
1.1 Features ........................................................................................................................................ 22
1.2 Intended Use ................................................................................................................................ 22
1.3 Standard Configuration ............................................................................................................... 23
The following safety notices are used to emphasize certain safety instructions. Follow the safety instructions
in this manual along with warnings and cautions symbols. Ignoring such warnings or cautions while handling
the product may results in serious injury or accident. It is important for you to read and understand the
contents of this manual before attempting to use the product.
Symbols Descriptions
Indicates a potential ly hazardous situation which will cause death, se vere personal injur y
or substantial property damage if the instructions are ignored.
Indicates a potentially hazardous situation which may cause minor personal
property damage if the instructions are ignored.
Provides additiona l inf ormation that is helpful to you. It may em phas i ze cert ain i nf ormation
regarding special tools or items to check before operating the product.
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Safety Information
This product is designed and manufactured to ensure maximum safety of operation and to meet all the
safety requirements applicable to electronic medical equipment. However, anyone attempting to operate the
system must be fully aware of potential safety hazards. It shou ld be opera ted and maintained in strict
compliance with the following safety precautions and operating instruments contained herein:
Caution: Federal law restricts this device to sale by or on the order of a physician or a
licensed practitioner.
Always be alert when operating this device. If a malfunction occurs, do not use this device
until qualified personnel correct the problems.
The product should be installed, maintained and serviced according to Vieworks
maintenance procedures and by Vieworks personnel or other qualified maintenance
personnel approved in writing by Vieworks. Operation and maintenance should be done in
strict compliance with the operation instructions contained in the manuals.
The system, in whole or in part, cannot be m odif ied in any wa y without wr itte n appr oval
from Vieworks.
Before authorizing any person to operate the system, verify that the person has read and
fully understand the Service Manual. The owner should make certain that only properly
trained and fully qualified personnel are authorized to operate the equipment. An
authorized operators list should be maintained.
Prevent unauthorized personnel from access to the system.
It is important that this Service Manual be kept at hand, studied carefully and reviewed
periodically by the authorized operators.
The owner should ensure continuous power supply to the system, with voltage and
current according to the product specifications. If power failures are frequent, an
Uninterrupted Power Supply (UPS) should be installed to avoid loss of data.
If the product does not operate properly or if it fails to respond to the controls described in
this manual, the operator should immediately contact Vieworks field service
representative.
User must not contact a fuse holder or contacts of connector (ex: Inlet connector) with a
patient simultaneously during operating the equipment and not allow patient to touch the
fuse holder or contacts of connector.
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The images and calculations provided by this system are intended to be used as tools for
the competent user. They are explicitly not to be regarded as a sole incontrovertible basis
for clinical diagnosis. Users are encouraged to study the literature and reach their own
professional conclusions regarding the clinical utility of the system.
The user should be aware of the product specifications and of the system’s accuracy and
stability limitations. These limitations must be considered before making any decision
based on quantitative values, in case of doubt, please consult a Vieworks representative .
Do not install the equipment in a location with the conditions listed below. Otherwise, it
may result in failure or malfunction, fall or cause fire or injury.
Close to facilities where water is used.
Locations exposed to direct sunlight.
Close to air-conditioner or ventilation equipment.
Close to heat source such as a heater.
Prone to vibration.
Insecure place.
Dusty environm ent.
Saline or sulfurous environment.
High humidity.
Ambient temperature is higher than the operating temperature stated in this Service
Manual.
Occasionally, this product may have defect pixels caused by TFT characteristics. When
the defect pixels are found, perform the Defect detection. For details about how to correct
defect pixels, refer to
5.4.3Defect Correction.
Do not inflict excessive shock and mechanical vibration. Otherwise, it may result in poor
image quality caused by noise.
Do not unscrew or loosen the screws on the detector surface since all the screws are
secured properly at the time of shipment. Otherwise, it may result in poor image quality or
damage to equipment.
This product may malfunction due to electromagnetic interference (EMI) caused by
telecommunication devices, transceivers, electronic devices, etc. To prevent the
electromagnetic wave from badly influencing the product, be sure to avoid placing it in
close proximity to the product. Or, change direction or position of the product or move into
the shielded place to reduce electromagnetic interference.
To reduce the risk of electric shock, do not remove cover. No user-serviceable part inside.
Refer servicing to qualified service personnel.
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Battery Pack and Battery Charger Safety Information
Before using the battery pack and battery charger dedicated to ViVIX-S Wireless, read all applicable
warnings and cautions.
Not following these instructions could result in electrical shock, fire, explosion or other conditions which may
cause death, injury or property damages.
Do not use the battery pack as a power source for equipment other than ViVIX-S Wireless
detectors. Be sure to use only the dedicated battery pack for the ViVIX-S Wireless
detector.
The battery charger is designed for the dedicated battery pack. Do not use the battery
charger other than the dedicated one. Otherwise, a battery explosion or a battery leak
may occur, resulting in fire or electrical shock.
Do not operate the battery charger using any type of power supply other than the one
indicated on the rating label.
Do not handle the product with wet hands.
Do not place heavy objects such as medical equipment on cables and cords, or do not
pull, bend, bundle, or step on them to prevent their sheath from being damaged.
Do not attempt to disassemble, alter, or apply heat to the product.
Avoid dropping or subjecting the product to severe impacts. To avoid the risk of injury, do
not touch the internal parts of the battery if it has been cracked or otherwise damaged.
Stop using the battery pack immediately if it emits smoke, a strange smell, or otherwise
behaves abnormally.
Do not let the battery pack and battery charger come into contact with water or other
liquids and do not allow them to get wet.
Do not clean with substances containing organic solvents such as alcohol, benzene,
thinner, or other chemicals. Otherwise, fire or electrical shock may result.
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Do not allow dirt or metal objects (such as hair pins, clips, staples or keys) to contact the
terminals. Otherwise, battery explosion or leakage of electrolyte may occur, resulting in
fire, injury or pollution of surrounding area. If the battery leaks and the electrolytes come
into contact with your eyes, mouth, skin or clothing, immediatel y wash it awa y with runnin g
water and seek medical attention.
Do not leave, store, or place the product in a location near heat sources, or in a place
subject to direct sunlight, high temperature, high humidity, excessive dust, or mechanical
shock. Otherwise, battery leakage, overheating or damage to the product may occur,
resulting in electrical shock, burns, injury or fire.
Do not attempt to use a battery pack that has deteriorated. Using a battery pack that has
exceeded its life cycle may lead to overheating, fire or explosion.
The Lithium ion/polymer battery is recyclable.
Battery slowly discharges even if not in use. The battery pack may have expired if it
discharges immediately after being fully charged. You can purchase an optional b atter y
pack to replace an exhausted one.
The battery pack is a consumable item. If a fully charged battery is consumed quickly, use
a new and fully charged battery pack.
Be sure to charge the battery periodically (once a year) if it is not used for an extended
period of time. The battery pack cannot be charged if it has been over discharged.
Before discarding the battery pack, cover the terminals with adhesive tape or other
insulators. Contact with other metal materials may cause fire or explosion.
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General Hazards
Radiation Hazards
This system can be connected to x-ray generating equipment. Be certain to follow the safety instructions and
specifications for wearing proper lead apron when x-ray exposures are planned or possible.
All personnel should wear protective equipment including dosimeters during all phases of installation,
operation and maintenance of the system.
Electric Shock Hazards
To reduce the electric shock hazard, the system must be connected to an electrical ground. A three
conductor AC power cable is supplied with this system to provide the proper electrical grounding. The power
cable must be plugged into an UL-approved three-contact electrical outlet.
Do not disassemble or modify the product as it may result in fire or electric shock. There are no operator
serviceable parts or adjustments inside the systems. Only trained and qualified personnel should be
permitted access to the internal parts of the system.
Explosion Hazards
Do not operate the equipment in the presence of flammable or explosive liquids, vapors or gases. Do not
plug in or turn on the system where hazardous substances are detected.
If flammable substances are detected after the system has been turned on, do not attempt to turn off the
system or unplug it. Evacuate and ventilate the area before turning the system off.
Implosion Hazards
Do not hit or drop the equipment. The equipment may be damaged if it receives a strong jolt, which may
result in fire or electric shock if the equipment is used without it being repaired.
Owner’s Responsibility
The owner is responsible for ensuring that anyone using the system reads and understands the Service
Manual and other relevant literature, and fully understands them. Vieworks makes no representation,
however, that the act of reading this manual renders the reader qualified to operate, test and calibrate the
system.
Do not use the system if unsafe conditions are known to exist. In case of hardware failure
that could cause hazardous conditions (smoke, fire and etc), turn the power OFF and
unplug the power cords of all sub-systems.
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Notes for Using the Equipment
System Diagnostic
The VXSetup software runs a system diagnostic. Run VXSetup software after installing the system and at
least once a year. If an error occurs, report the detailed error information to Vieworks local dealer or
distributor.
The owner is responsible for ensuring that the system diagnostic is performed every year.
Do not try to use the system if the system diagnostic is failed.
Calibration
To ensure optimal performance of the system, it is important to verify that the system is calibrated.
The owner is responsible for ensuring that the system calibration is performed after the
system installation is completed or the system is repaired. Do not try to use the system if
system calibration is not performed.
Distances measurements
Distances measurements in millimeters are possible only after distance calibration has been performed using
a reference object (refer to VXvue User Manual).
The operator is responsible for performing distance calibration with a reference object and
verifying the results of the distance calibration before taking any distance measurements
on an image.
Left/Right Marker
The operator is responsible for the correct and clear marking on the left or right side of the image to eliminate
possible errors.
The software includes an option to mark the image with L (left) or R (right) indicator from acquisition phase
through printing and archiving. If the operator chose, for any reason, not to use L/R markers, he must use an
alternative way to eliminate any possible mistake.
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Image Backup
To avoid missing images which might result in patient being exposed to additional doses of radiation, it is
important to backup the images by filming or by using a CD or DVD option. This should be done as a routine
operation for every patient.
If the hard disk of your workstation is about to full, the operator should backup images and delete the images
to make room on the hard disk for new patient.
User Limitations
The VXvue software has the technician mode which could only be operated with the inputting PASS WORD.
The technician mode should be operated by the personnel who are qualified by Vieworks.
Cleaning the System
Use a dry cloth to clean surfaces of the system. Do not use detergents or organic solvents to clean the
system. Strong detergent, and organic cleaners may damage the finish and cause structural weakening. Do
not clean the system with turning the power on.
Disposal
Disposal of this product in an unlawful manner may have negative effects on health and on the environment.
When disposing of this product, therefore, be absolutely sure to follow the procedure which is in conformity
with the laws and regulations applicable in your area.
The expected life span of ViVIX-S Wireless system is about 3 years.
Overheating
Do not block the ventilation ports of the detector to prevent overheating of the detector. Overheating can
cause system malfunction and damages.
Electrical fire
This equipment is not suitable for use in the presence of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide.
Conductive fluids that drain into the active circuit components of the system may cause short circuits
that can result in electrical fire. Therefore, do not place fluids or food on any part of the system.
To avoid electric shocks and burns caused by use of the wrong type of fire extinguisher, make sure that
the fire extinguisher at the site has been approved for use on electrical fires.
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Handling the Equipment
The Equipment must be handled with care to avoid personal injury damage to the internal image sensor.
Do not put pressure on the detector locally since it will cause permanent damage to
the internal image sensor.
Excessive weight on the equipment may damage the internal image sensor.
It is recommended to use the case, in case if a patient should be positioned to put
pressure on the detector while acquiring images.
Load Limit Specifications
Uniform Load
Local Load
150 ㎏ over the whole area of the detector surface
100 ㎏ on an area 40 ㎜ in diameter
Pediatric Application
Every request should be reviewed by the pediatric radiologist prior to beginning the examination to
insure correct study is being performed.
If the technologist notices an unusual request, they should contact the pediatric radiologist. An example
should be from pediatric clinic where they order a Full Cervical, Thoracic, and Lumbar Spine series. The
pediatric radiologist should contact ordering physician and decide which study is the best for this
pediatric patient.
The technologist should use the proper technique for the patient’s size to decrease the radiation dose
when the technologist acquires diagnostic images.
ALL Pediatric patients shall be shielded for their x-ray examinations, except for when the shield will
obscure the region of interest, as in a pelvic or SI joint xray for trauma or arthritis, or when it is physically
or clinically unreasonable to shield the patient. For routine Hip X-Rays, ALL male children shall have
their scrotum shielded using the small gonadal shield, females may not be shielded as this wou ld
obscure the hips.
To minimize motion in infants and young children, swaddle the infant. Use distraction tools to improve
cooperation and projectors with child-friendly themes, music, toys with flashing lights or music, childfriendly images on the ceiling or walls, singing, counting, and a parent reading and talking to the child
through the console all can help reduce anxiety and comfort the child.
A Scoliosis series will consist of a single frontal standing view of the spine. No lateral view or supine
view is needed, unless specifically asked for by the Orthopedist or Radiologist. If the female’s breasts
can be shielded without obscuring the spine, breast shields should be used.
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Regulatory
Medical Equipment Classifications
Type of protection against electrical shock
Degree of protection against ingress of water IPXO
Mode of operation Continuous operation
Flammable anesthetics NOT suitable for use in the presence of a flammable
Class Ⅰ equipment
anesthetic mixture with air or with oxygen or nitrous oxide.
Equipment Standards
IEC/EN/UL 60601-1 Medical electrical equipm ent
CSA C22.2 No. 601.1 Part 1: General requirements for safety
IEC/EN 60601-1-2 Medical electrical equipm ent
Part 2: Electromagnetic compatibility–requirements and tests
IEEE 802.11a/b/g/n Wireless Communications
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Guidance and Manufacturer’s Declaration for EMC Directive
This device has been tested for EMI/EMC compliance, but interference can still occur in an
electromagneticall y nois y location. Attempt to maintain a suitable distance between electrical devices to
prevent malfunction.
Electromagnetic Emissions
The Equipment Under Test (EUT) is intended for use in the electromagnetic environment specified below.
The customer or user of the EUT should assure that it is used in such an environment.
Immunity Test Compliance Electromagnetic Environment – Guidance
Group 1 The EUT 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 equi pment.
Class A The EUT is suitable for use in all establishments other than
domestic and those directly connected to the public low-voltage
Class A
power supply network that supplies buildings used for domestic
purposes.
Complies
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IEC 60601
Test Level
Compliance
Level
±6 ㎸
±6 ㎸
±2㎸ for
lines
±2㎸ for
lines
±1 ㎸
mode
±1 ㎸
mode
<5% Uт
Uт) for 5 sec.
<5% Uт
Uт) for 5 sec.
Electromagnetic Immunity
The EUT is intended for use in the electromagnetic environment specified below.
The customer or user of the EUT should assure that it is used in such an environment.
Immunity Test
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
contact
±8 ㎸ air
power supply
lines
± 1 ㎸ for
input/output
differential
mode
±2 ㎸
common
(>95% dip in
Uт) for 0.5
cycle.
40% Uт
(60% dip in
Uт) for 5
cycles.
70% Uт
(30% dip in
Uт) for 25
cycles.
contact
±8 ㎸ air
power supply
lines
± 1 ㎸ for
input/output
differential
mode
±2 ㎸
common
(>95% dip in
Uт) for 0.5
cycle.
40% Uт
(60% dip in
Uт ) for 5
cycles.
70% Uт
(30% dip in
Uт) for 25
cycles.
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
EUT image intensifier requires continued operation
during power mains interruptions, it is recommended
that the EUT image intensifier be powered from an
uninterruptible power supply or a battery.
Power frequency
(50/60 ㎐)
magnetic field
<5% Uт
(<95% dip in
3 A/m 3 A/m Power frequency magnetic fields should be at lev els
<5% Uт
(<95% dip in
characteristic of a typical location in a typical
commercial or hospital environment.
IEC 61000-4-8
NOTE: Uт is the a.c. mains voltage prior to application of the test level.
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IEC 60601
Test Level
Compliance
Level
3 Vrms 150
3 Vrms 150
Immunity Test
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
㎑ to 80 ㎒
3 V/m 80 ㎒
to 2.5 ㎓
㎑ to 80 ㎒
3 V/m 80 ㎒
to 2.5 ㎓
Electromagnetic Environment – Guidance
Portable and mobile RF communications equipment
should be used no closer to any part of the EUT,
including cables, than the recommended separation
distance calculated from the equation applicable to the
frequency of the transmitter.
Recommended separation distance
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
b
range.
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1: At 80 ㎒ and 800 ㎒, 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 EUT is used exceeds the applicable RF compliance level above, the EUT should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the EUT.
b
Over the frequency range 150 ㎑ to 80 ㎒, field strengths should be less than [V1] V/m.
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Label and Symbols
Detectors
FXRD-1417WA FXRD-1417WB
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System Control Unit
Battery Charger
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Symbols
Symbol Description
Wireless Service Manual
Direct Current
Alternating Current
Protective Earth (Ground)
Equipotentiality
Power Off
Attention, consult accompanying documents
Power On
Medical Equipment
With Respect to electric shock, fire, and mechanical hazards only
In accordance with UL60601-1 and CAN/CSA C22.2 No. 601.1.
This mark shows compliance of the equipment with Directive 93/42/EEC.
Read and understand all instructions and war nin g lab e ls in the produc t
documentation before using the equipment.
Keep manual for future reference.
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1. Overview
The ViVIX-S Wireless is advanced wire less flat panel X-ray imaging system designed for digital radiography.
The lightweight wireless digital radiography is designed to be compatible with conventional X-ray film
cassettes so that the users who are not familiar with Digital Radiography (DR) can easily understand and use
the ViVIX-S system. In addition, the wireless communication (IEEE 802.11a/b/g/n) feature improves the
operability and high-speed processing.
1.1 Features
Wireless LAN communication (IEEE 802.11a/b/g/n) feature
Supporting Conventional 35 × 43 X-ray film cassette
Compatible with not only new X-ra y generat ors based on DR inter f ace but also conventional X-ray
generators
Designed with simple wiring and lightweight for portable applications
Image digitization, image inversion, image processing, zooming, panning, window level adjustment,
contrast adjustment, and various features enable the operator to see diagnostic details th at is difficult to
see by using conventional non-digital techniques.
Depending on the operating environment, the Ether Con Cable (optional) enables the device to be used
through expansion to a wired connection.
1.2 Intended Use
The ViVIX-S Digital X-ray detector is indicated for digital imaging solution designed for providing general
radiographic diagnosis of human anatomy. This device is intended to replace film or screen based
radiographic systems in all general purpose diagnostic procedures. This device is not intended for
mammography applications.
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Detector
System Control Unit
ViVIX-S Viewer
Gigabit Ethernet
Cables supplied with equipment
X-ray System
Generator
Vieworks
Generator Interface
Tether Interface
Battery Charger
Stand
Viework
s
Viewo
rks
Please
~
1.3 Standard Configuration
Figure 1.1 ViVIX-S Wireless System Configuration
Wireless communication is established between the ViVIX-S Wireless detector and System Control Unit. The
ViVIX-S system is compliant with IEEE 802.11a/b/g/n (2.4 ㎓ / 5 ㎓). The available frequency band may
vary depending on local radio laws and system requirements. Consult your local dealer for the frequency
available in your area.
Use of multiple WLAN devices within the same frequency band may interfere with each
wireless communication and cause a decline in transmission speed.
Do not cover or block the wireless module of the detector. Otherwise, the transmission
speed or operable distance may be reduced.
Recommended maximum operating distance of wireless communication between the
detector and System Control Unit is 8 meters.
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2. Product Description
ViVIX-S Wireless system consists of detector, system control unit (SCU), battery charger, battery pack,
software and its accessories.
Viewer: VXvue
Calibration and Diagnostic: VXSetup
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Accessories (Cables)
AC Power Cable (2M)
Generator Interface Cable (15M)
Direct LAN Cable 15M (1000BASE-T)
Tether Interface Cable (3M)
The use of accessories and cables other than those specified, with the exception of
ViVIX-S Wireless accessories and cables sold by Vieworks Co., LTD. as replacement
parts for internal components, may result in increased emissions or decreased immunity
of the equipment.
Accessory equipment connected to the analog and digital interfaces must be certified
according to the respective IEC standards. All combinations of equipment must be in
compliance with IEC 60601-1-1 system requirements. Any person who connects
additional equipment to the signal input or signal output ports configures a medical
system, and is therefore responsible for ensuring that the system complies with the
requirements of the system standard IEC 60601-1. If in doubt, consult Vieworks technical
support representative.
Workstation (Recommended but NOT included)
Operating System Microsoft Windows XP 32 bit SP3 (Professional Edition),
Windows 7 32 bit SP1 (Pr of es siona l Edi tio n or higher) or
Windows 7 64 bit SP1 (Professional Edition or higher)
CPU Intel Core i5 2600 or higher (or equivalent AMD chips)
Memory 2 GB or higher
Hard Disk 1 TB or higher
Ethernet (NIC) Intel® PRO 1000 Series (PT, CT, etc)
Monitor 1280 × 800 or higher
CD-Rom CD or DVD R/W or blu-ray
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2.2 Detector
2.2.1 Detector Specifications
Item Description
Model FXRD-1417WA(B)
Purpose General radiography
Image Matrix Size
Pixel Pitch
Effective Imaging Area
2560 × 3072 pixels
140 ㎛
358 ㎜ ×430 ㎜
Grayscale 14 bit, 16,384 grayscale
Scintillator CsI (Cesium Iodide) or Gadox (Gadolinium Oxysulfide)
Image Acquire and Transfer Time Preview: 2 s, Image Processing: 6.5 s (2 s when using Tether Interface)
Spatial Resolution
Rated Power Supply
Wireless
Wired
Min. 3.5 line pair/㎜
DC +24 V, Max. 0.5 A
Powered by the battery pack (4,000 ㎃ h)
Powered by the SCU using tether interface
Power Consumption Max. 12 W
Wireless Communications
†
Tether Interface (Optional) Gigabit Ethernet (1000BASE-T) via ‡PoE
IEEE 802.11a/b/g/n (2.4 ㎓ / 5 ㎓)
Imaging Plate Carbon Fiber Plate
Cooling Air cooling
Dimensions (H × W × D)
384 ㎜ × 460 ㎜ × 15 ㎜
Weight
3.0 ㎏ (including battery pack)
Environmental Requirements
Operation Temperature: +10 ∼ +35℃
Humidity: 30 ∼ 85% (Non-Condensing)
Atmospheric pressure: 70 ∼ 106 ㎪
Altitude: Maximum 2000 meters
Storage and transportation Temperature: -15 ∼ +55℃
Humidity: 10 ∼ 90% (Non-Condensing)
Atmospheric pressure: 50 ∼ 106 ㎪
Altitude: Maximum 2000 meters
Tab le 2.1 Detector Specifications
†
Tether Interface: Allows the detector to communicate with SCU via Ethernet cabling when wireless communications is
not available or higher speed data transfer is necessary.
‡
PoE (Power over Ethernet): Delivers electrical power over LAN cablin g to the netw orked dev ice.
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2
1
A
B
C
D
3
4
2.2.2 Detector Components
Figure 2.1 Detector Components
No. Name Description
1 Status Indicators
Power button
2 Wireless Module Transmits data with wireless communications (IEEE 802.11a/b/g/n).
3 Tether Interface Allows the detector to communicate with SCU via PoE cabling (Gigabit Ethernet
A: Data LED, Indicates communication and transmission status. - Blue
B: Active LED, Indicates the detector is ready to work. - Orange
C: Power LED, Indicates power on/off status. - Green
D: Power button, Press to power on or off the detector.
1000BASE-T)
4 Battery Pack Supplies electrical power to the detector while communicating wirelessly.
Tab le 2.2 Detector Components Description
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2.2.3 Detector Dimension
Figure 2.2 Detector Dimension
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2.3 System Control Unit
2.3.1 System Control Unit Specifications
Item Description
Model FXRS-03A
Power Supply
Cabling Ports Gigabit Ethernet Ports – 3EA
Wireless Communications
Dimensions (W × H × D)
Weight
Environmental Requirements
Operation
Storage and transportation Temperature: -15 ~ +55℃
Input: AC100 to 240V, 50/60 ㎐, Max. 200VA
Output: DC +24V 3.3A, 80W
Power over Ethernet Ports – 2EA (Only for FXRD-1417)
IEEE 802.11a/b/g/n (2.4 ㎓ / 5 ㎓)
300 ㎜ × 235.8 ㎜ × 58 ㎜, Antenna Height – 105 ㎜
1 Power S w i tch Turns on or off the SCU.
2 Fan Expels heated air inside of the SCU.
3 Antenna Assists communi cations between the detector and SCU.
4 Status LED Indicates status of SCU operation and connection.
Blinking Green: Startup in progress
Blue: Connected to Wi-Fi network
Tab le 2.4 System Control Unit Components (Front)
Page 30 of 124 RA14-11A-022
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