Samsung Accuvix XG Ultrasound - Service Manual
Samsung Accuvix XG Ultrasound - Service Manual
Samsung Accuvix XG Ultrasound - Service Manual
ENGLISH
Document No. CSD-SMEXG
Revision 00
Classifications:
▶ Type of protection against electrical shock: Class I
▶ Degree of protection against electrical shock (Patient connection): Type BF equipment
▶ Degree of protection against harmful ingress of water: Ordinary equipment
▶ Degree of safety of application in the presence of a flammable anesthetic material with air or with
oxygen or nitrous oxide: Equipment not suitable for use in the presence of a flammable anesthetic
mixture with air or with oxygen or nitrous oxide.
▶ Mode of operation: Continuous operation
The company is shall not be held liable for any injury and damage caused by not following this
warning.
For safe use of this product, you should read ‘Chapter 2. Safety’ in this manual, prior to starting to
useing this system.
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Describes precautions necessary to prevent user hazards of great urgency. Ignoring a
DANGER warning will risk life-threatening injury.
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Used to indicate the presence of a hazard that can cause serious personal injury, or
substantial property damage.
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Indicates the presence of a hazard that can cause equipment damage.
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A piece of information useful for installing, operating and maintaining a system. Not related
to any hazard.
Contents
Chapter 1. General Information
Chapter 2. Safety
Contents
Contents
Chapter 3. Installing the Product
Contents
Contents
Chapter 4. Checking the Product
Contents
Contents
Chapter 5. Product Structure
Contents
Contents
Chapter 6. Basic Maintenance
Contents
Contents
Chapter 7. Troubleshooting
Contents
Contents
Chapter 8. Disassembly and Reassembly
8.1 Overview ...................................................................................................... 8-1
8.2 Disassembly and Reassembly of the Body Cover .................................. 8-4
8.2.1 Preparations.............................................................................. 8-4
8.2.2 Body Front Cover ..................................................................... 8-4
8.2.3 Body Rear Cover...................................................................... 8-5
8.2.4 Body Top Cover ....................................................................... 8-6
8.2.5 Handle AY ................................................................................. 8-7
8.2.6 Body Arch Front Cover ............................................................ 8-8
8.2.7 Body Arch Inner Right & Left Cover ....................................... 8-9
8.2.8 Body Side Right & Left Cover ...............................................8-10
8.2.9 Body Skirt Right & Left Cover ...............................................8-11
8.3 Disassembly and Reassembly of the Ultrasound System PCB Part ..8-12
8.4.1 Preparations............................................................................8-12
8.4.2 PSA ASSY ..............................................................................8-14
8.4.3 CW Board, BF Board, BE Board, MTR Board ....................8-13
8.4 Disassembly and Reassembly of the LCD & ARM...............................8-14
8.4.1 Preparations............................................................................8-14
8.4.2 LCD ..........................................................................................8-14
8.4.3 LCD ARM ................................................................................8-15
8.5 PC Part Disassembly and Reassembly of the...................................8-16
8.5.1 Preparations............................................................................8-16
8.5.2 PC ASSY.................................................................................8-16
8.5.3 PCI Board, DVI Board, VCRIn Board,VGA Card ...............8-17
8.5.4 Rear Board ..............................................................................8-18
8.5.5 PC Power ................................................................................8-19
8.5.6 HDD .........................................................................................8-20
8.6 Disassembly and Reassembly of the Power .........................................8-21
8.6.1 Preparations............................................................................8-21
8.6.2 AC to DC Power Module .......................................................8-21
8.6.3 DC to DC Power Module .......................................................8-22
Contents
Contents
8.7 Disassembly and Reassembly of the User Interface Part....................8-23
8.7.1 Preparations............................................................................8-23
8.7.2 Control Panel ..........................................................................8-23
8.7.3 Touch Panel ............................................................................8-24
8.7.4 Control Panel Board...............................................................8-25
8.7.5 Track Ball.................................................................................8-26
8.7.6 Alpha-Numeric Board ............................................................8-27
8.7.7 LCD IF Board ..........................................................................8-28
8.7.8 DVD .........................................................................................8-29
8.7.9 Speaker Right & Left ..............................................................8-30
8.7.10 ECG Module ...........................................................................8-31
8.8 Disassembly and Reassembly of the Rear Fan ....................................8-32
8.8.1 Preparations............................................................................8-32
8.8.2 Rear Fan .................................................................................8-32
Contents
Contents
Chapter 9. Probe
9.1 Overview ...................................................................................................... 9-1
9.2 Probe List ..................................................................................................... 9-2
9.3 Thermal Index (TI Table)............................................................................ 9-6
9.4 Ultrasound Transmission Gel .................................................................... 9-7
9.5 Sheaths ........................................................................................................ 9-7
9.6 Probe Precautions ...................................................................................... 9-8
9.7 Cleaning and Disinfecting the Probe ......................................................9-10
Contents
Chapter 1. General Information
1.1 Overview
Chapter 1 contains the information necessary to plan the Troubleshooting of ACCUVIX XG
The ACCUVIX XG is a high-resolution color ultrasound scanner with high penetration and a
variety of measurement functions
Contents
High-end Digital Beamforming : The ACCUVIX XG utilizes the newly developed Digital
Beam forming technology.
Various diagnostic Modes : 2D Mode, M Mode, Color Doppler Mode, Power Doppler
Mode, PW Spectral Doppler Mode, CW Spectral Doppler Mode, TDI Mode(Tissue
Doppler Image Mode), etc.
Measurement and Report Functions : Besides the basic distance, area, circumference
and volume measurement functions, the ACCUVIX XGalso provides application-specific
measurement functions. The report function collates measurement data.
Review of Scanned Images : The ACCUVIX XG displays Cine images of 5400 frames
and loop images of 8192 lines.
SonoViewTM : This is a total ultrasound image management system, which allows a user
to archive, view and exchange documents.
1.3.1 Console
The console consists of two parts – the inner unit and the outer unit. The interior of the
console mainly contains devices that produce ultrasound images. On the exterior of the
console are various connectors, probe holders, storage compartments, handles, wheels, etc.
LCD
LCD ARM
Control Panel
Probe Connectors
Caster
Dial Button
Button
Slide Volume
Track Ball
1.3.4 Probe
Probes are devices that generate ultrasound waves and process reflected wave data for the
purpose of image formation.
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For more information, refer to `Chapter 9 Probes’.
2D mode
M-Mode
Color Doppler
Pulsed Wave (PW) Spectral Doppler
Continuous Wave (CW) Doppler
Imaging modes
Tissue Doppler Imaging (TDI)
Power Doppler (PD)
Directional Power Doppler (DPD)
Color M-Mode
Anatomical M
Phased Array
P2-4BA, P3-8CA, P4-12
Linear Array
L3-8, L5-13IS, LF5-12, LS5-13
Curved Array
Probes
C1-4EC, C2-6IC, C4-9/10ED, VR5-9, EV4-9/10ED, ER4-9/10ED
3D
V4-8, 3DC2-6, V5-9, V6-12
CW
CW 2.0, CW 4.0
TGC control
Mode-independent gain control
Acoustic power control (adjustable)
Signal processing Dynamic aperture
(Pre-processing) Dynamic apodization
Dynamic range control (adjustable)
Image view area control
M-mode sweep speed control
Frame average
Edge Enhancement / Blurring
Signal processing Gamma-scale windowing
(Post-processing) Image orientation (left/right and up/down, rotation)
White on black/black on white
Zoom
VCR
Video Page Printer
Color Video Page Printer
USB Video Printer
USB Color Video Printer
Auxiliary
Inkjet Printer
Laser Printer
Foot Switch(IPX1)
USB Flash Memory Media
Monitor
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Operating: 10 C ~ 40 C
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Temperature Limits Storage & Shipping: -10 C ~ 50 C
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Transport: -20 ~ 60 C
2.1 Overview
Chapter 2 contains the information necessary to Safety
Please read this chapter before using the MEDISON ultrasound system. It is relevant to
the ultrasound system, the probes, the recording devices, and any of the optional
equipment.
ACCUVIX XG is intended for use by, or by the order of, and under the supervision of, a
licensed physician who is qualified for direct use of the medical device.
Contents
Stmbols Description
CAUTION
Identifies the point where the system safety ground is fastened to the
chassis. Protective earth connected to conductive parts of Class I
equipment for safety purposes
ECG connector
USB connector
Microphone connector
Probe connector
1) Front
3) Monitor
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As for US requirement, the LEAKAGE CURRENT might be measured from a center-
tapped circuit when the equipment connects in the United States to 240V supply system.
To help assure grounding reliability, connect to a “hospital grade” or “hospital only”
grounded power outlet.
Additional equipment connected to medical electrical equipment must comply with the
respective IEC or ISO standards (e.g. IEC 60950 for data processing equipment).
Furthermore all configurations shall comply with the requirements for medical electrical
systems (see IEC 60601-1-1 or clause 16 of the 3 Ed. of IEC 60601-1, respectively).
Anybody connecting additional equipment to medical electrical equipment configures a
medical system and is therefore responsible that the system complies with the
requirements for medical electrical systems. Attention is drawn to the fact that local laws
take priority over the above-mentioned requirements. If in doubt, consult your local
representative or the technical service department.
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The system has been designed for 100-120VAC and 200-240VAC; you should select the
input voltage of monitor, printer and VCR. Prior to connecting an OEM power cord, verify
that the voltage indicated on the power cord matches the voltage rating of the OEM
device.
An isolation transformer protects the system from power surges. The isolation
transformer continues to operate when the system is in standby.
Do not immerse the cable in liquids. Cables are not waterproof.
The auxiliary socket outlets installed on this system are rated 100-120V and 200-240V
with maximum total load of 200W. Use these outlets only for supplying power to
equipment that is intended to be part of the ultrasound system. Do not connect additional
multiple-socket outlets or extension cords to the system
Do not touch SIP/SOP and the patient simultaneously. There is a risk of electric shock
from leakage current
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This device is not intended to provide a primary ECG monitoring function, and therefore
does not have means of indicating an inoperative electrocardiograph.
Do not use ECG electrodes of HF surgical equipment. Any malfunctions in the HF
surgical equipment may result in burns to the patient.
Do not use ECG electrodes during cardiac pacemaker procedures or other electrical
stimulators.
Do not use ECG leads and electrodes in an operating room.
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The level of electrical energy discharged from a system user or patient to an ultrasound
system can be significant enough to cause damage to the system or probes.
The following precautions can help to reduce ESD:
- Anti-static sprays on carpets or linoleum
- Anti-static mats
- A ground wire connection between the system and the patient table or bed.
It is highly recommended that the user be given training on ESD-related warning symbols
and preventive procedures.
2.3.4 EMI
Although this system has been manufactured in compliance with existing EMI
(Electromagnetic Interference) requirements, use of this system in the presence of an
electromagnetic field can cause momentary degradation of the ultrasound image.
If this occurs often, MEDISON suggests a review of the environment in which the system
is being used, to identify possible sources of radiated emissions. These emissions could
be from other electrical devices used within the same room or an adjacent room.
Communication devices such as cellular phones and pagers can cause these emissions.
The existence of radios, TVs, or microwave transmission equipment nearby can also
cause interference.
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In cases where EMI is causing disturbances, it may be necessary to relocate this system.
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When connecting other customer-supplied accessories to the system, such as a remote
printer or VCR, it is the user’s responsibility to ensure the electromagnetic compatibility of
the system. Use only CISPR 11 or CISPR 22, CLASS B compliant devices.
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The use of cables, transducers, and accessories other than those specified may result
inincreased emission or decreased Immunity of the Ultrasound System.
IEC 60601 Electromagnetic environment -
Immunity test Compliance level
Test level guidance
Electrical fast ±2KV for power supply ±2KV for power Mains power quality should be that
lines supply lines of a typical commercial or hospital
transient/burst
environment.
±1KV for input/output ±1KV for input/
lines output lines
IEC 61000-4-4
Surge ±1KV differential mode ±1KV differential mode Mains power quality should be that
±2KV common mode ±2KV common mode of a typical commercial or hospital
IEC 61000-4-5 environment.
Voltage dips, short <5% Uт <5% Uт Mains power quality should be that
interruptions and (>95% dip in Uт) (>95% dip in Uт) of a typical commercial or hospital
voltage variations for 0.5cycle for 0.5cycle environment. If the user of this
on power supply product requires continued
input lines 40% Uт 40% Uт operation during power mains
(60% dip in Uт ) (60% dip in Uт ) interruptions, it is recommended
IEC 61000-4-11 for 5 cycle for 5 cycle that this product be powered from
an uninterruptible power supply or
70% Uт 70% Uт a battery.
(30% dip in Uт) (30% dip in Uт)
for 25 cycle for 25 cycle
<5% Uт <5% Uт
(<95% dip in Uт ) (<95% dip in Uт )
for 5 s for 5 s
Power frequency Power frequency magnetic fields
(50/60Hz) should be at levels characteristic
magnetic field 3 A/m 3 A/m of a typical location in a typical
commercial or hospital
IEC 61000-4-8 environment.
80MHz to 800MHZ
800MHz to 2.5GHz
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 Ultrasound System is used exceeds
the applicable RF compliance level above, the Ultrasound System should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the
Ultrasound System or using a shielded location with a higher RF shielding effectiveness and filter attenuation.
b Over the frequency range 150kHz to 80MHz, field strengths should be less than [V1] V/m.
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If the system is connected to other customer-supplied equipment, such as a local area
network (LAN) or a remote printer, Medison cannot guarantee that the remote equipment
will work correctly in the presence of electromagnetic phenomena.
A medical device can either generate or receive electromagnetic interference. The EMC
standards describe tests for both emitted and received interference.
Medison Ultrasound System does not generate interference in excess of the referenced
standards.
An Ultrasound System is designed to receive signals at radio frequency and is therefore
susceptible to interference generated by RF energy sources. Examples of other source of
interference are medical device, information technology products, and radio and television
transmission towers. Tracing the source of radiated interference can be a difficult task.
Customers should consider the following in an attempt to locate the source:
Is the interference intermittent or constant?
Does the interference show up only with one transducers operating at the
same frequency or with several transducer?
Do two different transducer operating at the same frequency have the
same problem?
Is the interference present if the system is moved to a different location in
the facility?
The answers to these questions will help determine if the problem reside
with the system or the scanning environment. After you answer the question,
contact your local MEDISON customer service department.
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The product weighs more than 100kg. Be extra careful when transporting it. Careless
transportation of the product may result in product damage or personal injury
Before transporting the product, check that the brakes on the front wheels are unlocked.
Also, make sure to retract the monitor arm completely so that it is secured in a stationary
position.
Always use the handles at the back of the console and move the product slowly.
This product is designed to resist shocks. However, excessive shock, for example if the
product falls over, may cause serious damage.
If the system operates abnormally after repositioning, please contact the MEDISON
Customer Service Department.
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Be aware of the castors, especially when moving the system. MEDISON recommends
that you exercise caution when moving the product up or down ramps
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Do not press the control panel excessively.
Never attempt to modify the product in any way.
Check the operational safety when using the product after a prolonged break in service.
Make sure that other objects, such as metal pieces, do not enter the system.
Do not block the ventilation slots.
To prevent damage to the power cord, be sure to grip the plug head – not the cord –
when unplugging.
Excessive bending or twisting of cables on patient-applied parts may cause failure or
intermittent operation of the system.
Improper cleaning or sterilization of a patient-applied part may cause permanent damage.
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Do not press on the control panel with excessive force or lean against it.
Do not sit on the control panel or apply too much force to it.
When adjusting the height or position of the control panel, be careful not to leave your
fingers or hand in area between the control panel and the lift - they may get trapped and
hurt
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Ultrasound waves may have damaging effects on cells and, therefore, may be harmful to
the patient. If there is no medical benefit, minimize the exposure time and maintain the
ultrasound wave output level at low. Please refer to the ALARA principle.
Do not use the system if an error message appears on the video display indicating that a
hazardous condition exists. Note the error code, turn off the power to the system, and call
your local MEDISON Customer Service Department.
Do not use a system that exhibits erratic or inconsistent updating. Discontinuities in the
scanning sequence are indicative of a hardware failure that should be corrected before
use.
The system limits the maximum contact temperature to 43 degree Celsius, and the
ultrasonic waves output observes American FDA regulations.
1) POWER
Power controls the system acoustic output. Two real-time output values are on the
screen: a TI and a MI. They change as the system responds to POWER adjustments.
In combined modes, such as simultaneous Color, 2D-mode and pulsed Doppler, the
individual modes each add to the total TI. One mode will be the dominant contributor to
this total. The displayed MI will be from the mode with the largest peak pressure.
2) Zoom
Increasing the zoom magnification may increase frame rate. This action will increase the
TI. The number of focal zones may also increase automatically to improve resolution. This
action may change MI since the peak intensity can occur at a different depth.
3) Persistence
A lower persistence will decrease the TI. Pulse voltage may be automatically increased.
An increase in pulse voltage will increase MI.
4) Focal no.
More focal zones may change both the TI and MI by changing frame rate or focal
depth automatically. Lower frame rates decrease the TI. MI displayed will correspond
to the zone with the largest peak intensity.
5) Focus
Changing the focal depth will change the MI. Generally, higher MI values will occur
when the focal depth is near the natural focus of the transducer.
4) Scale
Using the SCALE control to increase the color velocity range may increase the TI.
The system will automatically adjust pulse voltage to stay below the system
maximums. A decrease in pulse voltage will also decrease MI.
5) Sec Width
A narrower 2D-mode sector width in Color imaging will increase color frame rate. The
TI will increase. MI will not change. If pulsed Doppler is also enabled, then pulsed
Doppler will remain as the primary mode and the TI change will be small.
1) Probe
Each probe model available has unique specifications for contact area, beam shape,
and center frequency. Defaults are initialized when you select a probe. MEDISON
factory defaults vary with probe, application, and selected mode. Defaults have been
chosen below the FDA limits for intended use.
2) Depth
An increase in 2D-mode depth will automatically decrease the 2D-mode frame rate.
This would decrease the TI. The system may also automatically choose a deeper
2D-mode focal depth. A change of focal depth may change the MI. The MI displayed
is that of the zone with the largest peak intensity.
3) Application
Acoustic output defaults are set when you select an application. MEDISON factory
defaults vary with probe, application, and mode. Defaults have been chosen below
the FDA limits for intended use.
− ( 0.23 alf )
In Situ = Water [ e ]
where: In Situ = In Situ Intensity Value
Water = Water Value Intensity
e = 2.7183
a = Attenuation Factor
Tissue a(dB/cm-MHz)
Brain .53
Heart .66
Kidney .79
Liver .43
Muscle .55
l = skin line to measurement depth (cm)
f = Center frequency of the transducer/system/mode combination(MHz)
Since the ultrasonic path during an examination is likely to pass through varying lengths
and types of tissue, it is difficult to estimate the true In Situ intensity. An attenuation factor
of 0.3 is used for general reporting purpose; therefore, the In Situ value which is
commonly reported uses the formula:
− ( 0.069 lf )
In Situ (derated) = Water [ e ]
Since this value is not the true In Situ intensity, the term “derated” is used.
The maximum derated and the maximum water values do not always occur at the same
operating condition; therefore, the reported maximum water and derated values may not
be related to the In Situ (derated) formula. Take for example a multi-zone array transducer
that has maximum water value intensities in its deepest zone: the same transducer may
have its largest derated intensity in one if its shallowest focal zones.
1) Systematic Uncertainties
For the pulse intensity integral, derated rarefaction pressure Pr.3, center frequency and
pulse duration, the analysis includes considerations of the effects on accuracy of:
Hydrophone calibration drift or errors.
The systematic uncertainties Acoustic power measurements using a Radiation Force are
measured through the use of calibrated NIST acoustic power sources.
We also refer to a September 1993 analysis done by a working group of the IEC
technical committee 87 and prepared by K. Beissner, as a first supplement to IEC
publication 1161.
The document includes analysis and discussion of the sources of error / measurement
effects due to:
Balance system calibration.
Absorbing (or reflecting) target suspension mechanisms.
Linearity of the balance system.
Extrapolation to the moment of switching the ultrasonic transducer
(compensation for ringing and thermal drift).
Target imperfections.
Absorbing (reflecting) target geometry and finite target size.
Target misalignment.
Ultrasonic transducer misalignment.
Water temperature.
Ultrasonic attenuation and acoustic streaming.
Coupling or shielding foil properties.
Plane-wave assumption.
Environmental influences.
Excitation voltage measurement.
Ultrasonic transducer temperature.
Effects due to nonlinear propagation and saturation loss.
The overall findings of the analysis give a rough Acoustic Power accuracy figure of +/-
10% for the frequency range of 1 - 10 MHz.
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For disposing of the system or accessories that have come to the end of their lifespan,
contact the vendor or follow appropriate disposal procedures.
You are responsible for complying with the relevant regulations for disposing of wastes.
The lithium ion battery used in the product must be replaced by a MEDISON service
engineer or an authorized dealer.
This symbol is applied in the European Union and other European countries
This symbol on the product indicates that this product shall not be treated as household
waste. Instead it shall be handed over to the applicable collection point for the recycling of
electrical and electronic equipment. By ensuring this product is disposed of correctly, you
will help prevent potential negative consequences for the environment and human health,
which could otherwise be caused by inappropriate waste handling of this product. The
recycling of materials will help to conserve natural resources. For more detailed
information about recycling of this product, please contact your local city office, your
electrical and electronic waste disposal service or the shop where you purchased the
product.
Contents
3.1 Overview ...................................................................................................... 3-1
3.2 Transportation.............................................................................................. 3-3
3.2.1 Precautions for Transportation ....................................................... 3-3
3.2.2 Temperature and Humidity ............................................................. 3-3
3.2.3 Transportation of the Product ......................................................... 3-3
3.3 Unpacking .................................................................................................... 3-4
3.3.1 Unpacking the Box........................................................................... 3-4
3.3.2 Checking Package Contents .......................................................... 3-5
3.4 Precautions for Installation ......................................................................... 3-6
3.4.1 Precautions....................................................................................... 3-6
3.4.2 Installation Location .........................................................................3-6
3.5 Installation Procedure ................................................................................. 3-7
3.5.1 Installation Safety ............................................................................. 3-7
3.5.2 Connecting the Power Cord ........................................................... 3-8
3.5.3 Connecting the Network Cable ...................................................... 3-9
3.5.4 Connecting the Foot switch ............................................................ 3-9
3.5.5 Connecting the Probe...................................................................... 3-9
3.6 Starting the Product................................................................................... 3-11
3.7 Shutting down the Product .......................................................................3-12
3.7.1 Power Switch..................................................................................3-12
3.7.2 Cut-off Switch .................................................................................3-12
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Type Temperature [ C] Humidity [%]
Transportation -25 ~ 60 20 ~ 90
Care -10 ~ 50 20 ~ 90
Operation 10 ~ 35 30 ~ 75
[Table 3-1] Temperature and Humidity Requirements
3.4.1 Precautions
Please follow the precautions below.
1) Avoid installing the product where water may get into it.
2) Avoid installing the product in direct sunlight.
3) Avoid installing the product in places where there are high temperature fluctuations.
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4)Temperatures of 10 C ~ 35 C and a humidity of 30% ~ 75% are required for normal
operation..
5) Avoid installing the product near a heater.
6) Avoid installing the product in a dusty location, or where there is a lack of ventilation.
7) Avoid installing the product in a location subject to vibration.
8) Avoid installing the product where there are chemicals or gas.
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If you use the product near a generator, X-Ray equipment, or a broadcasting transmission
cable, the screen may not work normally due to interference.
In addition, sharing the same wall outlet with other electric equipment may cause noise.
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The product and the power cord may be connected before shipping.
Power Cable
[Figure 3-6] Product Power
Allowable Voltage
Voltage Current Frequency
Range
Connect the
network (LAN)
Connect the
foot switch
1) Connect probes when the probe handle is unlocked (when the knob is turned
counterclockwise).
2) Connect probes with the probe cable pointing downwards.
3) Turn the probe handle clockwise until it is fixed at the opposite direction of the cable.
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Although you can connect a probe when the power is on, do not connect or disconnect a
probe during the booting sequence of the product.
Cut-Off Switch
3) To start ACCUVIX XG, press the On/Off switch at the right side of the control panel
Power Switch
Power Switch
Cut-Off Switch
3.8.1.1 DVD-Multi
DVD-RW, DVD-RAM, DVD-R, DVD+R, DVD-ROM, CD-R, CD-RW, CD-ROM
3.8.1.1 Hard Disc Drive
500Gbytes.
3.10.1 Title
You can specify information displayed in the title area on the screen.
3.10.1.1 Institution
Enter the name of the hospital/institution where the product is installed. The current date is
displayed. To change the date, press
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You cannot input following characters; # [ “ ; : ? | ₩
3.10.1.2 Date
The current date is displayed. To change the date, press
˙ T˙ ˙ip˙ s˙ ˙! –˙ H
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˙ e˙
- HPRF: Select whether to activate HPRF (High Pulse Repetition Frequency) which is
supported in PW Spectral Doppler Mode. Check the checkbox to use the HPRF function.
- Color Map Auto invert: Check this checkbox to automatically highlight Color Map. This
is only applied when you change Steer in 2D/C/D mode, C mode, or DPDI mode in PD
mode.
- M/PW Loop Side by Side: Add Loop Side by Side display in M mode or Power Spectral
Doppler mode.
- Width Rescale: Automatically fit the image size to the screen size when the depth of a
2D image is adjusted. This function can be used only with Linear Probe.
3.10.5 Control
You can specify display-related options
3.10.5.1 Track Ball Speed for Scan Mode
Specify the Trackball speed as Slow, Normal or Fast.
3.10.5.2 Track Ball Speed for Management
Specify the Trackball speed as Slow, Normal or Fast. Slower speed allows more precise
measurement
3.11.2 Font
Specify the target for which you want to set the font. Choose from Document Font and
Measure Result Font.
1) Font Name : Select the font type to use.
2) Font Size : Select the font size to use.
3) Font Color : Select the font color to use.
4) Preview : Preview window displays the font you selected.
5) Default : Go back to the default setting like below.
3.12.2 BodyMaker
3.12.2.1 Size
Set the BodyMarker size (Small, Medium, Large).
3.12.2.2 Option
BodyMarker Auto Active: Set whether to activate BodyMarker mode automatically when
changing an active image region.
3.19.2.3 BodyMaker Edit
˙O
N ˙ T˙ E
˙
You can add or save between 1 and 100 BodyMaker(s) in each list
1) Adding a Bodymarker
Select and double-click a bodymarker in the left list (u). The selected bodymarker is
added to the right list (v). The list cannot have duplicated bodymarkers. In this case a
warning message was popped-up.
2) Removing a Bodymarker
Select and double-click a bodymarker in the right list (v).
3) Saving and Canceling Bodymarker list
Click Save to save the list. Click Close to cancel the list.
4) Resetting Bodymarker List
Click Reset. The Bodymarker list is reset to the system defaults.
3.12.2.4 Text setup
Select whether to use Quick Text, Auto Text Erase, Boot up Caps Lock on, Autotext, Edit
Text, Autotext Edit or Clear Annotation.
1) Quick Text
If the checkbox is selected, the Quick Text function is enabled. Quick Text switches the
system to the text input mode immediately after a character key in the Alphanumeric
Keyboard is pressed.
The system has a built-in abbreviation list for this function. You can add a new
abbreviation or edit the existing abbreviation as desired.
※ Tips˙ ˙! –˙ E
˙ ˙ ˙ ˙ ˙ d˙ ˙i˙t˙in˙ g˙ A
˙ b˙ b˙ ˙re˙ v˙˙ia˙ ˙t˙io˙ n˙ ˙l˙is˙ ˙t
To enable the abbreviation list stored in the system, press the Autotext Edit button. The
system will switch to the Autotext Edit screen.
To save the changes and finish editing, press the Close button.
① Modify Word
- Use the Trackball and the Set button to select a word to modify in the list. An
abbreviation for the selected word and its full word are displayed under the Abbreviation
and Full Word fields at the bottom of the screen.
- Modify words in the Abbreviation and Full Word fields. The abbreviation list is updated in
real time.
② Add Word
- Press the New button.
- Enter words to add in the Abbreviation and Full Word fields at the bottom of the screen.
The entered words are added to the abbreviation list.
5) Clear Annotation
Check this checkbox to delete the entered annotation when you change the mode.
6) Edit Text
Select an application to modify and edit the corresponding text page.
˙O
N ˙ T˙ E
˙
The User Knob 2 key is only used in Scan Mode
3.15.1 E-mail
You can specify a server through which you will send and receive e-mails.
1) Mail (SMTP) Server
Specify the e-mail server.
2) Port No.
Enter a port number.
3) ID
Enter an ID for the e-mail server.
4) Password
Enter a password for the e-mail server.
3.15.2 Buzzer Control
Generate a buzzer sound when a button or dial-button is use.
1) Buzzer Sound
Set this to on or off using the trackball. When this is set to on, the buzzer sounds each
time a button or dial-button is used.
2) Touch Screen Sound
Set this to on or off using the trackball. When this is set to on, it sounds each time the
touch screen is tapped.
3) Set / Exit Key Sound
Set this to on or off using the trackball. When this is set to on, it sounds each time the Set
or Exit button on the control panel is used.
3.15.3 Account
Register the user ID and password.
1) Name Formatting
Set the order in which patient names are displayed.
Default: Names are displayed in the order of last name, first name and middle name
(Ex. Smith, Robert L).
Custom: For ‘Item,’ specify the order as last name, first name and middle name. For
‘Separator,’ specify a symbol such as comma or space, or just omit it.
2) Representation Priority
Specify how patient names are displayed. Select the precedence of Roman,
Ideographic and Phonetic letters.
1) Option
It shows the types of optional software that can be installed on the product.
2) Status
It shows the current status of optional software.
Lock_Not Installed: No hardware is connected.
Lock_Unregistered: The software is not registered.
Lock_Installed: Hardware is installed but not registered.
Unlock_Permanent: Ready for use without any time limitation.
Unlock_Restricted: Ready for use for a certain period.
Lock_Expired: Use of the software is restricted and it cannot be used after a
specified period of use has expired.
3) Hardware Configuration
The list of optional hardware is displayed on the screen. Currently, only ECG is
supported.
Check the checkbox for hardware that will be used. Reboot the system to finish
settings.
3.17.1.1 AE Title
Enter the name of the DICOM AE (Application Entity). The title is used to identify devices
that use DICOM in a network.
3.17.1.2 Station Name
Enter the name of the system. Along with AE Title, it is often used to identify the system in
the DICOM network.
Include 3D Volume: Select whether to send 3D volume data together with the 3D images
˙NO
˙ T˙ E
˙
Select this only when you use a Storage service which supports the 3D volume data of
Medison.
3.17.7.1 Color
Specify whether to use colors. Select Grayscale or RGB.
3.17.7.2 Format
Specify the paper layout. Select from 1ⅹ1, 1ⅹ2, 2ⅹ2, 2ⅹ3, 3ⅹ3, 3ⅹ4, 3ⅹ5, 4ⅹ4,
4ⅹ5 and 4ⅹ6.
3.17.7.3 Orientation
Specify the paper orientation. Select Landscape or Portrait.
Status Description
˙O
N ˙ T˙ E
˙
The specified items will appear on the screen only when the Auto Calc dial-button on the
softmenu is pressed in Spectral Doppler Mode.
˙O
N ˙ T˙ E
˙
The S/W version of your system may be different from that in the figure above.
3.20.1 Utility
This menu is for system settings and for using ECG, Biopsy, and Histogram.
You can use the Utility menu as follows:
1) Tap Utility on the touch screen. The Utility screen appears on the touch screen.
2) Tap a button to select the desired item.
3) Tap Return to return to the Utility screen after using it. To exit the Utility screen and
switch to the scan mode, tap Exit on the touch screen or press the Exit button on the
control panel.
2) 2D Post
Select 2D Post
3) Color Map
Select Color Map
Brightness
Set the brightness of the screen. Select a value between 0 and 100 by using the dial-
button.
Contrast
Set the contrast of the screen. Select a value between 0 and 100 by using the dial-button.
Curve
Specify the focus curve. Select one from Type 1 to 5 or User 1 to 3 by using the dial-
button. You can edit the user type focus curves according to your preferences by using
Edit. They can be edited in the same way as for 2D Post.
Edit
When you set Curve as User, the Edit button on the touch screen is enabled. Tapping
Edit on the touch screen shows the screen and menu for setting a curve.
- Insert: Insert a point to the curve. The new point is added in the middle between the
presently selected point and the next point.
- Delete: Deletes the currently selected point.
- Save: Save the current curve.
- Picker Pos: Select a point in the curve. Select the position of the point using the dial-
button.
- Color: Select your choice of Red, Green or Blue for the color of the point on the curve.
˙O
N ˙ T˙ E
˙
It shows an image of the heart beat and appears in the menu for cardiac or Vascular
application only.
In Multi Image Mode such as Dual or Quad, ECG CINE can be used for each image.
3.20.4 Histogram
A histogram is a type of graph representing the distribution of echoes.
1. Tab Histogram on the touch screen.
2. Specify an area that a histogram is to cover. Use the Trackball and the Set button to
specify area 1, 2 and 3.
3. Histogram 1, 2 and 3 will appear on the screen.
3.20.5 Biopsy
Tab Biopsy on the touch screen.
˙CA
˙U˙ T˙ ˙IO
˙N˙
Before performing biopsy, you should specify the Biopsy Guide Line.
˙A
C ˙U˙ T˙ ˙IO
˙N˙
Note that the Biopsy Guide Line cannot be edited when the Trapezoidal function is in use
for the Linear Probe.
If the system is rebooted, the Biopsy Guide Line settings are restored to the default.
3.20.7 VCR
Tab VCR on the touch screen
˙CA
˙U˙ T˙ ˙IO
˙N˙
Connect the VCR on the system before using.
Check the capacity of the media before recording.
Only VCRs supported by MEDISON can be used.
˙O
N ˙ T˙ E
˙
Counter and Search may not be shown on the touch screen by VCR type.
1) Using VCR
Play: Play back recorded data. Rew: Perform rewind.
Pause: Stop playback temporarily. Stop: Stop playback.
Record: Start recording. FF: Perform fast forward.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
Return and Exit are not available during playback
2) Counter
The VCR Counter window appears on the monitor screen. Reset the counter.
3) Serach
The VCR Counter window appears on the monitor screen. Enter a specific time in the
counter to search the image.
4) VCR Volume
Adjust the VCR volume. Select a value between 0 and 100 by using the dial-button on the
touch screen.
Tab Exit on the touch screen or on the control panel to exit Storage Manager.
1) Refresh
Update the dislay on the touch screen to play of drives currently connected to the system.
˙O
N ˙ T˙ E
˙
When using Storage Manager, you should press Refresh to update information.
2) Eject / Remove
Disconnect the selected drive.
˙O
N ˙ T˙ E
˙
Before unplugging a USB Flash memory drive, make sure to disconnect it by using the
Eject / Remove button.
3) Format
Initialise the selected drive. Under the Format window, you can initialize various settings.
Press Start to start initialization. Press Close to cancel.
3.20.8 Presets
Tap Preset on the touch screen. The Pre. Load screen appears on the touch screen and
the probe settings supported by the current application appear as buttons.
Tap an application or App. Load on the touch screen to change to the selected application.
1) User 1 - 5
Select the image settings saved by the user previously.
[Rename]: Change the Userset name that was saved previously.
[App. Load]: Run the selected Userset.
2) Save
Pressing this button after making a selection saves the settings applied on the current
screen.
3.20.9 Help
Tap Help on the touch screen. The electronic manual appears on the monitor screen.
˙O
N ˙ T˙ E
˙
There is no Return key on the Help screen.
1. Tap Utility > Measure Setup on the touch screen. Or click Measure Setup on the Setup
screen.
2. When the Measure Setup screen appears, select a tab that has items to configure.
3. Specify settings for each item.
4. Save and finish the setting. Press the Close button on the touch screen or the Exit
button on the control panel to switch to scan mode. Press Return on the touch screen to
go back to the Utility menu
˙ T˙ ˙ip˙ s˙ ˙! –˙ S
※ ˙ e˙ ˙le˙ c˙ ˙t˙in˙ g˙ a˙ ˙ta˙ b˙
You can select a tab in either of two ways as desired.
- Use the trackball and the Set button to select a tab.
- Select a tab in the touch screen.
˙ T˙ ˙ip˙ s˙ ˙! –˙ S
※ ˙ e˙ ˙le˙ c˙ ˙t˙in˙ ˙f L˙˙in˙ e˙ T˙ y˙ p˙ e˙
If you select Hidden Dotted Line or Hidden Dotted Line after Set, you can keep images
from being interfered with by a measurement line.
4) Measurement Results
Transparent BK color: Set transparent background.
Number of Results Displayed: Set the number of lines in which to display the
measurement results. This is applied to the basic measurement results for all applications
except for obstetrics,cardiac, vascular, urology, and fetal heart.
˙O
N ˙ T˙ E
˙
Use the Setting tab of each application to set the Number of Measure Results Displayed
for obstetrics, cardiac, vascular, urology, and fetal heart.
3.21.2.5 Report
Select the Report tab under the General tab. Here you can set items related to the
measurement report.
2) Report Header
Specify header options for reports. You can specify more than one item and the specified
items appear in all measurement reports.
Hospital Info.
This is information about the hospitals in which the product is installed. You can select
Hospital name, Diag. Physician, Ref. Physician, and Sonographer.
Patient Info.
This is information about the patient. You can select ID, name, Gender, Heart Rate,
Birthday, Age, and BSA.
Others
This information concerns other comments. You can select Description and Accession
3.21.2.11 Caliper
Select the Caliper sub-tab under the General tab.
Specify whether additional information will be shown along with basic measurement
values when basic measurements are taken by pressing the Caliper button on the control
panel. If this option is selected, the additional information will be also saved and output
along with measurement results.
If Application is set to Cardiac, the D Velocity, D A/B and D Trace items are changed.
3.21.3 Cardiac
Select the Cardiac tab in the Measure Setup screen. You can specify settings for cardiac
measurement.
3.21.4 Vascular
Select the Vascular tab in the Measure Setup screen. You can specify settings for
vascular measurement.
Specify how the volume of the left ventricle is measured. For more information on
calculation formulae, please refer to reference manual.
3.21.5.3 Fetal Echo Measurement Result
Measurement Result Type
Set a measurement method. Select Avg, Last, Max or Min value.
3.21.5.4 Number of Measure Results Displayed
Number of Result Displayed
Specify the number of lines for measurement results that are displayed on the screen.
1) Percentile Info.
- Show Percentile Information
Check the checkbox to use the Percentile Information.
- Percentile Criteria
Select a value that will be used for percentile calculation.
▶ GA by LMP: GA is calculated based on the maternal LMP.
▶ Estab. Due Date: GA is calculated based on the Estab. Due Date that is entered in the
Patient Information.
▶ AUA (Average US GA): GA is calculated using the average value of several ultrasound
measurements.
- Rank Information Method
Specify how the growth range information will be displayed. Specify how the growth range
information will be displayed. The growth range information can be used to observe fetal
development and abnormality, if any.
6) OB Measurement Result
- Measurement Result Type
▶ Select the measurement result type from between average (Avg), the last measured
value (Last), maximum value (Max), and minimum value (Min).
1) Items
This setting is intended for measurement of the gestational age (GA) and fetal size
(Growth). Select items in the following order::
- Select a measurement item in the list on the left.
- Select a reference type from the GA table and Growth table.
- Select a reference in the list on the right.
2) Fetal Weight
This setting is intended for measurement of the estimated fetal weight (EFW). Select
items in the following order
- Select the EFW measurement method from EFW equation and EFW growth.
- Select a reference in the list on the below.
3) Add Reference
˙O
N ˙ T˙ E
˙
Observe the following directions when adding a table reference. If these conditions are
not met, a warning message appears and the reference is not saved.
- Input at least three types of data.
- If there are no Min and Max values, select Value Only for “Table Type.”
4. Press OK to go to the next step. The system will switch to the Editor screen.Press
Cancel to cancel.
5. Enter a reference.
6. Press Save to save the information. Press Cancel to cancel.
7. Press OK to finish. Press Cancel to cancel.
Specify the order of measurement items when measuring EFW using the User 1 or User
2 button.
Change the order of measurement item using arrow buttons.
3.20.6.3 Calc&Graph
Select the sub tab Calc & Graph under the OB tab. You can specify settings for calculation
and graphs.
1) Auto Calculations
Specify an item that will be calculated automatically. For example, if the MAD checkbox is
selected as shown below, when APD and TAD are measured, the measurements are
used to calculate MAD automatically and display the result on the screen. The results of
automatic calculation may affect GA and EDD information.
2) Ratio Calculations
Specify a measurement item for which a ratio will be calculated. For example, if the
FL/BPD checkbox is selected, when FL and BPD are measured, the ratio between them
is calculated and displayed on the screen. This ratio also appears in a report.
4) Trend Graph
Specify whether to include a graph for a certain item or ratio in an obstetrics report. Press
and the Editor screen for the selected graph will appear.
4.1 Overview
Chapter 4 describes how to check ACCUVIX XG and how to check if its major functions
and the power supply are working properly.
Contents
Cut-Off Switch
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
The product should be turned on about 10 seconds after the AC power switch at
the back of the product is turned on.
During booting the system, do not press any key of the alphanumeric keyboard.
It may cause malfunction.
If you turn on the power after turning off forcibly, the system can turn on and off
momentary. It is one of the character of Intel® PC main board, not system error.
3) To start ACCUVIX XG, press the On/Off switch at the right side of the control
panel(keyboard).
Power Switch
③
②
④
⑤
[Figure 4-3] Monitor Display
① Title Area.
Displays patient name, hospital name, application, frame rate and depth, probe
information,acoustic output information, and date and time.
② Measurement Menu Area
Displays the selected thumbnail image. During measurement, displays the
measurement menus.
The control panel consists of a keyboard, soft menus, buttons, dials, dial-buttons, a slide,
and a trackball.
The dial-button can be used both as a dial and a button.
End Exam Finishes the exam of the currently selected patient and
Button
resets the related data.
Protocol Displays the Protocol screen with which the StressEcho can
Button
be used.
TM
Review Button Runs SONOVIEW which is the image filing program.
Press this button to turn the Quick Scan function on. The
Q Scan Button ‘Q’ mark is displayed on the top of the image. It can be
used only in specific applications of specific probes.
Saves an image or a report displayed on the screen in the
Acquire Button system database.
Record Button Records image using the VCR connected to the system.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
Too large a difference in the gain value settings of adjacent TGC slides may lead
to the generation of stripes in an image.
˙ T˙ ˙ip˙ ˙! W
※ ˙ h˙ e˙ n˙ t˙h˙ e˙ r˙ e˙ a˙ r˙ e˙ t˙w
˙ o˙ S˙ o˙ ˙ft˙m
˙ e˙ n˙ u˙ s˙
When there are two menus available upper and lower, both menus can be adjusted
with the corresponding dial-button. Press a desired menu button on the touch screen
and then use the dial-button.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
Do not apply excessive force to the control panel.
Use the handle at the back of the body when moving the product.
6) 3D Mode
① Check if the loading is normal when Free Hand 3D Scan runs and it is skipped
by Freeze, check if the image is fragmented and if there is any noise during the
operation.
② Check if the loading is normal when Static 3D Scan runs, check if the image is
fragmented and if there is any noise during the operation.
Check if the probe and motor sounds are normal.
③ Check if the loading is normal when Live 3D Scan runs, check if the image is
fragmented and if there is any noise during the operation.
Check if the probe and motor sounds are normal.
④ Check if the ROI 3D, ABC 3D, and Full images are normal.
⑨ Select Step Angle, Rotation Angle, and Rot. Axis and check if Cine Loading is
done according to the settings made during Cine operation. Check if images
are properly displayed during the Cine operation.
5.1 Overview
Chapter 5 describes the internal structure and operation mechanism of ACCUVIX XG.
This chapter must be read for the product maintenance and upgrade.
ACCUVIX XG is Software DSC-applied ultrasound system.
It not only adopted 19 inch LCD monitor and provides high resolution ultrasound Image,
but also provides the premium grade system functions. To improve the processing
speed, MEDISON Co., Ltd. developed new interface to connect a latest PC and the
ultrasound system with its proprietary technology. The enhancement of processor
speed makes the system operations faster and reduces diagnosis time.
ACCUVIX XG can use up to 192 Element probes and adopted Digital Beamforming of
TX 128 Channels. Ultrasound image is displayed on the LCD through the Front End
Part and Back End Part (including PC Part).
The resolution of the LCD monitor is 1280 X 1024 pixels and various image formats are
provided. The wide view angle of the LCD panel provides convenient work environment
for diagnosis. In addition, the arm-type monitor controller enables users to control the
monitor easily.
The DVD RW drive and USB port are placed on the front panel of the system for easier
image backup and software service. Since this system supports various external
storage devices such as USB MO, USB Flash Memory and external-type USB HDD,
upgrade becomes more easier.
˙O
N ˙ T˙ E˙
“5.6.4.1 ~ 5.6.4.4” described Non-CW(Continuous Wave Board). Continuous
Wave Doppler function is a function added to CW(Continuous Wave Board).
5.6.4.8 CW TX Control
Controls the voltage of the CW(Continuous Wave)’s TX Pulser.
5.9.3 Specification
LCD Monitor Data Transmission
DVI 1 Port Input 2 Port Output
Analog RGB 1 Port Output
USB 2.0 1 Port to LCD IF
Power Control Interface
BW Printer Remote
Foot Switch
Video in/out, Audio in/out
Audio MIC
5.10.2 Picture
5.11.3 Specification
Video Decoding(S-VHS, VHS, Composite) Support
Audio Decoding Support
PCI Express slot Support
5.11.4 Operation Mechanism
If video data and audio data is input from the DVI Board, it processes the data to send
the data to the PC Mother.
DVI Board function interconnects the external data and the VCRIN Board and provides
interface function.
So, Decoding control functions also are executed in VCRIN board.
5.12.2 Picture
5.16.3 Specification
3D Probe Motor Drive
Voltage & Current Control Controller
Null Position Signal Sensing
DC Voltage supply (+12V, -12V, +3.3V, +5V)
3D Probe implements 3D Mode by driving the Stepping Motor. The Motor Board does
o
Feedback Control by using the SIN and COS waveform that has 90 phase difference from
the 3D Probe. 3D Probe provides Null Position signal to the Motor Board and the Motor
Board provides One Frame signal that is used as basis for 3D image acquisition to the BE
Board.
AC Power
Connector
AC Voltage Out
2) Output Voltage
AC/DC Output Voltage Use Range
110 ~ 120 V
External Device
AC 200 ~ 240 V
200 ~ 240 V PC Power
DC 24 V Ultrasound System Part
6.1 Overview
Chapter 6 describes basic ACCUVIX XG maintenance procedures.
How to upgrade and how to use Admin Mode (Service Mode) are described.
Contents
˙O
N ˙ T˙ E˙
The software version number in the above figure may differ from the actual software
version of the system.
st
6.4.1.1 1 CD
This is the Windows XP Embedded installation method. This method uses a 1st CD
st
1)Prepare a 1 CD provided by the service team of MEDISON Co., Ltd.
2)Turn on ACCUVIX XG.
st
3)Insert a 1 CD into the CD/DVD-ROM drive. Boot up system.
4)After 2 minutes passed, installation program will be shown up
5)Select 1 or 2 of program, 1 is set as default.
① Partitioning And Formatting ALL
② Delete every Partition. Create new Partition
③ Format every Drive. (Every data on the HDD will be deleted)
④ No Partitioning, Formatting Only OS Partition
⑤ Format OS Drive(C:\) only. (D,E,F Drive Data will be remained)
6)Exceptions
① If “ Network ID “ input message shows, just click “OK” or “Cancel”. It will
continue.
② If Track Ball or Keyboard does not work intermittently, restart the system.
7)After “Window XPE” installation completed, system restart, then screen shows.
8)When the software upgrade is complete, restart ACCUVIX XG.
9)Check if the software version in the start screen is changed to the new version.
rd
6.4.1.3 3 CD
rd
This is the Application up-grade method. This method uses a 3 CD
rd
1) Prepare a 3 CD provided by the service team of MEDISON Co., Ltd.
2) Turn on ACCUVIX XG.
3) When system booting is complete, enter Windows Mode and display the Windows
XP Desktop screen.
4) Exit the ultrasound program. To exit the program press the "Alt + F4" key
combination using the keyboard.
rd
5) Insert a 3 CD into the CD/DVD-ROM drive
6) Will show up automatically
7) Select the right product name, then click "Ok" button
8) System will shut down automatically after finishing installation.
9) Check if the software version in the start screen is changed to the new version.
˙O
N ˙ T˙ E˙
For information on software version up detail, refer to the “Technical information”
6.5.2.3 Restore
Using this function, you can restore settings with the backed-up user setting values. You
can use this function in Admin Mode only.
1)If you press [Restore], the ultrasound program is terminated and the Restore function
runs. If a message appears asking whether to exit the ultrasound program before
running the Restore function, click [OK].
2)In the [Restore] screen, you can select the User Setting Item and Backup Media.
3)If you press [Next], the Restore function is executed.
4)When the restoration is complete, the system will restart.
6.5.2.5 VGA
1) Video Out Format
You can select the scan type for Video Out through filter. Supported scan types are
NTSC and PAL.
6.5.2.6 Printer
Printer settings to adjust. Printer icon and you can adjust the settings using the printer
7.1 Overview
Chapter 7 describes basic troubleshooting procedures.
˙O
N ˙ T˙ E˙
Procedures for troubleshooting expected problems are described. Unexpected
situations may occur.
Procedures for troubleshooting normal problems are described.
Contents
8.1 Overview
Chapter 8 describes how to disassemble ACCUVIX XG.
Refer to this chapter when you upgrade or repair the hardware.
˙ A˙ R
W ˙N˙ ˙IN
˙G˙
The system contains dangerous high voltage. Never disassemble the system. There is a
risk of electric shock and injury.
The repair of the system and the replacement of parts must be carried out by an authorized
engineer or the customer service department of MEDISON Co., Ltd.
The company is not responsible for any injury and damage caused by not following this
warning.
When working with the system on, do not wear a static electricity protective wristband.
There is a risk of electric shock and injury.
˙O
N ˙ T˙ E˙
When disassembling or reassembling the system, wear static electricity protective gloves
and a wristband.
These will prevent any accidents due to carelessness, and damage to the system due to
static electricity.
8.2.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
1) 2)
4 Screws
3) 4) 5)
2 Screws
1)
Cable
2) 3)
6 Screws
1) 2)
1) 2)
8 Screws
1) 2) 4 Screws
4 Screws
3)
1) 2)
3) 4) 5)
3) 4) 5) 6)
7), 8)
3 Screws
3 Screws
5 Screws
[Figure 8-8] Body Side Right & Left Covr
1) 2)
3) 4) 5) 6)
7) 8), 9)
4 Screws
8.3.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
1)
2) 3)
18 Screws
3) CW Board
4) BF Board
5) BE Board
6) MTR Board
8.4.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
8.4.2 LCD
1) Remove the 2 screws from the Rear Back LCD Cover using the (+) screwdriver and
separate it.
2) Remove the 2 screws from the LCD Panel using the (+) screwdriver and separate it.
3) Hold the LCD Panel with both hands and disassemble it.
4) Separate the cable from the AD Board.
1) 2)
4 Screws
2 Screws
3) 4) Cable
1) 2) 4)
3)
①
5)
①
②
6) 7)
6)
2 Screws
2 Screws
LCD ARM
8.5.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
8.5.2 PC ASSY
1) Disassemble the Body Rear Cover referring to “8.2.3 Body Rear Cover”.
2) Separate all cables connected to the PC ASSY.
3) Remove the 3 screws of the PC ASSY using the (+) screwdriver.
4) Hold the handle of the PC ASSY and pull it to separate it.
1) 2)
3) 2 Screws 4)
Screw
1) 2) 3)
14 Screws
4)~9)
Screws
[Figure 8-15] PCI Board, DVI Board, VCR In board, VGA Card
1) 2) 3)
4) 5)
Cables 4 Screws
6)
1) 2) 3)
4)
5)
4 Screws
1) 2)
3)
Cables
4 Screws
8.6.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
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Since the ADM is heavy, take care when disassembling it. If the ADM falls suddenly,
it may cause an injury.
Cables
1) 2), 3)
2 Screws
4)
1) 2)
3)
4), 5)
4 Screws
Cables
8.7.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
1)
2) 3)
Cables
Screws
Cables
2)
3)
Screws
4)
2) 3)
4)
2) 3)
2 Screws
Track Ball
2) 8 Screws
3)
Cable
1) 2) 3)
4)
4 Screws
1)
2), 3)
Cable
Screws
4)
1) 2) 3) 4)
5) 6) 7)
8)
Cable
2 Screws
2 Screws
[Figure 8-28] Speaker Right & Left
1) 2)
Screw
3) 4)
ECG Module
Cable
8.2.1 Preparations
1) Prepare a (+) screwdriver and static electricity protective gloves.
2) Shut down the system referring to “3.7 System Shutdown (Power Shut Down)”.
1) 2)
3)
Cable
4)
Screw
9.1 Overview
The probe is a device that sends and receives ultrasound for acquiring image data. It is
also called a Transducer or Scanhead.
The system limits patient contact temperature to 43℃degrees Celsius, and acoustic
output values to their respective U.S. FDA limits. A power protection fuse circuit protects
against over-current conditions. If the power monitor protection circuit senses an over-
current condition, then the drive current to the probe is shut off immediately, preventing
overheating of the probe surfaces and limiting acoustic output. Validation of the power
protection fuse circuit is performed under normal system operation. For invasive probes,
additional protections are designed to keep patient contact surface temperature under
43℃ degrees Celsius in the event of a single fault failure.
Contents
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Do not use mineral oil, oil-based solutions, or other non-approved material as they
may cause damage to the probe.
Do not use gels that contain any of the following agents:
- Acetone
- Methanol
- Denatured Ethyl Alcohol
- Mineral Oil
- Iodine
- Lanolin
- Any lotions or gels containing perfume
9.5 Sheaths
Sheaths are recommended for clinical applications of an invasive nature, including
intraoperative, transrectal, transvaginal, and biopsy procedures.
MEDISON does not supply sheaths so that you should purchase appropriate ones on
your own.
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Always keep sheaths in a sterile state.
Sheaths are disposable. Do not reuse them.
If sheaths are torn or soiled after use, clean and disinfect the probe.
In neurosurgical applications, a disinfected probe must be used with sterile gel and a
sterile pyrogen-free sheath.
If the sterile sheath becomes compromised during neurosurgical applica-tions
involving a patient with Creutzfeldt-Jakob disease, the probe cannot be successfully
sterilized by any disinfection method.
Some sheaths contain natural rubber latex and talc, which can cause allergic
reactions in some individuals. Please refer to the FDA Medical Alert released on
March 29, 1991.
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Do not apply mechanical shock to the probe.
Do not place the probe cable on the floor where the cable can be run over by
equipment wheels, etc. Do not apply excessive force to bend or pull the cable.
Do not immerse the probe into any inappropriate substances such as alcohol, bleach,
ammonium chloride, and hydrogen peroxide.
Do not expose the probe to temperatures of 50°C or higher.
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No neurosurgical treatments or examinations should be carried out on a patient with
Creutzfeldt-Jakob disease (critical brain disease caused by virus). If the probe has
been used on such a patient, it cannot be sterilized by any method whatsoever.
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Sufficient washing and disinfecting must be carried out for preventing infection. This
is the responsibility of the user who manages and maintains the disinfection
procedures for the equipment. Always use legally approved detergents and sheaths.
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Regularly receive short-circuit examination from the MEDISON Customer Service
Department.
Do not immerse the probe into liquid.
Do not drop the probe or apply mechanical shocks.
Inspect the housing, strain relief, lens and seal for damage, and check for any
functional problem before and after each use.
Do not apply excessive force to twist, pull or bend the probe cable. It may result in a
short circuit.
The power protection fuse protects the probe and the product from excess current. If
the power monitoring protection circuit detects excess current, it immediately shuts
off the current to the probe in order to prevent the probe surface from overheating
and to restrict the ultrasound power output.
The temperature of the product for making contact with patients is limited under 43°C.
The ultrasound power output (AP&I) is in compliance with US FDA standards.
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Always use protective eyewear and gloves when cleaning and disinfecting probes.
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Do not use a surgical brush when cleaning probes. The use of even soft brushes
can damage the probe.
During cleaning and disinfection, keep the parts of the probe that must remain dry
higher than the other parts during wetting until all parts are dry. This will help prevent
liquid from entering non-liquid-tight areas of the probe.
1) Disconnect the probe from the system.
2) Remove any biopsy adapters or biopsy needle guides. (Biopsy adapters are
reusable and can be disinfected).
3) Discard sheaths. (Sheaths are single-use items).
4) Use a soft cloth lightly dampened with mild soap or compatible cleaning solution
to remove any particulate matter and body fluid that remain on the probe or cable.
5) To remove remaining particulates, rinse with water up to the immersion point.
6) Wipe with a dry cloth.
7) If necessary, wipe first with a water-dampened clothe to remove soap residue.
9.7.3 Disinfection
A 10-6 reduction in pathogens should be reached following the disinfection procedures
in this Manual and using the following MEDISON recommended solutions.
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If a pre-mixed solution is used, be sure to observe the solution expiration date.
The type of tissue it will contact during use dictates the level of disinfection required
for a device. Ensure that the solution strength and duration of contact are appropriate
for disinfection.
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Using a non-recommended disinfectant or not following the recommended
disinfection method can damage and/or discolor the probe and will void the probe
warranty.
Do not immerse probes for longer than one hour, unless they are sterilizable.
Only sterilize probes using liquid solutions. Avoid using autoclave, gas (EtO), or other
non-MEDISON-approved methods.
10.1 Overview
Chapter 10 describes how to extend the life of ACCUVIX XG.
It includes are how to maintain the product and how to backup information.
Make sure to read this chapter for proper maintenance of the product.
Contents
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Placing the system near generators, X-Ray machines, or broadcast cables may
result in screen noise and abnormal visual images. Using the power source with
other electric devices may also induce noise.
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Turn off the system and disconnect the system power cord from the wall outlet.
Otherwise, it may result in electric shock or fire.
Always use protective eyewear and gloves when cleaning and disinfecting the
equipment.
10.2.2.1 Cleaning
1) Console : Use a soft cloth lightly dampened in a mild soap or detergent solution to
clean exterior surfaces on the system
2) Cleaning Monitor : Wipe the LCD surface with a soft dry cloth. When the LCD panel
has dirt on it, wipe it 2 - 3 times or more in one direction system.
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For information on cleaning and disinfection of the probe & biopsy kit, please refer to
Chapter 8 "Probes." In User Manual
10.2.2.2 Disinfections
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Use only recommended disinfectants on system surfaces.
Active
Solutions Country Type FDA 510(k)
ingredient
1) Turn off the system and disconnect the system power cord from the wall outlet.
2) Mix the disinfection solution compatible with your system according to label
instructions for solution strength.
3) Wipe the system surfaces with the disinfectant solution, following the disinfectant
label instructions for wipe durations, solution strength, and disinfectant contact
duration.
4) Air dry or towel dry with a sterile cloth according to the instructions on the disinfectant
label.
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To avoid risk of electric shock, always disconnect the plug from the system prior to
fuse replacement.
1. Turn off the system and disconnect the system power cord from the wall outlet. (See ①)
2. Press the fuse holder in the direction of the arrow and pull it out. (See ② )
3. Remove the old fuse and replace it with a new one.
4. After installing the new fuse, connect the plug to the system.
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Be sure to lock the brakes on the front wheels before cleaning the air filters to avoid
injury by any unexpected movement of the product.
Air Filter
1) Pull the filter under the front of the console to away from the product.
2) Shake the filter to remove the dust and wash in a mild soapy solution.
3) Rinse and air dry or dry with a cloth.
4) Slide the filter back into the product.
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Allow the wet filter to dry thoroughly before installing. The wet filter can cause the
malfunction.
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The user must ensure that safety inspections are performed every 2 years according
to the requirements of safety standard EN 60601-1. Only trained persons are allowed
to perform these safety inspections.
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You may lose information files on user settings or patients, because of shock on the
product or internal error. Thus, back-up on a regular basis.
10.3.3 Software
The product software may be updated to enhance performance. The user cannot make
any changes to the software by himself/herself.. Please contact the MEDISON
customer service for help in software changes.
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Minor software updates may be carried out without the prior notice from the
manufacturer.
TM
Should errors occur in the operating system (Windows XP ), and should you desire to
upgrade the operating system, please follow the instructions of the operating system
manufacturer.
11.1 Overview
This chapter 11 contains information on the ACCUVIX XG Service Part.
Please refer to the ACCUVIX XG Part Catalogue to Check the replacement parts and their
software versions for each system configuration.
For installing and verifying system parts, please refer to figures and part table in this chapter.
Part numbers are indicated in the corresponding table.
Prior to ordering parts, please verify whether the existing parts can be replaced according to the
current service policy
Contents
11.1 Overview .................................................................................................... 11-1
11.2 Body Cover ................................................................................................ 11-2
11.3 Ultrasound System Part ......................................................................... 11-4
11.4 LCD & ARM ............................................................................................... 11-5
11.5 PC Part ....................................................................................................... 11-6
11.6 Power Part ................................................................................................. 11-8
11.7 User Interface Part .................................................................................... 11-9
11.8 ETC Part ..................................................................................................11-10
11.9 Options ..................................................................................................... 11-11
11
10
12 7
13
6
14
5
15
4
16
4 Body Skirt Right Cover A215-300A Body Skirt Right Cover EKO7
5 Body Side Right Cover A215-302A Body Side Right Cover EKO7
6 Body Arch Front Cover A215-299A Body Arch Front Cover EKO7
7 Body Arch Top Cover 215-M-569A Body Arch Top Cover EKO7
11 Base Lower Back Unit Arm Cover 215-M-513A Base Lower Back Unit Arm Cover
12 Base Lower Front Unit Arm Cover 215-M-514A Base Lower Front Unit Arm Cover
15 Body Side Left Cover A215-303A Body Side Left Cover EKO7
16 Body Skirt Left Cover A215-301A Body Skirt Left Cover EKO7
1 2
3 4 5 6
1 3
1 LCD19 Inch Monitor ASSY AY-353-LCD-19 LCD19 Inch Monitor ASSY EKO7
2 Rear Back LCD Cover 215-M-560A Rear Back LCD Cover EKO7
4 Base Lower Back Unit Arm Cover 215-M-513A Base Lower Back Unit Arm Cover
5 Base Lower Front Unit Arm Cover 215-M-514A Base Lower Front Unit Arm Cover
3 4
5 6 7
8
1 9
9 PC Power & Cable ASSY AY-POWER-PC-346 PC Power & Cable ASSY ACCUVIX V20
1 2
3
1
5 6
4
7
8
2
1
4
3
[Figure11-8] ETC Part
3 Caster Lock ASSY (Single) A374-021A Caster Lock ASSY (Single) EKO7
4 Caster Lock ASSY (Dual) A374-022A Caster Lock ASSY (Dual) EKO7
1 4D OPT-357-4D 4D
2 3DMXI OPT-357-3DMXI 3D XI
7 CW OPT-357-CW CW FUCTION