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AccuRay D5 6 Operating Manual E-3 20190515 º ¡
AccuRay D5 6 Operating Manual E-3 20190515 º ¡
HX-DxH Series
Operation Manual
HX-DxH Series
Operation Manual
Read this service & installation manual thoroughly before you use the product.
Keep this instruction manual for future reference.
Manual Notation
The number of this manual is entitled on the basis of the following standard:
X M X - Y Y Y Y - Z
(1) (2) (3) (4) (5)
(1) S : Service
O : Operation
(2) M : Manual
(3) K : Korean
E : English
(5) Z : Version
X-ray equipment, if not properly used, may cause injury. Accordingly, the
instructions herein should be thoroughly read and understood before
attempting to place this equipment in operation. We are glad to assist and
cooperate in placing this equipment in use.
In case of any changes in its user or location, ensure that this service & installation
manual is always kept together with the equipment. Periodically check to be sure
that the manual and the warning labels are not missing or damaged. If they are,
contact your DK Medical Systems service representative for replacement.
Notice
• All copyrights regarding this manual are property of DK Medical Systems.
Neither all nor part of these contents shall be reproduced or duplicated without the
express permission of DK Medical Systems.
• Content of this manual may be changed for improvement without prior notice.
Although every possible effort has been made to avoid errors while creating this
manual, immediate revision may not be possible in the event that errors or missing
information are detected.
• Screen images and illustrations contained in this manual may differ from those in
actual use, and are intended for example purposes only. Illustrations may also use
partial images.
DANGER
Indicates an imminently hazardous situation which, if not avoided, will result in serious
injury or death.
WARNING
Indicates a potentially hazardous situation which, if not avoided, could result in serious
injury or possibly death.
CAUTION
Indicates a potentially hazardous situation which, if not avoided, may result in minor to
moderate injury or equipment damage.
NOTE
Emphasizes additional information that is provided to ensure the proper use of this
product.
Preface 8
Operating Precautions
(for Both the Safety and the Prevention of Danger)
on Using Electric Medical Equipment
1. Only personnel with the following experience and knowledge can use the equipment.
1) Medical radiographic training (if particular qualifications are required in the country
concerned, those qualifications must be held).
2) A capacity to read and understand the instruction manual.
2. When installing the equipment, pay attention to the following items:
1) Do not install it near water faucet or similar equipment.
2) Install it away from potential sources of problems such as abnormal pressure, temperature,
humidity, drafts, direct sunlight, dust, chlorine or sulphur gas.
3) During transportation and operation of the equipment, avoid tilting, vibration and sharp
impact against it.
4) Keep the equipment away from area where chemical or gas is stored.
5) Use only correct electrical power source with matching frequency, voltage and current
(or wattage).
6) Check the conditions of the battery power source (power and polarity) before operating the
equipment.
7) Properly ground the equipment.
8) When using this equipment, an operator shall be in an X-ray protection room.
3. Before operating the equipment, pay attention to the following items:
1) Check the conditions of switch contacts, polarity, dial settings, and meters, and make sure
the equipment performs smoothly.
2) Confirm that the ground is connected properly.
3) Check all wirings for proper and correct connections.
4) Pay attention when using more than one unit at a time, because it may lead to an incorrect
diagnosis and cause a hazard.
5) Check the condition of external electric circuit, which will be directly connected to a patient.
6) Check the condition of battery power source.
4. While operating the equipment, pay attention to the following items:
1) Do not exceed the time or the amount of equipment use needed for a diagnosis or a therapy.
2) Observe the equipment and a patient continuously, for early detection of a problem.
3) When a problem is detected with the equipment or a patient, take proper actions to stop
the equipment without harming the patient.
4) Do not let a patient touch the equipment.
5) When using the equipment, a user must wear protective gear against X-ray.
WARNING
· The responsibility of proper use and maintenance of the machine lies with a user.
· Only a diagnostic radiography technician and/or any personnel with a certificate
indicating equal proficiency can use the machine.
· Since an inspection and a repair of the inside of the machine are dangerous, if an error
occurs, make sure to put up a sign of defect of the machine. Then, contact your DK
Medical Systems service technician or a personnel with a certificate indicating equal
proficiency to repair the apparatus.
· In general, modifications of the machine are strictly prohibited by the Regulatory
Requirements of the Law of the country where the device is installed. Nevertheless, if
any modification should be made, consult it first with the manufacturer and/or seller.
Preface 10
Perform Periodic Inspection
Preventive maintenance is required to maintain safety and performance of this system for a
long time. As to the maintenance and inspection that specially trained experts exclusively
can perform, utilize the maintenance agreement offered by our company.
Wa r r a n t y
The warranty of this system is valid for one (1) year as from the date of purchase.
Please note that our company is not responsible for the following failures and damages:
Service after the expiration of warranty is available at reasonable cost and should be performed
by your DK Medical Systems service representative.
In some jurisdictions, some of the foregoing warranty disclaimers or damage limitations may not
be applied. DK Medical Systems will be indemnified for any claim, liability, or damage arising out
of the misuse or non-compliance with this manual by the purchaser or lessee of the system.
WARNING
WARNING
WARNING
Preface 12
WARNING
Repair and maintenance of the inside of the equipment can only be performed by
an engineer assigned by DK Medical Systems.
Maintenance must be assigned to specially trained expert. Contact your DK Medical
Systems service representative for repair and maintenance.
WARNING
To ensure the safety of equipment when using it, thoroughly read the manual
provided with the equipment. Also, fully understand all of precautions written in
this manual regarding the equipment use.
WARNING
If connecting this equipment to another one, make sure that another equipment is
certified by DK Medical Systems, does not cause degrading any system
performance and/or guarantees its safety.
CAUTION
Make sure that operator and patient can communicate while taking X-ray
irradiation.
If the equipment use can put a patient in danger, stop the examination or treatment
immediately.
DANGER
WARNING
Preface 14
WARNING
Do not put this equipment in a place where any liquid may exist, nor put such
liquid into the equipment. Avoid letting any liquid be spilled on the surface of the
equipment, nor enter into the equipment.
Otherwise, an electric shock may occur.
In case of liquid being entered inside of the equipment, turn off the power immediately,
and contact DK Medical Systems Service Representative.
WARNING
In case when any abnormality is found during the system operation, stop operating it
immediately and contact our service agents. Repair and inspection of the system need to
be conducted by them.
WARNING
WARNING
When moving the equipment, always be very careful to avoid contact with a
patient or an operator and ensure that they do not become caught between the
equipment and any neighboring devices.
Otherwise, it may cause injury.
Do NOT use the equipment in a place where metal fragments may enter.
Otherwise, it may result in an electric shock.
WARNING
Prior to conducting a study, check that the equipment is functioning correctly and all
system components and attachments are securely fastened.
WARNING
WARNING
Preface 16
NOTE
Cautions on Storage
CAUTION
WARNING
Be sure to turn the equipment power OFF before cleaning and disinfecting the
equipment.
Otherwise, malfunction may occur in the equipment, or the equipment may operate in
an unintended way. Thoroughly ventilate the room before turning ON the power after
disinfection work is completed.
CAUTION
CAUTION
Do NOT directly apply rubbing alcohol or water nor spray it onto the equipment.
Wipe off the surface of the equipment with a cloth soaked with rubbing alcohol.
If rubbing alcohol gets inside the equipment, it can cause failure or accidents.
CAUTION
Observe the following precautions when cleaning and disinfecting a touch panel:
• Turn the equipment power OFF before cleaning and disinfecting.
• Clean and disinfect the touch panel periodically.
• Wipe the surface of the equipment with a cloth soaked with disinfectant or cleaner.
If liquid gets inside the equipment, it can cause failure or accident.
• Do NOT rub or hit the panel surface because it can be scarred easily.
• Wipe the panel gently with moistened soft cloth to remove the dust from the surface.
Preface 18
CAUTION
CAUTION
CAUTION
On completing the work, check the following points before switching the power ON
again.
WARNING
When turning the power ON after cleaning, make sure the examination room is
properly ventilated.
Turning the power ON when any flammable gas remains in the examination room could
lead to fire, smoke, explosion or electrocution.
CAUTION
Preface 20
Cautions on Electromagnetic Compatibility (EMC)
WARNING
WARNING
WARNING
Do NOT use this equipment adjacent to, or stacked with other equipment.
If adjacent or stacked use is necessary, be sure that this equipment works properly in
such environment.
WARNING
Do NOT bring any cellular telephone or related device into the examination room
with their power ON.
Such devices can exceed the EMC standard limitations, and under some conditions it
can impair the proper functioning of the equipment. In the worst case, it can cause
serious injury or clinical error.
Cautions on Radiation
WARNING
Do not allow any personnel to use the equipment unless he/she is a qualified one (such
as a doctor, X-ray technician or X-ray engineer). The equipment can only be used under
a supervision of such qualified personnel.
WARNING
Preface 22
WARNING
During X-ray irradiation, ensure that the X-ray irradiates the necessary region only.
To avoid unnecessary exposure to X-ray radiation, narrow down the area to be shoot by
a collimator, and take protective measures like wearing a lead apron.
WARNING
Always check the X-ray exposure region by using the collimator lamp.
If irradiating outside of the required region of a patient, there may be a risk of exposing
the patient to unnecessary radiation.
WARNING
A user of the equipment is liable for a patient and/or user’s injury or wound caused from
an X-ray exposure. Since the manufacturer provides all necessary information
regarding the equipment and its possible risk if not being properly used, the
manufacturer is not liable for managing the equipment after its installation nor for safety
practices that a user does.
Also, it is emphasized that the manufacturer has no responsibility of maintenance
and/or services of any equipment if it is not maintained properly along with the
instruction, or is modified and/or changed.
In this manual, there are proper information including warning, caution and product
labels attached to the surface of the equipment. And the manufacturer does not have
any liability for a user’s equipment use or violence against the safety rules/
recommendations.
Also, the manufacturer is not liable for any patient or individuals over-exposed to X-ray
resulted from a user’s misuse of the equipment.
This X-ray unit may be dangerous to both patient and operator unless safe exposure
factor, operating instruction and maintenance schedule are observed.
CAUTION
Do not exceed the maximum tube operation limits shown in the X-Ray tube data of its
manufacturer. Intended life and reliability may not be obtained unless a generator is
operated within published specifications.
WARNING
To avoid the risk of electric shock, this equipment must be connected to supply mains
with protective ground.
CAUTION
In order to minimize the absorbed dose, make the distance to the focal spot as far as
possible (Minimum 45 cm).
Preface 24
CAUTION
CAUTION
CAUTION
Keep pressing the radiography preparation button (or the first stage of hand switch) and
the radiography button (or the second stage of hand switch) until exposure time is
completed. Releasing them before completing X-ray irradiation will stop the procedure in
the middle, and thus a suitable radiography image will not be acquired.
WARNING
Do not allow operation of this apparatus by any person other than qualified personnel
(physician, radiotherapy engineer and clinical X-ray engineer), or allow a person to use
this equipment under the supervision of qualified personnel.
WARNING
The equipment can be operated only by qualified personnel, such as radiography
technician or a person with equivalent qualification.
WARNING
No person but only a patient is allowed to stay in the examination room during X-
ray irradiation.
If the equipment is not used correctly, operator, patient, and others may receive a greater
dose of radiation than necessary. If someone has to be in the examination room with a
patient for some reason, then that person must take adequate measures to protect
him/herself against the radiation (e.g., wearing a protective apron, screen, etc.).
* During radiography, the radiography indicator illuminates and the buzzer rings for
audible warning.
WARNING
Perform X-ray irradiation carefully according to doctor's direction when using the
equipment with expectant mother, woman who is suspected as pregnant, lactating
woman, or children.
Particular ways of using the equipment may increase the scatter dose absorbed into the
patient, which may cause a radiation hazard.
Preface 26
WARNING
Always check the X-ray exposure region by using the collimator lamp.
If irradiating outside of the required region of a patient, there may be a risk of exposing
the patient to unnecessary radiation.
WARNING
During X-ray irradiation, ensure that the X-ray irradiates the necessary region only.
To avoid unnecessary exposure to X-ray radiation, narrow down the shooting area of
collimator and take protective measures, such as wearing a lead apron.
WARNING
CAUTION
Be sure to carry out aging (running-in operation of the X-ray tube unit) before
taking an X-ray radiography.
Refer to the ‘aging’ procedure described in the X-ray high voltage generator manual.
CAUTION
CAUTION
In order to minimize the radiation dose on a patient, make the distance between
the focus and the patient's body surface as far as possible (Minimum 45 cm).
The shorter the distance becomes, the greater the amount of scatter dose will be
absorbed into the patient, which may cause a radiation hazard.
CAUTION
Pay extra attention, when irradiating X-ray for a long time or repeatedly.
It may cause a radiation hazard.
Preface 28
Cautions on Operation
CAUTION
NOTE
CAUTION
The activity called as ‘aging’ is efficient to check that X-ray tube does not have any
problem as well as to prevent the equipment from its electric discharge. If the equipment
runs abnormally, turn off the equipment and the main board. Then contact the client
service team of DK Medical Systems.
1. Select a large focus and conduct radiography in the following order. Take the interval
time around 60 secs between your shootings.
2. If any error occurs during the aging, wait for a while and reduce the X-ray tube
voltage to 30 kV before conducting X-ray shooting.
3. Check if the X-ray tube can change during X-ray shooing if the tube has two or more
focuses.
4. Perform aging for each unit if there are two or more X-ray tube units.
5. After radiating three times, an operator needs to spend five minutes to cool down the
X-ray tube.
Preface 30
Service Life
The equipment lifetime is 10 years (based on DK Medical Systems’ criteria) assuming the
specified maintenance checks are performed.
Disposal Precaution
CAUTION
Language(s) Provided
DK Medical Systems provides technical documents in English. Providing language(s) of
each country will be added at DOC and label and packaging chapter.
Software Revision
This manual applies to the software revision 1.0 ∗
Attenuation equivalent should not be greater than 1.6Vmm Al but thinner than 15mm
thickness. All parts of the cassette such as hinges, locks and marking device shall be
within the minimum radii for corners and edges. The flatness shall be 1mm warp or less.
WEEE Mark
Contact your DK Medical Systems service representative when the equipment has
reached the end of its life. They will advise you regarding the equipment take-back.
With your co-operation, we are aiming to reduce contamination from waste electronic and
electrical equipment and preserve natural resource through re-use and recycling. Do not
hesitate to ask your DK Medical Systems service representative, if you require further
information.
Preface 32
Abbreviations
Abbr. Full Description Abbr. Full Description
Acryl Acryl MOT Motor
ATR Actuator Off-CNT Off-Centered
Base Base PTM Potentiometer
BR Bearing PRS Pressure
BK Bracket Rail Rail
CRG Carriage SFT Shaft
CNT Center SOL Solenoid
CHN Chain SPG Spring
Clutch Clutch SPT Sproket
CSH Cushion STD Stand
DTR Detector STP Stopper
EMG Emergency SW Switch
EXT Extend TB Timing Belt
FXD Fixed TP Top Plate
Lock Lock WIT Weight
Mcr SW Micro Switch Wire Wire
Options
The "Options" described in this manual may be provided as standard, or may be
unavailable, depending on its sales format.
Preface 34
Warning and Caution Labels
The following safety labels, which describe handling precautions, are attached to the
equipment. With adequate understanding of the contents on these labels and the warning
/caution items in this manual, operate the equipment safely. Inspect the safety labels
periodically (once a year).
If any label is peeled or unreadable by stain or scratch, replace it with a new one. For
new labels, contact your DK service representative.
Following Labels are attached as seen on the Figure below.
z 2
Preface 36
This page is intentionally blank.
Precautions in Use 12
Be sure to Read the Following to Prevent Explosion, Electric 14
Shock, or Injury
Cautions on Storage 17
Cautions on Cleaning and Disinfection 18
Cautions on Electromagnetic Compatibility (EMC) 21
Cautions Relating to Cellular Telephones 22
Cautions on Radiation
Cautions on Radiography 26
Cautions on Operation 29
Cautions on X-ray Tube Aging 30
Service Life 31
Disposal Precaution
Language(s) Provided
Software Revision
Abbreviations 33
Options
Contents 38
01 Overview
1.1 Applications 45
1.2 Contraindications 46
02 Prior to Operation
2.1 Composition 57
2.2 Dimensions 60
03 Operation
3.1 Operation Procedure 69
05 Troubleshooting
5.1 Error/Check Code 87
5.2 Troubleshooting 89
07 Technical Data
7.1 Product Specification – HX-D5H 101
09 Appendix
9.1 Manufacturer Information 125
9.1.1 Regulatory Information
9.1.2 Company’s Quality System
9.1.3 International Standards
9.2 List of Components 126
9.2.1 Fuse List
9.2.2 Accessories
9.2.3 List of Cables 127
9.3 Attenuation Equivalent 128
9.3.1 Attenuation Equivalent Table
9.4 Connection Diagram 129
Contents 42
This page is intentionally blank.
1.1 Applications
1.2 Contraindications
1.1 Application
1. Intended Use
The generator provides manual mode (kV, mA, ms), semi-automatic mode (kV, mAs),
automatic mode (AEC). It can store various APR (Anatomical Programming Radiograph)
by using highly integrated memory, and it can acquire an image with proper kV, mA, ms
values by an automatic control method without worrying about the subject by giving AEC
function. AEC irradiation method is an automatic control, which is convenient for a user,
and has more accurate value and time settings, so to obtain excellent image quality.
In order to use the product safely and reliably for a long period of time, you should
thoroughly familiarize yourself with the functions and operation of the product and read
the maintenance instructions of this manual before using this equipment. Special
attention should be paid to all warnings and cautions of this manual.
The manufacturer is not responsible for any damage to the equipment or a user’s injury
caused by an improper use or a failure in maintaining the equipment.
The responsibility of the device’s use and maintenance lies with a user.
1.2 Contraindications
The HX-D5(6)H should not be used if any of the following contra-indications exists.
CAUTION
1. Overview 46
Chapter
The operation panel provides the function of setting the tube voltage and tube current
that are applied to the X-ray tube unit, as well as the irradiation time for performing
radiography.
2. Generator
The generator includes a power circuit. It controls the opening and closing of the main
circuit and manages the generation of high voltage to be applied to the X-ray tube
according to the tube voltage signal of the X-ray tube unit. The tube current and
irradiation time can be manipulated on the user panel.
The operating and the interface circuits are necessary ones for the external equipment
and the safety interlock, and these circuits are provided in the operation generator.
3. Essential Performance
Item Specification
Sex No limitation
Nationality No limitation
1. Overview 48
Chapter
1. Overview 50
Chapter
Use the equipment under the following ambient conditions in an examination room or
operating room.
· Temperature : 5 to 35°C
· Humidity : 45 to 85 % (Non-condensing)
· Air Pressure : 800 to 1060 hPa
· Environment Luminosity : 150 to 500 lx
· Ambient Noise Level : Under 70 dB
CAUTION
Avoid sudden changes in temperature and humidity, even if such changes are made
within the above range. Otherwise, it can cause condensation that may damage the
equipment. Condensation inside the equipment can cause rust and corrosion. Frost
resulted from low temperatures can damage internal circuits.
CAUTION
DANGER
Do not use a power supply other than the one specified below.
Using a power supply other than the one specified below may cause serious accident
such as a fire, smoke emission or an explosion.
• Frequency: 50/60 Hz
• Standard voltage and permitted voltage range and power-supply impedance under
non-load conditions.
Standard Permitted
Power Supply Impedance
Voltage Voltage Range
220 VAC ± 10 % 0.16 Ω max
• Relationship between cable length and cross-sectional area to match the transformer
capacity.
• Transformer capacity: 70 kVA (single phase)
• Frequency: 50/60 Hz
• Standard voltage and permitted voltage range and power-supply impedance under
non-load conditions.
Standard Permitted
Power Supply Impedance
Voltage Voltage Range
380V ± 10 % 0.16 Ω max
• Relationship between cable length and cross-sectional area to match the transformer
capacity.
• Transformer capacity: 75 kVA (3-phase)
1. Overview 52
• Safety Devices
CAUTION
If an earth leakage breaker is used for either power voltage, use an inverter type of earth
leakage breaker to prevent malfunction in high-frequency circuits.
Transport and store the equipment under the following ambient conditions:
· Temperature : -10 to 60 °C
· Humidity : 10 to 95 % (Non-condensing)
· Air Pressure : 800 to 1060 hPa
CAUTION
3. Applied Part: Wall-stand, floating top table, and vertical tube stand
1. Overview 54
This page is intentionally blank.
2.1 Composition
2.2 Dimensions
2.1 Composition
This chapter describes on compositions for HV generator.
15
8 16
17
9 18
13
1 10 11 12 3
14 2
Fig. 2.1.
14 Save APR Address Stores APR exposure condition to the APR address.
Enables adjustment of an exposure condition for a
15 Patient Size Selection
patient’s body size.
16 AEC Field Selection Enables selecting AEC field type and using photo timer.
5
4 6
1 2
Fig. 2.2.
2. Prior to Operation 58
3. HV Generator (HX-D5H / HX-D6H)
Fig. 2.3.
2.2 Dimensions
1. HX-5H
• HX-D5H Main Body
<Top view>
unit: mm
<Front view> <Side view>
• OP Console
<Top view>
unit: mm
2. Prior to Operation 60
2. HX-D6H
<Top view>
unit: mm
<Front view> <Side view>
• Mini Console
unit: mm
<Front view> <Side view>
4
2
Fig. 2.6.
No. Name Description
1 Status Display It shows technique factors.
It enables an operator to change size setting for a patient; small,
Patient Size
2 medium, and large. It is able to adjust condition of X-ray exposure
Change
by changing its size for a patient.
Technique It enables an operator to use general radiography technique. Also, it
3
Button can be used for saving and searching an APR .
It is illuminated when a user selects an APR address. If the APR
4 APR Address address is selected, the selected address and relevant technique
button are illuminated at the same time.
1 2 3
Fig. 2.7.
2. Prior to Operation 62
1
2
3
4
5
Fig. 2.8.
Sensitivity It is the button for changing a sensitivity level as Low (L), Medium
3
Settings (M), and High (H). A user can set the level by touching it.
Sec /mAs It enables changing condition settings for X-ray exposure (e.g. sec,
4
Settings or mAs).
Focal Spot
5 It is the button to modify the size of focus as small or large.
Change
3
Fig. 2.9.
2. Prior to Operation 64
2.3.2 How to Set Exposure Condition
1 2 3 4
Fig. 2.10.
No. Name
1 kV value adjustment
2 mA value adjustment
ms Velocity of ms·sec /mAs values will Setting values of ms·sec /mAs can be
sec increase or decrease rapidly, when a increased or decreased. Each time the
mAs user keeps pressing down this button. key is pressed, it will make them going
up or down by 1 step.
1. Radiography
1 2 3 4 5 6
Fig. 2.11.
Identify Focal It is illuminated when a focal spot size is selected by a user. The left
1
Spot Size side is for a large size, and the right is for a small one.
Ready
2 It is lit when preparations for X-ray radiography are completed.
Indicator
Standby It is lit approximately two seconds later, after the power is turned on.
4
Indicator It is possible to take a radiography only when this indicator is lit.
2. Prior to Operation 66
2. Technique factor
1 2 3 4
Fig. 2.12.
Fig. 3.1
The daily inspection comprises the starting and ending inspections. The daily inspection
is necessary in order to sustain the system performance for a long time. Check whether
all inspections and corrective actions are completed before using the system.
Use the "Starting Inspection Checklist" and "Ending Inspection Checklist" in 8.1
“Daily Checklist". We recommend that you fill out a copy of the "Starting
Inspection Checklist" and "Ending Inspection Checklist" and keep it for a certain
period of time.
CAUTION
Check that the safety of examination room, before turning the power ON.
3. Operation 70
Chapter
CAUTION
Contact your DK Medical Systems service representative if any of the following problems
occur when the power is turned ON:
• An operation panel display shows an abnormality, such as flickering.
• An operation panel makes an abnormal noise.
• an X-ray tube unit produces abnormal sounds or vibration.
1. Close the knife switch or non-fuse circuit breaker connected to the equipment power
cable.
2. Check that the power of operation panel is on or off.
3. Press the right arrow [Power on/off ] to turn the power on. If an internal battery of
operation panel is discharged, the power will not be turned on and an error code will
appear on the technique factor. In normal case, the stand-by indicator is illuminated
approximately two seconds after pressing the power switch.
[Power Switch]
Fig. 3.2.
When the unit is turned on, the operation console indicator will show the same
radiography condition that was used for the latest X-ray radiography.
CAUTION
• Except emergency, do not turn off the power if it has not been five minutes after an X-
ray irradiation, or while the starter brake is being applied to the X-ray tube. Otherwise, it
can reduce the life of the X-ray tube.
• Turn off the power when an emergency occurs or when no examination is conducted.
• Be careful when opening a knife switch or non-fuse circuit breaker to connect to
the equipment power cable.
1. Press the left arrow [Power ON/OFF ] to turn the power off.
2. Open the knife switch or non-fuse circuit breaker connected to the equipment power
cable.
[Power Switch]
Fig. 3.3.
3. Operation 72
Chapter
1. sec/mAs Transition
To transit ‘sec’ to ‘mAs’, press the sec <-> mAs transition button ( ). To change
mA, use the mA window. Depending on the changed technique conditions and
combination of ms/sec/mAs, it is possible to conduct the settings of conditions for a
radiography exposure.
2. Setting Method for kV, mA, and sec/mAs
By using the up/down arrow keys of operation panel, a user can adjust
exposure conditions easily. The operation panel provides the up/down arrow
keys for each unit [kV, mA, sec and mAs] for exposure conditions.
3. Description on Display and Arrow Button
No. Description
It displays a current kV value. The value can be modified by 1kV to 10kV. It is not
1
modified by a technical factor.
It displays a current mA value. It can be modified by a certain amount as programmed
2
on firmware. It is affected by a technical factor in mAs condition.
It displays current ms·sec / mAs values. They can be modified by a certain amount as
3
programmed on firmware.
By pressing a focus selection on the operation panel, a user can switch a focus as large
or small.
Status Description
CAUTION
The function of focus selection is not available when irradiating an X-ray by a registered
APR exposure condition.
3. Operation 74
3.4.3 Changing Patient Size
Press either of [Patient size change] keys according to the body thickness of a patient. This
function will be applied to technical factors to adjust exposure conditions. The below symbol
will be illuminated after a user selects a size of patient.
Fig. 3.4.
1. Settings of Photographic Density
Press the [Density-up] , or [Density-down] button to set a density.
The position ‘0’ is the standard density. Increasing the density as "+1" produces a
darker image by 15 %; "-1" produces lighter by 15 %.
Fig. 3.5.
2. Setting of Speed (Intensifying Screen Sensitivity)
The speed toggles among L, M, and H each time the [SENS] key is pressed.
Fig. 3.6.
Status Description
L Low intensifying-screen sensitivity (longer exposure time than the standard)
M Standard
H High intensifying-screen sensitivity (shorter exposure time than the standard)
2) Input 3sec. APR address under condition of selecting Save. When inputting,
memory is saved simultaneously with beep tone sound.
3) When using AUTO Memory, input 3sec. AUTO Memory Down under condition of
selecting Save.
4) Input 3 sec. AUTO Memory Down under condition of selecting Del (AUTO Memory).
4
5
6
2 1
Fig. 3.7. APR Memory :32*7 = 224
3. Operation 76
Chapter
CAUTION
CAUTION
Check messages related to the X-ray High Voltage Generator if the icon ( ) is lit.
NOTE
It is important to run-in (aging) the X-ray tube before commencing an actual X-ray
irradiation. Follow the aging procedure described in the section for ‘Aging an X-ray Tube’.
Insufficient aging can result in arc of the X-ray tube during the X-ray irradiation.
NOTE
If a radiographic operation does not occur when the [X-ray switch] key is pressed
down for five seconds, release the button and check if an error message is displayed.
1) Press the [Ready switch] key. The [Ready switch] key will be lit and the
[ready indicator] will appear on the display.
2) Press the [X-ray switch] key while holding down the [Ready switch] key. Then,
a radiographic operation will be conducted. The key will be lit and the X-ray
indicator will appear on the display window during the X-ray irradiation.
2. Press the hand switch as the second step. An radiographic operation will be
conducted. During the X-ray irradiation, the ( : X-ray indicator) appears on the
display.
Hand Switch
(X-ray Stand by)
Hand Switch
(X-ray Ready)
Hand Switch
(X-ray Irradiation)
Fig. 3.8.
NOTE
Hold down the hand switch until the X-ray irradiation is completed.
3. Operation 78
3.5.3 Additional Information for Radiographic Operation
NOTE
• The status of X-ray irradiation can be notified by sound during X-ray irradiation.
• A user can check the status of device by voice signals.
NOTE
An operator should use the provided DAP only. Otherwise, it might cause an error or
malfunctioning.
1. DAP Display
Dose value is displayed on the operation panel, after X-ray irradiation is completed.
This function can store up to thirty (30) memories in total.
[DAP Value]
1 234
If the DAP meter did not receive any DAP value nor irradiate an X-ray, it displays the
value like below.
-- ---
Fig. 3.9.
CAUTION
If a density value is not 0 or an APR gauge has already been charged as full in an APR
address, it is not possible to save a data.
CAUTION
Fig. 4.1.
Fig. 4.2.
4. Advanced Functions 82
3. Series & Routine APR
This button enables a function of series or routine APR. When this button is illuminated,
it is able to proceed a series or routine APR exposure in consecutive order that APR
addresses are saved.
Fig. 4.3.
Fig. 4.4.
Fig. 4.5.
Fig. 4.6.
4. Advanced Functions 84
Chapter
Fig. 4.7.
2. Changing AEC Field
HX-xH provides total five (5) sections of AEC field range. By pressing
the key button, a user can switch an AEC field easily.
Fig. 4.8.
85 HX-DxH Series Operation Manual OME-HX-DxH Series-3
05 Troubleshooting
This chapter explains error messages that is displayed on the screen of
equipment, and solutions for them.
5.2 Troubleshooting
Chapter
E.no 09 EP, IP Set Error The IC (U2, U29) are missing from the main board.
E.no 12 Zero Cross Low When a main power input is lower than 45Hz (50~60hz)
High Current When a current output exceeds 10% when switching a rotor
E.no 13
Detected on Rotor (Approximating 4.2V)
Low Current When a current output is lower than 10% when switching a
E.no 14
Detected on Rotor rotor (Approximating 4.2V)
High Current
It occurs when a value of filament current exceeds a standard
E.no 15 Detected on
value for protecting an X-ray tube unit.
STB Filament
Low Current
It occurs when a value of filament current is lower than a
E.no 16 Detected on
standard value for protecting an X-ray tube unit.
STB Filament
E.no 22 H/W +kV Level Error Measured kV value is +20% than the set +kV value.
E.no 23 H/W –kV Level Error Measured kV value is -20% than the set -kV value.
* Remarks
5. Troubleshooting 88
Chapter
5.2 Troubleshooting
Error No. Code Name Solution
1. Check whether resistors R20 and R32 on the rotor board are
normal. (1Ø: 3W-30Kohm /3Ø: 3W-47Kohm). If not, replace the
rotor board.
Charge Monitor 2. Check whether a diode D17 on the rotor board is normal.
E.no 10
Error (1Ø: 1N5375 /3Ø: 1N5955B). If not, replace the rotor board.
3. When exposing an X-ray, check the minimum voltage in CN14
(lower than 200VDC). It can be all different depending on a
condition. Upon checking it, calibrate the kV and mA.
1. If a frequency of main power measured by an oscilloscope is
normal, replace the rotor board.
E.no 11 Zero Cross Over 2. If the Error no. 11 still appears even though the rotor board has
been already replaced, contact DK Medical Systems service
representative.
If a frequency of main power measured by an oscilloscope is
E.no 12 Zero Cross Low
normal, replace the rotor board.
1. Check the rotor cable.
2. Check a resistor value in the rotor.
High Current
3. After removing the wiring from the rotor board, press the Ready.
E.no 13 Detected on
If the Err no.13 still shows up, replace the rotor board.
Rotor
4. After removing the wiring from the rotor board, press the Ready.
If the Err no.14 shows up, replace the X-ray tube.
1. Check the rotor cable.
2. If the wiring is normal, check the rotor rotation by pressing the
Low Current
Ready button. (If the Err no. 14 still shows up while rotating the
E.no 14 Detected on
rotor, replace the rotor board.)
Rotor
3. If the wiring is normal, check the rotor rotation by pressing the
Ready button. (If the rotor is not rotated, replace the X-ray tube.)
1. Check the ‘LED1 ON’ in the Filament board. If the LED1 is
turned OFF, check the power in SMPS.
2. Check the voltage between TP3 and TP5 on the filament board:
High Current If it exceeds 2.5V, replace the filament board; If lower than 2.5V,
E.no 15 Detected on STB replace the main CTRL board.
Filament If greater than 2.5V of voltage is detected in the HFG Filament
Current Feedback at the Standby status, check the output value
of main CTRL board and the status of filament DRV board.
3. If the problem still exists, replace the HV tank.
1. Check the filament board whether the LED1 is turned ON. If the
LED is turned OFF, check the power in SMPS.
2. Check the voltage between TP3 and TP5 on the filament board;
Low Current if it is lower than 0.5V, replace the filament board. If greater than
E.no 16 Detected on STB 0.5V, replace the main CTRL board.
Filament If lower than 0.5V of voltage is detected in the HFG Filament
Current Feedback at the Standby status, check the output value
of Main CTRL Board and check the status of filament DRV board.
3. If still the problem exists, replace the HV tank.
5. Troubleshooting 90
Error No. Code Name Solution
2. Check the current between TP15 and TP9 (GND) on main CTRL
board with an oscilloscope. If the measured current has 20% of
difference compared with the established current value, replace
EXPO Fil FB the main CTRL board.
E.no 17
Level Error 3. Check the current between TP13 and TP9 on the main CTRL
board with an oscilloscope; if the set current is lower than 100mA,
then 1V is 10mA. If greater than 100mA, 1V is 100mA.
If abnormal, replace the filament board.
4. If the problem still occurs, contact DK Medical Systems service
representative.
H/W +kV 1. Compare the voltage between TP6, TP8 and TP9 (GND) with
E.no 22
Level Error oscilloscope ch1 and ch2. If two waveforms are not in asymmetry,
H/W -kV it means the HV tank might have a problem.
E.no 23 2. If they are in symmetry, replace the control board.
Level Error
1. Check whether a LED1 on the IGBT board is turned ON. (If the
IGBT OCP LED1 is turned ON upon checking it, then check the status of
E.no 25
Fault Error IGBT board; whether IGBT is cracked. And, check the wire for
BASE INPUT.)
* Remarks
5. Troubleshooting 92
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Cleaning and
Operator or equipment manager As required
Sanitation
The daily inspection consists of the starting and ending inspections. Daily inspection is
necessary in order to use the system for a long time. Check whether all inspections
and correct actions have been completed, before using the system.
Refer to the “Starting Inspection Checklist” and “Ending Inspection Checklist” in 8.1
“Daily Checklist”. We recommend that you retain filled out copy of the “Starting
Inspection Checklist” and “Ending Inspection Checklist” for a certain period of time.
1. Turn off the power of HV generator, and cut down the electricity.
2. Conduct a visual inspection on the cable connection among component devices.
3. If any rust is found in chemical materials, increase the interval of cleaning component
devices. Use a cloth damped with warm, soapy water for sanitation. Just swipe a cover
or an enclosure of device. Do not use any solvent type of cleaner.
Be sure to turn OFF the system power before cleaning and disinfecting the
system.
Otherwise, a malfunction may occur in the system, or the system may operate in an
unintended way.
WARNING
WARNING
WARNING
Before turning on the power, thoroughly ventilate the room after cleaning a
device, in order to prevent it from accidents.
Flammable gases accumulated in the room may ignite, smoke, explode, or cause an
electric shock when the power is turned on.
WARNING
• Chlorine-based sanitizer
• Sanitizer that corrodes metal, plastic, rubber, or paint
• Sanitizer unsuitable for metal, plastic, rubber, or paint
• Spray-gas type sanitizer
• Volatile sanitizer
• Sanitizer that may enter the equipment
WARNING
Periodic inspection mainly affects the equipment performance and its internal
mechanism. The inspection requires a deep understanding about the internal
mechanisms which can be dangerous for an untrained personnel. Contact your DK
Medical Systems service representative if you wish to request a periodic inspection.
It is recommended to conduct periodic inspection every six (6) months. A fee is charged
for periodic inspection after a warranty is expired.
Item Description
6.2.1 Fuse
Manufacturer
No. Component Part No. Technical data
/ Type
Generator
1 Main Fuse (F1, F2, F3) 600V, 60A Buss (JT60060)
500V, 10A Cylindrical
2 Magnetic Fuse (F4, F5, F6) Legrand
type (10x38mm)
Generator: Rotor I/F Board
3 Fuse (F1, F4, F5, F6, F7) 250V, 10A (20mm) Glass type
Hand Switch
kV 40 to 125 kV (E7239X)
10 to 500 mA (E7239X)
mA Small : 10, 12.5, 16, 20, 25, 32, 40, 50 ,64, 80, 100, 125mA
Large : 200, 250, 320, 400, 500mA
Short Time Rating Single phase : E7239X: 40kW (125kV, 320mA / 80 kV, 500mA)
Coefficient of
CV (Coefficient Value) ≤ 0.05
Reproducibility
Operation Panel 3 kg
Control Cabinet 82 kg
Nominal Min.
AEC 1ms
Exposure Time
Radiography
mAs Limit 500mAs
mA Small : 10, 12.5, 16, 20, 25, 32, 40, 50 ,64, 80, 100, 125,
160mA
Large : 200, 250, 320, 400, 500, 630mA
Setting mAs 0.1 to 500 mAs
Range
0.001 to 10 sec
1ms ~ 10000ms (41 steps)
sec 1, 1.2, 1.6, 2, 2.5, 3.2, 4, 5, 6.3, 8, 10, 12.5, 16, 20, 25, 32, 40,
50, 63, 80, 100, 125, 160, 200, 250, 320, 400, 500, 630, 800,
1000, 1250, 1600, 2000, 2500, 3200, 4000, 5000, 6300, 8000,
10000 ms
Kv 100kV 150kV
mA 500mA 320mA
Coefficient of
CV (Coefficient Value) ≤ 0.05
Reproducibility
Operation Panel 3 kg
Control Cabinet 84 kg
Nominal Min.
AEC 1ms
Exposure Time
Radiography
mAs Limit 500mAs
GX-D5H
• Tube voltage range: 40 ~ 125kV (E7239X)
X-ray Controller • Tube current range: 10 ~ 500mA (E7239X)
1
(Optional)
• Exposure time range: 1ms ~ 10sec
• mAs range: 0.1mAs ~ 500mAs
• Functions: APR, DAP, AEC, DR available
• Internal software
GX-D5 - Model name: GX-D5
- Version: 1.0
• Internal software
HX-D5 - Model name: HX-D5
- Version: 1.0
• Internal software
GX-D6 - Model name: GX-D6
- Version: 1.0
• Internal software
HX-D6 - Model name: HX-D6
- Version: 1.0
CAUTION
· Pay attention to the electro-magnetic circumstances at the site since the device may
be affected depending on the electro-magnetic field at the site.
· Due to the installation this equipment, other devices may be affected. In this case, the
equipment needs to be moved to another location to avoid the problem.
CAUTION
Only accessories, transducers and cables sold by the DK Medical Systems need to be
used. If a user replace equipment’s parts as the ones from a different manufacturer, it
may cause emissions and/or immunity of HX-DxH to be increased or decreased.
CAUTION
· The HX-DxH should be used only in the specified type of shielded location.
· For radiated RF immunity test, a Medical Electrical Equipment has not all been tested
over the entire frequency range, which is from 80 MHz to 2,5 GHz.
· A Medical Electrical Equipment has been tested for radiated RF immunity only at
selected frequencies.
RF Emissions EN
Class A
55011/ CISPR 11
The HX-DxH is intended for use in the electromagnetic environment specified below. A customer
or a user of HX-DxH should assure that it is used in such environment.
Electrical Fast
±2 kV ±2 kV
Transient / Mains power quality should be
for power supply lines for power supply lines
Burst that of a typical commercial or
±1 kV ±1 kV
EN 61000-4-4/ hospital environment.
for input/output lines for input/output lines
IEC 61000-4-4
NOTE: UT is the A.C. mains voltage prior to application of the test level.
The HX-DxH is intended for use in the electro-magnetic environment specified below. The
customer or the user of the HX-DxH should assure that it is used in such an environment.
NOTE
• At 80 MHz and 800 MHz, the higher frequency range applies.
• These guidelines may not apply in all situations. Electromagnetic propagation is affected
by absorption and reflection from structures, objects and people.
*1: 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 HX-DxH is used
exceeds the applicable RF compliance level above, the HX-DxH should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the cables.
*2: Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
100 12 12 23
NOTE
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated using the equation applicable to the
frequency of the transmitter, where P is the maximum output power rating of the transmitter in
watts (W) according to the transmitter manufacturer.
• At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
• These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
kV mA E7239 kV mA E7239
40 10 40 10
50 8 50 8
63 6.3 63 6.3
40 80 5 90 80 4
100 4 100 2.5
125 3.2 125 1.6
160 2.5 160 0.63
40 10 40 10
50 8 50 8
63 6.3 63 6.3
50 80 5 100 80 2.5
100 4 100 2
125 3.2 125 0.8
160 2.5 160 0.4
40 10 40 10
50 8 50 8
63 6.3 63 5
60 80 5 110 80 2
100 4 100 1.25
125 3.2 125 0.4
160 2.5 160 0.1
40 10 40 10
50 8 50 6.3
63 6.3 63 4
70 80 5 120 80 1.25
100 4 100 0.25
125 3.2 125 0.12
160 1.6 160 0.1
40 10 40 10
50 8 50 6.3
63 6.3 63 4
80 80 5 125 80 1.25
100 3.2 100 0.25
125 3.2 125 0.12
160 1 160 0.1
kV mA E7239 kV mA E7239
125 2.5 125 1.6
160 2.5 160 1.6
200 2 200 1.6
250 1.6 250 0.63
40 100
320 0.5 320 0.2
400 0.5 400 0.1
500 X 500 X
630 X 630 X
125 2.5 125 1.25
160 2.5 160 1.25
200 2 200 1.25
250 1.6 250 0.5
50 110
320 0.5 320 0.16
400 0.5 400 X
500 X 500 X
630 X 630 X
125 2.5 125 0.8
160 2.5 160 0.8
200 2 200 0.8
250 1.6 250 0.32
60 120
320 0.5 320 0.1
400 0.5 400 X
500 X 500 X
630 X 630 X
125 2.5 125 0.8
160 2.5 160 0.8
200 2 200 0.8
250 1.6 250 0.32
70 125
320 0.5 320 0.1
400 0.4 400 X
500 0.16 500 X
630 X 630 X
125 2 125 X
160 2 160 X
200 2 200 X
250 1.6 250 X
80 150
320 0.4 320 X
400 0.25 400 X
500 0.1 500 X
630 X 630 X
125 2
160 2
200 2
250 1
90
320 0.32
400 0.16
500 X
630 X
Time mA Selected
(mS) 10 12.5 16 20 25 32 40 50 64 80 100 125 160 200 250 320 400 500 630
1 - - - - - - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63
1.2 - - - - - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8
1.6 - - - - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1
2 - - - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25
2.5 - - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6
3.2 - - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2
4 - - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5
5 - - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2
6.3 - - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4
8 - 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5
10 0.1 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3
12.5 0.125 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8
16 0.16 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10
20 0.2 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5
25 0.25 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16
32 0.32 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20
40 0.4 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25
50 0.5 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32
63 0.63 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40
80 0.8 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50
100 1 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63
125 1.25 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80
160 1.6 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100
200 2 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125
250 2.5 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160
320 3.2 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200
400 4 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250
500 5 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250 320
630 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250 320 -
800 8 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250 320 400 -
1000 10 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250 320 400 500 -
1250 12.5 16 20 25 32 40 50 63 80 100 125 160 200 250 320 400 500 - -
1600 16 20 25 32 40 50 63 80 100 125 160 200 250 320 400 500 - - -
2000 20 25 32 40 50 63 80 100 125 160 200 250 320 400 500 - - - -
2500 25 32 40 50 63 80 100 125 160 200 250 320 400 500 - - - - -
3200 32 40 50 63 80 100 125 160 200 250 320 400 500 - - - - - -
4000 40 50 63 80 100 125 160 200 250 320 400 500 - - - - - - -
5000 50 63 80 100 125 160 200 250 320 400 500 - - - - - - - -
6300 63 80 100 125 160 200 250 320 400 500 - - - - - - - - -
8000 80 100 125 160 200 250 320 400 500 - - - - - - - - - -
10000 100 125 160 200 250 320 400 500 - - - - - - - - - - -
* Abbreviations
CAUTION
The contents of table above were calculated and prepared by various theories, and data
that is actually calculated might be different slightly, depending on a clinical use.
Consider the above table as a data for assessing radiation risks.
8.1 Checklist
Chapter
8.1 Checklist
8.1.1 Starting Inspection Checklist
Always carry out the inspection described below, prior to using the system.
1. Check the following points visually before switching the power ON. Take proper
actions to correct a problem.
2. Check visually that connections have been made correctly, before switching the
power ON. Correct a nonconformity, if any.
3. Turn the power ON. Check the following points visually and aurally. Correct a
nonconformity, if any.
Always check the following points, before switching the power OFF. Correct a
problem, if any.
1. Check the following points visually before switching the power OFF. Correct a
nonconformity, if any.
2. Switch the power OFF. Check the following points visually. Correct a nonconformity,
if any.
8. Checklist 122
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The company's quality system satisfies the Annex II exclusion section of Annex IV of the
Directive 93/42/EEC as amended by 2007/42EC, which is certified by the Institute for
DNV NEMKO PRESAFE AS.
Manufacturer
No. Component Part No. Technical data EA
/ type
Generator
1 Main Fuse (F1, F2, F3) 600V, 60A Buss (JT60060) 3
500V, 10A
2 Magnetic Fuse (F4, F5, F6) Cylindrical type Legrand 3
(10x38mm)
Generator: Rotor I/F Board
3 Fuse (F1, F4, F5, F6, F7) 250V, 10A (20mm) Glass type 4
4 Fuse (F2, F3) 250V, 3.15A (20mm) Glass type 2
Generator: Auto-trans Fuse
5 Fuse (F4, F5, F6, F7, F8, F9) 250V, 2A (30mm) Glass type 6
6 Fuse (F1, F2, F3) 250V, 3A (30mm) Glass type 3
7 Fuse (F10, F11) 250V, 5A (30mm) Glass type 2
8 Fuse (F12, F13, F14) 250V, 10A (30mm) Glass type 3
CAUTION
To avoid causing a fire, it is recommend to use a product that is the same or equivalent
to the above-specified specification, when replacing a product.
9.2.2 Accessories
9. Appendix 126
9.2.3 List of Cables
Shielded
No Name Conduit Length Note
or Not
1 AC Input Power Cable Unshielded 16㎟ X 4C 4m
2 Console Cable(mini) Shielded 24AWG X 15C 16m
3 DC Power Cable(SF-80) Unshielded 0.75㎟ X 2C 10m
Handlebar Control
4 Unshielded 28AWG X 15Pr 7m
Cable(T3)
5 AC Power Cable(T3) Unshielded VCTF2.5 X 3C 18m
6 Sync Input Cable(T3) Shielded 24AWG X 3C 18m
7 High Voltage Cable Shielded 40㎜ X 3C 14m
8 Rotor Cable(SF-80) unshielded 1.0SQ X 10C 10m
9 Rotor Cable(T3) unshielded 1.0SQ X 10C 18m
10 AC Power Cable unshielded 0.75㎟ X 2C 0.5m
11 AC Power Cable unshielded 18AWG X 3C 12m
12 Moving Grid Cable unshielded 0.75㎟ X 2C 16m
13 AC Power Cable unshielded VCTF 2.5SQ X 3C 13m
14 Bucky Solenoid unshielded VCTF 0.75SQ X 2C 16m
15 AC Input Power Cable unshielded 0.75㎟ X 3C 2m
10 Core
16 RGB Cable shielded 2m
(3 X 2Core + 4Core)
17 Lan Cable shielded 24AWG, CAT5 15m
18 DC Power Cable shielded 18AWG X 4C 10m
Generator Inter Face
19 Cable(1717,1417 – shielded 26AWG X 9C 15m
Generator)
20 Tether Interface Cable shielded 26AWG X 8C 7m
CAUTION
Use a cable specified on the above list; if not, it may occur an error and/or obstacle
against operation. Also it may decrease immunity of the system.
Maximum Value of
No. Component Part Model
Attenuation Equivalent
1 Patient Table TE-90 1.0 mmAl
2 Patient Table TF-90 1.0 mmAl
3 Integration Table ST-90D 1.0 mmAl
4 Bucky Stand DS-90 0.5 mmAl
Fig. 9.1.
CAUTION
If an operator does not follow the Attenuation Equivalent of items for the X-ray Beam,
which is in accordance with sub-clause 203.10.101 of IEC 60601-2-54, it may cause
excessive X-ray exposure to the patient. The table 203.104 of Attenuation Equivalent of
items in the X-ray Beam is shown above.
9. Appendix 128
Chapter
9. Appendix 130
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