Veraview Ix: Operation Instructions
Veraview Ix: Operation Instructions
Veraview Ix: Operation Instructions
Prevent Accidents 2
Warnings and Cautions 4
Parts Identification 6
Usage 9
(1) Before Use 9
(2) Use 10
Selecting the exposure parameters 10
Selecting radiography conditions 11
Positioning the patient 12
Taking an exposure 14
Operation 2018-10-22 1
Prevent Accidents
Attention Customers
Do not fail to receive clear instructions concerning the various ways to use this equipment as described in this accompanying
Operator’s Manual.
Fill out and sign the warranty and give the dealer from whom you purchased the equipment his copy.
Attention Dealers
Do not fail to give clear instructions concerning the various ways to use this equipment as described in this accompanying
operator’s manual.
After instructing the customer in the operation of the equipment, have him fill out and sign the warranty. Then fill in your own
section of the warranty and give the customer his copy. Do not fail to send the manufacturer’s copy to J. MORITA MFG. CORP.
Prevent Accidents
Most operation and maintenance problems result from insufficient attention being paid to basic safety precautions and not being
able to foresee the possibilities of accidents. Problems and accidents are best avoided by foreseeing the possibility of danger
and operating the unit in accordance with the manufacturer’s recommendations. First thoroughly read all precautions and
instructions pertaining to safety and accident prevention; then, operate the equipment with the utmost caution to prevent either
damaging the equipment itself or causing bodily injury.
The following symbols and expressions indicate the degree of danger and harm that could result from ignoring the
instructions they accompany:
This warns the user of the possibility of extremely serious injury or complete destruction of the
equipment as well as other property damage including the possibility of fire.
This warns the user of the possibility of mild injury or damage to the equipment.
* The warning symbols ( ) and caution symbols ( ) that appear next to the main text on the
right hand side of the page refer to and are explained by the Warnings and Cautions at the bottom
of the page.
This alerts the user of important points concerning operation or the risk of equipment damage.
The user (e.g., healthcare facility, clinic, hospital etc.) is responsible for the management, maintenance, and use of medical
devices.
Disregarding the information on safety is considered ABNORMAL USE.
Do not use this equipment for anything other than its specified dental treatment purpose..
2 Operation 2018-10-22
Intended Operator Profile
a) Qualification:
Legally qualified person such as radiologic technician and dentists for X-ray device operation (it may differ among countries).
b) Education and Knowledge:
It is assumed that the user understands the risks of X-rays and the protective steps required. It is also assumed that the user
is thoroughly familiar with X-ray diagnosis, anatomy, and hygiene including the prevention of cross contamination.
c) Language Understanding:
English (Intended for professional use as described above).
d) Experience:
Experienced Person with operating X-ray devices.
No special training is required except in cases where this is required by legal regulations of the relevant country or region.
Related Documents
• Installation Instructions
Disclaimer
■ J. MORITA MFG. CORP. will not be responsible for accidents, equipment damage, or bodily injury resulting from:
1. Repairs made by personnel not authorized by J. MORITA MFG. CORP.
2. Any changes, modifications, or alterations of its products
3. The use of products or equipment made by other manufacturers, except for those procured by J. MORITA MFG. CORP.
4. Maintenance or repairs using parts or components other than those specified by J. MORITA MFG. CORP. and other than in
their original condition
5. Operating the equipment in ways other than the operating procedures described in this manual or resulting from the safety
precautions and warnings in this manual not being observed
6. Workplace conditions and environment or installation conditions which do not conform to those stated in this manual such
as improper electrical power supply
7. Fires, earthquakes, floods, lightning, natural disasters, or acts of God.
■ The useful life of the Veraview iX is 10 years (based on self-certification) from the date of installation provided it is regularly
and properly inspected and maintained.
■ J. MORITA MFG. CORP. will supply replacement parts and be able to repair the product for a period of 10 years after the man-
ufacture of the product has been discontinued.
Operation 2018-10-22 3
Warnings and Cautions
• This X-ray unit may be dangerous to PATIENT and OPERATOR unless safe exposure factors and operating instructions are
observed.
• Only dentists and other legally qualified and authorized personnel are allowed to operate this equipment.
• Do not use this equipment for patients when it is being maintained or serviced.
• Make sufficient space around the power switch so that it is easily accessible in case of emergency.
• Make sufficient space around the power plug so that it is easily unplugged in case of emergency (R-Type).
• Make sufficient space around the power distribution panel so that it is easily turned the breaker open in case of emergency
(WA-Type).
• To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
• To avoid the risk of electric shock, do not replace the power supply cord.
• The EQUIPMENT should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is neces-
sary, the EQUIPMENT should be observed to verify normal operation in the configuration in which it will be used.
• When an examination requires X-ray irradiation to implantable or wearable electronic medical device, the operator must take
proper care after referring to the operation manual (and related safety information) for such implantable or wearable electronic
medical devices because if a diagnostic X-ray device directly irradiates an implantable or wearable electronic medical device, it
can cause sufficient electronic interference to affect the function and operation of the medical device.
* For reference, U.S.A. FDA published about interference with cardiac implantable electronic devices (pacemakers and im-
plantable cardioverter defibrillators), insulin pumps, and neurostimulators on the following web site. (Accessed July 2018)
Title: Interference between CT and Electronic Medical Devices
URL: https://www.fda.gov/Radiation-EmittingProducts/RadiationSafety/ElectromagneticCompatibilityEMC/ucm489704.htm
• Do not use this unit for fluoroscopic examinations.
• Judgment and caution should be used in regards to radiographs of pregnant women. The decision should be based on “clinical
need of diagnostic information”.
• Do not use the wireless transmission devices listed below in the examination area; electromagnetic interference from these de-
vices could cause this X-ray unit to operate in a random, unexpected and dangerous manner.
1. Cell phone terminals.
2. Wireless transmitting devices such as ham radios, walkie-talkies, and transceivers.
3. Cell phones.
4. Routers for intra-building paging systems, wireless LAN, cordless analogue telephones, and other electric wireless devices.
• Interference from the Veraview iX, devices listed below might malfunction or operate in a random, unexpected and dangerous
manner.
1. Electric medical devices for examination, diagnosis and treatment.
2. Personal computers.
• The Unit must be installed in an X-ray shield location. Local regulation for radiation protection must be observed.
• The emission button must be operated in a radiation protected area.
• If the unit is not enclosed by an X-ray booth or other protective barrier, everyone except the patient must stay outside from a
distance not less than 2 m from tube head during X-ray emission.
• The user must restrict access to the equipment in accordance with local regulations for radiation protection.
• The operator must not enter the X-ray beam during exposure. The residual radiation exists even behind the radiography media
(film, sensor, and imaging plate).
• The patient and operator must be provided with appropriate X-ray protection gear such as lead-impregnated clothing that con-
forms to local regulations.
• The operator must be able to see the exposure emissions lights and hear the audible signal during operation of the equipment.
• The operator must be able to see and hear the patient during the operation of the equipment.
• Responsible organization in medical institution needs for providing means for audio and visual communication between the
operator and the patient.
• Proper radiation safety precautions must be established in accordance with local, state and governmental regulations in re-
gards to operator and patient protection. The ultimate responsibility lies with the owner/operator to ensure that the protection
requirements of national and local codes are met.
• Proper infection control procedures must be established and maintained for each patient.
• Do not use multiple portable socket outlet nor extension cord for the power supply.
4 Operation 2018-10-22
• Do not install the film processor (developer) in the same room as the unit; it could corrode the electric circuit.
• Infection control procedures must be observed when using accessories, such as film holders, X-ray tube guides, imaging
plates and CCD detectors. When using accessories always follow the manufacturer’s instructions on how to use the accessory
and prevent cross contamination from one patient to another.
• Do not hang onto the arm or lean on it etc. This could damage the arm or cause it to come off.
• Do not place your fingers in the moving section, or the spaces in between the arm,
head rest, X-ray head, and inverter box.
• Do not push the scissor arm towards the horizontal arm with excessive force; this
could damage it.
Operation 2019-04-22 5
Parts Identification
Parts Identification
Arm
Pole Brace
Head Rest
Support Column
Cone (Standard Cone)
(SSD: 200 mm)
⹅ Control Box
Emission Button
Control Panel
6 Operation 2019-04-22
Parts Identification
Scissor Arm
Horizontal Arm
Hand Switch
Cone
X-ray Head
Control Panel
Inverter Box
Operation 2018-02-20 7
Parts Identification
⹅ Control Panel
kV Indicator 60 kV or 70 kV
mGy .cm2 Up or Down Key
Display
Patient Key
Exposure Indicator
Emission Key
Ready Indicator
8 Operation 2017-02-24
Usage
* If the unit has not been used for some time, make sure it works properly before using it again.
R-Type WA-Type
ON
ON
Press the On side (-) of the switch to turn the unit on.
The timer display and the keys on the control panel will light up.
The control panel enters sleep mode if left for five minutes (default)
mGy .cm2
with no operation after the unit is turned on. At this time, the timer
display appears as shown at left.
To cancel sleep mode, press any key (except the Emission key)
on the control panel.
• In case of lightning, avoid the risk of electrical shock: stop using the equipment immediately and have the patient move away from it. Do not touch the equip-
ment or the main power cord.
Operation 2019-04-22 9
(2) Use
2 kV Indicator
mGy .cm2
Digital Film
10 Operation 2017-02-24
Selecting radiography conditions
Upper Jaw
Lower Jaw
Occlusion
mGy .cm2
The exposure time (in seconds) will be shown on the display. The exposure time for the selected parameters will
automatically appear on the display.
Operation 2017-02-24 11
Positioning the patient
Poor patient positioning may make it hard to make a correct diagnosis using the captured image.
Pole Brace
Slide the pole up or down to adjust the height of the X-ray head.
• Infection control procedures must be observed when using accessories, such as film holders, X-ray tube guides, imaging plates and CCD detectors. When us-
ing accessories always follow the manufacturer’s instructions on how to use the accessory and prevent cross contamination from one patient to another.
• When lowering the pole, do not pinch your fingers between the pole and the main support column.
• Maximum loading limit of Body Weight is 135 kg. Do not use this equipment for patients who weight more than 135 kg.
• Have patients remove glasses, earrings and any other accessories that might interfere with making a good exposure.
• When moving the light pole up or down or rotating the arm, do not use excessive fore, especially if the pole or arm reaches its stopper. This could damage the
equipment. (R-Type)
12 Operation 2019-04-22
Positioning the patient
Intersection of the blue and green pointers (the center of the radiation field)
Pull the X-ray head toward the patient to direct the cone toward the radiography media in the patient’s mouth so that
you can adjust the exposure point and angle.
You can adjust the exposure point by taking advantage of the pointers.
When Long SSD adaptor (option) is attached, the pointer is inoperable.
⹅ Pointers
Intersection of the blue
and green pointers
The pointer lights are turned on when the X-ray unit is turned on or when the pointer light switch is pressed.
The pointer lights will be turned off automatically in one minute.
The intersection of the blue and green pointers is the center of the radiation field.
• The pointer lights may damage the eye. Do not look into the X-ray tube or the lights may enter your eye.
• Operate with care to avoid hitting the tube head to the wall. Otherwise the tube head might possibly be destroyed.
• Do not use the unit if the arm or tube head moves abnormally (with abnormal noise) when positioning the tube head.
Operation 2018-10-22 13
Taking an exposure
1
Ask the patient not to move during the exposures.
The operator must stay outside the X-ray room or protect him/herself from exposure if staying in the room.
2
Emission Button
During exposure, the exposure buzzer is heard and the exposure indicator lights up.
Hold the Emission button or key until the exposure buzzer stops.
mGy .cm2
If you release the Emission button or key before exposure is completed, the radiography process is interrupted and the error message “E00” is
displayed on the timer display.
To clear the message, press any key (except the Emission key) on the control panel.
• Everyone except the patient must stay outside the X-ray room during X-ray emission. If the unit is not enclosed by an X-ray booth or other protective barrier,
everyone except the patient must stay outside from a distance not less than 2 m from tube head during X-ray emission.
• When it is required to stay in the X-ray room during the radiography, the operator must wear X-ray protective clothing.
• Always monitor the patient and the unit during X-ray radiography. Should an emergency occur, release your finger from the Emission button or key to stop the
unit.
• Hold the Emission button or key until the radiography is completed. If the Emission button or key is released before the radiography is completed, the radiogra-
phy process is interrupted.
• In the event that the unit does not respond to key operation, turn off the unit and have the patient leave the room. Power the unit on again after one minute or
more has elapsed after the unit was turned off.
14 Operation 2018-10-22
Taking an exposure
mGy .cm2
mGy .cm2
After exposure is completed, the exposure buzzer stops and the exposure indicator turns off.
In addition, the Ready indicator (green) blinks and the timer display alternately shows the exposure time taken and the Dose
area product.
* For more information on Dose area products, refer to page 22.
The unit occasionally discontinues operation for a period to protect the X-ray tube. During this time, no X-rays can be emitted. The time remaining
(in seconds) until the unit is ready for use is displayed as a countdown on the timer display if the Emission button or key is pressed. The timer
display alternately shows the exposure time taken and the Dose area product during the non-operating time or before pressing any radiography
condition selection keys after a non-operating time.
4
Remove the radiography media from the patient’s mouth.
⹅ Ready indicator
Operation 2017-02-24 15
(3) After Use
It takes approximately 10 seconds for the timer display to turn off after the power switch is turned off.
• Do not fail to turn the power switch off. This will avoid the risk of electric shocks, burns, or accidentally pressing a switch.
16 Operation 2018-10-22
(4) User Setting
mGy .cm2
To enter the setting mode, press and hold the kV key (approximately five seconds) until you hear beeps.
The timer display will show a blinking “5” (default).
kV Indicator
Up or Down Key
mGy .cm2
Sets the amount of time before entering sleep mode
(OFF to 60 minutes).
Press the up or down key to switch the value in increments
of five minutes.
* The default is 5 (minutes).
Operation 2017-02-24 17
Startup settings for radiography conditions and sleep mode time
To save all settings and exit the setting mode, press and hold the Occlusion key (approximately 5 seconds).
* Hold the key until you hear beeps.
At the next startup, the unit will be configured with the saved radiography conditions.
To not save the settings, press the Occlusion key for a short time or turn off the unit.
18 Operation 2017-02-24
Setting the timer table
To switch to the timer table setting mode, press and hold the Film/Digital key (approximately five seconds) until you hear
beeps.
The timer display will show “F. 08” * blinking (*Default for the standard cone. For the long cone, “F. 11” is shown.)
mGy .cm2
To save all settings and exit the timer table setting mode, press and hold the Occlusion key (approximately 5 seconds).
* Hold the key until you hear beeps.
The settable numbers are any of the table numbers (00 to 14).
To not save the settings, press the Occlusion key for a short time or turn off the unit.
Operation 2017-02-24 19
Timer table
The following timer table is based on the 60 kV setting with the use of the standard cone.
When switched to 70 kV, the unit will apply and display the timer table number two smaller than a selected timer table number.
When using the long cone, manually select the timer table number three greater than the timer table number you would normally want to choose.
No. 00 Adult (M) 0.04 0.05 0.06 0.03 0.03 0.05 0.08
Lady (S) 0.03 0.03 0.04 0.02 0.03 0.03 0.05
Child (C) 0.02 0.03 0.03 0.01 0.02 0.03 0.04
No. 01 Adult (M) 0.05 0.06 0.08 0.03 0.04 0.06 0.10
Lady (S) 0.03 0.04 0.05 0.02 0.03 0.04 0.06
Child (C) 0.03 0.03 0.04 0.02 0.02 0.03 0.05
No. 02 Adult (M) 0.06 0.08 0.10 0.04 0.05 0.08 0.13
Lady (S) 0.04 0.05 0.06 0.03 0.04 0.05 0.08
Child (C) 0.03 0.04 0.05 0.02 0.03 0.04 0.06
No. 03 Adult (M) 0.08 0.10 0.13 0.05 0.06 0.10 0.16
Lady (S) 0.05 0.06 0.08 0.03 0.05 0.06 0.10
Child (C) 0.04 0.05 0.06 0.03 0.03 0.05 0.08
No. 04 Adult (M) 0.10 0.13 0.16 0.06 0.08 0.13 0.20
Lady (S) 0.06 0.08 0.10 0.04 0.06 0.08 0.13
Child (C) 0.05 0.06 0.08 0.03 0.04 0.06 0.10
No. 05 Adult (M) 0.13 0.16 0.20 0.08 0.10 0.16 0.25
Lady (S) 0.08 0.10 0.13 0.05 0.08 0.10 0.16
Child (C) 0.06 0.08 0.10 0.04 0.05 0.08 0.13
No. 06 Adult (M) 0.16 0.20 0.25 0.10 0.13 0.20 0.32
Lady (S) 0.10 0.13 0.16 0.06 0.10 0.13 0.20
Child (C) 0.08 0.10 0.13 0.05 0.06 0.10 0.16
No. 07 Adult (M) 0.20 0.25 0.32 0.13 0.16 0.25 0.40
Lady (S) 0.13 0.16 0.20 0.08 0.13 0.16 0.25
Child (C) 0.10 0.13 0.16 0.06 0.08 0.13 0.20
No. 08 Adult (M) 0.25 0.32 0.40 0.16 0.20 0.32 0.50
Lady (S) 0.16 0.20 0.25 0.10 0.16 0.20 0.32
Child (C) 0.13 0.16 0.20 0.08 0.10 0.16 0.25
No. 09 Adult (M) 0.32 0.40 0.50 0.20 0.25 0.40 0.63
Lady (S) 0.20 0.25 0.32 0.13 0.20 0.25 0.40
Child (C) 0.16 0.20 0.25 0.10 0.13 0.20 0.32
(Unit: sec.)
20 Operation 2017-02-24
Timer table
No. 10 Adult (M) 0.40 0.50 0.63 0.25 0.32 0.50 0.80
Lady (S) 0.25 0.32 0.40 0.16 0.25 0.32 0.50
Child (C) 0.20 0.25 0.32 0.13 0.16 0.25 0.40
No. 11 Adult (M) 0.50 0.63 0.80 0.32 0.40 0.63 1.00
Lady (S) 0.32 0.40 0.50 0.20 0.32 0.40 0.63
Child (C) 0.25 0.32 0.40 0.16 0.20 0.32 0.50
No. 12 Adult (M) 0.63 0.80 1.00 0.40 0.50 0.80 1.25
Lady (S) 0.40 0.50 0.63 0.25 0.40 0.50 0.80
Child (C) 0.32 0.40 0.50 0.20 0.25 0.40 0.63
No. 13 Adult (M) 0.80 1.00 1.25 0.50 0.63 1.00 1.60
Lady (S) 0.50 0.63 0.80 0.32 0.50 0.63 1.00
Child (C) 0.40 0.50 0.63 0.25 0.32 0.50 0.80
No. 14 Adult (M) 1.00 1.25 1.60 0.63 0.80 1.25 2.00
Lady (S) 0.63 0.80 1.00 0.40 0.63 0.80 1.25
Child (C) 0.50 0.63 0.80 0.32 0.40 0.63 1.00
(Unit: sec.)
Operation 2017-02-24 21
Dose area product
The Dose area product displayed is the multiplication product of the air kerma end and the size of the radiation field at the cone.
These values are typical values and are not the measured Dose area products for each X-ray exposure. In addition, these
values differ between when the standard cone is used and when the long cone is used.
The air kerma is calculated by divided the Dose area product by the X-ray field size of diameter 58 mm.
The dosemeter to check and maintain the accuracy of the Dose area product indications shall be calibrated at the appropriate
energy.
Accuracy: Display value ±50%
1. After checking that the Ready indicator is lit, press and hold the Lady key (approximately
five seconds).
The dose area product is not affected by the SSD (Source Skin Distance) but;
• Air kerma (dose) is attenuated by inverse square of the SSD ratio.
• The radiation field diameter increases in proportion to the SSD ratio.
• The size of the radiation field (area) increases in proportion to the square of the SSD ratio.
22 Operation 2018-02-20
Disinfection, Replacement / Optional Parts and Storage
(1) Disinfection
After each use (patient), disinfect the cone, head rest, chair seat and seat height adjust lever by wiping them with Ethanol
for Disinfection (Ethanol 70 vol% to 80 vol%).
If it is not possible to obtain Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%), use one of the disinfectants listed
below; do not use any other type of disinfectant.
• DÜRR DENTAL’s FD 322 quick disinfectant
• DÜRR DENTAL’s FD 333 quick disinfectant
• DÜRR DENTAL’s FD 360 imitation leather cleaning and care
• DÜRR DENTAL’s FD 366 sensitive Rapid disinfection
Wipe the operation panel with Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%).
Use only Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%) or a neutral detergent to clean outer surfaces. Alkali or acidic solutions, cresol liquid
soap, and other chemicals can cause discoloration and surface damage.
Dampen a soft cloth with Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%) or a neutral detergent, and wring it out thoroughly. Make sure no
liquid seeps inside; this could cause mechanical or other malfunctions.
Use Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%) to immediately wipe off any water, detergent or other chemicals that get on the outer sur-
faces.
Do not directly spray Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%), neutral detergent or water on the unit. Make sure no liquid seeps inside;
this could cause mechanical or other malfunctions.
Do not use ozone water to clean the unit. Ozone water could damage to the unit.
Do not disinfect the clinic with ozone gas or ultraviolet light. This could damage plastic and rubber components.
The X-ray image receptor must be cleaned or disinfected for each patient in order to avoid cross infection between patients. For cleaning or disinfec-
tion of the receptor, follow the instructions of the receptor’s manufacturer.
• Do not fail to turn the power switch off. This will avoid the risk of electric shocks, burns, or accidentally pressing a switch.
Operation 2018-10-22 23
(2) Replacement Parts
* Replace the parts as necessary depending on degree of wear and length of use.
* Order parts from your local dealer or J. MORITA OFFICE.
* Fuses F1 and F2 for R-Type located on Filter PCB.
* Fuses F1 for WA-Type located on Filter PCB.
6112473 Main Fuse(For EX-2) F10 A 250 V Fast-acting, High Breaking Capacity, 1
Size: 5 × 20 mm
(4) Storage
* For transport and storage conditions, refer to page 32.
■ Do not expose to direct sunlight frequently or for long times.
■ If the unit has not been used for a long time, make sure it works properly before using.
• The Filter PCB remains live even if the Power Switch is turned off. Unplug the Power Cord or turn off the Power Breaker in the Power Distribution Panel before
servicing.
24 Operation 2018-10-22
Maintenance and Inspection
Regular Inspection
■ Maintenance and inspection are generally consider to be the duty and obligation of the user, but if, for some reason, the user
is unable to carry out these duties, they may be performed by the accredited service personnel. Contact your local dealer or J.
MORITA OFFICE for details.
■ Replace the parts listed in the Parts Lists as necessary depending on degree of wear and length of use.
■ This apparatus should be inspected every 6 months in accordance with the following maintenance and inspection items.
■ The inspection items marked * may only be performed by the service personnel for further preventive inspection and mainte-
nance during the life of the device.
Operation 2018-02-20 25
Service Life
Service life refers to the standard period the unit or individual components can be expected to be usable as long as inspection
and maintenance procedures specified by J. MORITA MFG. CORP. are followed.
Component Service Life List refers to components that can be expected to wear out, degrade or break depending on frequency
and conditions of usage, which greatly affects how long these components retain their performance standards.
The product warranty is good for 3 years after delivery.
The components on the Component Service Life List that are noted “Yes” are critical for safety. These components must be
inspected and replaced or have appropriate maintenance performed as necessary without fail before their standard service life
expires.
The user must pay for parts and repairs that are performed after the warranty expires or the part has passed its specified service
life. However, if a maintenance contract has been agreed to, this will depend on the contents of that contract.
For details concerning regular inspection and parts replacements, contact your local dealer or J. MORITA OFFICE.
Moving Parts (for Arm and Lift) 30,000 exposures or 4 years Yes Including cables, bearings,
whichever comes first. etc.
*1 The service life of the X-ray tube depends on the number and length of exposures it is used for as well as the output (tube
voltage and current) and the time between exposures. Of these factors, the most critical is the number of exposures which
degrades the anode. As the anode gradually degrades, stable output is lost, and the circuit protection system detects errors
and terminates X-ray emission.
⹅ Service
26 Operation 2018-10-22
Troubleshooting
If the equipment does not seem to be working properly, the user should first try to inspect and adjust it himself.
* If the user is unable to inspect the equipment himself or if the equipment fails to work properly after being adjusted or after
parts are replaced, contact your local dealer or J. MORITA OFFICE.
* The inside parts of the equipment are charged with high voltage. Do not attempt to perform maintenance or adjustment that is
not described in the troubleshooting table.
* If an accident occurs, the equipment must not be used until repairs have been completed by a qualified and trained technician
provided by the manufacturer.
No power when power • No power supply • Check the breaker on the distribution panel.
switch is turned on.
Cannot expose X-ray • Ready Indicator on the Control Panel is • Downtime until next emission operation.
even if emission key/ flashing. Wait until Ready Indicator lights up.
emission button is
pushed.
Beep sounds and • Turn off the power supply. After all LEDs on the control panel are turned off, turn on the power
setting value of supply. (Abnormality of software or breakdown of control panel’s board.)
exposure time will be
set 2.0 sec. or 0.01 sec.
Pole goes down by • Take out the screw in the back of the support column and
Spacer
itself. then remove the spacer. Replace the screw and use the
Screw
unit without the spacer.
(Do not use the unit this was too long; it could be damaged.
Have it repaired as soon as possible.)
⹅ Error Numbers
* Check the list below if an error number appears in the display on the control panel.
If other error No. is shown, turned the unit off, wait 1 minute, and then turn it on again
* Contact your local dealer or J. MORITA OFFICE if the apparatus does not work normally even after performing the steps
recommended below.
E00 Emission key/ emission button is To clear the message, press any key on the control panel (except
released before the exposure end the Emission key).
Hold the emission key/ emission button down until the exposure
is completed.
E05 Abnormal Head Temperature The internal temperature of the head is out of the range.
If the head overheats due to repeated use, turn the unit off and
wait for it to cool down.
If the ambient temperature is low, heat the room and wait for the
unit to warm up.
Operating Ambient Temperature: +10°C to +40°C
E09 Inverter overheated. It is the overheating of the inverter due to repeated use. Turn the
unit off and wait for it to cool down.
Operation 2018-10-22 27
Technical Specifications
Specifications
Model V080
Type EX-2
This unit is X-ray generator which includes X-ray source assembly and high-voltage generator.
Disinfection Methods By wiping with Ethanol for Disinfection (Ethanol 70 vol% to 80 vol%).
Intended Use
Model V080 is a Dental X-ray unit using with an intra-oral X-ray image receptor. Model V080 is used for dental radiographic
examination and diagnosis of teeth, jaw and oral structure by exposing an X-ray image receptor to ionizing radiation.
To obtain diagnostic images, an appropriate imaging receptor shall be used with this device.
- CCD/CMOS type receptor: Detector line pair resolution 5 lp/mm or more, low contrast resolution diameter 1.0 mm or more.
- Imaging Plate type receptor: Scan resolution 5 lp/mm or more, low contrast resolution diameter 1.0 mm or more.
- Film: ISO speed of D or higher. E or F recommended.
For the European market, the receptor shall bear the CE marking.
X-ray Tube
Manufacturer / Model Toshiba or Canon Electron Tubes & Devices / D-0711SB
Focal Spot 0.7 (IEC 60336)
Target Angle 16 degrees
Target Material Tungsten
Inherent Filtration At least 1.0 mmAl
Nominal Anode Input Power 940 W (1 sec.)
Maximum Anode Heat Content 7 kJ (10 kHU)
Nominal Tube Voltage 70 kV
Circuit (Center-Grounded) Constant Potential (DC)
Maximum Filament Current 3.0 A
Filament Voltage 3.0 V – 3.7 V (At max. Filament Current 3.0 A)
Filament Frequency Limits 0 kHz – 20 kHz
28 Operation 2018-10-22
Specifications
Operation 2018-10-22 29
Specifications
Power Requirements
Rated Nominal Voltage AC 220 – 240 V, 50 – 60 Hz single phase
*WA-Type: Permanently installation
*R-Type: Plug-connection
Measurement Bases
The kV is: Actual X-radiation is monitored by Non Invasive Evaluator of Radiation Output. The mA is measured by monitoring
current in the HT return line, which equals the tube current.
Exposure time: Starting point of exposure is determined at the time when the kV value reaches to 75% of average kV value.
Termination of exposure is determined at the time when the kV value decreases to 75% of average kV value.
30 Operation 2018-02-20
Specifications
Mechanical Parameters
Weight R-Type: Approximately 33 kg (net)
WA-Type: Approximately 25 kg (net)
R-Type
156 52
340° 540° 115 27
180°
255
360 280
300°
278
1480~2140
1350/1450
92
219
860~1520
385~485
375
535 515
WA-Type
57
105
250°
180 °
° 540
1850/2100/2300
550/800/1000 1300
700
100
1245
875
100
1200
333
∅25
275
120
105
175 48
Floor
Operation 2018-10-22 31
Specifications
Reference Axis
Standard Cone [Long Cone]
Focal Spot (0.7) Collimator
(Unit: mm)
Max. Φ60
151 [183]
SSD: 200 [303]
Environmental Data
Operating Conditions
Ambient Temperature +10°C to +40°C
Humidity 30% to 75% (without condensation)
Atmospheric Pressure 70 kPa to 106 kPa
Transportation and Storage Conditions
Ambient Temperature -10°C to +50°C
Humidity 5% to 85% (without condensation)
Atmospheric Pressure 50 kPa to 106 kPa
Original Language
English
Disposal
The package should be recycled. Metal parts of the equipment are disposed as scrap metal. Synthetic materials, electrical
components, and printed circuit boards are disposed as electrical scrap. Material must be disposed according to the relevant
national legal regulations. Consult specialized disposal companies for this purpose. Please inquire of the local city/community
administrations concerning local disposal companies.
This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted munici-
pal waste and must be collected separately. Contact your local dealer or J. MORITA OFFICE for details.
32 Operation 2018-10-22
Specifications
Heating: 4.9 W
Heat Storage (kJ)
Cooling
Time (min.)
Operation 2018-02-20 33
Specifications
Cooling
Heating
Time (min.)
34 Operation 2018-02-20
Symbols and Markings
⹅ R-Type
Power Switch
| : On
: Off
Rating Label
Long SSD Adaptor (option)
Focal Spot
(dimple)
⹅ WA-Type
X-ray Tube Head
Assembly Label
Long SSD Adaptor Label
Rating Label
Focal Spot
(dimple)
Power Switch
| : On
: Off
⹅ Package
Prescription Device
CAUTION: Federal law restricts this device to sale by or on the order of a dentist and a licensed healthcare practitioner. (Valid only for U.S.A.)
Operation 2019-04-22 35
Symbols and Markings
⹅ Rating Label, X-ray Tube Head Assembly Label, Long SSD Adaptor Label (option),
and Operating Instructions
Marking of electrical equipment in accordance with EU authorized representative under the European
the European Directive 2012/19/EU (WEEE) Directive 93/42/EEC
(Valid only for EU) (Valid only for EU)
● Indicated Items on the Rating Label, X-ray Tube Head Assembly Label, and Long SSD Adaptor
Label (option)
* For details, refer to “Technical Specifications” (p. 28).
* Some symbols described in this page may be included.
Exposure Time: Max. X-ray exposure time X-RAY FIELD: X-ray field size
Nom. Focal Spot Value: Nominal focal spot value Ser. No.: Serial number
36 Operation 2020-03-23
Electromagnetic Disturbances (EMD)
The Veraview iX (hereafter “this device”) conforms to IEC 60601-1-2:2014 Ed. 4.0, the relevant international standard for
electromagnetic disturbances (EMD).
The following is the “Guidance and Manufacturer’s Declaration” which is required by IEC 60601-1-2:2014 Ed. 4.0, the relevant
international standard for electromagnetic disturbances.
This device is intended for use in the electromagnetic environment specified below.
The customer or the user of this device should assure that it is used in such an environment.
Conducted disturbance Group 1 This device uses RF energy only for its internal function. Therefore, its
CISPR 11 Class B RF emissions are very low and are not likely to cause any interference in
nearby electronic equipment.
Radiated disturbance Group 1 This device is suitable for use in all establishments, including domestic
CISPR 11 Class B establishments and those directly connected to the public low-voltage
power supply network that supplies buildings used for domestic
purposes.
• The use environment of this device is the Professional healthcare facility environment.
• This device needs special precautions regarding EMD and needs to be installed and put into service according to the EMD information provided in the ACCOM-
PANYING DOCUMENTS.
• Use of parts other than those accompanied or specified by J. MORITA MFG. CORP. could result in increased electromagnetic emissions or decreased electro-
magnetic immunity of this device and result in improper operation.
• Do not use this device as adjacent or stacked as possible with other. When adjoining or stacking is necessary, use it after observing whether this equipment
and other equipment work properly.
• Portable and mobile RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30
cm to any part of the V080, including cables specified by the manufacturer.
Operation 2018-10-22 37
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
This device is intended for use in the electromagnetic environment specified below.
The customer or the user of this device should assure that it is used in such an environment.
Electromagnetic Environment
Immunity Test IEC 60601 Test Level Compliance Level
– Guidance
Electrical fast ±2 kV for power supply lines ±2 kV for power supply lines Mains power quality should be that
transients/bursts ±1 kV for input/output lines ±1 kV for input/output lines of a typical commercial or hospital
IEC 61000-4-4 environment.
Surge AC/DC power AC/DC power Mains power quality should be that
IEC 61000-4-5 ±0.5 kV, ±1 kV line(s) to line(s) ±0.5 kV, ±1 kV line(s) to line(s) of a typical commercial or hospital
±0.5 kV, ±1 kV, ±2 kV line(s) to ±0.5 kV, ±1 kV, ±2 kV line(s) to environment.
earth earth
Signal input/output Signal input/output*1
±2 kV line(s) to earth ±2 kV line(s) to earth
Voltage dips, short dips dips Mains power quality should be that
interruptions and 0% UT: 0.5 cycle (at 0, 45, 90, 0% UT: 0.5 cycle (at 0, 45, 90, of a typical commercial or hospital
voltage variations on 135, 180, 225, 270, 315°) 135, 180, 225, 270, 315°) environment.
power supply lines 0% UT: 1 cycle (at 0°) 0% UT: 1 cycle (at 0°) If user of this device requires
IEC 61000-4-11 70% UT: 25/30 cycles (at 0°) 70% UT: 25/30 cycles (at 0°) continued operation during
25 (50 Hz)/30 (60 Hz) 25 (50 Hz)/30 (60 Hz) power mains interruptions, it is
short interruptions short interruptions recommended that this device be
0% UT: 250/300 cycles 0% UT: 250/300 cycles powered from an uninterruptible
250 (50 Hz)/300 (60 Hz) 250 (50 Hz)/300 (60 Hz) power supply or a battery.
Power frequency 30 A/m (r.m.s.) 30 A/m (r.m.s.) Power frequency magnetic field
(50/60 Hz) 50 Hz or 60 Hz 50 Hz or 60 Hz should be at levels characteristic
magnetic field of a typical location in a typical
IEC 61000-4-8 commercial or hospital environment.
NOTE 1: UT is the a.c. mains voltage prior to application of the test level.
NOTE 2: r.m.s.: root mean square
*1: Not applicable because it does not connect directly to outdoor cable.
38 Operation 2018-10-22
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
This device is intended for use in the electromagnetic environment specified below.
The customer or the user of this device should assure that it is used in such an environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment – Guidance
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
(a) Field strengths from fixed transmitters, such as base stations for ratio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicated 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 this device is used exceeds the applicable RF compliance level above, this
device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting of relocating this device.
(b) Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
(c) The ISM (Industrial, Scientific and Medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553
MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
Operation 2018-02-20 39
Essential Performance
• No X-ray irradiation without an active operation of the emission button or emission key.
• X-ray termination is done by releasing the emission button or emission key.
NOTE:
If the essential performance is lost or degraded due to electromagnetic disturbance, X-ray termination would not be done by
releasing the emission button or emission key, or X-ray would be irradiated without an active operation of the emission button
or emission key.
40 Operation 2018-10-22
Pub. No.: X4081-EN-5 Printed in Japan