CS 2100 System User Guide
CS 2100 System User Guide
www.kodakdental.com
User’s Guide
The User Guide for the KODAK 2100 Intraoral X-ray System includes information on the usage of the equipment. We
recommend that you thoroughly familiarize yourself with this Guide in order to make the most effective use of your system.
No part of this Guide may be reproduced without the express permission of Carestream Health, Inc.
U.S. Federal law restricts this equipment to sale by or on the order of a dentist or physician.
In this Guide, all trademarks and registered trademarks are the property of their respective holders.
The Brand names and logos reproduced in this Guide are copyright.
KODAK is a trademark of KODAK used under Licence.
KODAK 2100 Intraoral X-Ray System complies with Directive 93/42/CEE relating to medical equipment.
0086
Manufacturer
Care stream Hea lth, Inc.
150 Verona Street
Roche ster NY 14 608
EC REP
TROPHY
4, Rue F. Pelloutier, Croissy-Beaubourg
77435 Marne la Vallée Cedex 2, France
Contents
1—About This Guide
Conventions in this Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–1
4—ACQUIRING AN IMAGE
Preparing for Image Acquisition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4–1
Launching the X-Ray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4–2
5—USER MODE
Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–1
Entering the User Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–1
Modifying Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–1
Exiting the User Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–2
Performing a Tube Seasoning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–2
6—TROUBLESHOOTING
Quick Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6–1
Information Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6–3
Error Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6–4
7—MAINTENANCE
Quarterly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7–1
Generator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7–1
Mechanical support. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7–1
2
Chapter 1
About This Guide
Conventions in this Guide
The following special messages emphasize information or indicate potential risk to personnel or
equipment:
WARNING
Warns you to avoid injury to yourself or others by following the
safety instructions precisely.
CAUTION
Alerts you to a condition that might cause serious damage.
IMPORTANT
Alerts you to a condition that might cause problems.
NOTE
Emphasizes important information.
TIP
Provides extra information and hints.
WARNING
Exposure to ionizing radiation
The KODAK 2100 unit has been designed to produce high-quality intraoral radiographies that:
The KODAK 2100 Intraoral X-ray system uses a high-frequency technology that allows:
• Reduced X-ray doses for patients because the KODAK 2100 unit emits fewer soft
rays absorbed by patients which are not used during image creation.
• Shorter exposure times which reduce the risk of motion blurr during exposure
The KODAK 2100 Intraoral X-ray system is equipped with a thermal safety system that prevents
the generator from overheating in case of intensive use. This prohibits any exposure as long as the
generator has not cooled down. The I01 error message appears on the display and an audible
beep is heard during the unit cooling period. The beep stops when the cooling period is over.
To obtain high-quality intraoral radiography with maximum details, you must be very careful when
performing the three steps of the radiography process:
• Positioning the patient, the X-ray generator, and the imaging system
• Setting the exposure parameters according to the imaging receptor used (film or
sensor)
• Processing the film (if a conventional film is used.)
General Overview
The KODAK 2100 Intraoral X-ray unit is composed of the following functional components
Extension R Span A
• A rectangular collimator. Its various sizes adapt to films and RVG sensors. It is
recommended to use such a collimator if possible, in order to limit the radiation absorbed
by patients.
The KODAK 2100 Intraoral X-ray unit is also composed of a remote exposure switch which is an
optional accessory.
7
8 5
2 1
4 3
6
7
8 5
2 1
NOTE
This configuration is an optional configuration
5
8
1
4
1
3
6 7
9
1 7
4
8
6 2
1
3 S
mGy 60 kV - 7 mA
+
8
_
2
7 digital - push
9
6
90°
Paralleling technique
The positioning tool used in the paralleling technique allows you to align the beam and the imaging
receptor. An appropriate collimator reduces the dosage by limiting the surface exposure.
Bisecting technique
When using the bisecting technique, do not use a rectangular collimator. This limits the risk of
X-ray beam and image receptor misalignment.
90°
If you do not position the film or the sensor correctly, this results in errors on the radiography, such
as distorted teeth and roots, elongation, magnification, and/or overlapping contacts. The
paralleling technique generally reduces the risk of such errors. However, if you do not position the
system correctly, angulation errors can occur (angulation of the receptor to the tooth itself).
If the beam exit pattern is not aligned with the imaging receptor, then part of the radiography will
not be exposed to radiation and the final radiography will have some clear (unexposed) areas. This
defect is called “cone cuts".
The imaging receptor is marked to indicate the tube side. If the orientation is not correct, the
resulting radiography is lighter and may show artifacts, such as foil pattern or sensor cable.
Exposure
Exposure Parameters
Since each receptor (film, phosphor plate or digital sensor) has its own sensitivity to X-ray
radiation. the sensor choice impacts the exposure parameters. For instance, the sensitivity class
for conventional dental films is characterized with the letter D, E, or F where F is more sensitive
than E, and E more sensitive than D. Consequently, the required dose for the correct exposure
goes down as sensitivity increases.
Due to the different sensitivity of the digital sensors, you also need to adjust the exposure
parameters to the used sensor type (film or digital equipment).
The KODAK 2100 Intraoral X-ray system allows you to select the exposure times. The exposure
times indicated in Tables 3-1 to 3-4 meet the manufacturer’s recommendations. Depending on the
used sensor type, you can change the mode by pressing and holding the selection knob for at
least three seconds. To set the exposure times, see the Preparing for Image Acquisition section.
Exposure Times
Exposure Times for Film
The indicated exposure times are given as a guideline.
60 kV - 7 mA - Cone 20 cm (8 in.)
Maxillary Mandibular Bitewing Occlusal
Anterior Premolar Molar Anterior Premolar Molar Anterior Posterior
KODAK Child 0.250 0.320 0.400 0.200 0.250 0.250 0.200 0.250 0.500
ULTRA-
SPEED Adult 0.400 0.500 0.630 0.320 0.400 0.400 0.320 0.400 0.630
(D)
KODAK Child 0.100 0.125 0.160 0.080 0.100 0.100 0.080 0.100 0.200
INSIGHT
(F) Adult 0.160 0.200 0.250 0.125 0.160 0.160 0.125 0.160 0.250
KODAK Child 0.250 0.320 0.400 0.200 0.250 0.250 0.200 0.250 0.500
D-SPEED Adult 0.400 0.500 0.630 0.320 0.400 0.400 0.320 0.400 0.630
KODAK Child 0.125 0.160 0.200 0.100 0.100 0.125 0.100 0.125 0.200
E-SPEED Adult 0.200 0.250 0.250 0.160 0.160 0.200 0.160 0.200 0.320
60 kV - 7 mA - Cone 20 cm (8 in.)
Maxillary Mandibular Bitewing Occlusal
Anterior Premolar Molar Anterior Premolar Molar Anterior Posterior
Child 0.250 0.320 0.400 0.200 0.250 0.250 0.200 0.250 0.500
CR7400
Adult 0.400 0.500 0.630 0.320 0.400 0.400 0.320 0.400 0.630
60 kV - 7 mA - Cone 20 cm (8 in.)
Maxillary Mandibular Bitewing Occlusal
Anterior Premolar Molar Anterior Premolar Molar Anterior Posterior
KODAK Child 0.100 0.125 0.160 0.080 0.080 0.100 0.080 0.100 0.160
RVG 5100 Adult 0.160 0.160 0.200 0.125 0.125 0.160 0.125 0.160 0.250
Child 0.100 0.125 0.160 0.080 0.080 0.100 0.080 0.100 0.160
KODAK
RVG 5000
Adult 0.160 0.160 0.200 0.125 0.125 0.160 0.125 0.160 0.250
TROPHY Child 0.100 0.125 0.160 0.080 0.080 0.100 0.080 0.100 0.160
RVG
Access Adult 0.160 0.200 0.200 0.125 0.125 0.160 0.125 0.160 0.250
KODAK Child 0.080 0.100 0.125 0.063 0.080 0.080 0.063 0.080 0.125
RVG 6500 Adult 0.125 0.160 0.200 0.125 0.160 0.160 0.100 0.125 0.200
KODAK Child 0.080 0.100 0.125 0.063 0.080 0.080 0.063 0.080 0.125
RVG 6100
(size 1& 2) Adult 0.125 0.160 0.200 0.125 0.160 0.160 0.100 0.125 0.200
Child 0.080 0.100 0.125 0.063 0.080 0.080 0.063 0.080 0.125
KODAK
RVG 6000
Adult 0.125 0.160 0.200 0.125 0.160 0.160 0.100 0.125 0.200
TROPHY Child 0.080 0.100 0.125 0.063 0.080 0.080 0.063 0.080 0.125
RVG
Ultimate Adult 0.125 0.160 0.200 0.100 0.100 0.125 0.100 0.125 0.200
TROPHY Child 0.080 0.100 0.125 0.063 0.063 0.080 0.063 0.080 0.125
RVG
Reference
High
Resolution Adult 0.125 0.160 0.160 0.100 0.100 0.125 0.100 0.125 0.200
mode
TROPHY Child 0.080 0.100 0.125 0.063 0.063 0.080 0.063 0.080 0.125
RVGui High
Resolution
mode Adult 0.125 0.160 0.160 0.100 0.100 0.125 0.100 0.125 0.200
TROPHY Child 0.020 0.025 0.032 0.016 0.020 0.020 0.016 0.020 0.040
RVG
Reference
High
Sensitive Adult 0.032 0.040 0.050 0.025 0.032 0.032 0.025 0.032 0.050
mode
TROPHY Child 0.020 0.025 0.032 0.016 0.020 0.020 0.016 0.020 0.040
RVGui High
Sensitivite
mode Adult 0.032 0.040 0.050 0.025 0.032 0.032 0.025 0.032 0.050
Child 0.040 0.050 0.063 0.032 0.040 0.040 0.032 0.040 0.080
TROPHY
RVG THD
Adult 0.063 0.080 0.100 0.050 0.063 0.063 0.050 0.063 0.100
KODAK Child 0.040 0.050 0.063 0.032 0.040 0.040 0.032 0.040 0.080
RVG 6100
size 0 Adult 0.063 0.080 0.100 0.050 0.063 0.063 0.050 0.063 0.100
The following table is a template that you may fill in according to your specific conditions.
60 kV - 7 mA - Cone 20 cm (8 in.)
Maxillary Mandibular Bitewing Occlusal
Anterior Premolar Molar Anterior Premolar Molar Anterior Posterior
Child
Adult
Child
Adult
Emitted Doses
To obtain the dose in mGy.cm2, multiply the values listed in Table 3-5 by the exposure surface. The
exposure surface depends on the used collimator type as indicated in Table 3-6.
60 kV - 7 mA
NOTE
Dose accuracy: +/- 30% (mGy)
Film Processing
When using conventional films, you must process the film according to the manufacturer’s
instructions. Process the film under safelight conditions manually or using an automatic processor.
If you use an automatic processor, see the processor’s manual. Check that the processor
maintenance is performed regularly.
If you process the film manually, follow precisely the manufacturer’s recommendations for solution
preparation, processing time, and solution temperature for both the developer and the fixer baths.
Any deviation from the manufacturer’s recommendations (such as a solution that would be too
concentrated or diluted, too hot or cold, or if the film processing duration is incorrect) will impact
the final radiography quality.
Before archiving, do not forget to wash the film correctly and to dry it in a clean place.
If necessary, for example after a long inactivity period of the KODAK 2100 system, we recommend
to start with the tube seasoning procedure. For more information, see the Tube Seasoning
Procedure.
When you switch ON the unit, a self-test starts automatically. It checks the display. When the test
is completed, a short beep sounds. If an error occurs, an error code appears. For error messages,
see the Troubleshooting section.
2. Select the exposure mode (film or digital) by pressing and holding for at least three
seconds until the correct mode is displayed. The indicator lights up if you use a digital sensor
wherreas it is OFF if you use a film.
NOTE
Depending on your local regulations, you may disable this function. See the User
Mode section.
For more information on exposure times, see Tables 3-1, 3-2, 3-3, and 3-4.
NOTE
- If you use a film or a storage phosphor plate, the exposure time ranges from 0.05
to 1.25 sec.
- If you use a digital sensor, the exposure time ranges from 0.010 to 0.063 sec.
IMPORTANT
The operator must instruct the patient to refrain from moving during the
entire exposure.
WARNING
1. Press from the control timer unit or from the X-ray exposure switch.
2. Keep pressing until the X-ray emission indicator is OFF and the beep stops.
During the X-ray emission, the exposure time counts off on the display.
CAUTION
If you release the button before the end of the X-ray, a manipulator alarm
(E01) is enabled.
This indicates that the X-ray emission was aborted prematurely. There is an
underexposure risk. Depending on the remaining time, you can decide to
process the image or start a new image acquisition.
+
When the acquisition is completed, the emitted dose is displayed in mGy. The “mGy” indicator
lights up. For information on the emitted doses based on the exposure times, see Table 3-5.
The latest parameter settings are kept until a new image acquisition is performed.
+
Parameters
Table 5–1 Parameters Available through the User Mode
The self-test is enabled. While the self-test is in progress, the software information (for
example, F718 2.1) is displayed.
2. Once F718 2.1 is displayed, press shortly on from the control timer unit.
You access the menu, when "USER" is displayed. The display intermittently shows the first
parameter (P 01) and its setting (for example, "ON").
+
Modifying Parameters
To modify parameters, follow these steps:
+
4. To validate, press and hold for at least 3 seconds until "COPY" is displayed and a
beep is heard.
+
5. To keep the initial value, press on shortly. "ABOR" is displayed. The system returns to
the parameter/program mode.
To exit the user mode, press on shortly. “QUIT” is displayed until the system returns to the
operational mode. The self-test continues until it is completed.
1 Go to the User Mode menu and change parameter P 05 from OFF to ON.
The self-test continues. After the self-test is completed, I 02 is displayed. This message means
that the seasoning process must be started.
+
2 Press on .
The display blinks,. The sequence step number and the required exposure settings (kV, time)
are displayed alternatively.
4. Launch an X-ray.
WARNING
When the exposure is completed, the display blinks. The cooling error code (I 01) and the
remaining time required before the next step are displayed alternatively.
When the cooling cycle is completed, the display blinks. The next step number and its
exposure settings are displayed alternatively.
IMPORTANT
If the malfunction persists or more serious conditions occur, contact your
representative and stop the equipment.
When you call your representative, you must have the following information ready:
Quick Troubleshooting
Quick troubleshooting guides you through the actions you need to take to correct the
malfunctions.
The following table lists the malfunctions and the actions to take.
Control unit doesn't light up. The control unit is Connect the control unit.
disconnected.
Fuse F1 burnt out or is
Change the fuse.
defective.
The control unit is defective Call your representative.
Wait until the I01message is no longer
No X-ray emission The generator is cooling displayed.
The radiology control key is
defective. Call your representative.
6–2 TROUBLESHOOTING
Information Messages
Information Messages
An information “I” error code with a message appears on the display.
The following table lists the information messages and the actions to take.
IMPORTANT
If you switch OFF the system, the microprocessor does not calculate the
cooling time.
For safety reasons, it considers that the system has not gone through the
cooling cycle.
I 02 Request for X-ray tube seasoning. See the User Mode section.
Error Messages
The following table lists the error messages and the actions to take.
6–4 TROUBLESHOOTING
Chapter 7
MAINTENANCE
This chapter describes the maintenance tasks you must perform for your KODAK 2100 Intraoral
X-ray system
Quarterly
Generator
Check that:
Mechanical support
Check that:
Operation
WARNING
Check that:
• The audible signal is heard and the X-ray emission indicator is visible when you launch an
X-ray (exposure time: 0.1 sec).
• The “E01” message is displayed when you launch an X-ray (exposure time:1.0 sec) and
you release the control button before the exposure end.
• The self-test starts with a simultaneous display and alarm light test.
• Then, the system test starts. After the test is completed (indicated by a short beep), the
firmware version and the total number of exposures (divided by 10) performed by the unit
since first installation are displayed.
IMPORTANT
If a check result is not satisfactory, stop using the equipment and
contact your representative.
Annually
We recommend that a general inspection of the unit be carried out by an authorized service
technician provided by your representative.
1 Clean the outside of the equipment with a damp paper towel or a soft cloth using an
alcohol-based, non-corrosive cleaner.
2 Wipe off surfaces with disinfectant.
CAUTION
•Liquids must not drip into the equipment.
•Do not spray cleaner or disinfectant directly on the equipment.
•Protect the equipment from contamination using barriers
available from dental distributors.
•Follow the manufacturer’s safety recommendations when using a
cleaner or a disinfectant.
7–2 MAINTENANCE
2100
Intraoral X-Ray System
User’s Guide