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User Guide
Notice
Congratulations on your purchase of the CS 2200. Thank you for your confidence in our products and we will do all in our
power to ensure your complete satisfaction.
The User Guide for the CS 2200 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.
0086
Manufacturer
Care stream Hea lth, Inc.
150 Verona Street
Roche ster, NY 1 4 60 8, USA
EC REP
TROPHY
4, Rue F. Pelloutier, Croissy-Beaubourg
77435 Marne la Vallée Cedex 2, France
Contents
4—ACQUIRING AN IMAGE
Preparing for Image Acquisition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4–1
Launching the X-Ray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4–2
Setting the Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4–2
5—USER MODE
Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–1
Entering the User Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–1
Modifying Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5–2
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
Control timer unit and electrical installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7–1
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 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 CS 2200 unit has been designed to produce high-quality intraoral radiographies that:
Reduced X-ray doses for patients because the CS 2200 unit emits fewer soft rays
absorbed by patients which are not used during image creation.
Shorter exposure times which reduce the risk of motion blur during exposure
The CS 2200 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, a red LED lights up on the control
timer unit 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,
phosphor plates or sensor)
Processing the film (if a conventional film is used.)
General Overview
The CS 2200 unit is composed of the following functional components
Extension R Span A
A rectangular collimator. Its various sizes adapt to films, phosphor plates and RVG
sensors. It is recommended to use such a collimator if possible, in order to limit the
radiation absorbed by patients.
7 8
5
2 1
3
6
Figure 2–3 Standard CS 2200 Unit. with Separate Control Timer Unit
7 8
5
3 1
4
6
8
5
1
3
2
7
5
8
1
4
7
6
9
3
1
7
6 2
3
2
6
4
8
5
9 7
10 11
13 12
90°
Paralleling technique
The positioning tool used in the paralleling technique allows you to align the beam and the image
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, digital sensor, or phosphor plate) has its own sensitivity to X-ray
radiation. the receptor 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.
The CS 2200 allows you to use two different modes with pre-set exposure times. These modes
are programmed when installing the equipment based on your local imaging systems, as indicated
in Tables 3-3 to 3-5. These tables meet the manufacturer's standard conditions and should only be
used as guidelines.
Adjust your exposure settings as needed, based on the results obtained from your system
exposure and processing.
Adjust your exposure settings after a change to your imaging system.
To modify the settings, start the “Setting the Mode” procedure.
The CS 2200 also allows you to use the manual mode where you select the exposure time directly.
Exposure Times
Tables 3-1 and 3-2 indicate exposure times that were defined based on a unit equipped with a
standard cone of 20 cm (8 in.) focus-to-skin distance.
70 kV - 7 mA) 60 kV - 7 mA
Mandibular
Incisor / Bicuspid 0.099 0.150 0.189 0.198 0.300 0.378
Premolar 0.106 0.160 0.202 0.211 0.320 0.403
Molar 0.119 0.180 0.227 0.238 0.360 0.454
Bitewing
Anterior 0.099 0.150 0.189 0.198 0.300 0.378
Posterior 0.119 0.180 0.227 0.238 0.360 0.454
Occlusal
Emitted Doses
To obtain the dose in mGy.cm2, multiply the values listed in table 3-6 by the exposed surface. The
exposed surface depends on the collimator type used as indicated in table 3-7.
70 kV - 7 mA 60 kV - 7 mA
D D D D D D D D
t(s) t(s) t(s) t(s) t(s) t(s) t(s) t(s)
mGy mGy mGy mgY mGy mGy mGy mgY
0.010 0.09 0.260 2.22 0.510 4.36 0.760 6.49 0.010 0.06 0.260 1.58 0.520 3.17 1.050 6.40
0.020 0.17 0.270 2.31 0.520 4.44 0.770 6.58 0.020 0.12 0.270 1.64 0.540 3.29 1.100 6.70
0.030 0.26 0.280 2.39 0.530 4.53 0.780 6.66 0.030 0.18 0.280 1.71 0.560 3.41 1.150 7.01
0.040 0.34 0.290 2.48 0.540 4.61 0.790 6.75 0.040 0.24 0.290 1.77 0.580 3.53 1.200 7.31
0.050 0.43 0.300 2.56 0.550 4.70 0.800 6.83 0.050 0.30 0.300 1.83 0.600 3.65 1.250 7.62
0.060 0.51 0.310 2.65 0.560 4.78 0.810 6.92 0.060 0.37 0.310 1.89 0.620 3.78 1.300 7.92
0.070 0.60 0.320 2.73 0.570 4.87 0.820 7.00 0.070 0.43 0.320 1.95 0.640 3.90 1.350 8.22
0.080 0.68 0.330 2.82 0.580 4.95 0.830 7.09 0.080 0.49 0.330 2.01 0.660 4.02 1.400 8.53
0.090 0.77 0.340 2.90 0.590 5.04 0.840 7.17 0.090 0.55 0.340 2.07 0.680 4.14 1.450 8.83
0.100 0.85 0.350 2.99 0.600 5.12 0.850 7.26 0.100 0.61 0.350 2.13 0.700 4.26 1.500 9.14
0.110 0.94 0.360 3.07 0.610 5.21 0.860 7.34 0.110 0.67 0.360 2.19 0.720 4.38 1.550 9.44
0.120 1.02 0.370 3.16 0.620 5.29 0.870 7.43 0.120 0.73 0.370 2.25 0.740 4.51 1.600 9.75
0.130 1.11 0.380 3.25 0.630 5.38 0.880 7.52 0.130 0.79 0.380 2.31 0.760 4.63 1.650 10.05
0.140 1.20 0.390 3.33 0.640 5.47 0.890 7.60 0.140 0.85 0.390 2.38 0.780 4.75 1.700 10.36
0.150 1.28 0.400 3.42 0.650 5.55 0.900 7.69 0.150 0.91 0.400 2.44 0.800 4.87 1.750 10.66
0.160 1.37 0.410 3.50 0.660 5.64 0.910 7.77 0.160 0.97 0.410 2.50 0.820 4.99 1.800 10.97
0.170 1.45 0.420 3.59 0.670 5.72 0.920 7.86 0.170 1.04 0.420 2.56 0.840 5.12 1.850 11.27
0.180 1.54 0.430 3.67 0.680 5.81 0.930 7.94 0.180 1.10 0.430 2.62 0.860 5.24 1.900 11.57
0.190 1.62 0.440 3.76 0.690 5.89 0.940 8.03 0.190 1.16 0.440 2.68 0.880 5.36 1.950 11.88
0.200 1.71 0.450 3.84 0.700 5.98 0.950 8.11 0.200 1.22 0.450 2.74 0.900 5.48 2.000 12.18
0.210 1.79 0.460 3.93 0.710 6.06 0.960 8.20 0.210 1.28 0.460 2.80 0.920 5.60 2.100 12.79
0.220 1.88 0.470 4.01 0.720 6.15 0.970 8.28 0.220 1.34 0.470 2.86 0.940 5.72 2.200 13.40
0.230 1.96 0.480 4.10 0.730 6.23 0.980 8.37 0.230 1.40 0.480 2.92 0.960 5.85 2.230 14.01
0.240 2.05 0.490 4.18 0.740 6.32 0.990 8.45 0.240 1.46 0.490 2.98 0.980 5.97 2.240 14.62
0.250 2.14 0.500 4.27 0.750 6.41 1.000 8.54 0.250 1.52 0.500 3.05 1.000 6.09 2.500 15.23
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 developer and 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 CS 2200 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. From the control timer unit, select the exposure mode using .
When the correct mode is displayed, the corresponding indicator lights up.
4. From the control timer unit, press on to select the patient type: Child, Adult
(standard), or Adult (large),
Tooth when using the automatic mode or the bitewing or occlusal program.
Exposure time when using the manual mode.
The unit is now ready for acquisition.
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 exposure, 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 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 3-6.
The latest parameter settings are kept until a new image acquisition is performed.
2. Press and hold simultaneously for at least three seconds until the display
blinks.
3. If necessary, modify the setting by rotating until the desired setting is displayed.
Parameters
Table 5–1 Parameters Available through the User Mode
NOTE
The specific country value is equal to the
international telephone country code.
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 03) and its setting (for example, "0").
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 .
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. The red light of the
cooling cycle is lit.
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.
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.
I 01 and red Cooling cycle: this message can appear during Do not switch OFF the equipment.
LED lights up intensive use period.
on the control The information message disappears
timer unit. as soon as the system reaches a
satisfactory temperature.
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 CS 2200.
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 make an
exposure (manual mode, 60 kV, 0.1 sec).
The “E01” message is displayed when you launch an X-ray (manual mode, 60 kV, 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 either an intermediate disinfectant or a low-level disinfectant.
CAUTION
Liquids must not drip into the equipment.
Do not spray cleaner or disinfectant directly on the equipment.
Follow the manufacturer’s safety recommendations when using a
cleaner or a disinfectant.
7–2 MAINTENANCE