Professional Documents
Culture Documents
Software 2.4X
Software
Ausgabe
Revision A
Datum
Date 07/07
Sprache Englisch
Language English
K1029084
Dornier Compact Alpha
Service Manual
English
Warning
No part of this Service Manual may be reproduced or transmitted in any form without
permission in writing from Dornier MedTech Systems GmbH.
All rights reserved in case of patent issue or design registration.
Manufacturer
Telephone: +49-8153-888-0
Fax: +49-8153-888-665
ii Compact Alpha.SM_GB_A
History of Revision
The list of the valid chapters indicates the last changes of the respective pages.
The designation of the revision of the changed or added chapters is shown at the bottom
of the pages (e.g.: Compact Alpha.SM_GB_A).
i -vi A
1 1.1 -1.6 A
2 2.1 - 2.16 A
3 3.1 - 3.4 A
4 4.1 - 4.10 A
5 5.1 - 5.32 A
6 6.1 - 6.20 A
7 7.1 - 7.24 A
8 8.1 - 8.38 A
9 9.1 - 9.16 A
10 10.1 - 10.28 A
11
12 12.1 - 12.18 A
13
14
15 15.1 - 15.16 A
A
B B.1 - B.4 A
C
D
G
I
iv Compact Alpha.SM_GB_A
WARNING The service instructions in this Service Manual are for use by qualified personnel
only. Perform no service unless you are qualified to do so.
Compact Alpha.SM_GB_A v
Table of Contents
NOTE Each chapter has its own table of contents.
Chapter Title
1 System Overview
2 Locate Components
3 Messages
4 Service Mode
5 Schematics
6 Shock-wave Positioning
7 Water Circuit
8 Shock-wave Circuit
9 Control Unit
10 Ultrasound Locating
11 Reserved
12 Computer
13 Reserved
14 Reserved
15 Patient Table
Appendices
A Reserved
B List of Parts
C FCO’s, EO’s and TIP’s
D Reserved
G Reserved
I Reserved
vi Compact Alpha.SM_GB_A
1 System Overview
Table of Contents
1.1 Introduction
NOTE An isocentric scanner guide is mounted at the therapy head for localization.
1.3.1 Dimensions
Frequency: 50/60 Hz ± 1 Hz
- during therapy 10 °C to 32 °C / 50 °F to 90 °F
- in storage (without water) -10 °C to 70 °C / 14 °F to 158 °F
- in storage (with water) 1 °C to 70 °C / 34 °F to 158 °F
Weight of patient:
- with Dornier Relax V1 – V3 max. 150 kg (330 lbs)
- with Dornier Relax + max. 180 kg (396 lbs)
NOTE The maximum load for the patient table Dornier Relax V3 in USA is increased to
204 kg (450 lbs) if the EO 75 is performed on the respective patient table.
The technical data are to see in the Operating Manual and in the Service Documentation
of the ultrasound device.
Table of Contents
Table of Figures
2.1 Introduction
Chapter 2 shows designators and locations for subassemblies and components of the
Dornier Compact Alpha.
2.2 Subassemblies
2.3 Components
Designator Component
1A1.A1 PCB Medico
1A1.A2 PCB Mediad
1A6 Shock wave generator
1A10 PCB Relay
1G1 Power Supply +5 VDC,+15 VDC, -15 VDC
1G2 Power Supply +24 VDC
1G3 Power Supply +24 VDC
1T1 Isolating transformer (Option)
1U1 Starting Current Limiter
1U2 Converter PCB
1X10 Power terminal
1Z1 Line filter
3U1 Converter PCB
Designator Component
1A4 Capacitor charging and trigger unit
1A5 Cooler
1A5/E1 Fan
1A7 Water circuit
Designator Component
1A1 Controller
1A1.A1 PCB Medico
1A1.A2 PCB Mediad
1A5 Cooler
1A5/E1 Fan
1A7 Water circuit
1A11 Diode module
1K1 – 1K6 Relays for brakes
1R2 Varistor, over voltage protection
1S1 Main switch ON/OFF
1X1 Power plug
1X2 Interface control unit
1X3 Interface ultrasound
1X5 Interface ECG
3U2 DC/DC converter (option for X-ray RTFI)
3X2 Interface isocentric scanner guide
Designator Component
1A7 Water circuit
1A7/B1 Temperature sensor
1A7/E1 Heater 500 W
1A7/M0 Circulation pump
1A7/S1 Level switch air separation
1A7/S2 Level switch refill container
1A7/S3 Flow switch
1A7/S4 Over temperature switch
1A7/VA2 Drain valve
1A7/VA3 Drain valve
1A7/VA4 Drain valve
1A7/Y2 Valve circulation
1A7/Y3 Valve filling
1A7/Y4 Valve air separation
Designator Component
1A7 Water circuit
1A7/B1 Temperature sensor
1A7/E1 Heater 500 W
1A7/F1 Filter
1A7/F2 Filter
1A7/M0 Circulation pump
1A7/M1 Degassing pump
1A7/S1 Level switch air separation
1A7/S2 Level switch refill container
1A7/S3 Flow switch
1A7/S4 Over temperature switch
1A7/VA2 Drain valve
1A7/VA3 Drain valve
1A7/VA4 Drain valve
1A7/Y2 Valve circulation
1A7/Y3 Valve filling
1A7/Y4 Valve air separation
Designator Component
2A1 PCB switch
2S1 Switch for the brakes of joints 3 and 4
2S2 Switch for the brake of the Y axis
2S3 Switch for the brake of joint 1
2S4 Switch for the brake of the Z axis
2X1 Interface brakes
2Y1 Brake for joint 1
2Y2 Brake for joint 2
2Y3 Brake for joint 3
2Y4 Brake for joint 4
2Y5 Brake Z axis
2Y6 Brake Y axis
2Y7 Brake Z axis
3B1 EMSE
3B5 Pressure sensor
3S1 Interlock switch
3X9 Connection PE
Table of Contents
Table of Tables
3.1 Introduction
Chapter 3 contains the messages, which may occur during the operation of the
Dornier Compact Alpha.
3.2 Description
Display H1 of the control unit is used to display messages and errors. Messages/errors
are displayed as text or as numbers.
Table 3-1 shows text messages.
Table 3-2 to Table 3-4 show the message numbers and the corresponding meanings.
Message Meaning
Message Meaning
Message Meaning
Message Meaning
Table of Contents
4.1 Introduction
NOTE The setting/reset of the EMSE shock-wave counter is possible in Service Level 1 as
from software version V2.42.
To activate Service Level 1, press keys frequency pos. (S3), frequency neg. (S2) and
shock-wave release key (S9). The keys must be pressed simultaneously and held down
as long as the Service Mode activation is detected. To return to the user program, press
the same three keys again.
Service Level 2 is activated when the DIL switch S1/3 on the PCB Medico has been set
to ON before activating the Dornier Compact Alpha as shown in Figure 4-1.
To return to the user program, deactivate the Dornier Compact Alpha and set DIL
switch S1/3 to OFF. Then the Dornier Compact Alpha can be started again as usual.
After startup in Service Mode, “10” (Setting menu) appears in display H1 on the control
unit. Display H2 shows “tOP”.
To move up and down through the menus, press S3 (frequency pos.) and S2
(frequency neg.). Pressing the Reset key S1 activates the selected menu.
Table 4-1 shows the available menus and corresponding displays.
NOTE The sub menus are described in this paragraph or there is a note in which chapter they
are described.
Figure 4-2 Switches and Display Elements of the Control Unit (partly)
H1 S1
H2
S2 S3
S4
H3 S5
’51 ‘ Test of the single keys of the control unit (description in chapter 9, page
9.11)
Table of Contents
5.1 Introduction
Chapter 5 contains schematics, wiring diagrams and ground plans for the
Dornier Compact Alpha
5.2 Schematics
Figure 5-1 Block Diagram, Power Supply 100 VAC – 240 VAC
Table of Contents
6.1 Introduction
6.2 Description
The shock-wave positioning consists of two horizontally mounted rotating joints (joint
3 and 4), two vertically mounted rotating joints (joint 1 and 2), a horizontal movement
(Z axis) and a vertical movement (Y axis).
The magnetic brakes of the single axes are released by the switches 2S1, 2S2, 2S3, 2S4
and by the foot switch 2S6.
The flexibility of the single axes and movements cause a free positioning of the therapy
head.
NOTE The schematics of the shock-wave positioning are shown in chapter 5 of this Service
Manual.
Figure 6-1 shows the shock-wave positioning of the Dornier Compact Alpha.
1 Joint 3
2 Joint 4
3 Z Axis
4 Joint 1
5 Joint 2
6 Y Axis
This paragraph describes which switch is to use to release the single joints and
movements.
By pressing the switch 2S1 the brake of the joint 3 (1, Figure 6-1) and the brake of the
joint 4 (2, Figure 6-1) will be released.
Switch 2S1 (1, Figure 6-2) is mounted in the handle of the therapy head.
1 Switch 2S1
Pressing the switch 2S2 releases the brake of the Y axis (6, Figure 6-1).
Thus a horizontal movement of the shock-wave positioning is possible.
Switch 2S2 (1, Figure 6-3) is mounted in the support of the shock-wave positioning.
1 Switch 2S2
Pressing the switch 2S3 releases the brake of joint 1 (4, Figure 6-1).
Thus a horizontal rotation of joint 1 is possible.
Switch 2S3 (1, Figure 6-4) is mounted in the support of the shock-wave positioning.
1 Switch 2S3
Pressing the switch 2S4 releases the brake of the Z axis (3, Figure 6-1).
Thus a vertical movement of the shock-wave positioning is possible.
Switch 2S4 (1, Figure 6-5) is mounted in the support of the shock-wave positioning.
1 Switch 2S4
Pressing the foot switch 2S6 release the brake of joint 1 (4, Figure 6-1), the brake of
joint 2 (5, Figure 6-1), the brake of the Y axis (6, Figure 6-1) and the brake of the Z
axis (3, Figure 6-1).
This causes a complete movement of the shock-wave positioning, however without the
rotation of the therapy head. To rotate the therapy head switch 2S1 has to be pressed.
Foot switch 2S6 is fix connected to the rack of the Dornier Compact Alpha with a
cable.
6.5.1 Z Axis
CAUTION Prior to the dismounting of the brake magnets the shock-wave positioning has to
be supported with an appropriate object if step 3 is not possible.
1 Locking screws
2 Cable
NOTE The mounting of the brake magnets for the Z axis is to perform in the reversed
sequence.
NOTE The special tools shown in Figure 6-7 are necessary for the exchange of the brake
magnets for the joints 1 to 4.
6.5.2 Joint 4
1 Locking screws
2 Cable
5 Loosen the six locking screws of the pressure disk (2, Figure 6-9) and remove the
pressure disk.
6 Loosen the clamping sleeves (2, Figure 6-10) by lightly tapping onto the clamping
disk (1, Figure 6-10) and remove them.
1 Clamping disk
2 Clamping sleeves
7 Remove the clamping disk with braking disk (see Figure 6-11).
8 Loosen the shaft nut, which is below and remove the brake magnet.
NOTE The mounting of the brake magnet is to perform in the reversed sequence.
The adjustment of the brake takes place by the adjusting screws (1, Figure 6-9) on the
clamping disk. The distance between the clamping disk and the braking disk will be
adjusted with the screws.
The brake is to be adjusted that joint 4
- is not rotatable with normal force in braked condition
- is free rotatable in released condition
6.5.3 Joint 3
1 Cable
NOTE The mounting of the brake magnet is to perform in the reversed sequence.
The adjustment of the brake for joint 3 is to perform in the same way as for joint 4 (see
paragraph 6.5.2.2).
6.5.4 Joint 2
NOTE To change the brake magnet for joint 2 the Y axis, which is mounted above joint 2, has
to be dismounted.
1 Remove the support for the control unit and its collet.
2 Remove the cover of the Y axis.
3 Unsolder cable (1, Figure 6-13).
4 Loosen the locking screws (1, Figure 6-14) and remove plate.
1 Locking screws
5 Remove Y movement.
6 Loosen the six locking screws (1, Figure 6-15) for the slide of the Y movement
and remove the slide.
1 Locking screws
NOTE The mounting of the brake magnet is to perform in the reversed sequence.
The adjustment of the brake for joint 2 is to perform in the same way as for joint 4 (see
paragraph 6.5.2.2).
6.5.5 Joint 1
1 Cable
NOTE The mounting of the brake magnet is to perform in the reversed sequence.
The adjustment of the brake for joint 1 is to perform in the same way as for joint 4 (see
paragraph 6.5.2.2).
6.5.6 Y Axis
1 Brake magnet
2 Holder
3 Cable
4 Cover
NOTE The mounting of the brake magnet is to perform in the reversed sequence.
NOTE The Laser Aiming Device QuickLinX can be refitted with the FCO 6013.
The Laser Aiming Device QuickLinX enables the localization of concretions and the
application area in conjunction with the Dornier Compact Alpha and any preferred
X-ray C-arm, which can be moved along the X, Y (horizontal), Z (vertical) and the
CC (swivel) axis.
Basically the Laser Aiming Device QuickLinX consists of the DC/DC converter, of the
four laser pointers and the on/off switch for the laser pointers.
The DC/DC converter is mounted in the rack and provides +5 VDC, which are
necessary for the operation of the laser pointers.
The four laser pointers and the on/off switch are integrated in the cover of the therapy
head.
Table of Contents
7.1 Introduction
Chapter 7 describes the functional groups of the water circuit (WKL) in the
Dornier Compact Alpha.
NOTE A water circuit without active degassing is mounted in a Dornier Compact Alpha up to
SN 80. The degassing of the water circuit is realized with an air separator where the
heating cartridge 1A7/E1 is installed.
For degassing of the water circuit in a Dornier Compact Alpha with a SN ≥ 81 or with
the installed FCO 7001 a degassing pump and two filters are installed.
7.2 Description
7.3.1 Description
WKL 1A7 is mounted in the rack on the left side (view from the therapy head). All
electrical function elements are supplied with a voltage of +24 VDC.
Exceptions are the heater and the fans of the cooling system which are supplied with
230 VAC:
Figure 7-1 shows the functional overview of the WKL (without active degassing).
Figure 7-2 shows the functional overview of the WKL (with active degassing).
NOTE The schematics of the water circuit control are shown in chapter 5 of this Service
Manual.
The water is heated, circulated and aerated in the main circuit. The main circuit also
eliminates residual air bubbles from the water cushion.
Heating cartridge 1A7/E1 and level switch 1A7/S1 are integrated in LA.
LA is where the water is heated and air bubbles are eliminated from the complete
system (system is aerated when container is refilled).
Aerating valve 1A7/Y4 is installed at the highest level of LA to ensure safe aeration.
Level switch 1A7/S2 is located in the refill container. The water necessary for coupling
is filled into NB. Level switch 1A7/S2 indicates when the water level is below the
minimum level and thus when a refill is necessary.
The heating cartridge is installed near the bottom of LA. The flow into LA occurs at the
level of the heating cartridge in order to ensure appropriate water heating.
The heating cartridge consists of heating element E1 and the over temperature fuse.
NOTE Table 7-1 shows the limit values of the temperature control.
An over temperature fuse is integrated in the heating cartridge. When the switch-off
temperature (95 °C) is exceeded, the heating cartridge is deactivated. The temperature is
measured in the heating cartridge. In the case of a dry run of the LA heating, the over
temperature sensor prevents overheating damages to functional elements in the water
circuit. When the over temperature fuse is released, the heating cartridge becomes
useless and must be replaced.
Level switch 1A7/S1 in LA controls aerating valve 1A7/Y4 via the PCB Medico. When
there is too much air in LA, the liquid level decreases and level switch 1A7/S1 opens.
Valve 1A7/Y4 is then activated by the PCB Medico. The valve opens. The excessive air
can escape, the liquid level increases and level switch 1A7/S1 closes.
Level switch 1A7/S2 prevents dry running of the pump when coupling the coupling
cushion. When the level switch opens, “FILL” appears in display H1 of the control unit.
“FILL” is also a prompt for the operator to refill NB with water.
Flow switch 1A7/S3 monitors the flow in the main circuit. When the flow in the water
circuit is insufficient for 30 seconds, 1A7/S3 opens and the error message “E011”
appears in display H1. The water circuit is deactivated and shock-wave operation
stopped.
Temperature switch 1A7/S4 monitors the water temperature in the coupling cushion.
When the water temperature exceeds 41 °C, the temperature switch opens and
shock-wave generation is interrupted. The message “C022” appears in display H1.
The PCB Medico controls the activation and deactivation of heating and cooling via
temperature sensor 1A7/B1.
Valves 1A7/Y2 and 1A7/Y3 allow the operator to switch between filling and draining
of the coupling cushion and also circulation of the WKL.
When the water level in LA is too low, PCB Medico opens valve 1A7/Y4 so that the
excessive air can escape.
The coupling cushion is decoupled also via valve 1A7/Y4.
Circulation pump 1A7/M0 is a magnetically coupled pump which ensures sufficient and
even flow through the WKL.
The aerating screw is to open when the coupling cushion is emptied in order to prevent
the coupling foil from adhering to the rubber lens and to separate air out of the coupling
cushion during filling.
The drain valve is opened to drain the water from the therapy head. Drain valve VA2 is
also used to aerate the coupling cushion and water circuit during refill.
The drain valve is opened to drain the water in case of water change.
The water in the circulation circuit is also pumped via the cooler in order to ensure
water cooling if necessary.
When the water reaches a certain temperature, the fan is activated to cool the cooling
circuit.
NOTE Table 7-1 shows the limit values of the temperature control.
In relation to a WKL without active degassing a degassing pump and two filters are
mounted additionally.
Furthermore the air separator LA is replaced by the degassing container EB.
NOTE Only the differences to a WKL without active degassing are described in
paragraph 7.3.4.
The heating cartridge 1A7/E1 and the level switch 1A7/S1 are mounted in the
degassing container.
The water is heated in the EB and the WKL is aerated with the valve 1A7/Y4.
The degassing pump makes a water-air bubble mixture which is nearly under
atmospheric air pressure after it is evacuated from the degassing pump. Since the gas
re-absorption process is slower than the degassing itself, the water-air bubble mixture
can be routed into the EB and separated by means of air separation (1A7/S1 and
1A7/Y4).
The main components of the therapy head are: EMSE 3B1, acoustic lens and coupling
cushion. The interlock switch 3S1 and the high voltage sockets are integrated in the
lower part of the therapy head.
Pressure sensor 3B5 is mounted at the outside of the therapy head to determine the
pressure in the coupling bellows. It is connected to the WKL with a hose.
The brake switch 2S1 is integrated in the handle of the therapy head.
The temperature in the WKL is measured via the temperature sensor (PT100) 1A7/B1.
The R/U converter 1U2 converts the resistance value corresponding to the temperature
into a voltage value (temperature coefficient: 0.1 V/°C).
Relay PCB 1A10 contains the relays with which the potential separation is transmitted
from the system to the patient subassemblies.
The analog value of the R/U converter 1U2 (AN12 SENS, TMP) is transmitted to the
PCB Medico.
When the temperature goes below the lower limit value for “heating on”, PCB Medico
activates heating element 1A7/E1 with the exception of the cases mentioned in
paragraph 7.3.2.3.
When the temperature exceeds the upper limit value for “heating off”, PCB Medico
deactivates heating element 1A7/E1.
Table 7-1 shows the limits of the temperature values.
Cooler on 36.0 °C
Cooler off 34.0 °C
Heating off 33.4 °C
Heating on 33.0 °C
Shock-wave release > 18.0 °C
When the actual water temperature in the therapy head exceeds or remains under the
preset limit values, the water circuit control generates an error message.
Over temperature is monitored by temperature switch 1A7/S4. When the water
temperature exceeds 41 °C, the temperature switch opens. This causes relay K1 on relay
PCB 1A10 to drop out. The heating is deactivated. Circulation pump 1A7/M0 is also
switched off. These safety switch-offs do not depend on the temperature-control circuit.
The temperature control circuit reports under temperature. The water circuit control
monitors the admissible temperature range.
Pressure sensor 3B5 is connected to the WKL by a hose. Thus pressure changes will be
detected directly.
The measured values are determined by resistance changes in the sensor, as a function
of the pressure. The resistance value corresponding to the pressure is converted to a
current value by the electronic integrated in the pressure sensor housing.
The automatic test runs from the Service Menu ’30 ‘ (Water system test menu) in the
Service Mode.
After activating the “Water system test menu”, press key S2 (frequency -) and key S3
(frequency +) on the control unit to select functions. The selected function is indicated
in display H1. Press S1 (Reset) to activate the selected function. The functions are:
- ’31 ‘ (start of the tests)
- ’37 ^’ (back to the main Service Menu)
The tests run automatically. The corresponding test number is indicated on display H2.
“PASS” is indicated on display H1 to show that a test has been successfully completed.
The temperature (in °C) is indicated on display H1.
In case of error, the corresponding error number (instead of “PASS”) is indicated on
display H1. The test routine stops at the displayed test number when an error occurs.
Press Reset to return to the Service Menu ’30 ‘.
After activating the test (pressing Reset) the status of temperature switch 1A7/S4
(SW_TMPOR) is checked. If the temperature switch is open (over temperature), the
cooler will be activated. When the water is cooled down, the temperature switch closes
and the cooler will be switched off. During the cooling phase message “C022”
(WK_OVERTEMP) is alternated with a display of the temperature (on display H1).
If the temperature switch does not close within 10 minutes, the test is not started and
message “E156” (WK_OR_SWITCH_WONT_CLOSE) is indicated on the display.
“End” is indicated on display H2 if all tests are successfully finished.
Table 7-2 shows the sequence of the test routine.
2 Flow switch 1A7/S3 Activate pump and check whether 1A7/S3 closes E150
3 Pressure sensor 3B5 Check whether the water pressure can be reduced E157
to minimum value.
4 Pressure sensor 3B5 Check whether the water pressure can be increased E158
to maximum value.
6 Heating 1A7/E1 Activate heating and check whether water circuit E152
can be heated to the maximum operating
temperature within 15 minutes.
7 Heating 1A7/E1 Activate heating and check whether water circuit E153:
can be heated within 15 minutes up to the point 1A7/S4 does not
Temperature switch 1A7/S4
where temperature switch 1A7/S4 opens open
(approx. 41 °C).
E152:
The test can activate two error messages. Heating cannot
heat water circuit
up to over
temperature
8 Cooler 1A5 Activate cooler fan and check whether water circuit E155:
can be cooled within 15 minutes up to the point Cooler not
where temperature switch 1A7/S4 closes. running.
The test can activate two error messages. E156:
Temperature
switch does not
close.
Use Service Menu ’60 ‘ for manually set and reset of several components of the WKL.
After activating the “Water system output setting/resetting menu”, press key S2
(frequency -) and S3 (frequency +) on the control unit to select functions. The selected
function is indicated in display H1. Press S1 (Reset) to activate the selected function.
The functions are:
- ’61 ‘ Pumps 1A7/M0 and 1A7/M1 on/off
- ’62 ‘ Open/close valve 1A7/Y4
- ’63 ‘ Open/close valve 1A7/Y2
- ’64 ‘ Open/close valve 1A7/Y3
- ’65 ‘ not used
- ’66 ‘ Cooler fan 1A5/E1 on/off
- ’67 ‘ not used
- ’68 ^’ (back to the main Service Menu)
NOTE If there is no refill after draining the WKL, the following steps 1 to 3 don’t have to be
performed on newer systems.
There are three connecting pieces at the underside of this systems where hoses can be
connected to drain the WKL. The three hoses are stored in the measuring and testing
device.
8 Press S1.
Service Menu ’41 ‘ is indicated on display H1.
10 Press S9.
Display H1 indicates “44 S” (submenu active).
Valves 1A7/Y2, Y3, and Y4 open.
11 Hang hoses in an appropriate container. Open drain valves VA2, VA3 and VA4.
12 Open aerating screw VA1 at the therapy head.
13 Drain water (approx. 5 liters) into an appropriate container.
14 Blow into the refill socket to check whether the refill container is empty.
15 Press S9 to deactivate submenu “44”.
16 Deactivate the Dornier Compact Alpha.
NOTE When no refill is required after draining, mount the housing covers.
The WKL has to be cleaned and rinsed during the maintenance or if the WKL is dirty.
Tap water is to use for cleaning and rinsing.
NOTE Measure and record the conductivity of the tap water using a conductivity meter before
filling the WKL of the Dornier Compact Alpha.
2 Rinse the water circuit with tap water until the conductivity of the water, measured
at drain valve VA2, is the same as the recorded one.
3 Drain WKL completely.
NOTE When no refill is required after rinsing mount the storage box and the housing covers.
The filling of WKL has to be done with the Service Mode, level 1.
7 Press S1.
Service Menu ’41 ‘ is indicated on display H1 (Filling).
9 Press S9.
Display H1 indicates “44 S” (submenu active).
Valves 1A7/Y2, Y3, and Y4 open.
10 Fill approx. 4 to 4½ liters of deionized and degassed water through the refill
socket. Then blow strongly into the refill socket in order to evacuate air bubbles
from the pump.
11 Press S9 to deactivate submenu “44”.
12 Turn the therapy head as shown in Figure 7-6 and press air out of the coupling
cushion via the aerating screw.
13 Move therapy head into under table position (coupling cushion up).
NOTE Turn the therapy head as shown in Figure 7-6 if there are still air bubbles in the
coupling cushion. Press air out of the coupling cushion.
4 Hold S9 and carefully refill small quantities (cupfuls) of deionized and degassed
water through the refill socket, until “Pr” is indicated on display H3.
5 Release S9.
CAUTION Verify that the coupling cushion will not be sucked too much to the lens. In this
case the lens can be pressed out of the support.
NOTE If there is too much water in the system, drain the surplus amount of water by opening
the drain valve VA2.
2 The deactivation of the degassing mode is to be done with the same key
combination.
1 Cable
2 Assembly block
3 Temperature switch with PG screw joint
Service Menu ’30 ‘ is used to adjust and store the regulation factors.
- ’32 P’ – ’36 t’ (Water pressure regulation factors)
- ’37 ^’ (back to the main Service Menu)
After activating Service Menu ’30 ‘, press S2 (frequency -) and S3 (frequency +) on the
control unit to select functions to change a regulation factor. Press S1 (Reset) to activate
the selected function. To change a regulation factor, use keys S2 (frequency -) and S3
(frequency +). The regulation value will be indicated on display H2. Table 7-4 shows
the functions.
Simultaneously pressing the keys S4 (SW intensity -) and S1 (Reset) will store the
factor value of the selected function in the NVRAM. If the menu option is changed
before the factor is stored then the original factor value will be restored.
During the adjustment the coupling pressure can be set with the keys S6/S7 whereby
the current regulation factors are considered.
33 d Set the range for the pressure over range valve 1A7/Y2 to open and 0 to 98
close, when regulating the coupling pressure Default 27 (=2.7mbar)
34 I Set the range between options 32 and 33. A negative value -98 to +98
decreases the range, a positive value increases the range. Default -11
(= -1.1mbar)
35 O Sets the zero pressure offset. This is the value from the pressure -30 to +70
sensor 3B5, when the coupling pressure level is set to 0. Default
Procedure: (= 16.2mbar)
1 Set the coupling pressure level to 0 and set the offset value to 0.
2 Bring therapy head in under table position;
Set the offset value to the pressure value shown on display H1.
3 Bring therapy head in over table position;
Set the offset value to the pressure value shown on display H1.
4 Store the average of these two values.
36 t Set the "Quick stop time". After coupling the system causes the 0 to 255
pressure to continue increasing for a couple of seconds. To Default 0
overcome this problem, the over pressure valve is momentarily
opened.
The valve activating time can be set in 10ms steps.
Table of Contents
8.1 Introduction
The shock-wave circuit supplies the shock-wave energy needed for the treatment of
pain and for the shock-wave lithotripsy.
Chapter 8 describes the subassemblies of the shock-wave circuit.
8.2 Description
NOTE Two different types of Capacitor Charging and Trigger Unit can be used on a Dornier
Compact Alpha.
- CCT (type LC475IG)
- CCT (type C4)
However the signals to the computer and the connections to the shock-wave generator
are the same on both types.
NOTE Type LC475IG is shown as the Capacitor Charging and Trigger Unit on Figure 8-1 to
Figure 8-2.
However the block diagram and the overviews are the same with the type C4.
After the power supply is switched on, 230 VAC is supplied to the CCT. The CCT is
activated by the signal LGON.
Relay K5 on the PCB Medico switches the signal LGON through to CCT. Relay K5 is
activated by the signal LGO when the signal SWINTL arrives at PCB Medico.
For high voltage build-up to occur, the signal CHARGE ON must be on and a nominal
value LOADVSOLL available for the charging voltage.
The high voltage build-up is reported to the PCB Medico by the signals LOADVIST
and EOC (End Of Charge).
The capacitor in the shock-wave generator 1A6 is charged from CCT via the charging
resistor.
The trigger signal TRIG IN from the PCB Medico triggers the pulse amplifier stage of
the trigger module in the CCT.
- ECG triggering
In the case of ECG triggering, trigger signal TRIG IN is delayed 30ms of the
ECG trigger signal by the PCB Medico.
- fixed frequency triggering
In the case of fixed frequency triggering, the PCB Medico generates a 60 to
180 SW/min. trigger signal, depending on the setting.
The pulse (TRIG IN) is amplified on the trigger module. The pulse then ignites a
thyristor which discharges its capacitor via the pulse transformer into the shock-wave
generator.
The pulse transformer increases the pulse voltage from 500 V to approx. 8 kV to 16 kV
and routes the voltage to the spark gap. The resulting ignition spark switches the
capacitor energy at the anode of the spark gap to the cathode.
Depending on the type of unit and on the shock-wave intensity setting, an impulse of
approx. 8 kV to 16 kV is generated. By means of induction, the impulse causes the
membrane of EMSE 3B1 to deflect and releases the resulting shock wave.
- Shock-wave circuit is enabled. This means that the signal CHARGEO activates
relay K7 on the PCB Medico
- Shock-wave release button is pressed
The interlock switches 3S1 in the therapy head and 1A6/S1 in the shock-wave
generator must be activated (closed). When the interlock circuit is closed, signal
SWINTL is simultaneously at PCB Medico and at the CCT.
The nominal preset value for the CCT (1A4) is reported back simultaneously to PCB
Medico as LOADVCTL.
The display on the control unit shows the ESWT/ESWL operating status.
During startup, the total number of shock waves is scrolled on the display (tOtAL
PULSES). Message “C049” appears when shock-wave release button is pressed.
After startup is completed, “C050” appears for approx. 2 seconds on the display.
If an error occurs in the shock-wave circuit during startup, pressing the shock-wave
release button will cause the error message “E032” to appear.
WARNING In order to ensure safety during servicing, the charging capacitor in the
shock-wave generator 1A6 has to be discharged via a safety discharge plug.
8.3.1 Description
The shock-wave intensity set by the operator is transmitted to the CCT as nominal
value. During shock-wave release, the control system continuously checks whether the
nominal value has been exceeded and whether the desired charging status has been
achieved at the time of shock-wave release.
The tasks of ESWT/ESWL control are to monitor and control the CCT and the water
circuit during shock-wave generation.
NOTE When one of the above conditions is fulfilled, shock-wave operation is interrupted and
the corresponding error message displayed.
If the intensity will be reduced during operation the signal LOADVSOLL is set to a
lower level for 230 ms and then to the correct level. This avoids an incorrect
comparison of LOADVSOLL and LOADVIST.
To avoid the increasing of the signal LOADVSOLL with reducing of the intensity level
with pressed shock-wave release button in ECG mode and no ECG signal, the signal
LOADVSOLL is set immediately to the new value.
The automatic test runs in Service Mode with Service Menu ’20 ‘
(ESWT auto test).
NOTE The “ESWT INIT TESTS” have to be performed first, otherwise the “ESWT SHOOT
LOOP” is not working.
2 Press S1.
“H20” is indicated on display H2
Water cushion automatically decouples and couples. This is to ensure that the
water cushion foil is not in focus F2. Flow switch 1A7/S3 is checked
simultaneously.
In case of an error, “C011” appears in display H1. ESWT test can not be started.
When the water cushion test has been successfully completed, “ESL” appears in
display H2.
When test 5 has been successfully completed, “End” appears in display H2.
NOTE It is essential that as from test 9 the shock-wave release button (S9) is pressed and is not
released until test 16 is concluded. Otherwise the ESWT SHOOT LOOP is not executed
properly!
When test 16 has been successfully completed, “End” appears in display H2.
8.4 EMSE
8.4.1 Description
1 Cover
2 Assembly block
3 Allen screws
CAUTION Three pressure springs are located on the underside of the pressure disk.
11 Remove pressure disk (2, Figure 8-7). Take care not to damage pressure springs.
12 Remove coil carefully (1, Figure 8-8).
13 Remove both Kapton foils.
1 Coil
2 Tension ring
15 Remove membrane.
16 Check lens for cracks.
If there are any cracks the lens must be replaced.
WARNING Cracks in the lens may lead to defocussing and may cause injury to patients.
5 Insert screws into tension ring with screw-locking varnish (medium strength) and
tighten.
6 Press lightly against coupling cushion in order to check tightness.
7 Clean membrane with alcohol.
8 Put Kapton foils (one or two) in place (avoid kinking).
CAUTION Only one Kapton foil is allowed on a coil with HD wire. Otherwise the power of the
shock-wave circuit will be affected (see TIP 107009).
CAUTION After changing EMSE, perform Model Stone Test according to paragraph 8.4.3.
The preparation and the performance of the Model Stone Test is described in the
current revision of EO 46.
The evaluation of the Model Stone Test is described in the current revision of EO 46.
The pressure test determines the shock-wave pressure of the Dornier Compact Alpha.
NOTE The pressure test has to be performed only, if there is an instruction of the Medical
Device Reporting Officer.
The preparation and the performance of the pressure test is described in the current
revision of EO 46.
The evaluation of the pressure test is described in the current revision of EO 46.
NOTE The test container, which is delivered together with the measuring and testing device is
to use for the paragraphs 8.4.3 and 8.4.4.
8.5.1 Description
Shock-wave generator 1A6 supplies the energy required for shock-wave release. The
shock-wave generator is connected to EMSE 3B1 via a coaxial cable. The shock-wave
generator is designed for operation with an inductive load.
The charging capacitor is charged by the charging unit of the CCT via a charging
resistor. A trigger signal from the triggering unit of the CCT is stepped up by the pulse
transformer and transmitted to the trigger pin of the spark gap. The resulting ignition
spark switches the charging voltage (capacitor energy) at the anode of the spark gap to
the cathode. The impulse causes a membrane deflection on EMSE 3B1 by means of
induction.
For greater efficiency, the return line of EMSE 3B1 is connected directly to the
negative side of the charging capacitor. A discharging resistor is connected in parallel
to the charging capacitor. The discharging resistor is used to discharge the charging
capacitor when shock-wave operation is interrupted. Since the discharging resistor
operates at a very high impedance (50 MOhm), there can still be high voltage at the
capacitor a long time after deactivation of the Dornier Compact Alpha.
WARNING When performing maintenance work, always plug safety discharge plug
completely into the shock-wave generator, as shown in Figure 8-11. The charging
capacitor is discharged to the housing of the shock-wave generator.
CAUTION If the charging capacitor was charged to a high energy level, arcing can occur
when inserting the safety discharge plug. This causes damage to the safety
discharge plug and/or the spark gap. Then a complete discharging is not ensured.
In order to avoid damage to the contact surface of spark gap or to the safety discharge
plug during discharging, make sure that the last shock-waves are released with
minimum intensity before the Dornier Compact Alpha is switched off.
If there are signs of arcing at the safety discharge plug it has to be exchanged.
1 Trigger connection
2 Connection to charging and discharging resistor
3 Locking screws (4 pieces)
4 Connection to energy cable
CAUTION When working on the spark gap, do not touch the ceramic structure and keep it
grease-free in order to avoid a flashover.
Switch on the Dornier Compact Alpha and active high voltage in ECG mode after
booting. The indicated value of the voltage accords to the high voltage in kV.
Table 8-3 and Table 8-4 show the EMSE power level.
Table 8-5 shows the acceptable trigger frequencies to the intensity levels during
shock-wave release.
Table 8-3 Power Levels of EMSE for the Dornier Compact Alpha
1 10.00
2 11.50
3 12.75
4 14.00
5 15.00
6 16.00
Table 8-4 Power Levels of EMSE for the Dornier Compact Alpha IPP
A 8.00
b 9.00
C 10.00
1 11.00
2 12.00
3 13.00
4 14.00
5 15.00
6 16.00
8.6.1 Description
The logic unit isolates electrically the input and output signals from the control
computer with an optocoupler. The complete LC475IG unit is controlled and monitored
by a microprocessor.
The power unit supplies the adjustable primary energy for high voltage generation with
a switching power supply which works as push-pull converter in half-bridge
configuration. Also the 500 V ignition pulses for the pulse transformer in the shock-
wave generator are generated.
The 20 kV high voltage unit consists of the high voltage switching power-supply
transformer with integrated voltage multiplier and the two high voltage dividing
resistors which supply the actual high voltage values for the logic unit.
Connector X1 is the interface to PCB Medico 1A1. In all, 6 control inputs and 3 report
outputs run through X1.
Table 8-6 describes the inputs.
Table 8-7 describes the outputs.
8.7.1 Description
The comparison between LOADVSOLL and LOADVIST takes place on the PCB
Interface. The comparison is adjustable with potentiometer.
The trigger generator used for the ignition of the spark gap is located on the PCB
Converter.
Furthermore the tact frequency, the short-circuit current for the HV-chopper and the
high voltage are adjusted on the PCB Converter.
The connections of the interface to the PCB IO 2000 are the same as in paragraph 8.6.3.
Table of Contents
9.1 Introduction
The most important functions of the Dornier Compact Alpha are executed via the
control unit. The control unit is integrated in a housing and connected to Dornier
Compact Alpha via a helix cable. While not in use, the control unit can be placed in a
holder on the Dornier Compact Alpha support.
Figure 9-1 Control Unit of the Dornier Compact Alpha with the most important elements
8 H6 Status display
Status LED Green: Device is working properly
Orange: C-message
Red: Error message
9 S9 Release of shock-waves
Shock-wave release
button
The data interface is a serial interface according to RS 422 standard (CCITT/X27 resp.
DIN 66259, part 3). The receiving lines are terminated in a 68-Ohm impedance to
ground.
The interface parameters are the following:
Transmission: asynchronous, full duplex
Transfer rate: 9600 Baud
Character length: 8 bit
Frame: 1 start bit, 1 stop bit, parity even
Handshake: software handshake XON/XOFF
The XOFF signal is sent by the controller as soon as the receiving buffer is almost full.
The receiving buffer has a total depth of 20 bytes.
The test is executed in Service Menu ’50 ‘. During the test “51” is indicated in
display H1.
NOTE Press S1 last, because pressing S1 ends the test and switches automatically back to the
main Service Menu.
1 Press S3.
2 Press S2.
3 Press S5 .
4 Press S4.
5 Press S7 .
6 Press S6.
7 Press S8.
8 Press S1.
+
9.7 Repair
The keyboard foil respectively the upper cover can be exchanged completely in case of
damage. An exchange of the complete control unit is only necessary in case of defective
electronics and / or lower cover.
NOTE The function of the single keys can be tested in Service Menu ’50 ‘, the user
functionality in User Mode.
1 Lower cover
2 Fastening frame
3 Screws
1 Electronics
2 Keyboard foil connector
3 Cable fixing
4 Helix cable
5 Connector
Table of Contents
10.1 Introduction 10.2
10.1 Introduction
Chapter 10 describes the ultrasound locating of the Dornier Compact Alpha with
ultrasound units from Kontron or B-K Ultrasound.
10.2 Description
High resolution ultrasound units which are put to the system are used for the stone
localization and diagnosis.
NOTE Operating and service procedures for these ultrasound systems are described in the
respective Operating Manual or Service Documentation.
The isocentric fastening (4, Figure 10-1) serves to mount the isocentric scanner guide
onto the therapy head. In addition it serves to mount the bellows on the therapy head via
the screwed on press ring (3, Figure 10-1).
The isocentric fastening is mounted ball bearing in such a manner that is rotatable on
the therapy head. Because of the construction an adjustment of the isocentric fastening
is not possible.
In order to lock the isocentric fastening in a certain position a segment (2, Figure 10-1)
is available. The segment locks the rotatable part of the fastening via a brake lever
(1, Figure 10-1).
1 Brake lever
2 Segment
3 Press ring
4 Isocentric fastening
CAUTION The press ring also serves to fix the O-ring of the coupling cushion, resp. the
sealing of the coupling cushion.
Make sure the O-ring will not be damaged during mounting or dismounting the
isocentric fastening.
The adjustment of the brake force is to be done by adding or removing shim washers
below the brake lever.
Adjust the brake so that the isocentric fastening
- can be rotated easily, without mechanical resistance and noiseless, when the
brake is released
- can not be rotated by normal force, when the brake is locked
The scanner is mounted on the isocentric scanner guide. The isocentric scanner guide
serves to carry, guide and lock the scanner. The locating arm is mounted in such a
manner that it is rotatable on a bogie track on the therapy head.
The isocentric scanner guide consists of the isocentric swivel unit (joint arms) and the
linear movement with scanner holder.
Joints A, B, C are coupled by means of two joint rods. This ensures that all joints
realize the same rotating angle. The scanner thus carries out isocentric movements
around the focus.
Locating precision is determined by the exactness of the isocentric scanner guide. The
lower joint arm must be parallel to the linear movement in each position.
Figure 10-2 shows the isocentric scanner guide.
CAUTION The isocentric scanner guide should not be exposed to mechanical stress (impact,
jolt, etc.).
The isocentric scanner guide should be secured in every position with the brake
lever.
The linear movement with the scanner can be moved. As a result, the variable distance
from the therapy focus (stone) to the patient surface is equalized. The scanner is pressed
onto the patient by a spring so that smaller, relative movements made by the patient can
be compensated for with respect to the mechanical locating system.
A linear potentiometer is integrated in the linear movement of the isocentric scanner
guide in order to ascertain the current scanner position and display the therapy focus
(crosshair) on the ultrasound image.
NOTE If the isocentric scanner guide is not mounted, the crosshair is not displayed on the
ultrasound image. The software detects the missing jumper (PIN 6 and 7) in the plug
(3X2) of the connecting cable.
1 Switch on the Dornier Compact Alpha in the Service Mode and the ultrasound
system.
2 Select Service Menu ’40 ‘.
3 Select Service Menu ’45 ‘.
4 Activate Service Menu ’45 ‘ by pressing once the shock-wave release key.
5 Depending on the communication status one of the following messages is
indicated on display H2 of the control unit:
nOr = communication OK
US? = no communication
L-r = change of image position on ultrasound unit (left - right)
U-d = change of image position on ultrasound unit (up - down)
L-U = change of image position on ultrasound unit (left - right & up - down)
When the isocentric scanner guide was exchanged, re-adjusted or the crosshair is not
faded in even with correct communication the isocentric scanner guide must be
calibrated.
If the converter PCB 3U1 was exchanged or re-adjusted the calibration has to be
performed as well.
1 Switch the ampere meter in the signal line to connector X2:1 of converter PCB.
2 Push the linear movement to the mechanical front stop.
3 Turn potentiometer P1 on converter PCB to adjust the current value to 3 - 8 mA.
4 Push the linear movement to the mechanical back stop (including spring travel).
5 Turn potentiometer P2 on converter PCB to adjust the current value to 16 - 20 mA.
6 Unclamp the ampere meter.
7 Connect the signal line to converter PCB.
Depending on the setting of the DIL switches on the PCB Medico the calibration can be
performed as follows:
- with OA_TOOL (PCB Medico, DIL switch S1/7 ON)
- without OA_TOOL (PCB Medico, DIL switch S1/7 OFF)
NOTE The calibration should be performed with the OA_TOOL. The calibration with
OA_TOOL is more precisely than the calibration without OA_TOOL.
1 Set DIL switches S1/3 (Service Mode), S1/7 (with OA_TOOL) and S1/8
(US installed) to “ON”.
2 Switch on the Dornier Compact Alpha.
3 Select Service Menu ’10 ‘.
4 Select Service Menu ’11 ‘.
NOTE The actual current value of the linear movement (mA x 10) is indicated on display H2
of the control unit. The current value must change, when the position of the linear
movement changes.
5 Insert the calibration sleeve (4, Figure 10-6) into the scanner holder.
6 Insert the short calibrating pin (3, Figure 10-6) into the calibration sleeve.
7 Attach the calibration device (2, Figure 10-6) including the support
(1, Figure 10-6) to the therapy head.
1 Support
2 Calibration device
3 Calibrating pin, short
4 Calibration sleeve
8 Move linear movement of isocentric scanner guide forward and position the short
calibrating pin (3, Figure 10-6) onto the ball of the calibration device, as shown in
Figure 10-6.
9 Store the actual current value by simultaneously pressing the keys RESET (S1)
and SHOCKWAVE INTENSITY- (S4) on the control unit.
NOTE If the entry was within the tolerance range “FIn” is indicated on display H2 of control
unit, otherwise “nO” appears.
1 Support
2 Calibration device
3 Calibrating pin, long
4 Calibration sleeve
13 Move linear movement of isocentric scanner guide forward and position the long
calibrating pin (3, Figure 10-7) onto the ball of the calibration device, as shown in
Figure 10-7.
14 Store the actual current value by simultaneously pressing the keys RESET (S1)
and SHOCKWAVE INTENSITY- (S4) on the control unit.
NOTE If the entry was within the tolerance range “FIn” is indicated on display H2 of control
unit, otherwise “nO” appears.
1 Set DIL switches S1/7 (without OA_TOOL) to “OFF”, S1/3 (Service Mode) and
S1/8 (US installed) to “ON”.
2 Switch on the Dornier Compact Alpha.
3 Select Service Menu ’10 ‘.
4 Select Service Menu ’11 ‘.
NOTE The actual current value of the linear movement (mA x 10) is indicated on display H2
of the control unit. The current value must change, when the position of the linear
movement changes.
NOTE If the entry was within the tolerance range “FIn” is indicated on display H2 of control
unit, otherwise “nO” appears.
NOTE If the entry was within the tolerance range “FIn” is indicated on display H2 of control
unit, otherwise “nO” appears.
NOTE If it is not possible to perform the calibration with or without the OA_TOOL, check the
current values from converter PCB (see paragraph 10.7.1) and re-adjust, if necessary.
If both values are stored correctly in the NVRAM of PCB Medico the crosshair is
displayed on the monitor of the ultrasound unit after reaching the appropriate water
temperature.
The maximum deviation is:
- 2 mm with therapy head in under table position
- 3 mm with therapy head in over table position
The ultrasound phantom is used to check the locating precision of the isocentric scanner
guide. The ultrasound phantom (1, Figure 10-8) is supplied with the system and has to
be mounted with the support (2, Figure 10-8) on the therapy head.
1 Ultrasound phantom
2 Support
In order to check the locating with the ultrasound phantom, the Dornier Compact Alpha
and the ultrasound system have to be activated. In addition, all conditions for crosshair
fade-in have to be fulfilled, as described in paragraph 10.5.
Apply ultrasound gel to the ultrasound phantom and move the scanner to the phantom
until the scanner surface touches the ultrasound phantom in order to estimate the
locating precision of the isocentric scanner guide. Move the isocentric scanner guide in
coupled condition along the movement range.
The stone phantom inside the phantom must appear in the center of the crosshair (ideal
adjustment) on the ultrasound image.
The mechanical adjustment of the isocentric scanner guide is within the tolerances,
when the stone phantom is displayed inside the crosshair range, resp. in the area of the
edge of the crosshair. Otherwise, a mechanical re-adjustment is necessary (see Figure
10-9).
The isocentric scanner guide has to be checked mechanically and adjusted when the
stone phantom was displayed out of the tolerance range during the check with the
ultrasound phantom (see paragraph 10.8.1).
Proceed as follows:
1 Pull the scanner out of the scanner holder.
2 Insert the calibration sleeve (4, Figure 10-10) into the scanner holder.
3 Insert the calibration tip (3, Figure 10-10) into the calibration sleeve.
4 Attach the calibration device (2, Figure 10-10) including the support
(1, Figure 10-10) to the therapy head.
5 Move linear movement of isocentric scanner guide to max. forward position.
1 Support
2 Calibration device
3 Calibration tip
4 Calibration sleeve
When the adjustment was done correctly, the distance in the complete movement area
of the isocentric scanner guide between both tips is maximum
- 2 mm, when TH is in under table position or
- 3 mm, when TH is in over table position.
If this is not the case, proceed with the following adjustments in relation to the
deviation (direction). The adjustment of the linear movement has to be checked first.
The other adjustments are depending on the deviation and are interactive.
The linear movement must be parallel to the lower joint arm at each position. This
ensures that there are isocentric movements around the therapy head in all positions of
the isocentric scanner guide.
The parallelism of the linear movement can be adjusted by loosening the four locking
screws.
1 Bring lower joint arm into horizontal position (check with water level).
2 Loosen the locking screws (1, Figure 10-11).
3 Rotate the linear movement (2, Figure 10-11) so that it runs parallel to the lower
joint arm (horizontal position).
1 Locking screws
2 Linear movement
The parallelism to focal point F can be adjusted by means of the dovetail guide
(1, Figure 10-12) of the isocentric fastening (2, Figure 10-12).
1 Loosen the locking screws (3, Figure 10-12) on the dovetail guide.
1 Dovetail Guide
2 Isocentric fastening
3 Locking screws
4 Screw in the center of rotation
The vertical adjustment to focal point F can be realized by means of the screw in the
center of rotation of the clamp block of the isocentric scanner guide. The clamp block is
used to mount the isocentric scanner guide on the dovetail guide of the isocentric
fastening.
1 Lightly loosen the screw in the center of rotation (4, Figure 10-12) on the clamp
block.
2 Move the isocentric scanner guide upwards or downwards, depending on the
deviation.
3 Tighten the screw, when the distance between both tips is within the tolerance.
The horizontal adjustment to focal point F can be realized by means of the screw in the
joint A. For that purpose open cover of housing.
1 Lightly loosen the screw (1, Figure 10-13).
1 Screw
2 Move the isocentric scanner guide towards the therapy head or away from the
therapy head, depending on the deviation in the joint.
3 Tighten the screw, when the distance between both tips is within the tolerance.
4 Mount the cover.
If it is not possible to adjust the rotating movement of the isocentric scanner guide
within the tolerance the joint rods have to be checked. Adjust the joint rods, if
necessary.
Remove both housing covers of the joint arms in order to adjust the joint rods.
Figure 10-14 shows the joint arms.
In order to achieve an isocentric rotating movement the difference in length of both
joint rods in a joint arm should be maximum 0.2 mm.
In addition the joint rods of the other joint arm have to be adjusted to the same length.
The distances have to be measured with a proper caliper.
NOTE If the difference in length of both joint rods in a joint arm is out of tolerance, rotate the
joint rod supports resp. the joint rods in order to adjust a permissible length.
The scanner holder (1, Figure 10-15) is mounted on the linear movement
(3, Figure 10-15) via a slide with brake lever (4, Figure 10-15).
The clamping lever (2, Figure 10-15) is used to lock the scanner holder. The scanner
holder can be removed from the linear movement. For this purpose, the clamping lever
must be released.
The clamping lever has to run parallel with the upper plain side of the linear movement
(see Figure 10-15) in order to ensure a proper handling of the linear movement. In this
position the scanner holder must be locked. If the scanner holder is not locked, the
clamping lever has to be re-adjusted.
If the scanner holder has become loose, the locking can be re-adjusted by an eccentric.
1 Remove the scanner holder by releasing the clamping lever (1, Figure 10-16).
2 Loosen the locking screw (2, Figure 10-16) of the clamping lever.
3 Rotate the eccentric (3, Figure 10-16).
4 Apply screw varnish to the locking screw and tighten the screw.
5 Mount the scanner holder on slide of the linear movement.
6 Close the clamping lever.
1 Clamping lever
2 Locking screw
3 Eccentric
NOTE It is not possible to adjust the scanner support of a scanner holder Kontron.
A clamping lever, as realized at the scanner holder Kontron, is used to fix the scanner
holder B-K at the linear movement. The clamping lever is adjustable with an eccentric.
The scanner holder B-K can be adjusted with adjusting screws (1, Figure 10-17) to
avoid incorrect localization. Both adjusting screws are pressing a plate to the scanner to
ensure a play free locking of the scanner in the scanner support with the clamping lever
(2, Figure 10-17).
1 Adjusting screws
2 Clamping lever
NOTE The adjustment for scanners on ultrasound units B-K is described in the Service
Documentation of the ultrasound unit.
When using mechanical Kontron scanners together with Dornier MicroEnvision and a
Dornier Compact Alpha an Offset value has to be set in the ultrasound unit. This
ensures a fault-free focussing in combination with the isocentric scanner guide.
CAUTION Make the Offset adjustment when a new mechanical scanner is used. The Offset
notifies the "internal" deviation of the scanner to the ultrasound unit.
NOTE There are different offset ranges but they are directly proportional.
Menu DORNIER, Offset 1 to 15 is equal to menu CROSS, Offset -7 to +7.
With the Offset adjustment small target deviation of the scanner can be compensated.
However, the Offset adjustment does not replace the mechanical adjustment of the
isocentric scanner guide.
The Offset adjustment is not necessary for electronic scanners.
NOTE See the relevant documentation for the ultrasound units for further information.
Table of Contents
12.1 Introduction
The PCB Medico is a processor system consisting of one micro controller. The
processor has no internal program memory and is operated with an external EPROM
(64 kByte). An external data memory (32 kByte RAM) is supplied for the processor.
The integrated A/D converters run with an 8-bit accuracy.
The address ranges of the peripheral modules operated from the micro controller via
address and data bus can be programmed via PAL.
Figure 12-1 shows the PCB Medico.
Figure 12-2 to Figure 12-8 show overviews of the PCB Medico.
The PCB Mediad converts digital values (signals and voltage) into single signals which
can be displayed via LEDs.
Jumper X1 (see Figure 12-9) can be set to check LEDs, even during operation.
Figure 12-10 and Figure 12-11 show overviews of the PCB Mediad.
NOTE As from SW V2.42 the software version number (e.g. 2_42) is shown on display H1 of
the control unit during the initialization.
System startup is initiated automatically after activation. When the startup runs
faultless, no user intervention is required until system is ready for operation.
A defined sequence is run through:
- System initialization (reset interfaces resp. inputs/outputs, delete certain
memory areas)
- System startup (execute system test, start water circuit, activate CCT)
NOTE After finishing the start up display H1 indicates “C050” and a beep occurs to message
that the system is ready.
Error messages can require a specific reaction from the operator (limited treatment
procedure, interruption of treatment, reset, etc.). The objective is to continue treatment
as long as the errors are not critical.
The user messages consist of a defined kit of messages which can be indicated on the
display of the control unit.
NOTE Operator messages resp. error messages with the respective texts are listed in chapter 3.
During system startup, the system configuration is determined via the DIL switches
integrated on the computer PCB.
Figure 12-12 shows the position of the DIL switch Sl.
Table 12-1 shows the system configuration.
Table 12-1 Assignment of the DIL Switch S1 for software as from V2.41
1 not used
2 not used
3 ON Service Mode
OFF OFF User Mode
Table of Contents
15.1 Introduction
In order to perform general urological measures, the patient tables are designed
X-ray transparent. The required supporting structures are located outside of the area of
radiation.
The patient table is available in four different variants:
- Dornier Relax V1 (patient table standard)
- Dornier Relax V2 (patient table with Z and K axes movement)
- Dornier Relax V3 (patient table with X, Y, Z and K axes movement)
These patient tables are movable and are equipped with a standstill brake. The standstill
brake locks the patient table during the therapy and parking.
The standstill brake is activated by means of a brake lever. The brake lever actuates the
brake linkage via a deflecting mechanism. The brake linkage locks the patient table.
Head and foot parts of all these tables can be lifted up.
- Dornier Relax +
NOTE A separate Service Manual is available for the patient table Dornier Relax +.
1 Table surface
2 Head/foot part
3 Locking of head/foot part
4 Table wheel
5 Table wheel with integrated brake
6 Brake lever of standstill brake
The table surface is attached to the chassis by means of two electrical lifting columns
(Z axis). The table surface can be tilted (K axis) to max. 20° ± 3° by raising or lowering
of one lifting column.
Z and K axes are moved using the hand control.
The hand control can be attached on both sides of the patient table by means of a Velcro
fastening. Optionally it can be attached in a support which is mounted on the rails of the
table.
The Z axis can be moved additionally with the foot switch.
Hand control and foot switch are connected to the patient table permanently and cannot
be unplugged.
A repair of the lifting columns is not possible.
The voltage supply for the patient table is 120 VAC or 230 VAC.
In addition, an accumulator package (24 V) is integrated in the control unit. The
accumulator package consists of four accumulators (6 V) connected in series.
Z and K axis can be moved without external power supply. The operating time of
accumulator operation is depending on the frequency of axis movements.
The accumulator package is charged via the integrated charging set when the patient
table is connected to the external power supply. The charging time is approx. 12 hours
with accumulator package discharged completely.
CAUTION Do not disconnect the accumulator package from the control unit.
If the accumulator package needs to be replaced, the complete control unit has to
be exchanged.
Figure 15-2 shows the patient table with Z and K axes movement.
1 Table surface
2 Head/foot part
3 Hand control
4 Table wheel with integrated brake
5 Locking of head/foot part
6 Foot switch
7 Brake lever of standstill brake
The table surface is attached to the chassis by means of a floating table (X and Y axis)
and two electrical lifting columns (Z and K axis).
The table surface can be tilted (K axis) to max. 15° ± 2° by raising or lowering of one
lifting column.
Z and K axis are moved using the hand control.
The hand control can be attached on both sides of the patient table by means of a Velcro
fastening. Optionally it can be attached in a support which is mounted on the rails of the
table.
The floating table can be moved in X direction (longitudinal axis) by minimum 100 mm
and in Y direction (lateral axis) by minimum 90 mm.
X and Y axis can be moved manually after activation of both release buttons for the
appropriate axis. The locking of the floating table is achieved by means of magnetic
brakes, which are voltage supplied by the control unit. The supply voltage for the
magnetic brakes is 24 VDC.
1 Table surface
2 Release button for floating table
3 Head/foot part
4 Locking of head/foot part
5 Hand control
6 Table wheel
7 Table wheel with integrated brake
8 Brake lever of standstill brake
1 LED K axis
2 LED X axis
3 LED Y axis
4 Handle with release buttons
The zero positions of the X and Y axis are determined by the position of the micro
switches and the accompanying switching elements and are not adjustable.
The axes movements are limited by rubber stops.
NOTE Proceeding from zero position, the floating table must be movable in directions X+ and
X- by a minimum 50 mm.
6 Install the rubber stops (1, Figure 15-7), so that movement distances of minimum
50 mm in both directions can be achieved.
NOTE Proceeding from zero position, the floating table must be movable in directions Y+ and
Y- by a minimum 45 mm.
6 Install the rubber stops (2, Figure 15-7), so that movement distances of minimum
45 mm in both directions can be achieved.
NOTE The foot switch is available only on patient tables with Z and K axes movement.
The lifting columns contain all functional components and are connected externally to
the control unit only. The lifting columns contain the end switches that are used for
deactivation of movement when reaching the lower or upper end position. The
switching positions are pre-defined and are not adjustable. In case of defect, the lifting
column has to be replaced completely.
The motion of the brake lever is transferred to the brake tappet via the deflecting
mechanism.
New brake tappets (Figure 15-10) and brake tappets with rubber buffers (Figure 15-11)
are available for the patient table.
NOTE Old brake tappets have to be replaced by new brake tappets in case of a defect.
CAUTION If old brake tappets need to be replaced by new ones, it has to take place on both
table wheels.
1 Lift-up the patient table until the affected table wheel is free to remove.
2 Loosen both Allen screws in the wheel support.
3 Pull down the wheel out of the support.
4 Dismount the brake tappet.
NOTE The rubber buffer can be replaced at old brake tappets as follows:
4a Hold the brake tappet at the upper end using a suitable wrench.
4b Remove screw of rubber buffer, be careful that the spring does not get lost.
4c Install new rubber buffer and tighten the screw.
1 Table wheel
2 Brake tappet
Figure 15-11 Assembly of Standstill Brake (Brake Tappet with Rubber Buffers)
1 Table wheel
2 Brake tappet
3 Rubber buffer
Table of Contents
B1 Introduction B.2
B1 Introduction
B2 List of Parts
B 2.1 Rack
B 2.2 Brakes