Service Manual Perfusor® Space, German . . . . . . . . . . 8713 9010
Service Manual Perfusor® Space, English (US). . . . . . 8713 9020U
Service Manual Perfusor® Space, French . . . . . . . . . . . 8713 9030
2 Perfusor® Space, 1.2 gb
1.01.0
0-Table of Contents
0
Important Preliminary RemarksService Work Page 0 - 5
Technical Safety Checks Page 0 - 5
Current Versions Page 0 - 5
Revision Service Page 0 - 5
Quality Management Page 0 - 6
Checks and Repair Page 0 - 6
Notes on ESD Page 0 - 6
Spare Parts and Test Equipment Page 0 - 7
Setting Off Page 0 - 7
Contact PersonsTechnical Training Page 0 - 11
Entry for Technical Training Page 0 - 11
Ordering of Spare Parts and Test Equipment Page 0 - 11
Service Hotline International Page 0 - 11
Return of Spare Parts and Test Equipment Page 0 - 11
Safety Officer
(§ 30 MPG) Page 0 - 11
Translation Page 0 - 11
System OverviewDescription Page 1 - 1
System Overview Page 1 - 1
Physical Construction Page 1 - 2
Function Page 1 - 3
Unit Software Page 1 - 6
Service Program Page 1 - 7
Technical Data Page 1 - 12
Options Page 1 - 12
Accessories Page 1 - 12
Unit Diagnosis / CalibrationGeneral Page 2 - 1
Alarms and Error Codes Page 2 - 3
The Most Important Error Modes Page 2 - 8
Device Check Page 2 - 9
Calibration Page 2 - 14
Procedural Instructions for Calibration Page 2 - 14
Trouble Shooting Page 2 - 29
Procedural Instructions on the TSCVisual Inspection Page 7 - 1
Electrical Safety
according to IEC/EN 60601-1
or VDE 0750 and VDE 0751 Page 7 - 2
Functional Inspection Perfusor® Space Page 7 - 3
Functional Inspection Power Supply SP Page 7 - 6
Test Equipment and Special ToolsTest equipment Page 8 - 1
Special Tools Page 8 - 3
Spare Parts ListPage 9 - 1
Revision DocumentationDescription of Version Page 10 - 1
Version List of the Individual Pages Page 10 - 1
IndexPage 11 - 1
0- 4 Perfusor® Space, 1.0 gb
1.11.0
0-Important Preliminary Remarks
0
Service WorkThe present manual is for your information only. The possession of
this manual does not authorize the performance of service work.
Service tasks may only be executed by persons, who
-have received appropriate training on the system from
B. Braun
-are included in the revision service
-possess the necessary test equipment and mechanical aids,
and
-fulfill the personal requirements (training and knowledge).
Technical Safety ChecksThe user is obliged to perform or to have performed the Technical
Safety Checks on those medial products for which these checks
have been prescribed by the manufacturer and to carry them out
according to the indications of the manufacturer as well as the
generally approved technical standards while adhering to the
periods stated (§ 6 MP BetreibV).
B. Braun also recommends training on the Technical Safety
Checks, or to perform at least the steps indicated in the current
version of the manual, as:
-the TSC requires that the instructions in the manuals are
observed
-the manuals are a reference for measurements
-depending on the unit type, the Service Program must be
called which may lead to a dangerous unit condition in case
of inappropriate operation. Furthermore, a special service
connector may be necessary.
Current VersionsThis manual version corresponds to the state when the manual
was written. B Braun reserves the right to make technical
modifications. The state of the revision is indicated by the index
number in the footer of every page.
Revision ServiceThe possession of this manual does not automatically mean
inclusion in the revision service. You will be included in the
revision service after:
-technical training by B. Braun Melsungen or
-a written order placed with the sales department of B. Braun
(fee required).
Perfusor® Space, 1.1 gb 0- 5
1.11.0
0
Important Preliminary Remarks
Responsibility of the ManufacturerThe manufacturer, person who assembles, installs or imports the
device can only be held responsible for safety, reliability and
performance if
-mounting, enhancements, new settings, changes or repairs
are carried out by duly authorized persons,
-the electrical installation in the corresponding room meets
the requirements of the VDE 0107, VDE 0100 part 710 or
IEC 60364-7-710 and the national standards,
-the device is used in accordance with the instructions for use
and the Service Manual,
-the Technical Safety Checks are performed at regular
intervals,
-a current manual which corresponds to the revision state is
used when carrying out maintenance, repair and service,
-the service technician takes part in the revision service,
-the technician has participated in a technical training course
for the specific B. Braun unit.
Quality ManagementB. Braun is certified in accordance with DIN EN ISO 9001 and
ISO 13485. This certification also includes maintenance and
service.
The unit has the CE label. The CE label confirms that the device
corresponds to the “Directive of the Council for Medical Products
93/42/EC” of June 14, 1993.
Checks and RepairTraining may only be performed by B. Braun. The possession of the
manual does not authorize the performance of repairs. The
instructions on electrostatic sensitive components (ESD
standards) must be observed.
After repair a device check or diagnosis is to be carried out.
Notes on ESDSemiconductors can be destroyed by electrostatic discharge.
Especially MOS components can be damaged by interference from
electrostatic fields, even without discharge via contact. This type
of damage is not immediately recognizable. Unit malfunctions
can even occur after a longer period of operation.
0- 6 Perfusor® Space, 1.1 gb
1.1
Fig.: 0 - 1
Important Preliminary Remarks
Each workstation must be equipped according to the
recommendations with the necessary static protective measures,
if ESD components or boards are handled.
Each workstation must be equipped with a conductive table
surface. The conductive surface, the soldering iron or the
soldering stations must be grounded via protective resistors.
Chairs must be of antistatic design. The floor or floor mats should
be of electrically conductive material.
Personnel must wear conductive wristbands which are connected
to a central ground potential via protective resistors, e.g. the
ground contact of a wall outlet. Furthermore it is recommended
that personnel wear cotton clothing and electrically conductive
shoes to prevent electrostatic charge.
0
Spare Parts and Test EquipmentOnly use original spare parts from the manufacturer. Do not
tamper with assembly groups which can only be exchanged
completely. The spare parts required are listed in the repair
descriptions.
Service personnel are responsible for the calibration of their test
equipment. Original test equipment can be calibrated at the
works of B. Braun. Further information is available upon request.
Setting OffAdditional notes and warnings are set off as follows:
Note
Is used for additional or special notes concerning information and
working steps.
CAUTION
Is used for working steps which may result in damage to the unit,
system or to a connected device.
WARNING
IS USED FOR WORKING STEPS WHICH MAY RESULT IN PERSONAL
INJURY.
Perfusor® Space, 1.1 gb 0- 7
1.11.0
0
Important Preliminary Remarks
References to chapters are shown as follows
(see “Setting Off“ ➨ pg. 0 - 7)
References to figures and tables are shown as follows
Fig.: 2 - 3 or Table 2 - 1
References to item numbers in figures are shown as follows
(Fig.: 1 - 1 / Item 1)
In this case “Fig.: 1 - 1“ is the figure number and “Item 1“ the item
number within the figure.
When the Service Manual is stored as pdf-file, these references
are displayed green. Click with the mouse button on a reference
to jump to the corresponding source.
Menu commands are described as:
Menu
File
.
0- 8 Perfusor® Space, 1.1 gb
1.2
Important Preliminary Remarks
0
List of AbbreviationsAbbreviations which are not generally known, but are used in this
manual, are listed below.
CAN Controller Area Network
CE Communauté Européenne
(European Communities)
CSCalibration Step
DIN Deutsche Industrie Norm
(German Industrial Standard)
EN European Standard
ESD Electrostatic Discharge
FuPFunction Microprocessor
IEC International Electrotechnical
Commission
ISO International Standardization
Organization
ISPInfusomat® Space
ISPSInfusomat® Space, Silicon
ISPPInfusomat® Space, PVC
KuPMonitoring Microprocessor
LCD Liquid Crystal Display
MOS Short for the following
company name:
MOS Technology, Inc.
(Commodore Semiconductor
Group)
PCA Patient-Controlled Analgesia
PSPPerfusor® Space
SPSpace (System)
SPCSpaceCover
SPCCSpaceCover comfort
SPCSSpaceCover standard
SPCOSpaceCom
SPCTSpaceControl
SPSSpaceStation
TEMP Temperature
TSTroubleshooting Step
TSC Technical Safety Checks
Perfusor® Space, 1.2 gb 0- 9
1.21.0
0
Important Preliminary Remarks
UTSUnit Test Step
VDE Verband der Elektrotechnik,
Elektronik und
Informationstechnik e.V.
(German electrical engineering
association)
0- 10 Perfusor® Space, 1.2 gb
1.3
0-Contact Persons
0
Technical TrainingVia local representative.
Entry for Technical TrainingApplication for a technical training course must be made via the
responsible representative.
Ordering of Spare Parts and Test EquipmentPlease contact your local B. Braun subsidary.
Return of Spare Parts and Test EquipmentB. Braun Melsungen AG
Schwarzenberger Weg 73-79
Wareneingang Werk C
34 212 Melsungen
Germany
Safety Officer
(§ 30 MPG)
TranslationCs2 Informatik GmbH & Co. KG, Germany
Dr. Ludwig Schütz
e-mail: ludwig.schuetz@bbraun.com
Perfusor® Space, 1.3 gb 0- 11
1.0
0
For your notes:
Contact Persons
0- 12 Perfusor® Space, 1.0 gb
1.0
Description
System Overview
1
2
3
4
Fig.: 1 - 1 Space system
Legend of fig. 1 - 1:
ItemDesignation
1SpaceCover
2Infusion pump Infusomat® Space
3Infusion syringe pump Perfusor® Space
1-System Overview
The Perfusor® Space (PSP) is according to IEC/EN 60601 resp. IEC/
EN 60601-2-24 a transportable infusion syringe pump for
administrating fluids in the nutritional therapy and infusion
technique as well as for home care applications.
The medical specialist must decide on suitability for application
on the basis of the warranted properties and the technical data.
The Space system is a modular design of modern infusion
technology for stationary, mobile or private use. The key modules
and their connection to the peripheral devices are shown in
Fig.: 1 - 1.
All the pump types, Perfusor® Space, Infusomat® Space and
Infusomat® Space P, as well as the other devices of the system are
of modular design. Up to three pumps can be connected together
mechanically using L rails on the bottom of the unit and grooves
on the top. They can then be fastened to a drip stand or
appropriate rail using the pole clamp.
The SpaceControl module can be used to extend operation. One
single pump can be inserted onto this module. The pump is then
connected via connectors to the module.
The SpaceStation module allows the set-up of a complete pump
system with up to 24 pumps. Up to four pumps can be installed in
every SpaceStation. The pumps are supplied with power via the
integrated power supply and the built-in connectors. The pumps
5
are connected to the optional SpaceCom via these connectors.
SpaceControl can also be integrated into the system.
Up to six SpaceStations can be set-up as a column with a total of
24 pumps. SpaceStation placed next to each other can be
connected via special connection cables, if the maximum number
of 24 pumps in maximum three columns is not exceeded.
SpaceCover Standard or SpaceCover Comfort forms the top of
each column. Alarms are signalled by a row of LEDs and a
loudspeaker in the SpaceCover Comfort.
1
4SpaceControl
5SpaceStation
Perfusor® Space, 1.0 gb 1- 1
1.0
1
System Overview
Physical Construction
1
2
5
4
3
Fig.: 1 - 2 Perfusor® Space
Legend of fig. 1 - 2:
ItemDesignation
1Perfusor® Space
2Drive head
3Syringe holder with piston brake
4Operating Unit
5Syringe area
6
78
6Connector “P2“ for SpaceStation module, external 12 V DC
and accessories
7Connector “P3“, connection to SpaceControl module
8Battery compartment cover
1- 2 Perfusor® Space, 1.0 gb
1.0
System Overview
The Perfusor® Space housing mainly consists of the bottom part
and the upper part.
The battery module is inserted in the rear of the housing upper
part. The opening is covered by the battery compartment cover.
The operating unit is attached to the front of the bottom part with
two hinges. This operating unit covers the area for the syringes.
The complete drive assembly, consisting of lead screw and drive
head with driving tube is located directly behind the syringe area
in the bottom part of the housing. The housing bushing for the
driving tube is located in the side of the housing.
The syringe holder is mounted in the right side of the housing
bottom part.
The processor PCB with the permanently connected external
connectors “P2” and “P3” is located at the bottom of the housing
bottom part.
1
Function
There are two power options for the Perfusor® Space:
-via the inserted battery module
-via an external 12 V DC power supply (e.g. SpaceStation,
SpaceControl, an external power supply or from an
ambulance car) connected to connector “P2”
The voltage supplied is converted to the internal voltages required
through a voltage transforming and monitoring circuit on the
processor PCB.
An independent circuit in the battery module monitors the battery
cells and controls their charge condition.
The Perfusor® Space is connected to a SpaceControl by connector
“P3”.
The function processor controls all the functions of the Perfusor®
Space. Data is stored in a non-volatile memory which also
controls the external data transfer.
The control microprocessor monitors all important responses of
the function processor to incoming information. If a response
does not correspond with that expected by the control
microprocessor, an error message is generated and the device is
switched to a safe stop state.
The drive motor is monitored by a detector for speed and direction
of rotation. The extended end position of the drive head is
detected by a switch on the processor PCB.
Perfusor® Space, 1.0 gb 1- 3
1.0
1
System Overview
The pressure in the infusion system is measured through a strain
gauge measuring in the drive head and monitored in the device
electronics. The data from the strain gauge is continuously
compared with the limit values which are calculated dependent
on the selected syringe type and the pressure settings. When the
limit values are exceeded an alarm is automatically triggered and
the pressure in the infusion system is reduced. The maximum
pressure is additionally limited by a second, independent system.
This maximum pressure limitation is performed using the motor
current control.
The syringe size detection is performed via the syringe holder. The
syringe holder is connected to a potentiometer. The syringe size is
determined from the resistance of the potentiometer.
The syringe is fixed with the syringe holder and the axial fastening
device. The syringe piston is fastened with two claws in the drive
head. When a syringe is inserted the syringe piston is held by the
piston brake, until the piston has been caught by the claws.
Keyboard and display as well as the syringe area are illuminated.
1- 4 Perfusor® Space, 1.0 gb
1.0
System Overview
1
Fig.: 1 - 3 Block diagram Perfusor® Space
Perfusor® Space, 1.0 gb 1- 5
1.0
1
System Overview
Unit Software
Position12345678910
Digit688C030001
Revision level
Hardware
Software group
Device type: Perfusor® Space
Fig.: 1 - 4
Approved Software Versions
688A030032
-Basic software
688A030035
-Improved functions
688A030040
-Improved functions
-Languages French and Swedish added
688B030002
-Improved functions
688B030003
-CAN bus functioning
688C030001
-Dose calculation
-Changed CAN log
688D030001
-Drug list data base
-Changed user language
688E030003
-Improved functions
-Piggyback
-Soft limits
688F030006
-PCA
-Changed claw configuration
-Optimized alarm handling
688G030002
-Improved functions
1- 6 Perfusor® Space, 1.0 gb
1.0
Service Program
System Overview
Software Update of the Unit
The instructions for updating the software are supplied with the
software itself.
CAUTION
If the device is disconnected while the software is being updated
or the device or PC is switched off, a component of the software
may be seriously damaged so that repairs are no longer possible.
In such a case the software cannot be updated via the PC and the
device must be returned to B. Braun.
Approved Version
Note
Please note that text and / or functions of the Service Program
may change depending on the software version. The following
screen illustrations are only examples and represent the state
when the manual was printed.
1
-0.0.28
-1.0.0
-1.1.2
-1.1.3
-1.1.4
-1.2.1
-1.3.5
-1.5.0
-2.0.1
-3.1.0
-4.0.0
-5.1.0
Starting the Service Program
Note
Installation and further operation of the Service Program is
described in its separate instructions for use.
Perfusor® Space, 1.0 gb 1- 7
1.0
1
System Overview
1. Start the “HiBaSeD.exe” program (History, Barcode, Service,
D
rug list) on the PC. The Service Program is loaded and
started and the initial window of the Service Program is
displayed.
2. Read the notes carefully.
3. Mark the field “I accept all conditions” and then the field
“Yes” to confirm that you have read the notes.
Note
Click the field “English” to switch the language of the notes over
to English.
Fig.: 1 - 5
Fig.: 1 - 6
4. Enter the password and confirm it by clicking the field “Start”.
The Service Program checks the PC interfaces for connected
devices of the Space system. Units that were found are
displayed for a short moment on the screen.
Fig.: 1 - 7
1- 8 Perfusor® Space, 1.0 gb
1.0
System Overview
The work window of the Service Program appears on the
screen. All devices recognized are listed in the left column.
1
Fig.: 1 - 8
5. Activate the desired device from the list on the left in the
work window with a double-click. The device data is then
displayed below the device name.
Perfusor® Space, 1.0 gb 1- 9
1.0
1
Fig.: 1 - 9
System Overview
If the unit software version is not compatible with the Service
Program version, a window opens prompting the operator to
change the Service Program version. This window displays a
compatibility list of the Service Program- and unit software
versions.
If Service Program- and unit software versions are
compatible, all the Service Program functions are activated.
Fig.: 1 - 10
1- 10 Perfusor® Space, 1.0 gb
1.0
Fig.: 1 - 11
System Overview
Service Program Version
1. Open the “HiBaSeD“ window via
version of the Service Program is shown in this window.
2. Close the window by clicking “OK”.
Compatibility List
1. Open the “Unit - Compatibility” window via
Compatibility
HiBaSeD-version and the unit software version.
2. Close the window by clicking “OK”.
. This window displays the compatibility of the
Help ➨ Info ...
Help ➨
1
. The current
Fig.: 1 - 12
Quit the Service Program
1. Exit the Service Program via
2. Disconnect a power supply which might be connected from
the unit.
3. Switch off the unit.
4. Remove the battery module.
5. The device can be restarted after appr. 10 seconds.
Application ➨Quit
.
Perfusor® Space, 1.0 gb 1- 11
1.3
1
System Overview
Technical Data
Options
All technical data is indicated in the instructions for use.
The functions of the individual options are detailed in the
instructions for use.
WHILE TESTING THE UNIT AND TROUBLE SHOOTING THE
OPERATOR/SERVICE TECHNICIAN MUST WORK WITH VOLTAGES
UP TO 115 / 230 V AC. THESE VOLTAGES MAY CAUSE INJURIES
WHICH ARE DANGEROUS TO LIFE AND LIMB. THE NATIONAL AND
INTERNATIONAL SAFETY REGULATIONS ARE TO BE ADHERED TO.
Before each disassembly and assembly of a unit subsystem check
the connectors, plug contacts and connections for corrosion and
tight fit. These fault types are not described again in the following
trouble shooting list.
The following equipment and gauges are necessary for testing the
unit and/or performing troubleshooting:
2
-PC
-Service connector SP
-Service Program HiBaSeD
-Interface cable
-Syringe 2 ml / 3 ml
-Syringe 10 ml
-Syringe 30 ml
-Diameter gauge 32.0 mm
-Diameter gauge 23.4 mm
-Diameter gauge 15.7 mm
-Diameter gauge 9.0 mm
-Length gauge PSP
-Syringe gauge “#Lehre OPS 50“with push-button plate and
motor power test adapter for Perfusor® Space
There are pictures of the gauges in Chapter “Special Tools“ (➨
pg. 8 - 3).
CAUTION
Take special care when carrying out measurements on an open
and switched-on unit. Short circuits and wrong measuring
methods can cause serious damage to or destroy the subsystems
of the device.
Perfusor® Space, 1.1 gb 2- 1
1.0
2
Unit Diagnosis / Calibration
The unit check, calibration and trouble shooting are subdivided
into numbered working steps (Unit Test Step UTS, Calibration Step
CS, Trouble Shooting TS) and are based on each other.
Beginning with UTS 1 the operation described here has to be
executed. The consequences of the steps performed are listed in
the “Function“ column. If the result corresponds to the
consequence, the working step must be carried out to which
reference is made in the column “If yes”. If the result does not
correspond with the function described, the working step in
column “If no” is to be executed.
One example is given in Fig.: 2 - 1.
UTSActivityFunctionIf yesIf no
1UTS 2
2UTS 3TS 1
3UTS 4
4UTS 5TS 4
5
Model table 1
TSActivityFunction
1UTS 3TS 2
2TS 3TS 4
3UTS 3
4UTS 4TS 4
5UTS 4
Model table 2
Fig.: 2 - 1 Model tables
Steps for which additional information is required are described
after the table in detail.
2- 2 Perfusor® Space, 1.0 gb
1.0
Alarms and Error Codes
Unit Diagnosis / Calibration
The alarms of the Perfusor® Space are classified in 5 categories.
These categories are listed hereafter according to their
importance.
-Alarm advice
In case of unacceptable inputs corresponding messages are
displayed (e.g. “Caution! Rate out of range“, “The parameter
cannot be changed“) and a beep sounds.
-Pre-alarm
Pre-alarms are triggered several minutes (depending on the
service settings) before the operating alarms.
-Reminder alarm
A reminder alarm is triggered if the device is not operated for
two minutes when input or operation was not finished.
-Operating alarm
In case of an operating alarm the infusion is stopped. An
audible signal is released, the red LED flashes and a staff call
is triggered. The message “Alarm” and the cause of the alarm
appear on the display.
-Device alarm
The most important alarms and error codes as well as their
meaning and possible fault clearance are specified in the
following lists.
2
Note
The device should be checked after every repair or service (see
“Device Check“ ➨ pg. 2 - 9).
Perfusor® Space, 1.0 gb 2- 3
1.0
2
Unit Diagnosis / Calibration
Alarms
AlarmPossible CauseFault Clearance
1Battery nearly discharged (type: pre-
alarm)
2Battery discharged (type: operating
alarm)
3Battery cover open (type: operating
alarm)
4Drive blocked (type: operating alarm)❒ The drive was manually blockedEliminate blockage
5Malfunction of claws (type: operating
alarm)
6Push-button has no contact (type:
operating alarm)
7Device alarm (type: device alarm)A serious internal fault was detected in
The device was not connected to the
mains long enough
Battery module defective or too oldReplace battery module
The device was not connected to the
mains long enough
Battery module defectiveReplace battery module
❒ The battery compartment cover is
not correctly closed
❒ The magnet in the battery
compartment cover is missing
❒ The battery compartment cover is
not recognized by the battery
module
❒ Driving force too lowConnect the unit to the mains for at least
❒ The drive is physically damagedReplace drive.
❒ The syringe piston was not
recognized
❒ The claws or the claw drive are/is
damaged
❒ Negative pressure in the syringe
system
❒ Syringe was removed without
opening the syringe holder
❒ Push-button sensor defectiveReplace drive head
the system
Operate the device with battery until the
message “Battery discharged“ is
displayed and the unit is switched off.
Then connect the unit to the mains for at
least 6 hours.
Connect the unit to the mains for at least
6 hours
Insert the battery compartment cover
correctly
Exchange the battery compartment cover
Replace battery module
6 hours and charge battery
Re-calibrate the device
Select or insert correct syringe type
Loosen the syringe via the emergency
release button in the drive head and
insert again
Re-calibrate the device
Replace drive head
See instructions for use
See instructions for use
Switch device off and on
Carry out a device check (see “Device
Check“ ➨ pg. 2 - 9)
Table 2 - 1 Alarms
2- 4 Perfusor® Space, 1.0 gb
1.0
Unit Diagnosis / Calibration
2
Device Alarms of the Function Processor
Error CodeDefinitionPossible CauseFault Clearance
11001 ... 1013Internal Error
21014Loudspeaker not offLoudspeaker connectorCheck the loudspeaker connector
LoudspeakerCheck the loudspeaker
31015Loudspeaker lostLoudspeaker connectorCheck the loudspeaker connector
LoudspeakerCheck the loudspeaker
41016Loudspeaker shortedLoudspeaker connectorCheck the loudspeaker connector
LoudspeakerCheck the loudspeaker
51017KuP switchoff path defect
(K_SM_CLK)
61018ADC pressure out of rangePressure measurement in drive
71019Internal Error
81020FUP Flash Memory Error Software SoftwareUpdate unit software
91021FUP different version KuP to FuPSoftwareUpdate unit software
101022 FUP pressure zero test failPressure measurement in drive
111023 FUP pressure offset test failPressure measurement in drive
121024FUP EA key closed too long 20sec Keyboard defectiveCarry out device check
131025Internal Error
Switch off path
Carry out calibration
head
Carry out calibration
head
Carry out calibration
head
Table 2 - 2 Device alarms of the function processor
Perfusor® Space, 1.0 gb 2- 5
1.0
2
Unit Diagnosis / Calibration
Device Alarms of the Control Microprocessor
Error CodeDefinitionPossible CauseFault Clearance
11100Timebase too fastQuartz of the processor PCBExchange processor PCB
21101Timebase too slowQuartz of the processor PCBExchange processor PCB
31102Timebase failQuartz of the processor PCB Exchange processor PCB
41103Keyboard HighKeyboard defectiveCarry out device check
51104EA_KEY defect 25secKeyboard defectiveCarry out device check
61105No keydecode Keyboard defectiveCarry out device check
71106ROM Romtest defect SoftwareSoftwareUpdate unit software
81107ROM Program defectSoftwareUpdate unit software
91108CM State without set
K_V_KM_ON
101109MPU_Test failedSoftwareUpdate unit software
111110RAM_Test failedSoftwareUpdate unit software
121111active resetVoltage supply during operation
interrupted
131112 ... 1114Internal Error
141115Drive too fastMotor drive
Recognition of direction of
rotation
151116Drive too slowMotor drive
Recognition of direction of
rotation
161117 ... 1118Internal Error
171119lcd backlight on defectLC display defectiveExchange operating unit
181120lcd backlight off defectLC display defectiveExchange operating unit
191121red led on defectLC display defectiveExchange operating unit
201122red led off defectLC display defectiveExchange operating unit
211123key pressed too long (without EA-