MELAG MELAtherm 10 User manual

User manual
MELAtherm® 10
Washer-Desinfector
as of software version 1.309
EN
Dear doctor,
We thank you for your confidence demonstrated by the purchase of this MELAG product. As an owner-run and operated
family concern founded in 1951, we have a long history of successful specialization in hygiene products for practice-
based use. Our focus on innovation, quality and the highest standards of operational reliability has established MELAG
as the world’s leading manufacturer in the instrument treatment and hygiene field.
You, our customer are justified in your demand for the best products, quality and reliability. Providing "competence in
hygiene" and "Quality – made in Germany", we guarantee that these demands will be met. Our certified quality
management systems is subject to close monitoring: one instrument to this end is our annual multi-day audit conducted
in accordance with ISO13485 and ISO9001. This guarantees that all MELAG products are manufactured and tested in
accordance with strict quality criteria.
The MELAG management and team.

Contents
Contents
1 General safety information..................................................................................................................................................5
2 Scope of delivery..................................................................................................................................................................7
3 General Guidelines...............................................................................................................................................................8
User group and validity ........................................................................................................................................................8
Intended use ........................................................................................................................................................................8
Symbols used.......................................................................................................................................................................8
Formatting rules ...................................................................................................................................................................8
Symbols on the device.........................................................................................................................................................9
Disposal ...............................................................................................................................................................................9
4 Performance specifications ..............................................................................................................................................10
User Benefits......................................................................................................................................................................10
Program sequence.............................................................................................................................................................11
Approved process agents ..................................................................................................................................................11
5 Description of the device...................................................................................................................................................13
Views of the device ............................................................................................................................................................13
Operating panel and acoustic signals ................................................................................................................................15
Menu structure ...................................................................................................................................................................16
Water softening unit ...........................................................................................................................................................17
6 Settings ...............................................................................................................................................................................18
SETUP menu .....................................................................................................................................................................18
Setting the water supply.....................................................................................................................................................18
Setting automatic logging...................................................................................................................................................18
Setting date and time .........................................................................................................................................................19
Setting the display contrast................................................................................................................................................20
Selecting the language.......................................................................................................................................................20
Setting the water hardness ................................................................................................................................................21
7 First steps ...........................................................................................................................................................................22
Setup and Installation.........................................................................................................................................................22
Testing in daily operation ...................................................................................................................................................22
Switching the device on and off .........................................................................................................................................22
Opening and closing the door ............................................................................................................................................22
Emergency release of the door..........................................................................................................................................23
Inserting the basis basket ..................................................................................................................................................24
Filling the regeneration salt................................................................................................................................................24
Regenerating the water softening unit ...............................................................................................................................25
Metering process agents....................................................................................................................................................26
Holding process agents ready............................................................................................................................................26
Bleeding the metering hoses..............................................................................................................................................28
8 Cleaning and Disinfection .................................................................................................................................................30
The nature of the load........................................................................................................................................................30
Arranging the load..............................................................................................................................................................30
Decontaminating hollow-bodied instruments .....................................................................................................................31
Decontaminating dental transfer instruments.....................................................................................................................32

Contents
Decontaminating ophthalmological instruments.................................................................................................................32
Overview of programs........................................................................................................................................................33
Selecting, starting and following the program ....................................................................................................................34
Manual program abort........................................................................................................................................................36
Removing the load after program end................................................................................................................................37
9 Logging ...............................................................................................................................................................................38
Batch documentation .........................................................................................................................................................38
Output media......................................................................................................................................................................38
Outputting logs immediately and automatically..................................................................................................................40
Subsequent log output .......................................................................................................................................................41
Deleting the saved logs......................................................................................................................................................41
Determining the format for the program logs .....................................................................................................................41
Finding the logs..................................................................................................................................................................44
10 Function tests...................................................................................................................................................................45
Automatic and manual functional check.............................................................................................................................45
Measuring conductivity.......................................................................................................................................................45
11 Maintenance......................................................................................................................................................................46
Daily checks and cleaning..................................................................................................................................................46
Cleaning on demand..........................................................................................................................................................48
Avoiding staining................................................................................................................................................................48
Changing the filter in the drying fan ...................................................................................................................................48
Maintenance.......................................................................................................................................................................49
(Process) validation............................................................................................................................................................50
12 Pause times ......................................................................................................................................................................51
Decommissioning...............................................................................................................................................................51
Transport within the practice..............................................................................................................................................52
13 Malfunctions .....................................................................................................................................................................53
General events...................................................................................................................................................................53
Warnings............................................................................................................................................................................54
Malfunction messages .......................................................................................................................................................56
14 Technical Data ..................................................................................................................................................................62
15 Accessories and Spare Parts..........................................................................................................................................63
Accessories........................................................................................................................................................................63
16 Documentation and approval..........................................................................................................................................64
Glossary .................................................................................................................................................................................65

1 General safety information
5
1 General safety information
When operating the device, comply with the following safety instructions as well as those
contained in subsequent chapters. Use the device only for the purpose named in these
instructions. Failure to comply with the set-up conditions can result in malfunctions or
damage to the device and/or human injury.
Power cable and power plug
nObserve the legal regulations and supply conditions of your local electricity company.
nNever operate the device if the mains cable or power plug are damaged.
nThe power cable and plug should only be replaced by authorized persons.
nNever damage or alter the plug or mains cable.
nNever unplug by pulling on the power cable. Always take a grip on the plug.
nMake sure that the power cable is not clamped.
nNever install the cable along a source of heat.
nNever fix the power cable with sharp objects.
Set-up installation and commissioning
nCheck the device for any damage suffered during transport after unpacking.
nOnly have the device set up, installed, and started up by people authorized by MELAG.
nThe connections for electrical provision and water supply and discharge must be set-up by trained per-
sonnel.
nIn accordance with current VDE specifications, the device is unsuitable for operation in explosive at-
mospheres.
nThe device is conceived for use outside patient surroundings. The device should be located at least
1.5 m away (radius) from the treatment area.
nThe documentation media (computer, CF card reader etc.) must be placed in such a way that they
cannot come into contact with liquids.
nObserve all the information contained in the technical manual during commissioning.
Daily operation
nUse only those instruments designed by their manufacturer for automatic treatment in a washer-disin-
fector. Comply with the instructions issued by the instrument manufacturer in accordance with
DINENISO17664. It is especially important to observe the manufacturer's information when treating
newly purchased instruments for the first time.
nUse only original MELAG accessories or those from other suppliers authorized for use by MELAG.
nWhen using additional accessories to accept instruments, especially hollow-bodied instruments, it is
necessary to observe the information contained in the manufacturer's operating instructions.
nObserve the relevant standards and directives applicable to the treatment of instruments in your coun-
try as well as the treatment information from the instrument manufacturer.
nThe personnel responsible for instrument treatment must be sufficiently trained and schooled.
nThe fore ventilation slits must not be covered.
nOnly operate the device with the basis basket provided for this purpose.
Process agents
nHandle all process agents with care. The cleaning, neutralization and rinsing aids contain irritants and
even caustic substances.
nUse only those process agents approved by MELAG for this device. Observe the operating and safety
information from the process agent manufacturer. If, despite observation of the manufacturer's inform-

1 General safety information
6
ation, the process agents have a negative effect on the material of the instruments or the device, liabil-
ity lies with the manufacturer of the process agents.
nThe use of process agents not approved by MELAG absolves MELAG of all liability whatsoever for
any damage to the device or the instruments.
nShould you have any questions concerning the compatibility of the process agents with the instru-
ments, please consult the manufacturer. MELAG provides information for the application of the pro-
cess agents in the device but does not take any responsibility for their effects on the instruments.
nAny fluids in the drawer and the floor tank underneath can also contain process agents in case of
damage. Ensure that you observe the information of the respective process agent manufacturer.
Maintenance
nHave the maintenance done only by authorized persons.
nMaintain the specified servicing intervals.
Transport and storage
nInstall and operate the device in a frost-free environment.
nStore and transport the device in a generally frost-free environment.
nAvoid strong vibrations.
Malfunctions
nShould the device issue the same malfunction message repeatedly, turn off the device
and if necessary, inform your stockist.
nOnly have the device repaired by authorized persons.

2 Scope of delivery
7
2 Scope of delivery
Please check the scope of delivery before setting up and connecting the device.
Standard scope of delivery
▪ Washer disinfector MELAtherm®10
▪ User manual
▪ Technical manual
▪ Record of installation and set-up
▪ Manufacturer's inspection report
▪ Certificate of Conformity
▪ Warranty certificate
▪ Instructions for the use and care of the accessories
▪ MELAflash CF card for documentation
▪ 1 L container for rinse aid
▪ 5 L container for cleaning agent
▪ Feed funnel for the regeneration salt
▪ Starter package of regeneration salt
▪ Open-end wrench for injector rail
▪ Transfer spigot for process agent containers
▪ Effluent hose with hose clamp Ø 16-25/9 mm
Optionally
▪ Accessories according to the delivery note

3 General Guidelines
8
3 General Guidelines
Please read this user manual carefully before commissioning the device. The operating manual includes
important safety information. The functionality and value-retention of this device depend primarily on the
care accorded to it. Make sure to keep the User Manual close to the device. It represents a component of
the product.
User group and validity
This manual applies for the devices MELAtherm® 10 DTA and MELAtherm® 10 DTB. This manual is
addressed to doctors, their assistants and service departments.
Intended use
In accordance with DIN EN ISO 15883-1 and -2, this device is designed for application in a medical
context, e.g. clinics and medical and dental practices. You can subject thermo-stable medical instruments
(i.e. instruments which are heat resistant to a temperature of 95°C) to automatic cleaning as long as they
are suitable for this purpose. The cleaning is undertaken via the use of water and a chemical cleaning
agent. Subsequent disinfection is performed by thermal disinfection.
This device is NOT suitable for treatment of:
▪ Thermo-instable instruments, e.g. flexible endoscopes
▪ Wastes for disposal and in the lab area
▪ Dishes
▪ Bedpans
Symbols used
Symbol Explanation
Indicates a dangerous situation, which if not avoided, could entail slight to life-
threatening injuries.
Draws your attention to a situation, which if not avoided, could result in damage to the
instruments, the practice fittings or the device.
Draws your attention to important information.
Formatting rules
Example Explanation
see Chapter 2 Reference to another text section within this document
Settings Words or phrases appearing on the display of the device are marked as display text.

3 General Guidelines
9
Symbols on the device
Manufacturer of the medical product
Date of manufacture of the medical product
Medical product serial number from the manufacturer
Article number of the medical product
Refers to the lowest and highest water temperature to which the device can be safely
subjected.
Flow pressure on the water inflow connected from min. to max.
Internal device fuse, rated in amperes [A]
The operating manual includes important safety information. Failure to comply with these
instructions can result in injury and material damage.
Please read this user manual carefully before commissioning the device.
In affixing this CE mark, the manufacturer declares that this medical product fulfils the
basic requirements of the Medical products directive. The four-digit number confirms that
this is monitored by an approved certification agency.
The device may not be disposed as domestic waste. The vendor is responsible for
appropriate disposal of the device - it must be delivered to the vendor to be disposed of.
By the designation of an apparatus with this symbol, the manufacturer furthermore
declares that he satisfies all requirements of the law concerning the release, redemption
and environmentally sound disposal of electric and electronic appliances.
Disposal
MELAG devices are synonymous for long-term quality. When you eventually need to decommission your
MELAG device, we offer a special disposal service. Simply contact your stockist.
The packaging protects the device against transport damage. The packaging materials have been
selected for their environmentally-friendly and recycling properties and can be recycled. Returning the
packaging to the material flow reduces the amount of waste and saves raw materials. Dispose of all non-
required packaging materials at the collection points of the dual system.
Dispose of waste from process agents in accordance with the specifications from the manufacturer of the
process agents. Information regarding this topic is provided by the safety data sheets or can be obtained
directly from the manufacturer of the process agents.
Dispose of accessories and consumption media which you no longer require (e.g. used filters) in the
appropriate manner. Comply with all relevant disposal specification in terms of possibly contaminated
waste.

4 Performance specifications
10
4 Performance specifications
User Benefits
Universal use
The device cleans and disinfects. The disinfection phase is conceived so as to reach an A0-value of at
least 3000. This eliminates vegetative bacteria and fungi/fungal spores and disables viruses (inc. HBV,
HCV) thus reaching the effective range AB in according to the (German) RKI directive.
Active drying
The device has an active drying facility. This means that after cleaning and disinfection, the instruments
are dried inside (interior lumen) and out via an integrated drying fan. The HEPA-Filter guarantees drying
with contamination-free air. Automatic treatment of hollow-bodied instruments is also possible. This
protects the instruments from stain accretion and rusting. The geometry of some hollow-bodied
instruments such as turbines, requires additional drying.
Automatic sieve recognition
The device recognizes automatically before a program start whether the fine sieve has been inserted in
the base of the washing chamber. Thus it avoids a situation in which instrument components enter the
opening of the drain pump or the circulation pump and thus compromising the function of the pumps, rinse
arms and the injector rail.
Internal water softening
The device has an internal softening plant. The water hardness of the local drinking water is set in the
device. The internal water softening unit then automatically adjusts itself to the best solution. This ensures
a optimal instrument decontamination result.
Monitoring the rotation speed of the rinse arms
The rotation speed of the rinse arms is subject to permanent monitoring during a program run. This
ensures that the cleaning process proceeds properly and the rinse arms do not become blocked e.g. by
protruding instruments in the washing chamber.
Monitoring the cleaning pressure
The cleaning pressure is monitored during a program run via a pressure sensor. This ensures effective
cleaning. Excess foam generation results in the interruption of the program run.
Metering monitoring
The required amounts of cleaner and neutralizer are measured out using a hose measuring pump. A
measurement turbine performs flow monitoring. The rinse aid is metered using a hose metering pump
subject to monitoring for rotation speed.
Drawer for process agents
The drawer in the lower area of the device provides storage space for the process agents cleaning agent,
neutralizer and rinse aid.
Automatic conductivity measurement
If the device is provided with DI water in the final rinse, the DI water is subject to automatic, internal
conductivity measurement.
Emergency opening of the door
The door can be opened manually via the emergency release following a power outage or malfunction.

4 Performance specifications
11
Program sequence
The program steps are indicated on the display during the program run:
Pre-cleaning
Pre-cleaning is performed with softened water and without process agents. It is temperature controlled. All
proteins on the instruments must be removed entirely. It is necessary to avoid denaturation resulting from
too a high water temperature. These and other coarse organic deposits are removed during pre-cleaning.
Cleaning
The actual cleaning is performed during the cleaning process. The washing chamber is heated until
reaching the program-specific temperature. This is then held during the holding time. The cleaner is added
automatically before the holding time begins.
Neutralization
The main cleaning is followed immediately by neutralization. Neutralization reduces alkalinity and frees the
instruments from acid-soluble deposits such as lime scale and extraneous rust etc. During this process, a
specified amount of cold process water is pumped into the washing chamber. This is followed by the
addition / mixing of a measured amount of neutralizer.
Intermediate rinsing
Intermediate rinsing is a preparatory step to disinfection to reduce the residual concentration of the
process agents.
Disinfection
Intermediate rinsing is followed by thermal disinfection at a temperature of over 90°C.
Drying
The instruments are then dried by the integrated drying fan from inside and out. This prevents rust
accretion on the instruments.
Displaying the batch counter
The display shows the last batch number run and the total batch counter after a program end or the end of
a program abort.
Approved process agents
NOTICE
Observe the operating and safety information from the process agent manufacturer.
Process agents from different manufacturers may not be mixed. Any change to another
authorized combination may only be performed by trained service partners. The metering
concentration must be adapted to local conditions. This is to be performed by the service
technician during setup in accordance with the manufacturer's information.
NOTICE
Observe the operating and safety information from the process agent manufacturer. If,
despite observation of the manufacturer's information, the process agents have a
negative effect on the material of the instruments or the device, liability lies with the
manufacturer of the process agents. The use of process agents not approved by MELAG
absolves MELAG of all liability whatsoever for any damage to the device or the
instruments.
The following combinations of process agents were tested for suitability for use with MELAtherm 10,
brought into circulation since 01-07-2012:

4 Performance specifications
12
Manufacturer Cleaner Neutralizer Rinse aid
Alpro* TR-3 TR-Neutralizer TR-Clear
B. Braun Helimatic cleaner alkaline Helimatic neutralizer C Helimatic rinse neutral
Bode Dismoclean 21 clean Dismoclean 25 acid Dismoclean 64
neutra-dry
Borer* deconex 28 ALKA ONE-x
deconex 22 LIQ-x
deconex 25 ORGANACID
deconex 26 MINERALACID
deconex 64 NEUTRADRY
Dr. Schumacher Thermoton Cleaner Thermoton N Thermoton clear
Dr. Weigert neodisher MediClean forte
neodisher MediClean Dental
neodisher N
neodisher Z
neodisher N dental
neodisher Z dental
neodisher MediKlar
neodisher MediKlar dental
neodisher MediKlar special
Schülke+thermodent alka clean
thermosept RKF forte
thermosept alka clean forte
thermodent neutralizer
thermosept NKP
thermosept NKZ
thermodent clear
thermosept BSK
Henry Schein Eurosept Thermo Cleanser Eurosept Thermo
Neutralizer
Eurosept Thermo Rinse
*When using process agents of manufacturers Alpro or Borer, it is absolutely essential and regardless of
the maintenance message after twelve month to replace all hoses of the dosing unit during maintenance.
Ensure that the process media selected are suitable for your instruments. Please address any questions to
the manufacturer of the process agents. Please observe and comply with the notes specific to the process
agents contained in the maintenance record.
Preset metering concentrations1)
Program Cleaner Neutralizer Rinse aid
Universal-Program 6 ml/l 1.5 ml/l 0.3 ml/l
Quick-Program 6 ml/l 1.5 ml/l 0.3 ml/l
Intensive Program 8 ml/l 1.5 ml/l 0.3 ml/l
Ophthalmo-Program 6 ml/l 1.5 ml/l --------
1) For using drinking water (hardness range medium - hard) we recommend the dosage concentrations
specified above. The metering concentration must be adjusted individually depending on the local
conditions. The pre-set metering quantities can be used for various combinations of process agents.
Observe the operating and safety information of the process agent manufacturer. This information can be
read-off from the canister in the units "ml/l" or on separate data sheets provided by the manufacturer. The
process-relevant parameters must be adapted depending on the nature of the soiling, the quality of the tap
water and other framework conditions. Please contact the manufacturer of the process agents regarding
this question.

5 Description of the device
13
5 Description of the device
Views of the device
2
1
3
5
6
4
7
10
8
9
Fig.1: Fore view
1 Operating and display field
2 Cover plate (optional)
3 Power switch
4 Cover for CF card slot and
Ethernet data interface (for
service)
5 Door grip
6 Hinged door, opens forwards
7 Drawer handle
8 Drawer for process agents
9 Ventilation slots
(air outlet with active drying)
10 Device foot
13
14
11
12
Fig.2: Cover cap CF card slot open
11 Card slot
12 LED
13 Ejection button
14 Ethernet data connection

5 Description of the device
14
20
19
18
15
16
17
Fig.3: View from rear
15 Connection for de-ionised water
(DI water)
16 Connection for cold water
17 Effluent connection
18 Transport rollers
19 Ethernet data connection for
permanent network connection
20 Mains power cable
25
21
22
23
24
Fig.4: View inside
21 Connection tube for injector rails
22 Cold water inflow (CW) and
deionised water (DI)
23 Salt container
24 Lower rinse arm
25 Coarse and fine sieve

5 Description of the device
15
31
27
30 29
28
26
Fig.5: Process agent drawer, open
26 Drying filter
27 Assignment of the process agents
28 Suction lance bracket
29 Container for rinse aid with suction
lance
30 Container for neutralizer with
suction lance
31 Container for cleaning agent with
suction lance
Operating panel and acoustic signals
The control panel consists of a two-line LED display and four membrane keys.
Key 1234
MELAG
MELAtherm 10
Fig.6: 2-row LED display
Table1: Key functions
Key Function/Explanation
1...2 or Navigation: BACKWARDS - FORWARDS
to adjust a value: REDUCE, INCREASE
3 Unlocking door, BACKWARDS, CANCELLATION
Leave menu
4 Confirming messages (ENTER, OK, YES, SELECTION).
QUIT with warning or malfunction messages
1+2 and The system status is displayed with information relating to the device e.g.
serial number, software version, daily and total batches etc.
1+3 and QUIT + DOOR, i.e. to acknowledge the program abort and unlock the door
3...4 or Deletes all logs located in the internal log memory

5 Description of the device
16
Acoustic Signals
The device issues acoustic signals for information purposes.
Table2: Acoustic Signals
Signal / tone Meaning
1x Confirmation, warning or message
3x Refill with salt soon; program abort; end of the abort after drying abort reached
5x Program completed successfully
10x Malfunction
Menu structure
P01 Universal-Program
P02 Quick-Program
P03 Intensive-Program
P04 Ophthalmo-Program
Z01 Rinsing
Z02 Emptying
Z03 Conductivity measurement DI
Z04 Air removal
Z05 Regeneration
Z06 Time metering 60s
M01 DOCU MENU (Output of a saved log via the following output media)
Select output medium: Automatic, CF card, MELAprint, PC
01 Log list
02 Last log
03 Logs of day
04 Logs of week
05 Logs of month
06 All logs
07 Last malfunction log
08 Malfunction logs Day
09 Malfunc. log Week
10 Malfunc. log Month
11 All malf. logs
12 Caption log
13 Status log
14 System log
15 Format CF card
M02 SETUP-MENU
01 DI water
02 Automatic logging
└
03 Date
04 Time
05 Display contrast
06 Language
07 Water (hardness) °dH
08 DIAGNOSIS + SERVICE
> AC outputs (AC-OUT)
> DC outputs (DC-OUT)
> Analogue inputs
> Counter inputs
> Digital inputs
SERVICE MENU
└
Maintenance Counter Date
DEMO mode
MAIN MENU
├
├
├
├
├
├
├
├
├
├
└
├
├
├
├
├
├
├
├
├
├
├
├
├
├
└
├
├
├
├
├
├
├
├
└
├
├
├
├
├
├
├
├
└
+
+

5 Description of the device
17
Water softening unit
The tap water is processed in a water softening unit to produce optimal cleaning results.
uUse coarse-grain regeneration salt (NaCl) to regenerate the water softening unit.
NOTICE
The fitted water softening unit has been optimized for a degree of hardness of 0–40°dH.
For higher degrees of hardness than 40°dH, you will require a dedicated water softening
unit.
NOTICE
An incorrectly set degree of hardness can result in a higher salt consumption or limes-
cale deposits on the instruments.
When using a dedicated water softening unit, the residual hardness of the dedicated
water softening unit must also be set in the setup menu.
Table3: Water hardness conversion table
°dH mmol/l °f °e °dH mmol/l °f °e °dH mmol/l °f °e
1 0.2 2 2 15 2.7 27 19 28 5.0 50 36
2 0.4 4 3 16 2.9 29 20 29 5.2 52 37
3 0.5 5 4 17 3.1 31 22 30 5.4 54 38
4 0.7 7 5 18 3.2 32 23 31 5.6 56 39
5 0.9 9 7 19 3.4 34 24 32 5.8 58 41
6 1.1 11 8 20 3.6 36 25 33 5.9 59 42
7 1.3 13 9 21 3.8 38 27 34 6.1 61 43
8 1.4 14 10 22 4.0 40 28 35 6.3 63 44
9 1.6 16 12 23 4.1 41 29 36 6.5 65 46
10 1.8 18 13 24 4.3 43 31 37 6.7 67 47
11 2.0 20 14 25 4.5 45 32 38 6.8 68 48
12 2.2 22 15 26 4.7 47 33 39 7.0 70 49
13 2.3 23 17 27 4.9 49 34 40 7.2 72 51
14 2.5 25 18

6 Settings
18
6 Settings
SETUP menu
The setup menu contains settings for the date, time and display contrast.
Navigate in the setup menu as follows:
1. Press to navigate in the main menu to M02->SETUP-MENU.
2. Press to open the setup menu.
3. Press to leave the setup menu.
4. Press to save changes or hold depressed to discard the changes.
Setting the water supply
If the device is connected to a DI water supply e.g. MELAdem 53/MELAdem 53 C or another water
treatment unit, this must be set on the device. In its delivery state, the water supply has been set to DI
water YES.
To alter this setting proceed as follows:
1. Press to open the setup menu.
ÊThis display registers the option 01 DI-Water YES.
2. Press in order to change the option.
ÊThe value YES flashes.
3. Press or to switch between YES and NO.
4. Press to accept Yes o No.
ÊThe value no longer flashes.
5. Press to leave the setup menu.
ÊThe selected value is automatically saved when leaving the setup menu.
Setting automatic logging
Settings relating to log output are made in Menu 02 Automatic logging. The settings made here are
saved for the respective output medium. The display image shows whether the option for log issue is
ACTIVE. Detailed information regarding logging is provided in chapter Logging [}page 38].
Determining the output medium
You are able to output the logs of the completed programs on various media: Comply with the
specifications of the manufacturer’s operating manual of the respective device.
The example shows how to use the CF card as an output medium. Proceed in a similar manner to set a
different output medium.
Working in the SETUP menu [}page 18] set the output medium as follows:
1. Press to navigate to 02 Automatic logging.

6 Settings
19
2. Press to open the menu 02 Automatic logging.
ÊThe selectable output media are displayed consecutively.
3. Press repeatedly to navigate in the setup menu to 01 CF card YES .
ÊThe display of YES indicates that the log is to be saved on the CF card.
4. Press if this value is to be changed.
ÊThe value YES flashes.
5. Press or to switch between YES and NO.
6. Press to save the new value.
ÊThe value no longer flashes.
7. Press to leave setup menu 02 Automatic logging.
ÊThe selected value is automatically saved when leaving the setup menu.
Determining the log format
You can find more detailed information regarding the log formats 0001 and 0002 here: Determining the
format for the program logs [}page 41].
Setting date and time
Date and time of the device must be correctly set for proper batch documentation.
PLEASE NOTICE
The time is not set automatically.
nThe time setting to summer or winter time must be performed manually.
Setting the date
Working in the SETUP menu [}page 18] set the output medium as follows:
1. Press to navigate to 03 Date.
2. Press to change the date.
ÊThe display changes to 03 Change date.
3. Press repeatedly to choose between day, month and year.
4. Press to activate the selected parameters (day, year).
ÊThe current value flashes.
5. Press or to reduce or increase the value.
6. Press to save the new value.
ÊThe value no longer flashes.
7. Press to change the month next. Proceed in a similar fashion here.
8. Press to leave the setup menu.
ÊThe selected value is automatically saved when leaving the setup menu.

6 Settings
20
Setting the time
Working in the SETUP menu [}page 18] set the time as follows:
1. Press repeatedly to navigate to 04 Time.
2. Press in order to change the language.
ÊThe display changes to 04 Change date.
3. Press to activate the selected parameters.
ÊThe current value flashes.
4. Press or to reduce or increase the value.
5. Press to save the new value.
ÊThe value no longer flashes.
6. Press to leave the setup menu.
ÊThe selected value is automatically saved when leaving the setup menu.
Setting the display contrast
Working in the SETUP menu [}page 18] set the display contrast as follows:
1. Press repeatedly to navigate to 05 Display contrast.
2. Press to activate the selected parameters.
ÊThe current value flashes.
3. Press or to reduce or increase the value.
4. Press to save the new value.
ÊThe value no longer flashes.
5. Press to leave the setup menu.
ÊThe selected value is automatically saved when leaving the setup menu.
Selecting the language
You can choose between two languages. Language 0001 is usually the local language or English,
Language 0002 is English or other required language Working in the SETUP menu [}page 18] set the
language as follows:
1. Press repeatedly to navigate to 06 Language.
2. Press to activate the selected parameters.
ÊThe current value flashes.
3. Press to change to language 0002.
4. Press to save the new value.
ÊThe value no longer flashes.
5. Press to leave the setup menu.