Tuttnauer T-Edge AMS10-230-PED-T User manual

1
Operation and Maintenance
Manual
Pre-vacuum B-class Steam Sterilizer
T-Edge
REF: AMS10-230-PED-T, AMS10-230-W-PED-T,
AMS10-230-T, AMS10-230-W-T
Cat. No. MAN205-0502001EN Rev G May 2020
Tuttnauer Ltd. Har –Tuv B Industrial Zone, P.O. Box 170, Beit Shemesh 9910101, Israel
Tel: [phone]
Tuttnauer Europe b.v., Hoeksteen 11, 4815 PR Breda, P.O. Box 7191, 4800 GD Breda,
Netherlands.
Tel: [phone], Fax: [phone]
To Purchase, Visit Avobus.com or call 1-800-674-3655

2
Table of Contents
1 GENERAL INFORMATION...................................................................................................................5
MANUFACTURER AND EUROPEAN AUTHORIZED REPRESENTATIVE INFORMATION........................................5
APPLICABLE REGULATION AND QUALITY STANDARDS ............................................................................5
1.2.1 And in consideration with: .....................................................................................................6
LEGEND FOR SYMBOLS APPEARING ON THE LABELS AND IN THIS MANUAL..................................................7
GENERAL DESCRIPTION OF THE DEVICE...............................................................................................9
INTENDED USE ............................................................................................................................10
INTENDED USERS .........................................................................................................................10
WARRANTY DESCRIPTION ..............................................................................................................10
WARRANTY STATEMENT................................................................................................................11
CUSTOMER INSPECTION UPON RECEIVAL OF THE DEVICE .....................................................................11
TYPICAL PRESSURE AND TEMPERATURE VERSUS TIME DIAGRAMS FOR THE OPERATING CYCLES....................12
DEVICE SPECIFICATIONS.................................................................................................................13
1.11.1 Device Overall Dimensions:................................................................................................13
1.11.2 Device Properties................................................................................................................14
1.11.3 Device Electrical Data.........................................................................................................15
1.11.4 Utility Requirements............................................................................................................15
DEVICE ENVIRONMENTAL INFORMATION ..........................................................................................16
DEVICE ENVIRONMENTAL INFORMATION ..........................................................................................16
REQUIREMENTS WITH CONCERN TO WATER QUALITY..........................................................................16
1.14.1 Tap water supply.................................................................................................................17
2SAFETY.......................................................................................................................................18
PRINCIPLE SAFETY WARNINGS AND PRECAUTIONS..............................................................................18
SAFETY NOTES.............................................................................................................................19
SAFETY FEATURES INCORPORATED IN THE DEVICE................................................................................19
3CONTENT OF THE DEVICE PACKAGE ...........................................................................................20
4DEPICTION OF SYSTEM PARTS ...................................................................................................21
FRONT VIEW ...............................................................................................................................21
REAR VIEW .................................................................................................................................22
5INSTALLATION INSTRUCTIONS...................................................................................................23
LIFTING AND CARRYING .................................................................................................................23
DEVICE PLACEMENT AND OPERATING CONDITIONS.............................................................................23
CONNECTIONS TO UTILITY SUPPLIES.................................................................................................24
STORAGE....................................................................................................................................24
INITIAL OPERATION OF THE DEVICE..................................................................................................24
6PRE-STERILIZATION CLEANING AND DISINFECTION OF INSTRUMENTS AND THEIR LOADING INTO
THE DEVICE ........................................................................................................................................26
7OPERATING INSTRUCTIONS .......................................................................................................29
TURNING ON THE DEVICE...............................................................................................................29
FILLING WATER ...........................................................................................................................30
FILLING WATER IN THE RESERVOIR....................................................................................................31
SEE THE REQUIREMENTS CONCERNING WATER QUALITY,IN SECTION 1.14..............................................33

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SETTING DATE AND TIME...............................................................................................................33
SET DATE AND TIME .....................................................................................................................34
8CONTROL PANEL........................................................................................................................35
HOME SCREEN DESCRIPTION AND FUNCTIONS ...................................................................................36
OPENING THE DEVICE DOOR ..........................................................................................................37
STARTING A CYCLE........................................................................................................................38
AVAILABLE STERILIZATION PROGRAMS AND TEST PROGRAMS ...............................................................42
8.4.1 List of available Sterilization and Test Programs (refer to sec.8.4.2 for maximal allowed
weight of load)..................................................................................................................................42
8.4.2 Maximum Load Weight per Load type.................................................................................43
8.4.3 Description of the Sterilization Cycle Stages.......................................................................43
8.4.4 Description of the Vacuum Test Stages..............................................................................43
8.4.5 Description of Bowie-Dick Test Stages ...............................................................................44
8.4.6 Information on Prion sterilization program...........................................................................44
CYCLE SUCCEEDED /CYCLE FAILED NOTIFICATIONS AND FOLLOW-ON.....................................................45
8.5.1 Cycle Succeeded................................................................................................................45
8.5.2 Cycle Failed ........................................................................................................................46
ABORTING A CYCLE .......................................................................................................................47
OPENING THE DOOR AND UNLOADING .............................................................................................48
CHECKING WASTE WATER LEVEL ....................................................................................................49
DRAINING THE RESERVOIRS............................................................................................................49
9PREVENTIVE AND SCHEDULED MAINTENANCE TO BE PERFORMED BY THE OPERATOR .............51
DAILY MAINTENANCE ...................................................................................................................51
WEEKLY MAINTENANCE ................................................................................................................51
MONTHLY MAINTENANCE .............................................................................................................52
PERIODIC MAINTENANCE...............................................................................................................53
9.4.1 Replacing the Air Filter........................................................................................................53
9.4.2 Cleaning the Drain Filter......................................................................................................55
9.4.3 Replacing the Drain Filter....................................................................................................56
10 FULL LIST OF INFORMATIVE SCREEN DISPLAY SYMBOLS, OPERATING MESSAGES, ERROR
MESSAGES AND TROUBLESHOOTING.................................................................................................58
SYMBOLS....................................................................................................................................58
ERROR MESSAGES &TROUBLESHOOTING..........................................................................................59
11 TSC PRINTER INSTALLATION (OPTIONAL)...................................................................................62
GENERAL PRINTER INFORMATION ....................................................................................................62
11.1.1 Printer Output:.....................................................................................................................62
IMPORTANT SAFETY INSTRUCTIONS ..................................................................................................64
INSTALLATION FOR THE FIRST TIME...................................................................................................65
OPEN THE PRINTER TOP COVER .......................................................................................................66
LOADING THERMAL PRINTER PAPER ROLL/LABEL ROLL .........................................................................67
CONNECTING THE INTERFACE CABLES TO THE PRINTER .........................................................................69
CONNECTING POWER AND INTERFACE CABLES ....................................................................................70
STARTING THE PRINTER..................................................................................................................71
SETTING PRINTER DEFINITIONS........................................................................................................72
12 FACTORY CODES FOR END USER ................................................................................................74
13 APPENDIX: TYPICAL PRESSURE AND TEMPERATURE VERSUS TIME DIAGRAMS FOR THE
OPERATING CYCLES............................................................................................................................76

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List of Tables
Table 1 - Device labeling.............................................................................................................................8
Table 2 -Device Properties ........................................................................................................................14
Table 3 - Device Electrical Data ................................................................................................................15
Table 4 - Utility Requirements ..................................................................................................................15
Table 5 - Water Quality ............................................................................................................................16
Table 6 - Safety Warnings and Precautions..............................................................................................18
Table 7 - Device Package ..........................................................................................................................20
Table 8 - Front View..................................................................................................................................20
Table 9 - Rear View...................................................................................................................................22
Table 10 - Home screen Description and Functions..................................................................................36
Table 11 - Home screen Description and Functions..................................................................................40
Table 12 - Maximum Load Weights..........................................................................................................43
Table 13 - Symbols....................................................................................................................................59
Table 14 - Error messages & Troubleshooting..........................................................................................61
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5
1 General Information
Manufacturer and European Authorized Representative
Information
T-Edge Autoclave is manufactured by Tuttnauer Ltd., Located Har –Tuv B
Industrial Zone, P.O. Box 170, Beit Shemesh 9910101, Israel. Tel: +972-2-
9904611
The European Authorized Representative is Tuttnauer Europe b.v., Hoeksteen
11, 4815 PR Breda, P.O. Box 7191, 4800 GD Breda, Netherlands. Tel: +31/76-
5423510, Fax: [phone]
Applicable Regulation and Quality Standards
The life cycle of Tuttnauer's T-Edge is in compliance with the following
regulation and quality standards:
93/42/EEC, Council Directive, concerning medical devices
2014/68/EU, Directive, concerning pressure equipment.
2006/42/EC Machinery Directive.
2014/35/EU, Directive, Low Voltage Directive (LVD)
2014/30/EU, Electromagnetic compatibility.
2012/19/EU WEEE and EU (2017/2102 Restriction of the use of certain
hazardous substances (RoHS Directive)
Canadian MDR (CMDR) SOR/98-282 (2018), consolidated.
ISO 9001: 2015 Quality Management System.
EN ISO 13485:2016 Quality Management System –Medical devices.
ISO 14001:2015 environmental management system
EN ISO 14971:2012 Medical devices –Application of risk management.
Chinese Regulations on Safety Technology for Pressure Vessel.
MEDDEV 2.12-1 Rev 8 Medical Devices Vigilance System
MEDDEV 2.12/2 Rev 2 Post Market Clinical Follow Up
MEDDEV 2.7.1 Rev 4 Clinical Evaluation
MEDDEV 2.5.2 Rev 8 Reporting of design changes of the quality
system
ASME Code section I and section VIII. Div.I
EN 13060:2014 Small steam sterilizer
ANSI/AAMI ST55:2016 Tabletop steam sterilizers

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IEC 61010-1 3.1 Edition, January 2017 Safety Requirements for
electrical equipment for measurement control and laboratory use.
EN 61010-2-40: 2015 Safety requirements for sterilizers and washer-
disinfectors used to treat medical materials.
EN ISO 15223-1: 2016 Symbols for use in the labeling of medical
devices.
EN 1041: 2008 + A1:2014 Information to be supplied by the
manufacturer of medical devices
EN 60529:1992 + A2:2013 Degrees of protection provided by
enclosures (IP Code)
EN 61326-1: 2013 for EMC Requirements for Electrical Equipment.
IEC 62304:2014 + A1: 2015 –Medical Device Software –Software life
cycle processes.
EN 62304:2006/AC:2008–Medical Device Software –Software life
cycle processes.
IEC 62366-1: 2015 –Part1: Application of Usability Engineering to
Medical Devices
EN 62366:2008 - Application of Usability Engineering to Medical
Devices
1.2.1 And in consideration with:
FDA QSR 21 CFR part 820 & part 11

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Legend for Symbols appearing on the Labels and in this
Manual
Manufacturer
European Authorized Representative
Year of Manufacturing
Catalog Number
Serial Number
Consult the Operation and Maintenance Manual (User
Manual) before use
IP31
Ingress Protection
European compliance Mark of compliance with the
European Medical Device Directive (Number xxxx identifies
the Notified Body that performed the examination)
European compliance Mark of compliance with the
European Pressure Equipment Directive (Number xxxx
identifies the Notified Body that performed the examination)
Keep away from sunlight and protect from heat.
For Indoor Use Only
Keep dry
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8
Disposal according to electronic scrap ordinance
This side up (during transport and shipment)
Fragile (during transport and shipment)
OR
A warning or precaution as detailed in the Operation and
Maintenance Manual (User Manual)
OR
Caution! Hot Surface
Table 1 - Device labeling

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General Description of the Device
The autoclave is fully automatic (a computerized control unit ensures a fully
automatic sterilization cycle, control and monitoring of physical parameters and
a clear documentation of the sterilization cycle. Drying is performed with the
door closed)
This autoclave uses steam as a sterilizing agent.
The steam is produced by warming up a controlled amount of water inserted to
a pipe heating element, and then to the chamber. This technique saves energy
and water consumption.
The autoclave is equipped with a Pipe heating element and with chamber
heaters to maintain the steam inside the chamber.
The autoclave is equipped with a vacuum system which supports and
improves:
Removal of residual air from packs and porous load and most kinds of
tubes (rubber, plastic etc.) by vacuum at the first stage of the cycle.
Steam penetration into the load; resulting in effective sterilization.
Temperature uniformity.
Post sterilization drying phase
A touchscreen is used for monitoring and control purposes.
The device has a built -in USB port to enable the operation of an external
optional barcode printer:
The barcode printer can print labels with a unique cycle ID barcode,
operator name, sterilization and expiry dates
One barcode printer can be connected to the machine.
The printer connection to the machine, by using a USB sockets, with a
dedicated cable.
Barcode printer power supply voltage can range between 100-240V.
A barcode printer is an optional addition to the autoclave
The device features built-in memory to record up to 999 sterilization cycles.
These can be exported to a USB device to be transferred to a PC.
The device has a built-in Network Port for use with optional Tuttnauer’s
R.P.C.R software when connected to your local network.
The autoclave has two optional configurations (available upon request):

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Basic: Demineralized water is supplied by a manually filled reservoir,
demineralized water overflow outlet on the rear cover (device catalog
number: AMS10-230-PED-T and AMS10-230-T)
Automatic (optional): Demineralized water direct inlet from the water
supply system, demineralized water overflow, and waste water outlet on
the rear cover (device catalog number: AMS10-230-W-PED-T and
AMS10-230-W-T)
Intended Use
The T-Edge Table-top autoclave is designed for sterilization of medical and
surgical goods such as wrapped and unwrapped solid, hollow, and porous
loads used in dental and medical clinics, first aid rooms, hospitals, and
laboratories etc.
Intended Users
The T-Edge tabletop autoclave is intended for use by hospital personnel and
other medical personnel as well as laboratory personnel.
All autoclave users must receive training in proper usage from an experienced
employee. Every new employee must undergo a training period under an
experienced employee.
Warranty Description
This warranty does not include routine cleaning and preventive
maintenance, to be performed according to instructions in chapter 8.
Tuttnauer warrantees all new autoclaves to be free from defects in material
and workmanship for a period of one full year, covering the parts (except door
gaskets and air filters –they are considered wear items).
Tuttnauer warrantees all chambers for a period of ten (10) years against
defects in materials and workmanship. This chamber warranty went into effect
January 1997.
This warranty does not apply to any product that has been subjected to
misuse, neglect, accident or improper installation or application, nor shall it
extend to autoclaves that have been repaired or altered outside the factory
without prior authorization from Tuttnauer.
Tuttnauer’s obligation is limited to the repair or replacement of parts for the
autoclave. This warranty will be void if the unit is not purchased from an
authorized Tuttnauer dealer. No other warranties or obligations are expressed
or implied.
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11
Warranty Statement
The warranty registration must be completed and returned to our service
departments; within fourteen (14) days of purchase or the warranty will be void.
Our European Representative’s Technical Service Department can be reached
at:
Tuttnauer Europe B.V., Hoeksteen 11 4815 PR P.O. Box 7191 4800 GD
Breda, The Netherlands
Tel: [phone], Fax: [phone], Email: [email protected]
Note: If there is any difficulty with this autoclave, and the solution is not
covered in this manual, contact our representative or us first. Do not attempt to
service this autoclave yourself. Describe the difficulty as clearly as possible so
we may be able to diagnose the problem and provide a prompt solution.
If replacement parts are needed, stipulate the model and serial number of the
machine.
No autoclaves will be accepted for repair without proper authorization from us.
All transportation charges must be paid both ways by the owner.
For technical information or service please contact us at:
Tuttnauer Europe B.V., Hoeksteen 11 4815 PR P.O. Box 7191 4800 GD
Breda, The Netherlands
Tel: [phone], Fax: [phone], Email: [email protected]
Or at:
Tuttnauer Ltd., Har –Tuv B Industrial Zone, P.O. Box 170, Beit Shemesh
9910101, Israel
Tel: [phone]
Customer Inspection Upon Receival of the Device
Upon receiving your Tuttnauer Autoclave, carefully inspect the outside of the
shipping carton for signs of damage. If any damage to the carton is found, note
the location with respect to the autoclave and check that area of the autoclave
carefully once it is fully unpacked. Observe packing method and retain packing
materials until the unit has been inspected. Mechanical inspection involves
checking for signs of physical damage such as: scratched panel surfaces,
broken knobs, damaged gasket etc.
If any damage is found, contact your dealer as soon as possible so that
they can file a claim with the shipping carrier and also notify Tuttnauer.
All Tuttnauer products are carefully inspected prior to shipment and all
reasonable precautions are taken in preparing them for shipment to assure
safe arrival at their destination.

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Manufacturer Sterilization Performance Validation
The sterilization performance validation of all sterilization programs and test
programs were performed by the manufacturer according to EN 13060.
Typical Pressure and Temperature versus Time Diagrams for
the Operating Cycles
The diagrams are shown in Appendix A

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Device Specifications
1.11.1 Device Overall Dimensions:
Front view Side view
Top View
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14
1.11.2 Device Properties
Property
Dimension
External size
Width
48cm
Height
49 cm
Depth
58 cm (supporting common install base
carry a 60 cm counter top)
Chamber
Diameter
25 cm
Depth
46 cm
volume
23lit
Usable chamber space
75% (~17 L)
Max. Allowable Working Pressure (MAWP)
2.8 bar
Maximum load per item
0.2kg
Maximum load per tray
Unwrapped
1.2kg
Wrapped
0.72kg
Maximum Solid load
Unwrapped
6kg
Wrapped
3.5kg
Maximum textile load
1.5kg
Tray dimensions
42.1 x 18.9 x 2.05
No. of trays
5
Net weight
50kg.
Shipping weight
60kg.
Floor loading requirements
75kg.
Mineral-free water reservoir
Max. water volume
Overflow (up to the float) -- 3.8lit
Min. water volume
1lit.
the volume used by the
sterilization cycle/load having the
highest steam consumption
Recorded 800ml were required to
sterilize full load of porous type using
"wrapped 121".
Recorded 1400ml were required to
sterilize full load of wrapped
instruments/porous type using "Prion
134".
Used (waste) water
reservoir
Max. water volume
Max vol. –4.0 lit.,
Float –3.7lit. (max allowed for start
cycle)
Safety relief valve
40 PSI
Load No. counter
Counting from 0 to 999 and nullifies.
Table 2 -Device Properties

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1.11.3 Device Electrical Data
Property
Value
Total Power
2000W
Voltage
1Ph / 230 VAC
Amperage
10A
Protection against
electrical shock
Class I (IEC 60601-1)
Mains supply fluctuation
+/- 10%
Frequency (Hz)
50Hz
Table 3 - Device Electrical Data
1.11.4 Utility Requirements
Property
Value
Mineral free water
See table in Water Quality
Mineral-free water inlet
Optional - 1/2" automatic
Drain
Optional - 3/4", withstanding temp. of
80°C
Power supply
* 1 phase, /230VAC ±10%, 50Hz, 10A.
Recommended circuit breaker
16A
Table 4 - Utility Requirements
* According to the local network.
Caution!
In order to avoid any injury by electrical hazard, it is recommended that a
ground fault protection device (GFCI) be installed in the electrical panel
feeding the autoclave (local codes may make this mandatory).
The electrical network must comply with local rules and regulations.
Verify that there is an easy access to the main power switch and to the
current leakage safety relay (GFCI). The voltage supplied to the device
must comply with the label ± 10%.

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Device Environmental Information
The peak sound level generated by the autoclave is 67dBa with
background noise of 48 dBa during sterilization stage, and 65 dBa
during drying stage.
The total heat per hour transmitted by the autoclave is <200Wh.
Device Environmental Information
The peak sound level generated by the autoclave is 67dBa with
background noise of 48 dBa during sterilization stage, and 65 dBa
during drying stage.
The total heat per hour transmitted by the autoclave is <200Wh.
Requirements with concern to Water Quality
The distilled or mineral-free water supply to the autoclave shall be according to
the table below:
TABLE1: Suggested Maximum Limits of Contaminants in Water for Steam
Sterilization per EN13060
Substance
Feed Water
Condensate
Evaporate residue
≤ 10 mg/l
≤ 1.0 mg/l
SiO2
≤ 1 mg/l
≤ 0.1 mg/l
Iron
≤ 0.2mg/l
≤ 0.1mg/l
Cadmium
≤ 0.005 mg/l
≤ 0.005 mg/l
Lead
≤ 0.05 mg/l
≤ 0.05 mg/l
Rest of heavy metals
except iron,
cadmium, lead
≤ 0.1 mg/l
≤ 0.1 mg/l
Chloride (Cl)
≤ 2 mg/l
≤ 0.1 mg/l
Phosphate
≤ 0.5 mg/l
≤ 0.1 mg/l
Conductivity (at
20°C)
≤15 µs/cm
≤ 3 µs/cm
pH value
5 to 7.5
5 to 7
Hardness
≤ 0.02 mmol/l
≤ 0.02 mmol/l
Appearance
Colorless, clean, without sediments
Table 5 - Water Quality
Compliance with the above data should be tested in accordance with
acknowledged analytical methods, by an authorized laboratory.
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17
Caution:
The use of water for autoclaves that do not comply with the table above
may have severe impact on the working life of the sterilizer and can
invalidate the manufacturer’s guarantee.
Use only deionized water, having a maximum conductivity of 15 µs/cm.
Conductivity greater than 15 µs/cm may cause failures.
1.14.1 Tap water supply
The range of hardness value 0.7-2.0 mmol/l (70- 200 mg/l CaCO3)
The use of soft water is strictly forbidden!
Please consult a water specialist!
Note: We recommend testing the water quality once a month. The use of water
for autoclaves that does not comply with the table above may have severe
impact on the working life of the sterilizer and can invalidate the manufacturer’s
guarantee.

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2Safety
Principle Safety Warnings and Precautions
Caution!
Always operate the autoclaves strictly as instructed in this
user manual.
Caution!
Instruments should not be loaded into the autoclave to be
sterilized unless Steam Sterilization is instructed in their User
Manual. The instructed Steam Sterilization Program should
be verified against the programs available in this autoclave.
Caution!
Never use the autoclave to sterilize corrosive products
(acids, bases, or phenols) volatile compounds or solutions
(ethanol, methanol or chloroform), or radioactive substances.
Warning!
Always wear heat resistant gloves before unloading and
avoid touching hot load and hot surfaces.
Warning!
Don't place your hand or head, etc. above the door while
opening it as hot steam is escaping the chamber.
Warning!
Do not stand near the back panel of the autoclave while the
device is operating as the pressure safety valve may release
steam.
Warning!
Do not touch hot surfaces, such as the top enclosure and
area adjacent to the chamber opening! Hot surfaces are
indicated with a label (see sec. 1.3 above)
Caution!
Only technical personnel having proper qualifications and
holding technical documentation (including a technician
manual) and adequate information are authorized to install
and serve the apparatus
Caution!
In order to assure proper operation of the autoclave, it should
not be placed in the vicinity of electrical equipment which is
not certified for Electromagnetic Compatibility according to
IEC/EN 61326-1.
Table 6 - Safety Warnings and Precautions

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Safety Notes
All new autoclave users must undergo a period of training in proper
usage under an experienced employee.
Before initial use, check the autoclave chamber to ensure that no
packaging materials have been left inside.
Before use, check inside the autoclave chamber to ensure that no items
have been left from the previous cycle.
Always verify that you have chosen the appropriate sterilization program
After the cycle, open the door slowly to allow steam to escape and wait
20 seconds before you remove the load.
A certified inspector must perform a periodic pressure chamber safety
test according to the local regulations.
Once a year, or more frequently, effectiveness tests must be performed,
i.e., calibration and validation.
Make sure there are no leaks, breaks, blockages, whistles or strange
noises.
Perform maintenance operations as instructed. The owner of the
autoclave is responsible to perform the maintenance operations.
Notify the person in charge immediately of any deviation from the
normal functioning of the device.
Protective equipment and clothes and other safety instructions should
be implemented in accordance with local and national regulations and/or
rules.
Safety features incorporated in the device
The pressure vessel chamber door has the following features protecting
personnel from hazards:
Two door switches indicate that the door is closed. Without this
indication steam is not introduced into the chamber.
An electrical door locking pin that blocks door opening during operation.
The following safety devices are installed in the autoclave to optimize its safe
operation:
Safety thermostat, to prevent over-heating of the chamber heating elements.
Safety cut-off switch to prevent over-heating of the pipe heating element.
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20
Safety pressure valve to prevent over-pressurizing of the chamber.
Warning!
Mind the Power socket. Keep it and its vicinity dry. Danger
of electrocution.
3Content of the Device Package
Table 7 - Device Package
Part Number
Part Description
Quantity
Supplied
AMS10-230-W-PED-T
T-Edge Autoclave
1
0663-DEV000
Aluminum Tray for 10”
5
TRH511-0001
Wire Tray holder for trays or
Cassettes
1
TRH511-0004
tray stoppers (to be assembled
on tray holder)
8
CMT240-0002
Tray Handle
1
PIP411-0042
Tube for Reservoir Drain
2
PIP511-0029
Tube for Auto reservoir drain+
Angular connector for the rear
drain pipe
1
WIR040-0003 Power cable
10A, 250V, EUR
Power cable
1
THE002-0117
Blank labels roll for barcode
printer
1
MAN205-0502001EN Rev.E
Operation and Maintenance
Manual (Europe)
1