Sirona teneo User manual

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Sirona Dental Systems GmbH
Operating Instructions TENEO Table of contents
Table of contents
1General information ................................................................................... 9
1.1 Dear Customer, ................................................................................ 9
1.2 Contact data ..................................................................................... 9
1.3 Notes on these Operating Instructions ............................................. 9
1.4 Other valid documents ..................................................................... 10
1.5 Warranty and liability ........................................................................ 10
1.6 Intended use ..................................................................................... 11
1.7 Formats and symbols used .............................................................. 11
2Safety information ...................................................................................... 12
2.1 Identification of danger levels ........................................................... 12
2.2 Information on the unit ...................................................................... 12
2.3 On-site installation ............................................................................ 12
2.4 Media quality .................................................................................... 12
2.5 Maintenance and repair .................................................................... 13
2.6 Trouble-free operation ...................................................................... 13
2.7 Vacuum system ................................................................................ 13
2.8 Patient chair ..................................................................................... 14
2.9 Ventilation slots ................................................................................ 14
2.10 Intermittent operation ....................................................................... 14
2.11 Touchscreen ..................................................................................... 14
2.12 Care and cleaning agents ................................................................ 14
2.13 Modifications and extensions of the system ..................................... 15
2.14 Electromagnetic compatibility ........................................................... 15
2.15 HF surgery ........................................................................................ 15
2.16 Dismantling/Installation .................................................................... 16
3System description .................................................................................... 17
3.1 Standards/Approvals ........................................................................ 17
3.2 System overview .............................................................................. 18
3.3 Patient chair ..................................................................................... 19
3.4 Headrest ........................................................................................... 19
3.4.1 Motor-driven headrest .......................................................... 19
3.4.2 MultiMotion headrest............................................................ 20
3.5 Foot control ...................................................................................... 21

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Table of contents Operating Instructions TENEO
3.6 Dentist element ................................................................................ 22
3.6.1 Instrument positions ............................................................. 23
3.6.2 EasyTouch user interface .................................................... 23
3.6.3 Touchscreen ........................................................................ 24
3.6.4 Fixed keys on the dentist element........................................ 25
3.7 Assistant element ............................................................................. 27
3.7.1 Instrument positions ............................................................. 28
3.7.2 User interface....................................................................... 28
3.7.3 Fixed keys on the assistant element .................................... 28
3.8 Water unit ......................................................................................... 29
3.9 External device connection .............................................................. 30
4Operation .................................................................................................... 32
4.1 Starting up the treatment center ....................................................... 32
4.1.1 Initial startup......................................................................... 32
4.1.2 Switching the treatment center on/off................................... 32
4.1.3 Selecting a user profile......................................................... 33
4.2 Control concept of touchscreen ....................................................... 34
4.3 Foot control ...................................................................................... 35
4.3.1 Wireless foot control............................................................. 35
4.3.2 Operating the foot control..................................................... 36
4.3.3 Using the cursor control ....................................................... 38
4.4 Patient chair ..................................................................................... 40
4.4.1 Safety information ................................................................ 40
4.4.2 Safety stop ........................................................................... 41
4.4.3 Triggering an immediate movement stop............................. 42
4.4.4 Armrests............................................................................... 43
4.4.5 Simple/Advanced Start program operating mode ................ 44
4.4.6 Adjusting the motor-driven headrest .................................... 46
4.4.7 Adjusting the MultiMotion headrest ...................................... 47
4.4.8 Moving the patient chair via chair programs ........................ 49
4.4.9 Moving the chair manually ................................................... 52
4.4.10 Creating chair and shock positioning programs ................... 55
4.4.11 Setting the Massage/Active lumbar support functions ......... 55

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Operating Instructions TENEO Table of contents
4.5 Dentist element ................................................................................ 56
4.5.1 Maximum load capacity........................................................ 56
4.5.2 Height adjustment ................................................................ 56
4.5.3 Motor-driven travel track....................................................... 56
4.5.4 Fixed keys on the dentist element........................................ 57
4.5.5 Quick setting keys and function levels ................................. 62
4.5.6 Saving instrument settings ................................................... 63
4.5.7 Placing the instruments in their holders ............................... 64
4.5.8 General instrument functions ............................................... 64
4.5.9 Electric motor ....................................................................... 69
4.5.10 Turbine ................................................................................. 73
4.5.11 SPRAYVIT L multifunctional syringe .................................... 73
4.5.12 SIROSONIC TL scaler ......................................................... 76
4.5.13 SIROTOM HF electrosurgical handpiece............................. 78
4.5.14 Implantological and endodontic treatments.......................... 84
4.6 Assistant element ............................................................................. 100
4.6.1 Maximum load capacity........................................................ 100
4.6.2 Height adjustment ................................................................ 100
4.6.3 Positionability ....................................................................... 100
4.6.4 Fixed keys on the assistant element .................................... 100
4.6.5 Suction handpieces.............................................................. 102
4.6.6 SPRAYVIT L multifunctional syringe .................................... 103
4.6.7 Mini L.E.D. curing light ......................................................... 104
4.6.8 Hydrocolloid.......................................................................... 107
4.7 Water unit ......................................................................................... 109
4.7.1 Swiveling the cuspidor bowl ................................................. 109
4.7.2 Tumbler filling with automatic sensor control ....................... 109
4.7.3 Adjusting the water amount for flushing ............................... 110
4.8 Tray .................................................................................................. 111
4.9 X-ray viewer ..................................................................................... 111
4.9.1 Attachment versions............................................................. 111
4.9.2 Switching the X-ray viewer on/off ......................................... 112
4.9.3 Attaching the anti-glare film.................................................. 112
4.10 SIROLUX FANTASTIC operating light ............................................. 113
4.10.1 Switching the operating light on/off and adjusting it ............. 113
4.10.2 Switching the composite function on/off............................... 113
4.11 SIVISION digital video system ......................................................... 114
4.11.1 SIVISION monitor................................................................. 114
4.11.2 SiroCam digital intraoral camera.......................................... 115

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4.12 External PC ...................................................................................... 119
4.12.1 SIVISION program ............................................................... 119
4.12.2 Open USB port..................................................................... 123
4.13 Configuration of the treatment center (setup) .................................. 123
4.13.1 Opening the setup programs................................................ 123
4.13.2 Configuring the EasyTouch user interface ........................... 124
4.13.3 Setting the date and time ..................................................... 125
4.13.4 Configuring control options .................................................. 126
4.13.5 Configure instruments .......................................................... 129
4.13.6 Configuring the network connection..................................... 131
4.13.7 Opening the Service domain................................................ 133
5Care and cleaning instructions for the practice team ............................ 134
5.1 Basics ............................................................................................... 134
5.1.1 Intervals................................................................................ 134
5.1.2 Care and cleaning agents .................................................... 135
5.1.3 Microbiological water test..................................................... 135
5.2 Surfaces ........................................................................................... 136
5.2.1 Cleaning/disinfecting surfaces ............................................. 136
5.2.2 Disinfect the EasyTouch ...................................................... 137
5.2.3 Disinfecting handles ............................................................. 137
5.2.4 Disinfecting the tray.............................................................. 138
5.2.5 Disinfect, clean and care for the upholstery ......................... 139
5.2.6 Disinfecting the MultiMotion headrest .................................. 139
5.2.7 Thermally disinfect the instrument holder of the dentist element
140
5.2.8 Thermally disinfect the instrument holder of the assistant element
141
5.2.9 Clean the foot control ........................................................... 141
5.3 Instruments and instrument hoses ................................................... 141
5.3.1 Rinsing water lines ............................................................... 141
5.3.2 Purge water lines (purge function) ....................................... 142
5.3.3 Automatically purge water lines (autopurge function) .......... 144
5.3.4 Care for, disinfect and sterilize the treatment instruments ... 148
5.3.5 Changing the cotton wool roll on the turbine hose............... 150
5.4 Vacuum system ................................................................................ 150
5.4.1 Purge the vacuum system.................................................... 150
5.4.2 Sterilize and disinfect the suction handpieces ..................... 150
5.4.3 Cleaning and disinfecting the vacuum system ..................... 151
5.4.4 Cleaning and disinfecting the suction hoses ........................ 153
5.4.5 Thermodisinfecting suction hoses........................................ 154

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Operating Instructions TENEO Table of contents
5.5 Components of the water unit .......................................................... 155
5.5.1 Clean the gold trap............................................................... 155
5.5.2 Clean and disinfect the cuspidor bowl.................................. 155
5.5.3 Adding disinfectant for water................................................ 156
5.5.4 Change the water and air filters ........................................... 157
5.5.5 Changing the amalgam rotor................................................ 157
5.5.6 Emptying the sediment container ......................................... 159
5.5.7 Cleaning the filter insert of the wet suction device ............... 160
5.6 Sanitize the treatment center ........................................................... 162
5.7 Foot control and connection box ...................................................... 168
5.7.1 Changing the battery of the wireless foot control ................. 168
5.7.2 Changing the fuse of the external device connection........... 169
6Maintenance by the service engineer....................................................... 170
6.1 Inspection and maintenance ............................................................ 170
6.2 Safety checks ................................................................................... 170
6.3 Safety tests for systems with HF surgical equipment ....................... 171
6.4 Maintenance Manual ........................................................................ 171
7Malfunctions ............................................................................................... 172
7.1 Error messages ................................................................................ 172
7.2 Remote maintenance ....................................................................... 173
8Spare parts and consumables .................................................................. 174
9Technical data............................................................................................. 176
10 Disposal....................................................................................................... 178
11 Overview of all function keys.................................................................... 179
11.1 Fixed keys ........................................................................................ 179
11.1.1 Dentist element .................................................................... 179
11.1.2 Assistant element................................................................. 180
11.2 Start program ................................................................................... 181
11.3 Instrument program .......................................................................... 182
11.4 Treatment program ........................................................................... 183
11.4.1 Treatment selection.............................................................. 183
11.4.2 Implantology......................................................................... 184
11.4.3 Endodontics.......................................................................... 185
11.4.4 Endodontics administration .................................................. 185

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11.5 Other dialogs .................................................................................... 186
11.5.1 Timer screen ........................................................................ 186
11.5.2 SPRAYVIT program ............................................................. 186
11.5.3 Tumbler filling settings screen.............................................. 186
11.5.4 Flushing settings screen ...................................................... 187
11.6 SIVISION program ........................................................................... 187
11.6.1 SIDEXIS ............................................................................... 187
11.6.2 PowerPoint........................................................................... 189
11.6.3 Media Player ........................................................................ 189
11.7 Setup program ................................................................................. 189
11.7.1 User interface....................................................................... 189
11.7.2 Date and time....................................................................... 190
11.7.3 Control options ..................................................................... 190
11.7.4 Instruments .......................................................................... 191
11.7.5 Network connection.............................................................. 192
11.7.6 Service domain .................................................................... 192
Index ............................................................................................................ 193
NOTE:
For quick navigation within this document, we have provided an index starting
from page 193.

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Sirona Dental Systems GmbH 1 General information
Operating Instructions TENEO Dear Customer,
1General information
1.1 Dear Customer,
We are pleased that you have equipped your practice with the TENEO®
treatment center.
Our claim is to recognize our customers' demands in good time and to create
innovative solutions. Together with your trade partner, you have configured
the unit to suit your individual taste. The new hub of your treatment room is
tailored to your personal needs.
With TENEO®you have a treatment center that stands for easy operation,
innovative comfort and high quality design. With TENEO®we have enhanced
proven functions and turned customer requirements into innovations. In
conjunction with the EasyTouch user interface, the reliable travel track
concept now makes treatment more pleasant and efficient than ever before.
These Operating Instructions are designed to assist you prior to initial use and
whenever you require information later on.
We wish you much success and pleasure with TENEO®.
Your TENEO®Team
1.2 Contact data
Customer Service Center Our German and English speaking Product Service staff are ready to answer
your technical questions by telephone from 7:30 a.m. to 5:30 p.m. CET. Of
course, you can also contact us by fax or e-mail outside of these working
hours as well.
Phone: [phone]
Fax: [phone]
E-Mail: [email protected]
To speed up the processing of your letter, be sure to specify "Bereich
Behandlungseinheiten" (Treatment Center Division) in the subject line of your
e-mail or fax.
Manufacturer's address Sirona Dental Systems GmbH
Fabrikstrasse 31
64625 Bensheim
Germany
Phone: [phone]
Fax: [phone]
E-Mail: [email protected]
www.sirona.com
1.3 Notes on these Operating Instructions
Observe the Operating Instructions Please familiarize yourself with the unit by reading through these Operating
Instructions before putting it into operation. It is essential that you comply with
the specified warning and safety information.

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1 General information Sirona Dental Systems GmbH
Other valid documents Operating Instructions TENEO
Keep documents safe Always keep the Operating Instructions handy in case you or another user
require(s) information at a later point of time. The technical documentation
supplied in a corresponding binder is also part of the product. File any other
operating instructions which may be required in this binder as well.
In case you sell the unit, make sure that the Operating Instructions and all
other technical documents are attached to it so that its new owner can
familiarize himself with its functioning and the specified warning and safety
information. The technical documents are a component of the product.
Help If you reach an impasse despite having thoroughly studied the Operating
Instructions, please contact your dental depot.
1.4 Other valid documents
You treatment center can be equipped with additional components that are
described in separate sets of operating instructions. The instructions as well
as any warning and safety information contained therein also must be
observed.
A separate manual of operating instructions exists for each of the following
Sirona products:
zTreatment instruments and accessories
zSIROLUX FANTASTIC operating light
z19" flat-screen monitor
zHUGO dental working stool
1.5 Warranty and liability
Warranty Passport To safeguard your warranty claims, please complete the attached "Installation
Report / Warranty Passport" together with the service engineer immediately
after the installation of your unit.
Maintenance Maintenance must be performed at scheduled intervals to ensure the
operational and functional reliability of your product and to protect the safety
and health of patients, users and other persons. For more information, please
refer to "Maintenance by the service engineer" [170].
The system owner is responsible for making sure that all maintenance
activities are performed.
As manufacturers of medical electrical equipment, we can assume
responsibility for the safety properties of the system only if maintenance and
repairs on the system are performed either by us or by agencies which we
have expressly authorized and if components affecting safe operation of the
system are replaced by original spare parts in case of failure.
Exclusion of liability In the event that the system owner fails to fulfill its obligation to perform
maintenance activities or ignores error messages, Sirona Dental Systems
GmbH and its authorized dealers cannot assume any liability for any damage
thus incurred.
NOTE: Brief operating instructions
A manual containing brief operating instructions has been provided to help
you look up functions quickly.

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Sirona Dental Systems GmbH 1 General information
Operating Instructions TENEO Intended use
1.6 Intended use
This dental treatment center is intended for the diagnosis, therapy and dental
treatment of humans by properly trained and qualified personnel.
This unit is not intended for operation in areas subject to explosion hazards.
Proper use also includes compliance with the present operating instructions
and the relevant maintenance instructions.
1.7 Formats and symbols used
The symbols and character formats used in the present manual have the
following meaning:
Instructions for action
References
Lists
Designations, commands, menu items
and quotes.
9Prerequisite
1. First action step
2. Second action step
or
¾Alternative action
ªResult, reaction of treatment
center
Prompts you to do something.
See "General information" Identifies a reference to another text
passage.
[11] Indicates the page being referred to.
List Designates a list.
Designation (in italics) Denotes key, button and program
designations
"Command/menu item" Identifies commands, menu items or
quotations.

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Sirona Dental Systems GmbH 2 Safety information
Operating Instructions TENEO Identification of danger levels
2Safety information
2.1 Identification of danger levels
Lead text
To prevent personal injury and material damage, please observe the warning
and safety information provided in the present operating instructions. Such
information is highlighted as follows:
Warning, Ca ution, Note
2.2 Information on the unit
The following symbol can be found on the unit rating plate:
Observe accompanying documents. They are attached to the unit.
2.3 On-site installation
The on-site installation must have been performed according to our
requirements. The details are described in the document "Installation
Requirements."
2.4 Media quality
The air and water supplies must meet the requirements specified in the
installation instructions. Use only drinking water and dry, oil-free and
hygienically clean air for the water and air supplies of the treatment center.
To ensure compliance with the medical and national legal requirements for
water from treatment centers, the treatment center must be equipped with a
disinfection system.
As the owner of the treatment center, you are responsible for the water
quality.
For this reason, you should check the water quality at regular intervals, see
"Microbiological inspection of the water" [135]. Please contact your
specialized dealer or your relevant dental association for the respective
national requirements and measures.
Highly immunosuppressed patients should not come in contact with water
from the treatment center. The use of sterile solutions is recommended.
WARNING: Warning of bodily injury
For a possible danger that could result in light to serious bodily injury.
CAUTION: Caution against damage
For a possibly harmful situation which could lead to damage of the product or
an object in its environment.
NOTE: Information to make work easier
For application information and other useful information.

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Maintenance and repair Operating Instructions TENEO
2.5 Maintenance and repair
Authorized technical personnel and
spare parts
As manufacturers of dental medical equipment and in the interest of the
operational safety of your system, we stress the importance of having
maintenance and repair of your treatment center performed only by ourselves
or by agencies expressly authorized by us. Furthermore, safety-critical
system components must always be replaced with original spare parts upon
failure.
We suggest that you request a certificate, showing the nature and extent of
the work performed, from those who carry out such work, and specify that the
certificate show any changes in rated parameters or working ranges, as well
as the date, the name of the firm and a signature.
Maintenance intervals Despite the outstanding quality of your treatment center and regular care by
the practice team, in the interest of operational safety, it is essential to have
preventive maintenance performed at scheduled intervals.
In order to ensure the operational safety and reliability of your treatment
center and to avoid damage due to natural wear, you as the system owner
must have your system checked regularly by an authorized service engineer
from your dental depot. Furthermore, safety checks must be performed.
Please contact your dental depot to obtain a maintenance offer. For more
information, please refer to "Maintenance by the service engineer" [170].
2.6 Trouble-free operation
Generally valid
The use of this unit is permissible only when the unit is functioning flawlessly.
If failure-free operation of the unit cannot be guaranteed, the unit must be
taken out of service. The unit must be checked for faults by authorized
technical personnel and repaired if necessary.
2.7 Vacuum system
The suction removal of aluminum and other metal oxides from blasting
devices via the automatic separator and the amalgam separator integrated in
the treatment center is prohibited! This would cause extreme wear and
clogging of the suction and water paths.
A separate vacuum system must be used in connection with metal oxide
blasting devices. Treatment centers equipped with a central wet suction
system are generally suitable for suction removal of the above material.
However, make sure to observe the instructions provided by the manufacturer
of your vacuum system.
No restrictions apply when using salt blasting devices in connection with
Sirona treatment centers. However, in such cases, make sure that the system
is subsequently flushed with an adequate amount of water.

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Sirona Dental Systems GmbH 2 Safety information
Operating Instructions TENEO Patient chair
2.8 Patient chair
Please observe the maximum load capacity of the patient chair of 165 kg.
The weight distribution complies with ISO 6875. The safety test is performed
with multiple safety factor according to
IEC 60601-1.
The maximum permissible weight of accessories mounted on the patient
chair is 5 kg.
The patient’s arms and legs must be resting on the upholstery of the chair.
2.9 Ventilation slots
Under no circumstances may the ventilation slots on the unit be covered,
since otherwise the air circulation will be obstructed. This may cause the unit
to overheat.
Do not spray liquids such as disinfectants into the ventilation slots. This could
cause the unit to malfunction. Use only wipe disinfection in the vicinity of the
ventilation slots.
2.10 Intermittent operation
The motors of the treatment center and of the treatment instruments are
designed for intermittent operation corresponding to the dental mode of
treatment.
Drive motors for patient chair and backrest: Max. 6% on-load factor, cycle
duration 425s
Other motors: ≥ 6% on-load factor, cycle duration 250s
SiroCam digital intraoral camera: 1min on / 3min off
2.11 Touchscreen
The monitor of the dentist element is equipped with touch-sensitive control
technology.
The touchscreen must not be operated with pointed objects such as ball-point
pens, pencils, etc. Such objects could damage or scratch its surface. Always
operate the touchscreen by pressing it gently with your fingertip.
2.12 Care and cleaning agents
Unsuitable care and cleaning agents may corrode the surface of the unit.
Therefore, use only care and cleaning agents which have been approved by
Sirona. For more information, please refer to "Care and cleaning agents" [
135].

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Modifications and extensions of the system Operating Instructions TENEO
2.13 Modifications and extensions of the
system
Modifications to this system which might affect the safety of the system
owner, patients or other persons are prohibited by law.
For reasons of product safety, this product may be operated only with original
Sirona accessories or third-party accessories expressly approved by Sirona.
The user assumes the risk of using non-approved accessories.
If any devices not approved by Sirona are connected, they must comply with
the applicable standards, e.g.:
zIEC 60950 for information technology equipment (e.g. PC) and
zIEC 60601-1 for medical electrical equipment.
The treatment center monitor must fulfill the requirements of IEC 60950 and
IEC 60601-1.
The loudspeaker port of the monitor may be connected only to a device that
complies with IEC 60950 (e.g. a PC) or
IEC 60601-1. Under no circumstances may it be connected e.g. to a stereo
system, etc.
If a system is created during the installation process, the requirements of IEC
60601-1-1 must be fulfilled.
2.14 Electromagnetic compatibility
Medical electrical equipment is subject to special precautionary measures
regarding electromagnetic compatibility (EMC). It must be installed and
operated as specified in the document "Installation Requirements."
Portable and mobile RF communications equipment may interfere with
medical electrical equipment. Therefore, the use of such devices (e.g. mobile
phones) in practice or hospital environments must be prohibited.
The presence of electromagnetic interference in the vicinity of the treatment
center may cause image degradation and interruptions in the data
transmission via the USB interface to the PC. In those cases, repeat the
image acquisition or other actions.
In the event of heavy interference, it may be necessary to restart the PC. It is
therefore not recommended to use the PC for controlling other devices that
provide essential performance components.
2.15 HF surgery
This dental treatment center is available with a high-frequency surgical
device.
Only in the Federal Republic of Germany: The system owner is obliged to
keep a “Medical Product Log” if any HF surgical equipment is installed! For
more information, refer to "Safety tests for systems with HF surgical
equipment" [171].

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Sirona Dental Systems GmbH 2 Safety information
Operating Instructions TENEO Dismantling/Installation
2.16 Dismantling/Installation
Observe the installation instructions
When dismantling and reassembling the system, proceed according to the
installation instructions for new installation in order to guarantee its
functioning and stability.

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Sirona Dental Systems GmbH 3 System description
Operating Instructions TENEO Standards/Approvals
3System description
3.1 Standards/Approvals
Certification
The TENEO®treatment center complies with the following standards:
zIEC 60601-1 (electrical and mechanical safety)
zIEC 60601-1-2 (electromagnetic compatibility)
zIEC 60601-1-4 (software)
zIEC 60601-1-6 (serviceability)
zIEC 60601-2-2 (HF surgery)
zISO 6875 (Patient chair)
zISO 9680 (Operating light)
zISO 11143 (Amalgam separator), see also below
zEN 1717 (Connection to the drinking water system), see also below
Original language: German
This product bears the CE mark in accordance with the provisions of the
Council Directive 93/42/EEC of June 14, 1993 concerning medical devices
(MDD).
The treatment center meets the requirements of the Canadian Standards
Association (CSA) according to CAN/CSA-C22.2 No. 601.1-M90
(AM 1 + AM 2), provided the CSA mark is attached on the type plate.
The amalgam separator achieves a separation efficiency of >98%. It therefore
meets the requirements of the standard ISO 11143 and the German Institute
for Structural Engineering (DIBT). The amalgam separator bears the Ü mark
of the DIBT and the AFNOR mark (of the French Standards Institute).
The treatment center complies with the technical rules and requirements on
safety and hygiene for connection to the public drinking water supply. The unit
is certified according to the requirements of the DVGW (Deutscher Verein für
Gas und Wasser = German Gas and Water Association). The unit thus fulfills
the requirements of EN 1717.
The current approvals are listed on the rating label of the patient chair.
The wireless modules in the wireless foot control and in the treatment center
meet the requirements of the R&TTE directive 1999/5/'EC. Standards:
zEN 60950-1
zEN 301489-1, EN 301489-17, EN 300328
The modules meet the requirements of the Federal Communications
Commission (Part 15 of the FCC Rules).
FCC ID: SIFNANOLOCAVR0108
TENEO®is a registered trademark of Sirona Dental Systems GmbH.
0123

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3 System description Sirona Dental Systems GmbH
System overview Operating Instructions TENEO
3.2 System overview
The treatment center comprises the following main components:
A Patient chair [19]
B Motor-driven headrest [19] (shown here) or MultiMotion
headrest [220]
C Foot control [21] (with cable or wireless link)
D Dentist element [22]
E Assistant element [27]
F Water unit [29]
G Media block [30] and power switch [232]

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Sirona Dental Systems GmbH 3 System description
Operating Instructions TENEO Patient chair
3.3 Patient chair
The patient chair features a variety of motor adjustment options to optimally
adapt the patient's position to the given treatment.
3.4 Headrest
3.4.1 Motor-driven headrest
The headrest allows for the following adjustment options:
zMotor-driven extension/retraction to adapt to the patient's stature
zMotor-driven tilting for maxillary/mandibular treatment
A Motor-driven headrest (shown here) or MultiMotion headrest
B Backrest
CSeat
D Armrest
E Toeboard
F Chair base
G Travel track for dentist element
H4-wayfootswitch
I Foot control cable port
J Rotary joint for assistant element
JIHG
F
E
C
B
AD

61 93 556 D3509
20 D3509.201.01.02.02 19.09.2008
3 System description Sirona Dental Systems GmbH
Headrest Operating Instructions TENEO
zManual tilting via quick mechanical adjustment
zShifting/rotation of the head support via the magnetic holder
For details, see "Adjusting the motor-driven headrest" [46].
3.4.2 MultiMotion headrest
The MultiMotion headrest enables optimal access to the patient. The
following settings are possible:
zRetraction/extension of the headrest extension to adjust the headrest to
the patient's stature
zAdjustment of head inclination for maxillary/mandibular treatment
zRotation of patient's head about the longitudinal axis of his body
zLateral inclination of the patient's head
A Removable head pad with magnetic holder
B Quick mechanical adjustment of headrest tilt
C Upper 4-way switch for headrest functions
D Lower 4-way switch for chair functions
D
C
B
A