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 GmbH1 General information
Operating Instructions TENEODear 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
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
you have a treatment center that stands for easy operation,
®
.
®
Team
1.2 Contact data
Customer Service CenterOur 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.
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.
Observe the Operating InstructionsPlease 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 safeAlways 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.
NOTE: Brief operating instructions
A manual containing brief operating instructions has been provided to help
you look up functions quickly.
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.
HelpIf 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 PassportTo safeguard your warranty claims, please complete the attached "Installation
Report / Warranty Passport" together with the service engineer immediately
after the installation of your unit.
MaintenanceMaintenance 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 liabilityIn 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.
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Sirona Dental Systems GmbH1 General information
Operating Instructions TENEOIntended 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.
9 Prerequisite
Prompts you to do something.
1. First action step
2. Second action step
or
¾ Alternative action
ª Result, reaction of treatment
center
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
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"Command/menu item"Identifies commands, menu items or
quotations.
11
Sirona Dental Systems GmbH2 Safety information
Operating Instructions TENEOIdentification 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, Caution, Note
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.
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.
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Highly immunosuppressed patients should not come in contact with water
from the treatment center. The use of sterile solutions is recommended.
12
2 Safety information Sirona Dental Systems GmbH
Maintenance and repair Operating Instructions TENEO
2.5 Maintenance and repair
Authorized technical personnel and
spare parts
Maintenance intervalsDespite the outstanding quality of your treatment center and regular care by
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.
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 GmbH2 Safety information
Operating Instructions TENEOPatient 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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2 Safety information Sirona Dental Systems GmbH
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.:
z IEC 60950 for information technology equipment (e.g. PC) and
z IEC 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 GmbH2 Safety information
Operating Instructions TENEODismantling/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 GmbH3 System description
Operating Instructions TENEOStandards/Approvals
3System description
3.1 Standards/Approvals
Certification
The TENEO® treatment center complies with the following standards:
z IEC 60601-1 (electrical and mechanical safety)
z IEC 60601-1-2 (electromagnetic compatibility)
z IEC 60601-1-4 (software)
z IEC 60601-1-6 (serviceability)
z IEC 60601-2-2 (HF surgery)
z ISO 6875 (Patient chair)
z ISO 9680 (Operating light)
z ISO 11143 (Amalgam separator), see also below
z EN 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).
0123
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:
z EN 60950-1
z EN 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.
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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:
APatient chair [ 19]
BMotor-driven headrest [ 19] (shown here) or MultiMotion
headrest [2 20]
CFoot control [ 21] (with cable or wireless link)
DDentist element [ 22]
EAssistant element [ 27]
FWater unit [ 29]
GMedia block [ 30] and power switch [2 32]
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Sirona Dental Systems GmbH3 System description
Operating Instructions TENEOPatient 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.
A
J
AMotor-driven headrest (shown here) or MultiMotion headrest
B
I
H
C
D
E
G
F
BBackrest
CSeat
DArmrest
EToeboard
FChair base
GTravel track for dentist element
H4-way foot switch
IFoot control cable port
JRotary joint for assistant element
3.4 Headrest
3.4.1 Motor-driven headrest
The headrest allows for the following adjustment options:
z Motor-driven extension/retraction to adapt to the patient's stature
z Motor-driven tilting for maxillary/mandibular treatment
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3 System description Sirona Dental Systems GmbH
Headrest Operating Instructions TENEO
z Manual tilting via quick mechanical adjustment
z Shifting/rotation of the head support via the magnetic holder
A
B
C
D
ARemovable head pad with magnetic holder
BQuick mechanical adjustment of headrest tilt
CUpper 4-way switch for headrest functions
DLower 4-way switch for chair functions
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:
z Retraction/extension of the headrest extension to adjust the headrest to
the patient's stature
z Adjustment of head inclination for maxillary/mandibular treatment
z Rotation of patient's head about the longitudinal axis of his body
z Lateral inclination of the patient's head
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Sirona Dental Systems GmbH3 System description
S
0
Operating Instructions TENEOFoot control
ARemovable head pad
BOperating handle for tilt adjustment
CRelease button (concealed) for rotation and lateral tilt
DHeadrest extension for stature adjustment
ERelease button for removing the headrest
For details, see "Adjusting the MultiMotion headrest" [ 47].
3.5 Foot control
The foot control enables hand-free control of the treatment instruments. Via
the integrated cursor control, virtually all functions of the treatment center can
be controlled via the foot control as an alternative to hand control.
E
A
B
C
D
F
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3 System description Sirona Dental Systems GmbH
Dentist element Operating Instructions TENEO
AFoot pedal as speed foot control or direct starter
BLeft button (program key S or spray)
C4-way foot switch plate for cursor control
DRight button (program key 0 or chip blower)
EPositioning bar
FConnecting cable
The foot control is also available with radio transmission. The connecting
cable has been omitted for the wireless foot control. The power supply is
provided by a battery.
3.6 Dentist element
All functions of the treatment center can be controlled via the EasyTouch
control panel on the dentist element. The dentist element is moved via a
motor-driven travel track.
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Sirona Dental Systems GmbH3 System description
Operating Instructions TENEODentist element
ARemovable instrument holder (max. 6 instruments)
BRemovable handles (left/right)
CTouchscreen for display and operation
DFixed keys
EMain switch
FX-ray viewer
GSkid-proof silicone mat
HAdditional holder for intraoral camera
ISupport arm, height-adjustable
JSlide of motor-driven travel track
3.6.1 Instrument positions
The following instrument position assignments are possible:
The SL motor and the motors from the BL line cannot be combined.
2
A maximum of one SIROSONIC TL scaler can be connected.
3.6.2 EasyTouch user interface
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3 System description Sirona Dental Systems GmbH
Dentist element Operating Instructions TENEO
ATouchscreen (pressure-sensitive user interface)
BFixed keys (membrane keyboard)
3.6.3 Touchscreen
The touchscreen displays virtual function keys according to the program
selected. A list of all function keys is provided in the Appendix of this
document, see "Overview of all function keys" [ 179].
Some programs are divided into a main program and sub-screens. The main
programs are briefly introduced below:
Start programThe Start program can be displayed in the Simple Start program or Advanced
Start program operating mode. Details on both operating modes, see "Simple/
Advanced Start program" [ 44].
Simple Start program operating mode (left) and Advanced Start program
operating mode (right)
Instrument programThe Instrument program matching the instrument currently removed is
displayed. The Instrument programs can be displayed either with the quick
setting keys or via the function levels. For details, see "Quick setting keys and
function levels" [ 62].
Motor screen with quick setting keys (left) and function levels (right)
SIVISION programThe SIVISION program enables the control of certain computer programs
running on the external PC directly from the treatment center. For details, see
"External PC" [ 119].
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Sirona Dental Systems GmbH3 System description
Operating Instructions TENEODentist element
SIVISION program
3.6.4 Fixed keys on the dentist element
NOTE: Detailed description
For a more detailed description of the fixed key functions, see "Fixed keys on
the dentist element" [ 57].
Fixed keys on the dentist element
Main switch
Switches the treatment center on/off.
To switch off, press and hold the key until an acoustic signal sounds. Then
release the key.
NOTE: Power switch
The treatment center also features a power switch on the base of the chair
that separates the treatment center from the power supply, see "Switching the
treatment center on/off" [ 32].
Timer function
Opens the Timer Function screen where any of six preset timers can be
activated. The time lapse is displayed in the footer of the touchscreen.
When the Timer Function key is pressed (> 2 s), the Timer Function settings
screen appears.
Shock positioning
Immediately moves the patient chair to a position for shock positioning of the
patient.
Operating light
Switches the operating light on/off.
Light intensity > 24,000 lux at 100%
When the operating light key is pressed (> 2 s), the Light Intensity settings
screen appears.
Composite function
Switches the composite setting for the operating light on/off.
This function is required to prevent premature curing of composite fillings.
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Reduced light intensity < 8,000 lux
Tumbler filling
Starts the tumbler filling function.
25
3 System description Sirona Dental Systems GmbH
Dentist element Operating Instructions TENEO
When the Tumbler filling key is pressed (> 2 s), the filling time and water
heating settings screen appears.
Flushing
Starts the flushing of the cuspidor bowl.
When the Flushing key is pressed (> 2 s), the Flushing Time settings screen
appears.
Freely selectable function
e.g. call key
freely available relay 230 VAC, 6 A
(connected by the service engineer).
This function can be preset as a button or as a switch in the Setup program.
Freely selectable function
freely available relay 230 VAC, 6 A
(connected by the service engineer).
This function can be preset as a button or as a switch in the Setup program.
Clean key
Pressing this key deactivates the complete user interface of the dentist
element. Pressing it again > 3 s reactivates the control panel.
This is used to make sure that no unwanted functions can be accidentally
triggered while cleaning the surface.
Setup key
Used for individual configuration of the treatment center by the user and for
reading out messages by the service engineer, see "Configuration of the
treatment center (Setup)" [ 123].
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Sirona Dental Systems GmbH3 System description
Operating Instructions TENEOAssistant element
3.7 Assistant element
The functional scope of the assistant element is adapted to the dental
assistant's field of activity. It can, however, also be positioned so as to enable
unassisted treatment by the dentist.
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AHolders 1 to 4 (from left to right) for instruments
BPosition of the hydrocolloid connection (concealed, under the
assistant element)
CUser interface
DSkid-proof silicone mat
ERemovable instrument holder
F3 rotary joints for flexible positioning (partially concealed)
GSupport arm, height adjustable by service engineer
27
3 System description Sirona Dental Systems GmbH
Assistant element Operating Instructions TENEO
3.7.1 Instrument positions
The following instrument position assignments are possible:
Holder 1Holder 2Holder 3Holder 4
Mini L.E.D. curing light
Surgical suction device
SPRAYVIT L multifunctional
syringe
If the assistant element is equipped with a hydrocolloid connection, the
surgical suction device cannot be installed.
3.7.2 User interface
3.7.3 Fixed keys on the assistant element
Spray aspiratorSaliva ejector
NOTE: Detailed description
For a more detailed description of the fixed key functions, see "Fixed keys on
the assistant element" [ 100].
Fixed keys on the assistant element
Tumbler filling
on/off
Flushing of the cuspidor bowl
on/off
X-ray viewer
on/off
This key has no function on the version not equipped with an X-ray viewer.
Timer function
Triggers the time lapse of the first timer. The timer is set on the dentist
element.
Chair program S
Mouth rinsing position with memory function (freely programmable)
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Sirona Dental Systems GmbH3 System description
Operating Instructions TENEOWate r uni t
Chair program 0
Entry/exit position (freely programmable)
Chair programs 1 and 2
(freely programmable)
Headrest
Moves the motor-driven headrest out/in for size adjustment. These keys do
not function if a MultiMotion headrest is installed.
Composite function
Switches the composite setting for the operating light on/off.
Reduced light intensity < 8,000 lux
Operating light
on/off
Light intensity > 24,000 lux at 100%
3.8 Water unit
The water unit is equipped with a disinfection system. It adds a disinfectant to
the water the patient comes in contact with. This reduces the amount of germs
in the water lines.
Germs in water lines
WARNING: Microorganisms can multiply in the water.
These microorganisms could increase the risk of damage to one's health.
¾ Never operate the treatment center without disinfectants.
The water unit can be optionally equipped with an automatic separator
(separation of suction air and waste water) combined with an amalgam
separator/sediment container or with a wet suction device.
BTumbler filler (depicted) or tumbler filler with automatic sensor
control for automatic filling of the tumbler
CMaintenance cover for disinfectant
DMount for support arm of operating light
EMount for tray support arm
FMaintenance flap for accessing flushing valve, amalgam
separator, sediment container or filter insert for wet suction
3.9 External device connection
External medical accessories can be connected to the external device
connection. They must comply with the requirements of Medical Device
Directive 93/42/EEC.
Connecting additional de vices
CAUTION: Additional devices connected to the external device
connection are exposed to a hydrogen peroxide concentration of 0.1‰-
0.2‰.
If the additional devices are not suitable for the specified hydrogen peroxide
concentration, they may be damaged.
¾ Before connecting any additional devices, check to make sure that they
can be exposed to a hydrogen peroxide concentration. Contact the
manufacturer of the relevant additional device, if necessary.
¾ Additional devices must not be sanitized with the treatment center, see
"Sanitizing the treatment center" [ 162].
NOTE: DVGW approval
Due to the design of the treatment center according to EN 1717/DIN 1988
(DVGW requirements) the connected additional devices fulfill the above
standards.
NOTE: Self-contained power supply
The inlet connector remains live when the power switch is turned off. The
connected external devices must therefore possess their own power switch.
However, the air and water connections are switched off.
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