Smart Touch r7

SMART TOUCH
R7
97050649
rev.006
10/2016
EN
R7 - OPERATING INSTRUCTION
TABLE OF CONTENTS
1. Safety guidelines........................................................... 4
5.5. Micromotor.................................................................... 43
1.1. Symbol definition............................................................. 4
5.5.1. RESTORATIVE operating mode................................... 46
1.2. Intended use.................................................................... 4
5.5.2. ENDODONTIC operating mode.................................... 46
1.2.1. Classification and reference standards........................... 5
5.6. Scaler............................................................................ 48
1.2.2. Environmental conditions................................................ 5
5.7. T LED curing light ......................................................... 51
1.2.2.1. Transport and packaging conditions............................... 5
(not available for the American and Canadian markets).51
1.2.3. Warranty.......................................................................... 5
5.8. C-U2 dental camera...................................................... 54
1.2.4. Disposing the equipment when no longer used.............. 5
5.9. ZEN-Xi integrated sensor ............................................. 58
1.3. Safety rules..................................................................... 6
1.4. Cleaning and disinfecting................................................ 7 6. Assistant’s board operation....................................... 59
1.5. Sterilization...................................................................... 8 6.1. Assistant’s touchpad..................................................... 59
6.2. Syringe on assistant’s board......................................... 60
2. Description of the CLASSE R devices........................ 9
6.3. Curing lamp on assistant’s board.................................. 60
2.1. Nameplate....................................................................... 9
6.4. Intraoral camera on assistant’s board........................... 60
2.2. Dental units................................................................... 10
6.5. Suction tubes................................................................. 61
2.3. Dental chair................................................................... 13
6.6. Hydraulic saliva ejector ................................................ 62
2.4. Turning on the dental operatory.................................... 13
7. Hydrogroup operation................................................ 63
3. Warnings for models R7 CART and R7 M CART....... 13
7.1. Fill cup and bowl............................................................ 63
3.1. R7 line operating unit conversion.................................. 14
3.2. R7 M line operating unit conversion.............................. 15 7.2 S.H.S./S system ( Semplified Hygienization Sistem ).......65
7.3. Manual SHS system...................................................... 66
4. Dental chair operation ................................................. 15 7.3.1. Disinfection cycle with oxygenated water...................... 67
4.1. Safety devices............................................................... 15 7.4. BIOSTER/S automatic disinfection system.................. 68
4.2. Emergency devices....................................................... 16 7.5. Automatic instrument FLUSHING CYCLE
4.3. Adjustable headrest....................................................... 16 (FLUSHING) ............................................................ 70
4.4. Dental chair control panel.............................................. 17 7.6. ACVS system (Automatic Cleaning Vacuum System)... 71
4.5. Movable armrests (optional).......................................... 17 7.7. Opening/closing the side hydrogroup cover.................. 72
4.6. Seat rotation (optional).................................................. 17
8. Accessories................................................................. 73
5. Instrument board operation....................................... 18 8.1. Operating lamp ............................................................. 73
5.1. Doctor’s control console................................................ 20 8.2. Monitor on lamp pole..................................................... 73
5.1.1. User interface................................................................ 22 8.3. Negatoscope for panoramas......................................... 73
5.1.1.1. Operator selection......................................................... 23 8.4. Air/water/230V quick-connect couplers......................... 73
5.1.1.2. General settings............................................................ 23 8.5. Auxiliary tray holder....................................................... 74
5.1.1.2.1. Hygiene system settings .............................................. 24
9. Maintenance ................................................................ 75
5.1.1.2.1.1. BIOSTER /S disinfection cycle setting.......................... 24
9.1. Instrument maintenance................................................ 75
5.1.1.2.1.2. Flushing CYCLE SETTING.......................................... 25
9.2. Draining condensate..................................................... 75
5.1.1.2.2. Hydro unit settings......................................................... 26
9.3. Cleaning the surgical suction filter................................. 75
5.1.1.2.2.1. Bowl water delivery setting............................................ 26
9.4. Surgical suction....................................................................76
5.1.1.2.2.2. Cup water delivery setting............................................. 27
9.5. CATTANI surgical separator.......................................... 77
5.1.1.2.2.3. Automatic bowl movement setting................................. 27
9.6 Cleaning the turbine return air filter............................... 78
5.1.1.2.3. Foot control adjustment................................................ 28
9.7. METASYS amalgam separator..................................... 78
5.1.1.2.4. Operating lamp adjustment .......................................... 28
9.8. DÜRR amalgam separator............................................ 78
5.1.1.2.5. Other settings................................................................ 29
9.9. Dental chair................................................................... 78
5.1.1.2.6. Time and date setting ................................................... 29
5.1.1.2.7. Chronometer ................................................................ 30 10. Fault messages........................................................... 79
5.1.1.2.8. Personalization of favourite keys................................... 30
5.1.1.2.9. Operator data entry ...................................................... 31 11. Specifications.............................................................. 80
5.1.1.2.10. LANGUAGE selection................................................... 31 11.1. Overall dimensions: R7 CONTINENTAL...................... 81
5.1.3. Programming the chair positions A, B, C and D........... 32 11.2. Overall dimensions: R7 INTERNATIONAL................... 82
5.1.4. Emergency stop button................................................. 32 11.3. Overall dimensions: R7 CART..................................... 83
5.1.5. SMART TOUCH screen disable button......................... 32 11.4. Overall dimensions: R7 M CONTINENTAL.................. 84
5.2. Foot control................................................................... 33 11.5. Overall dimensions: R7 M INTERNATIONAL............... 85
5.2.1. "Multifunction” foot control............................................. 33 11.6. Overall dimensions: R7 M CART.................................. 86
5.2.2. "Push-pedal” foot control............................................... 34 11.7. Overall dimensions: R7 P.............................................. 87
5.2.3. "Power Pedal" foot control............................................. 36 11.8. Overall dimensions: R7 SINGLE HYDRO GROUP...... 88
5.2.4. Wireless foot control...................................................... 38 12. Dental Unit maintenance plan.................................... 89
5.3. Syringe.......................................................................... 40
5.4. Turbine.......................................................................... 41
EN 3
1. Safety guidelines
• These instructions explain how to correctly use the following dental units:
R7 CONTINENTAL, R7 INTERNATIONAL, R7 CART , R7 SINGLE HYDROGROUP
R7 M CONTINENTAL, R7 M INTERNATIONAL, R7 M CART, R7 P
Carefully read and become familiar with the content of this manual before using the equipment.
• These instructions describe all the versions of the operating units with the maximum possible accessories, therefore not all the paragraphs are
applicable to the unit you have purchased.
• No part of this manual is to be reproduced, stored in a retrieval system or transmitted in any form or by any means, i.e. electronic, mechanical,
photocopying, translation or otherwise, without the prior written permission of CEFLA s.c..
• The information, specifications and illustrations contained in this publication are not binding.
CEFLA s.c. reserves the right to make technical improvements and changes without modifying the instructions contained herein.
• The manufacturer has a company policy of continual development. Although every effort is made to keep technical documentation up-to-date at all
times the manual may not correspond exactly to current specifications. The manufacturer reserves the right to make changes without prior notice.
• The original version of this manual is written in Italian.
• This equipment is equipped with a device that prevents liquid back up
1.1. Symbol definition

List of symbols used in this document to denote certain conditions:
1) Type of protection against direct and indirect contact: Class I.
Type of protection against direct and indirect contact: Type B.
2) WARNING!
Failure to observe may result in equipment damage or injury to the
user and/or patient.
3) OPERATING INSTRUCTIONS:
This symbol indicates that the user should read and become familiar
with the content of the User’s manual before attempting to use the
relative part of the equipment.
4) NOTE:
Identifies information that is especially important for the user and/or
assistant.
5) Earth ground. Functional earth connection.

6) Alternating current
7) Part sterilised in a steam autoclave up to 135° C.
8) On (a part of the apparatus)
9) Off (a part of the apparatus)
10) Equipment in accordance with essential requirements of directive EEC
93/42 and subsequent changes (Class II equipment).
11) Equipment in accordance with essential requirements of directive EEC
93/42 and subsequent changes .
12) Waste disposal symbol in accordance of Directive 2012/19/UE.
13) “Warning biological hazard”.
It provides information about possible risks of contamination deriving
from contact with fluids, storage of infected biological waste.
14) Manufacturer
15) Month and year of constructions
16) Apparatus serial number

17) Product/equipment identification code.
18) ON / OFF button.
19) "Refer to the instruction manual"
Means that for reasons of safety you need to consult the instruction

manual before using the device.
20) Do not push.
21) Foot crushing hazard.
22) Device equivalent to Class 2 light source.
23) Quality marking c(MET)us (USA and CANADA).
1.2. Intended use
• The R7 series of operatories are medical devices intended for dental treatment.
• The instrument board may hold up to 6 instruments.
• The assistant’s board can hold 2 suction tubes and 3 instruments.
• This equipment must be used only by adequately trained personnel (doctors and paramedics).
• The device is intended for non-continuous operation (see the operating times of the individual parts in the dedicated sections).
• The device is classified as pollution degree 2.
• Overvoltage class: II.
WARNING! (only for the American and Canadian markets)

The R7 series dental units and the relative accessories are intended for dental treatment, providing the dentist with a user interface to control functio-
ning of the dental chair and all the connected instruments. The dental unit supplies air and water, and a suction and electrical energy system allows
the dentist to intuitively control all the patient treatment procedures normally performed in a dentist’s surgery.
Federal law restricts the sale of this device exclusively to dentists.
4 EN
1.2.1. Classification and reference standards
• MEDICAL DEVICES classification

Classification of the dental unit in accordance with the indications given in annex IX of directive 93/42/EEC and subsequent changes: Class IIa.
• ELECTRICAL MEDICAL EQUIPMENT classification
Classification of the dental unit in accordance with standard IEC 60601-1 for safety of medical equipment: Class I - Type B.
• Reference standards: R7 series operatory units are designed and constructed in compliance with IEC 60601-1 3.a Ed. - 2007, IEC 60601-1-6 3.a
Ed. - 2010, IEC 62366 1.a Ed. - 2007, IEC 80601-2-60 1.a Ed. - 2012, IEC 60601-1-2 3.a Ed., ISO 6875 3.a Ed. - 2011, ISO 7494-1 2.a Ed. - 2011 and
EN 1717 (type AA and AB) standards as far as the water mains safety devices are concerned.
• Classification of RADIO DEVICES AND COMMUNICATION TERMINALS (only when the WIRELESS foot control is present)
Equipment classification according to Directive 99/05/EC Art.12: Class I.
1.2.2. Environmental conditions
The equipment is to be installed in rooms that satisfy the following requirements:

• temperature between 10 and 40°C.
• relative humidity between 30 and 75%.
• atmospheric pressure ranging from 700 to 1060 hPa.
• altitude ≤ 3000 m;
• air pressure entering equipment ranging from 6 to 8 bar.
• water hardness entering equipment not over 60 mg/l.
• water hardness at the equipment inlet must not be above 25 °f (French degrees) or 14 °d (German degrees) for untreated drinking water. For water
with a higher hardness degree, it is recommended to soften water until it reaches a hardness degree between 15 and 25 °f (French degrees) or
between 8.4 and 14 °d (German degreees);
• water pressure entering equipment ranging from 3 to 5 bar.
• water temperature entering equipment not higher than 25°C.
1.2.2.1. Transport and packaging conditions
• Temperature: from -10 to 70°C;

• Relative humidity: from 10% to 90%;
• Atmospheric pressure: from 500 to 1060hPa.
1.2.3. Warranty
CEFLA s.c. stands behind its products warranting safety, reliability and performance.
The warranty is valid only under the following terms:
• The conditions given on the warranty certificate are observed.
• The equipment is used only as instructed in this manual.
• The electrical wiring in the room in which the equipment is installed must conform to IEC 60364-7-710 (standards for electrical wiring in medical
and dental offices).
• A 3x1.5 mm2 line protected by a bi-polar cut-out that conforms to applicable standards (10 A, 250 V, distance between contacts at least 3 mm) must
be used to feed the equipment.
WARNING!
The color of the three wires (POWER, NEUTRAL and EARTH) should satisfy the requirements of current standards.
• Installation, repairs and, in general, any other operations requiring the casing to be opened are to be performed exclusively by personnel authorized
by ANTHOS.
1.2.4. Disposing the equipment when no longer used
In compliance with Directives 2011/65/EU and 2012/19/EU regarding restriction of the use of certain hazardous substances in electrical and electronic
equipment along with waste electrical and electronic equipment, it is forbidden to dispose of this equipment in the municipal waste stream as unsorted
municipal waste. When new equipment of equivalent type is purchased the waste equipment should be returned to the distributor on a one-to-one
basis for disposal. As far as reuse, recycling and other forms of waste recovery mentioned above are concerned, the manufacturer is responsible
for the actions specified by individual local laws. Efficient collection of sorted waste separately to recycle and treat waste electrical and electronic
equipment aids in preventing negative environmental impacts while protecting human health. In addition it facilitates recycling of the materials used
to construct the equipment. Illegal waste disposal carries heavy fines defined by local laws.
WARNING!
The crossed out wheeled bin placed on the equipment indicates that the waste equipment must be collected separately from other waste.
EN 5
1.3. Safety rules
WARNING!
• All equipment is permanently installed.
Depending on the type of chair the unit comes with, refer to the installation DATA given in paragraph “Specifications”.
CEFLA s.c. shall not be held liable for any personal injury or equipment damage resulting from failure to heed the precaution given above.
• Floor condition
The floor conditions (continuous type) must meet design load standards set forth in DIN 1055 sheet 3.
The weight of the dental unit including a patient weighing 160 Kg, is approximately 350 Kg.
See the Installation manual for further details about installation.
The positions of delivery and drainage line connections comply with standard UNI EN ISO 11144. In case of floor installation without load reduction
plate, floor characteristics must ensure a breakage resistance of the anchor bolt not less than 1200 daN each (considering a RcK concrete resistance
of 20 MPa). In case of floor installation without load reduction plate, floor characteristics must ensure a resistance of the anchor bolt not less than
260 daN.
• This device may not be modified in any way without the authorisation of the manufacturer.
If the device is modified, appropriate examinations and tests need to be conducted in order to ensure continued safe use.
CEFLA s.c. shall not be held liable for any personal injury or equipment damage resulting from failure to heed the precaution given above.
• Dental chair
The maximum chair capacity is 160 Kg. This weight must never be exceeded.
• Tray holders
The maximum weights that can be held must never be exceeded:
- Instrument tray attached to the instrument board maximum allowable load 2 Kg, evenly distributed.
- Auxiliary instrument tray, maximum allowable load on tray 3.5 Kg (no x-ray film viewer) or 2.5 Kg (with x-ray film viewer).
• Connections to external instruments
The equipment can be hooked up only to other instruments that bear the CE mark.
• Electromagnetic interferences.
Use of electrical equipment that does not comply to standard IEC 60601-1 3.a Ed. - 2007 in the office or nearby may cause electromagnetic or
other types of interferences resulting in dental unit malfunctions.
In these cases, shut off power to the dental unit before using this equipment.
• Replacing the chucks
Operate the turbine release and contra angle only once the chuck has come to a complete stop. On the contrary, the locking system will wear down
and the chucks can slip off causing injury. Use only high quality chucks with gauged diameter attachment. To check the state of the locking system,
make certain the chuck is firmly secured to the instrument every day before starting work. Locking system defects caused by misuse are easily
identified and not covered by the warranty.
• Patients with pace makers and/or hearing aids.
When treating patients with pace makers and/or hearing aids, take into consideration the effects the instruments may have on pace makers and/
or hearing aids. Carefully read technical-scientific information available on this subject.
• Implants.
If the dental unit is used for implant operations using separate equipment designed for this purpose, shut off power to the dental chair to avoid
unwanted movements resulting from faults and/or accidental start up of the controls.
• Do not forget to turn off the office’s water supply and master switch on the equipment before leaving the surgery.
• The equipment is not protected against liquid penetration (IPX O).
• This equipment is not suitable for use in the presence of a mix of inflammable anaesthetic gas with oxygen or nitrous oxide.
• This equipment must be stored properly so that it is kept in top working order at all times. The manufacturer shall not be held responsible for misuse,
carelessness or improper use of the equipment.
• This equipment is to be used exclusively by qualified personnel (doctors and paramedics) with the proper training.
• The user must be present at all times when the equipment is turned on or ready for start-up. In particular, never leave the equipment unattended in
the presence of children/the mentally disabled or other unauthorised personnel in general.
Any companions must keep out of the area in which treatment is performed and in any case under the responsibility of the operator. The area in
which treatment is performed refers to the space around the dental unit plus 1.5 meters.
• Quality of the water delivered by the dental unit.
The user is responsible for the quality of the water delivered by the dental unit and must adopt measures to maintain it.
To ensure that you meet the water quality requirements, CEFLA s.c. advises you to equip the dental unit with an internal or external disinfection system.
Once installed, the dental unit is exposed to contaminants originating from the water supply. For this reason, it is recommended to install and put it
into operation only when you begin using it daily and to perform the decontamination procedures described in the relative chapters right from the first
day of installation.
If the dental unit is equipped with a device for separation from the open water supply system (EN 1717), make sure that it also continuously adds
disinfectant as required and check that the relative tank contains an adequate quantity (see the relative paragraph).
NOTE: Contact your local dealer or Dental association for more detailed information about national laws and requirements.
• Applied Parts.
The parts of the device that during normal use necessarily come into contact with the patient for the device to be able to perform its functions
are: Dental chair upholstery, armrest, polymerising lamp fibre optics, terminal part of the syringe, single-use camera protection, scaler bits, drill
handpieces, cannula suction terminals.
Non applied parts that may come into contact with the patient are: dental chair armrest support, dental chair lower casing, patient-side hydro unit
casing, cup water delivery spout, bowl, suction tubes, handpiece body.
• WARNING! Moving the dental chair.

Make sure that the patient is ready to collaborate: ask him/her to keep his/her hands and feet close, avoiding incorrect postures.
Check that the patient is sitting properly when moving the dental chair (see figure).
6 EN
1.4. Cleaning and disinfecting
Cleaning is the first step of any disinfecting process. Physically scrubbing with detergents and surface-active substances and rinsing with water
removes a considerable amount of micro organisms. If a surface is not clean first, the disinfecting process cannot be successful. If a surface cannot
be adequately cleaned, it should be protected with barriers.
The outer parts of the equipment must be cleaned and disinfected using a product for hospital use with indications for HIV, HBV and tubercolocide
(medium-level disinfectant) specifically for small surfaces.
The various drugs and chemical products used in dentist’s surgeries may damage the painted surfaces and the plastic parts.
Research and tests run show that the surfaces cannot be fully protected against the harsh action of all products available on the market. We therefore
recommend protecting with barriers whenever possible. The harsh actions of chemical products also depend on the amount of time they are left on
the surfaces. It is therefore important not to leave the product on the surfaces longer than the time specified by the manufacturer.
It is recommended to use the specific medium-level disinfectant, STER 1 PLUS (CEFLA s.c.), which is compatible with:
• Coated surfaces and plastic parts.
• Upholstery.
WARNING!
Any splashes or spots of mordant will stain the MEMORY FOAM upholstery. Immediately rinse with plenty of water if acid spatters on the
upholstery.
• Uncoated metal surfaces.
If you do not use STER 1 PLUS, it is recommended to use products that contain at maximum:
• Ethanol. Concentration: maximum 30 g per 100 g of disinfectant.
• 1-propanol (N-propanol, propyl alcohol, N-propyl alcohol). Concentration: maximum 20 g per 100 g of disinfectant.
• Combination of ethanole and propanole. Concentration: the combination of the two should be maximum 40 g per 100 g of disinfectant.
WARNING!
• Do not use products containing isopropyl alcohol (2-propanol,iso-propanol).
• Do not use products that contain sodium hypochlorite (bleach).
• Do not use cleaners that contain phenol.
• Do not spray the selected products directly on the surfaces.
• All products must be used as directed by the manufacturer.
• Do not mix the STER 1 PLUS disinfectant with other products.
WARNING!
The products suggested are compatible with the materials of the equipment, however damages may occur to surfaces and materials re-
sulting from the use of different products, even if not included in the above list of excluded products.
Cleaning and disinfecting instructions.

Clean and disinfect with single-use non-abrasive paper (avoid using recycled paper) or sterile gauze.
Do not use sponges or in any case, any material that can be reused.
WARNING!
• Shut off the dental unit prior to clean and disinfecting the external parts.
• All material used to clean and disinfect must be thrown away.
EN 7
1.5. Sterilization
Each instrument is supplied NOT STERILE and must be sterilized in a steam autoclave (max 135°C) before use, avoiding any form of chemical
sterilization.
Sterilization must be performed using suitable packaging materials checked during the sterilization process validation.
We recommend sterilizing in steam autoclave (moist heat) using a pre-vacuum (forced air removal) cycle.
Autoclaves must comply with the requirements of, be validated by and maintained in accordance with EN 13060 (or ANSI/AAMI ST55), EN ISO
17665-1 and ANSI/ AAMI ST79.
See below for recommended minimum sterilization parameters for re-usable medical devices that have been validated to provide a 10^-6 sterility
assurance level (SAL):
• Cycle Type with pre-vacuum (Pre-vac).
• Method: "overkill" moist heat sterilization in compliance with ISO 17665-1.
• Minimum temperature: 134°C (273°F) for heat-resistant materials (instruments and metallic handpieces, etc); 121°C (250°F) for heat-labile materials
(rubber products, etc.).
• Minimum exposure time (1): 4 minutes (at 134°C), 20 minutes (at 120°C).
• Minimum drying time (2) : defined to ensure compliance with the requirements of EN 13060 (or ANSI/AAMI ST55).
Exposure time: period of time during which the load and the entire chamber are maintained above sterilization temperature.
(1)
DRYING TIME: period of time during which steam is removed from the chamber and the chamber's pressure is reduced to allow evaporation of
(2)
condensate from the load either by prolonged evacuation or by the injection and extraction of hot air or other gases.
The drying time varies according to load configuration, type of packaging and materials.
8 EN
2. Description of the CLASSE R devices
• R7 line dental units: they are equipped with a hydro group vertically integral with the dental chair; both the assistant’s board and the dentist’s in-
strument board are mounted on two articulated arms of which one is self-balanced, which allows adjusting them in height.
The hydrogroup, instrument and assistant’s boards can be turned to quickly change from the version for right-handed operators to the version for
left-handed operators.
• R7 M line dental units: they are not equipped with a hydro group and the load-bearing structure of the assistant’s board is positioned in the rear
area of the dental chair.
Both the assistant’s board and the dentist’s instrument board are mounted on two articulated arms of which one is self-balanced, which allows
adjusting them in height
Both the assistant’s board and the dentist’s instrument board can be turned to quickly convert them from a right-handed to a left-handed operator
version.
• R7 P line dental units: they are not equipped with a hydro group nor with a dentist’s instrument board.
The load-bearing structure of the assistant’s board is positioned in the rear area of the dental chair and it is mounted on two articulated arms of
which one is self-balanced, which allows adjusting it in height.
The assistant's board can be turned to quickly convert it from a right-handed to a left-handed operator version.
2.1. Nameplate
Models: R7 CONTINENTAL, R7 INTERNATIONAL and R7 SINGLE

HYDRO GROUP.
The ID plate is located on the link between patient chair and unit body.
Data given on plate:
• Manufacturer’s name
• Name of equipment
• Voltage
• Type of current
• Frequency
• Maximum power absorbed
• Serial number
• Year of manufacture
Models: R7 M CONTINENTAL and R7 M INTERNATIONAL.

The nameplate is found on the mount for the instrument board arms.
• Voltage
• Type of current
• Frequency
• Serial number
Models: R7 CART and R7 M CART.

The nameplate is found underneath the instrument board.
• Voltage
• Type of current
• Frequency
• Serial number
EN 9
Model R7 P.
The nameplate is found under the seat.
• Voltage
• Type of current
• Frequency
• Serial number
2.2. Dental units
Dental units R7 are available in the following versions:

Model R7 CONTINENTAL
Description of equipment.
a Hydrogroup
b Adjustable arm
c CONTINENTAL version instrument board
d Doctor’s console
e Tray holder
f Assistant’s board

g Assistant’s control console
h Utility service center
i Multifunction foot control

l Water to cup
m Turnable and removable bowl
n Autobalancing arm
o Canister for independent supply of instrument sprays and water to cup
u Load reduction plate.
z ANTHOS R1.0. dental chair

Model R7 INTERNATIONAL
a Hydrogroup
b Adjustable arm
c INTERNATIONAL version instrument board
e Tray holder (optional)
l Water to cup
n Autobalancing arm
r X-ray film viewer for panoramic x-rays (optional)

Model R7 CART
a Hydrogroup
mounted on height-adjustable cart
l Water to cup
m Removable and turnable bowl
o Canister for independent instrument spray and
water to cup supply
p Height-adjustable cart

10 EN
R7 SINGLE HYDRO GROUP

Version without instrument board.
a Hydrogroup
b Adjustable arm
e Auxiliary tray holder
l Water to cup
n Autobalancing arm

Model R7 M CONTINENTAL

b Adjustable arm
c CONTINENTAL version instrument board
e Tray holder
n Self-balancing arm
q Operating lamp support adjustable arm.

Model R7 M INTERNATIONAL
b Adjustable arm
e Tray holder
n Self-balancing arm


EN 11
Model R7 M CART

b Adjustable arm.
mounted on height-adjustable cart
e Tray holder table.
n Self-balancing arm.
o Canister for independent supply of instrument

sprays and water to cup.
p Height-adjustable cart
Model R7 P
b Adjustable arm.
e Tray holder table.
n Self-balancing arm.
o Bottle for supplying syringe on assistant's board

12 EN
2.3. Dental chair

Description of the chair
a Headrest
b Back
c Push-button panel chair movements
d Movable seat (optional)
e Movable arm (optional)

Operating times
The operating and rest times are as follows:
work 25 sec. - rest 10 min.
Maximum weight capacity.

The maximum chair capacity is 160 Kg.
WARNING!
Do not exceed this value.
Warnings for use.
WARNING: FOOT CRUSHING HAZARD

Pay attention to the patient and the staff during dental chair descent
(on both sides).
2.4. Turning on the dental operatory
Press the main switch ( f1 ) on the dental chair casing and check on the
control console that:
• “POWER” led ( g ) on
- equipment on
- pneumatic system connected
- water system connected.
• “POWER” led ( g ) off
- equipment off
- pneumatic system disconnected
- water system disconnected
WARNING!
The main switch must be pressed by hand.

3. Warnings for models R7 CART and R7 M CART.
WARNING!
While moving the cart, pay attention to steps and/or horizontal obsta-
cles as the cart may become unstable and/or overturn.
EN 13
3.1. R7 line operating unit conversion
To convert the operating unit from the right-handed operator

version to the left-handed operator version, proceed as follows:

• First of all, set up the operatory unit for conversion by moving
the backrest completely up, raising the dental chair at least more
than half of its vertical stroke and placing the instrument board’s
arm and body in the middle in relation to the dental chair seat
so that it is out of the way.
WARNING!
At this point, shut off the operatory unit so that it cannot
accidentally be turned on, creating hazardous situations.
• Take off the cover (a) that protects the hydrogroup’s short support
arm and blocks movement.
• Lift the element ( k ) locking the short arm in place.
NOTE: slightly move arms on their pivot points so as to
make element release easier.
• Turn the assistant’s board’s arms until they are compact in

relation to the hydrogroup.
• Start turning the hydrogroup and relative arm.
WARNING!
During this operation, avoid extending the arms of the
operating lamp, if any, to the outside so as to prevent any
excessive imbalance of the equipment.
• Once the hydrogroup is aligned with the dental chair, turn the
assistant’s board’s arms (b) bringing them into the new work
position.

WARNING!
Be extremely careful not to pinch the suction tubes and
instrument cords while performing this operation.
• Finish turning the hydrogroup to the left bringing it to the normal

work position for left-handed operators.
NOTE: make sure that element ( k ) is correctly locking short
arm in the new position.
• Turn the bowl to the new home position by hand.
• Place the pin ( c ), that stops rotation of the instrument board’s

arm, in the opposite hole to correctly set the arm’s work area.
WARNING!
If the stop pin is not used, the arm may bang against the
hydrogroup damaging it during regular operation.

• Put the cover ( a ) back on making sure the cover’s pins are
properly placed in the seats in the short arm thereby blocking
the hydrogroup.
• The operatory unit is now ready to be used by left-handed ope-

rators.
WARNING!
Before attempting to turn on the operatory unit, verify all
the equipment is in the correct work condition.
14 EN
3.2. R7 M line operating unit conversion
To convert an R7 M line operating unit from the right-handed operator

version to the left-handed operator version, simply invert instrument’s table
arm position with operating lamp support arm after having removed the
anti-rotation stopper pin ( c ). Once both arms have been turned, insert anti-
rotation stopper pin ( c ) back in place to lock the operating lamp support
arm in the new position.
4. Dental chair operation

The dental chair can be moved as follows:
• Chair seat up/down,
• Back up/down with inclination of the chair seat (Tren-
delemburg compensated),
• 30° clockwise or counter-clockwise seat rotation
(optional).
The dental chair can be operated from the following

places:
• Instrument board (a) (see par. 5).
• Multifunction foot control (b) (see par. 5.2).
• Assistant’s board (c) (see par. 6).
• Dental chair side control panel (see par. 4.4)
Dental chair movement shutdown

With the instruments in rest position, you can di-
sable the dental chair movements (see paragraph
5.1.1.2.5.).
The movement disabling is shown on the control
panel display by the relevant icon ( A ).
4.1. Safety devices
The equipment is supplied with the following safety devices:

• Dental chair footboard is equipped with a device ( l ) that immediately
stops the dental chair down movement in the presence of an obstacle

and automatically moves the seat up to free the obstacle.
• The dental chair back rest is equipped with a device ( m ) which immediately
stops the back rest or dental chair from moving down when an obstacle is
encountered and automatically moves it back up to clear the obstacle.
• The support arms of the assistant’s module feature a safety device ( n )
which stops downward chair movement if an obstacle is encountered. The
chair will then automatically move upwards so the user can remove the
obstruction.

• The hydrogroup support arms are equipped with a safety device ( o )
which immediately stops the dental chair from moving down when an
obstacle is encountered and automatically moves it back up to clear the
obstacle.
• Dental chair movements:
- with the instrument extracted NOT working: manual movements allowed,
automatic movements inhibited, but if they are already in progress at
the moment of extraction they are not interrupted;
- with instrument extracted and working: all the dental chair movements
are inhibited.

EN 15
4.2. Emergency devices

WARNING!
Use the devices below when movement of the equipment
needs to be blocked:
• Dental chair control buttons (a), (c) or (d).
Pressing any dental chair button blocks all movements are
blocked.
• Foot control ( b )
Foot control actuation: all movements are blocked.
4.3. Adjustable headrest
The headrest may be of two types:
1 with manual cushion lock lever

2 with pneumatic cushion lock lever
Adjusting headrest height.

• with manual locking ( 1 ):
The head rest blade is positioned through a magnetic clutch. The operator
should pull up and/or push down the headrest until it is in the desired
position.
• with pneumatic locking ( 2 ):
Press and hold down the locking button ( u ) to position the headrest as
desired. Once you have reached the desired position, release the button
( u ) to lock the headrest in place.

Adjusting the cushion:
• with manual lock ( 1 ): rotate the lock knob ( k ) anti-clockwise, position
the cushion as desired and then retighten the lock knob.
• with pneumatic lock ( 2 ): press the lock button ( u ) and keep it pressed
as you adjust the cushion as desired. Once the cushion is oriented as
desired just release the button ( u ) to lock in place.
Proper positioning of the headrest.
WARNING!
For correct use of the headrest, position the patient's head as shown in the
figure.
Important information.
WARNING!
• Maximum on-headrest load: 30 Kg.
• Do not attempt to move cushion while patient is resting against it.

• Do not attempt to modify the position of the cushion without first
releasing the lock mechanism.
• The pneumatic locking device is active only when the air circuit is
pressurized and the dental unit is on.
16 EN
4.4. Dental chair control panel
Description of the buttons:
Button to save dental chair functions
Button to reach home position
Button to reach rinse position
Button to raise seat
Button to raise back rest Button to retrieve programmed position “A”
Button to lower seat Button to retrieve programmed position “B”
Button to lower back rest Button to disengage dental chair seat brake
(operative only with turnable seat)
4.5. Movable armrests (optional)
Both arm rests are movable and can be turned downwards so that the patient
can more conveniently get on and off the chair.
WARNING!
• Maximum weight supported by armrest: 68 kg.
4.6. Seat rotation (optional)
The dental chair may be equipped with a pneumatic device that allows the seat
to be turned 30° clockwise or counter-clockwise to give the doctor or assistant
more free space under certain work conditions.
Follow the directions given below to turn the seat:
• Hold down the brake key, located on the control panel on the side of the
dental chair, for at least 2 seconds to release the seat.

NOTE: a buzzer rings intermittently and an icon ( A ) appears on
the top right side of the display screen to signal the seat is released. When
released, all the controls used to move the dental chair are disabled.
NOTE: operation of the foot control can be modified so that when
pressing the "Automatic chair return" button for at least 2 seconds (see
paragraph 5.2), chair seat release/locking is activated.
To activate this function, call Technical Service.
• Turn the seat to the desired position.
WARNING!
Be extremely careful not to accidentally bang the hydrogroup when
performing this operation.
• Press the brake key again to block the seat.

WARNING!
Before attempting to lower the patient, always verify that the seat is
actually blocked.

EN 17
5. Instrument board operation
Layout of instruments.
The positions the instruments are placed in on the board are determined by the customer at the time of order.
Starting the instruments.

• The syringe is always on (see paragraph 5.3.).
• The curing light is turned on with the key when the instrument is withdrawn (see paragraph 5.7.)
• Intraoral camera turn on when the instrument is extracted (see paragraph 5.8.).
• If connected to an external PC, the integrated ZEN-Xi sensor is always operative (see paragraph 5.9.).
• Once picked up, all the instruments are operated with the foot control. (see paragraph 5.2.).
Simultaneous use of the instruments.

A device sees that the instruments cannot be used simultaneously.
The first instrument removed is operative while those removed there after
are deactivated by this device.
This device allows the chuck to be replaced in one instrument while another
is used on the patient.
Putting the instrument board place.

The instrument board can be moved in all directions.
To adjust the height of the board and/or direct it horizontally, simply grasp
the handle ( a ).
NOTE (only for pantograph arm with pneumatic brake): to
adjust the height of the dentist’s instrument board, you first need to press
the brake release button .
NOTE model R7 CART / R7 M CART: o adjust the height of
the dentist’s instrument board, you first need to press the brake release
button .
Pantograph arm.
There are two types of pantograph arm:
with manual locking (only A5 series)
with pneumatic locking
Adjusting the pantograph arm with manual brake.

Balancing of the pantograph arm is determined at the time of installation.
Any future adjustments can be made using the knob ( b ) found on the
pantograph arm.
Turn clockwise: to increase clutching of the pantograph arm.
Turn counter-clockwise: to decrease clutching of the pantograph arm.
Instrument return arm stopping device (only for CONTINENTAL ver-

sion instrument boards).
If this device is provided, the instrument return arm can be locked in the
instrument extracted position.
When the device is used a click is heard about 2/3 of the total arm travel.
To go back to the original condition, simply move the arm to the end of its
travel ( B ).
Tray holder module for CONTINENTAL version dentist’s instrument board.

The tray holder module ( f ) is made of stainless steel and can easily be
removed from its support.
WARNING!
Maximum permitted load on the tray holder module ( f ): 2 kg distri-
buted.
Tray holder module for INTERNATIONAL version dentist’s instrument board.
The stainless steel tray holder (e) can be easily removed from its mount.
The tray holder can be turned both clockwise and counter-clockwise so
that it can be placed in the most convenient position for the operator. The
tray holder arm can be turned both clockwise and counter-clockwise for a
total of 60° passing through 8 set positions.
WARNING!
Maximum permitted load on the tray holder module ( e ): 2 kg distri-
buted.

18 EN
Inverting the console unit position for left-handed operators
WARNING!
BEFORE CARRYING OUT THIS OPERATION, TURN OFF THE DENTAL
UNIT. DO NOT REMOVE THE CONSOLE FROM THE DENTIST’S MO-
DULE IF THE DENTAL UNIT IS ON.

To invert the position of the console unit on the dentist’s module,
operate as follows:
• Remove the console unit after unscrewing the fastening ring nut ( g ) by
turning it anticlockwise.
• Remove the protective snap-on cap ( s ) of the quick-coupling on the left-
hand side and fit it on the coupling on the right-hand side.
• Turn the console unit brace 180°.
• Fit the console unit to the quick-coupling on the left-hand side.
To correctly position the console unit, push the brace fully into place in the
support and at the same time turn the ring nut by about 1/3 turn until it locks
without forcing tightening.
NOTE: to prevent the dentist’s module from slipping out on the
opposite side during this operation, it is advisable to beforehand turn it
about 90° with respect to its support arm (see figure).
• At this point, you can turn the dental unit on again.
WARNING!
During the console cleaning operations do not exert excessive pressure
on the pushbutton panel to prevent damaging stress on the connection.
Cleaning the dentist’s instrument board.

Clean the dentist’s instrument board using a suitable product (see para-
graph 1.4).
NOTE for CONTINENTAL version dentist’s instrument boards:
the instrument holder ( x ) can be removed to facilitate the cleaning ope-
rations; to remove it, simply pull it out of its seat as it is only secured with

magnets.
The silicone instrument holder ( u ) can also be sterilized in an autoclave
at 121°C (see paragraph 1.5.).
Removable instrument cords

All the instruments have removable cords to ease cleaning.
NOTE for CONTINENTAL version dentist’s instrument boards:
to remove the tubings you first need to remove the instrument holder and
then unscrew the relative plastic fastening ring nuts.
NOTE for INTERNATIONAL version dentist’s instrument bo-
ards: to remove the tubings, unscrew the relative plastic fastening ring
nuts below the dentist’s instrument board.
WARNING!
• Shut off the operatory unit before attempting to take off the cords.
• After shutting off the operatory unit, empty the syringe’s ducts by
pressing and holding down the relative air and water buttons directly
on the bowl until water spray is no longer present.
• The cords of the TURBINE, MICROMOTOR and SCALER contain
water, therefore hold the end of the cord on the handpiece side over
the bowl when removing the cord.
• When putting a cord back on, make certain the contacts are perfectly
dry and the plastic ring nut is tight.
• Each cord may be remounted only in the position for the correspon-
ding instrument.
Clean the instrument cord using a suitable product (see Paragraph 1.4).
WARNING!
The instrument cords are NOT suitable for autoclave or cold disin-
fection.
EN 19
5.1. Doctor’s control console
The R7 series dental units have a R7 “hybrid” dentist’s console consisting

of a membrane pushbutton panel and a resistive touchscreen display.
4.3” Wide colour TFT display with LED backlighting, resolution 480x272
pixels and 262k colours.
Pushbutton panel for the following models:

R7 CONTINENTAL
R7 M CONTINENTAL
Pushbutton panel for the following models:

R7 INTERNATIONAL
R7 M INTERNATIONAL
R7 CART
R7 M CART
Dentist’s instrument board brake release button

(INTERNATIONAL models)
SMART TOUCH screen disable button
Operatory light on/off button
Water to cup button
Auxiliary function button (available)
Bowl counter-clockwise button

( active only with powered bowl).
Bowl clockwise button

( active only with powered bowl)
Water to bowl function button
Dental chair functions save button
Emergency position button.
Automatic return button.
Rinse position button.
Chair seat up and set position “A” button.
Chair back up and set position “B” button.
Chair seat down and set position “C” button.
Chair back down and set position "D" button.
NOTE: Operation of dental chair buttons:

• Button pressed shortly: set position automatically reached.
• Button held down: positioned reached by hand.
20 EN
Warning icons.
Touching the icon button on the touch display, you can at any time
view the warning icons that show the operating status of the dental unit.
The warning icons viewable are the following:
Feeding with distilled water activated.
Feeding with mains water activated.
Distilled water level low.

( excluding models R7 M )
BIOSTER cycle in progress.
Suction tubes being washed.
Suction stopped due to full canister.
Wireless foot control battery charged.
Wireless foot control battery 50% charged.
Wireless foot control battery flat.
Wireless foot control connected and active.
Wireless foot control connected but not active.
Searching for connection to the wireless foot control.
Dental chair seat brake released (only with turnable seat ).
Rinse automated programme chair position.

COLD water-to-glass.
Home automated programme chair position.

WARM water-to-glass.
Emergency automated programme chair position.

HOT water-to-glass.
Dental chair save function on.

Dental chair position automated programme A.
Chair position manually set up.

Dental chair position automated programme B.
Dental chair position automated programme C.
Dental chair position automated programme D.
Dental chair movements blocked.
EN 21
5.1.1. User interface
When turned on, the dental unit performs a brief autodiagnosis cycle that ends
when the main screen containing the name of the operator last set is displayed.
As of this moment a number of settings can be edited from user-friendly
menus (see diagram).
Menu scrolling control.

• To access the setting menu, touch the icon button .
• To access the various submenus, touch the relative icon button.
• To change a setting in a menu, touch the relative icon button.
• To change a numerical value in a menu, touch the icon buttons or .
• To exit from a menu, touch the icon button .
Layout of the user interface menu.

The user interface menu is structured as shown in the diagram and includes
the following menus:
5.1.1.1. Operator selection.
5.1.1.2. GENERAL SETTINGS.
5.1.1.2.1. HYGIENE SYSTEM SETTING.
5.1.1.2.1.1. BIOSTER disinfection cycle setting.
5.1.1.2.1.2. FLUSHING cycle setting.
5.1.1.2.2. HYDRO UNIT SETTINGS.
5.1.1.2.2.1. Bowl water delivery setting.
5.1.1.2.2.2. Cup water delivery setting.
5.1.1.2.2.3. Bowl movement control.
5.1.1.2.3. FOOT CONTROL ADJUSTMENT.
5.1.1.2.4. OPERATING LAMP ADJUSTMENT.
5.1.1.2.5. OTHER SETTINGS.
5.1.1.2.6. TIME AND DATE SETTING.
5.1.1.2.7. CHRONOMETER.
5.1.1.2.8. FAVOURITE BUTTONS CUSTOMISATION.
5.1.1.2.9. OPERATOR DATA ENTRY.
5.1.1.2.10. LANGUAGE SELECTION.

Error messages.

During the initial self-diagnostic cycle, the dental unit may detect some mal-
functions in the internal system.
In this case, an error message is shown on the display (see paragraph 10)
which remains visible until the operator touches the TOUCH DISPLAY.
If the malfunction is not hazardous, the dental unit will continue to operate.
Stand-by mode.
The dental unit goes into power saving mode (stand-by) after approximately
10 minutes of non-use; this mode is shown by the ANTHOS logo on the
control panel display.
Normal operating conditions are restored as soon as any operation is
performed.
22 EN
5.1.1.1. Operator selection
The SMART TOUCH console of the R7 series dental units allows managing
3 different operators.
The following data can be set for each operator:
• Operator's name.
• Turbine and scaler power adjustment.
• 3 electric micromotor operating modes
• 4 scaler operating modes .
• Turning on and adjustment of the fibre optics of each instrument.
• Incremental or ON/OFF control of the turbine and the scaler power .
• Automatic dental chair movement programs.
• Hydro unit configuration parameters
Operator selection.
From the main page, repeatedly touch the icon button until finding the
desired operator.
NOTE: the operator is changed cyclically.
5.1.1.2. General settings
From the main page, carry out the following operations:

• Touch the icon button to access the GENERAL SETTINGS menu
containing the following icon buttons:
HYGIENE SYSTEM SETTINGS

(only if at least a hygiene system is present)
HYDRO UNIT SETTINGS
FOOT CONTROL ADJUSTMENT
OPERATING LAMP ADJUSTMENT
OTHER SETTINGS
TIME AND DATE SETTING
CHRONOMETER
PERSONALIZATION OF FAVOURITE KEYS
OPERATOR DATA ENTRY
LANGUAGE SELECTION
ACCESS SERVICE MENU

(FOR TECHNICAL SERVICE,ONLY)
EN 23
5.1.1.2.1. Hygiene system settings
NOTE: menu available only if at least a hygiene system is present.
From the GENERAL SETTINGS menu touch the icon button to

access the HYGIENE SYSTEM SETTINGS submenu containing the
following icon buttons:
BIOSTER /S disinfection cycle setting

(only if the BIOSTER /S system is present )
Flushing CYCLE SETTING

(only if the FLUSHING system is present)
5.1.1.2.1.1. BIOSTER /S disinfection cycle setting
This setting is shared by all users.

From the HYGIENE SYSTEM SETTINGS menu carry out the following
operations:
• Touch the icon button to access the BIOSTER/S DISINFECTION
CYCLE SETTING submenu.
• Withdraw the instruments to be treated (the corresponding icon will appear
on the display):
S1: syringe on instrument board.
A: instrument in position A
B: instrument in position B
C: instrument in position C
D: instrument in position D
F: instrument on assistant's board.
BC: water to cup duct. ( always operative )
The syringe on the assistant's board cannot be disinfected using
the BIOSTER S cycle.
• To start the disinfection cycle, touch the icon button (see Paragraph
7.4).
NOTE: the disinfectant contact time is preset and not modifiable
(600 seconds).
NOTE: the BIOSTER S cycle can only be activated if the SHS/S
system is on (see paragraph 7.2).
24 EN
5.1.1.2.1.2. Flushing CYCLE SETTING

From the HYGIENE SYSTEM SETTINGS menu carry out the following
operations:
• Touch the icon button to access the FLUSHING CYCLE SETTING
submenu .
NOTE: this submenu cannot be entered if the distilled water tank
is low (see paragraph 7.2.). A message on the control panel display and an
acoustic signal (BEEP) will signal the impossibility to enter the submenu.
• Set the flushing time by touching the icon buttons or .
NOTE: the time may range from at least 1 minute to at most 5

minutes, with 1 minute intervals.
NOTE: for the distilled water tank, it is advisable not to set a time
longer than 2 minutes.

• Withdraw the instruments to be treated (the corresponding icon will appear
on the display):
A: instrument in position A
B: instrument in position B
C: instrument in position C
D: instrument in position D
F: instrument on assistant's board.
NOTE: the syringe is always active, therefore as soon as it is in-

serted in the instrument container it will immediately start delivering water.
NOTE: the Flushing CYCLE does not start if at least one instrument
is not selected.
• To start the FLUSHING cycle, touch the icon button (see paragraph
7.6.).
EN 25
5.1.1.2.2. Hydro unit settings
From the GENERAL SETTINGS menu touch the icon button to access
the HYDRO UNIT SETTINGS submenu containing the following icon buttons:
Water to bowl settings
Water to cup settings
Automatic bowl movement setting

(only with motor-driven bowl)
5.1.1.2.2.1. Bowl water delivery setting
From the HYDRO UNIT SETTINGS menu touch the icon button to
access the BOWL WATER SETTING submenu containing the following
icon buttons:
Bowl flushing controller

with dental chair brought to rinse position
Bowl flushing controller

with dental chair brought to reset position
Cuspidor bowl flushing automatism

with return from the rinse position for the chair
A Bowl flushing controller with cup call
Setting of timed or ON/OFF bowl flushing
Bowl flushing time (in seconds )
• To select/deselect a function, touch the relative icon button.
• To change the bowl flushing time, touch the icon buttons or .
• To confirm the selected settings, it is sufficient to exit this submenu by
touching the icon button .
26 EN
5.1.1.2.2.2. Cup water delivery setting
From the HYDRO UNIT SETTINGS menu touch the icon button to access
the CUP WATER SETTING submenu containing the following icon buttons:
COLD cup water selection
WARM cup water selection
HOT cup water selection
Cup water delivery time

(in seconds )
Cup water delivery automatic function

with rinse position recall.
Cup detection sensor activation/deactivation

( only if the cup sensor is present )
Distilled water tank depressurization automatic function

with chair home position recall

• To change the cup water delivery time, touch the icon buttons or .
NOTE: the cup time of filling can be set up from a minimum of
1 second to a maximum of 10 seconds with increments of 0.1 seconds.

• To confirm the selected settings, exit this submenu by touching the icon
button .
5.1.1.2.2.3. Automatic bowl movement setting
From the HYDRO UNIT SETTINGS menu touch the icon button to
access the AUTOMATIC BOWL MOVEMENT SETTING submenu contai-
ning the following icon buttons:
Bowl rotation automatic function

with chair rinse position recall


with automatic dental chair program recall

EN 27
5.1.1.2.3. Foot control adjustment

access the FOOT CONTROL ADJUSTMENT submenu containing the
following icons:
Cable connection icon

(only with wireless foot control)
Wireless connection status icon

Battery percentage charge icon

Foot control joystick operation setting

with instrument removed
NOTE: the first 3 icons are just for signalling, while the fourth one al-
lows to select/deselect the operation mode of the foot control upper joystick.

• To select/deselect the type of foot control operation, touch the relative
icon button :
The joystick activates the chair manual movements (default).
The joystick is used for the following functions:
ON/OFF control for micromotor rotation direction inver-

sion, scaler ENDO function activation , camera MIRROR
function activation.
ON/OFF control for peristaltic pump activation.
ON/OFF control for operating lamp.
Instrument memory change.
button .
5.1.1.2.4. Operating lamp adjustment
From the GENERAL SETTINGS menu touch the icon button to ac-
cess the OPERATING LAMP SETTING submenu containing the following
icon buttons:
Light off automatism

with chair rinse position recall
Light off automatism

Lamp brightness reduction automatism

with curing lamp instrument removal
(only with VENUS PLUS –L LED lamp)
NOTE: with the off-control automatism activated, it is sufficient
to recall any chair movement to turn on again the operating light.
NOTE: with the brightness reduction automatism activated, it
is sufficient to replace the curing lamp instrument to reactivate the set
brightness.
• To select/deselect an automatic function, touch the relative icon button.
28 EN
5.1.1.2.5. Other settings
These settings are unique for all the operators.

access the OTHER SETTINGS containing the following icon buttons:
Touch display acoustic signal activation/deactivation
Dental chair movement activation/deactivation
Display brightness adjustment
• To activate or deactivate an acoustic signal each time the TOUCH DI-

SPLAY is touched.
• To enable/disable the dental chair movements, touch the relative icon
button.
NOTE: when the chair is locked, it is indicated by a dedicated
icon on the TOUCH DISPLAY (see paragraph 5.1.).
WARNING!
For greater working safety, this operation is obligatory if you need
to use an external electric scalpel.
• To adjust the display brightness, touch the relative icon buttons or .
NOTE: the settable value ranges from 1 to 10.

button .
5.1.1.2.6. Time and date setting

access the TIME AND DATE SETTING submenu.
• To change the data displayed, touch the relative icon buttons or .
button .
EN 29
5.1.1.2.7. Chronometer

access the CHRONOMETER SUBMENU.
• To change the various data displayed , touch the relative icon buttons
or .
NOTE: the time can bet set from 00:00:00 to 10:59:59.

• Once you have set the time, touch the icon button to start the
countdown.
NOTE: at this point, you can exit this menu by touching the icon
button without interrupting the countdown.
• To interrupt the countdown, touch the icon button .
NOTE: at this point, touching the icon button you can reset
the chronometer to the last time set.
• When the set time runs out, the dental unit emits an intermittent signal and
the CHRONOMETER menu is once again shown on the TOUCH DISPLAY.
To interrupt the intermittent signal, touch the icon button or any
button on the console.
NOTE: the last time set remains stored.
5.1.1.2.8. Personalization of favourite keys
This submenu allows you to select the function to attribute to the 3 lower
icons visible in the main page.
From the GENERAL SETTINGS menu touch the icon button to access
the FAVOURITE BUTTONS CUSTOMISATION submenu where you can
view the 3 positions modifiable with the icons of the functions currently set.
• To change the function for a specific position, touch the relative icon buttons
or .
• The settable functions are the following:
BIOSTER S DISINFECTION CYCLE SETTING

(position P1 only)
FLUSHING CYCLE SETTING

(position P1 only)
Hydro unit settings
Foot control adjustment
Operating lamp adjustment
Other settings
Time and date setting
Chronometer
Language selection
Independent water supply selection/deselection
button .
30 EN
5.1.1.2.9. Operator data entry

access the OPERATOR DATA ENTRY submenu.
NOTE: the data modified always refers to the operator set on the
main page.
• To enter the desired text, touch the icon buttons of the various letters (max.
20 characters).
• To enter capital letters, touch the icon button .
• To enter numbers or special characters, touch the icon button .
• To cancel any typing mistakes, touch the icon button cancelling from
left to right.
• Once you have entered the text, touch the icon button to exit from
the submenu and automatically save the data.
5.1.1.2.10. LANGUAGE selection

access the LANGUAGE SELECTION SUBMENU.
• To change the language, touch the icon button of the relative flag.
• To confirm the setting selected, exit this submenu by touching the icon
button .
5.1.2. Setting the dental chair’s “rinse” and “home” positions
This setting is specific for each operator.

Perform the following operations from the main screen:
• Bring the dental chair into the desired position with the manual movements
buttons.
NOTE: in the case of the “Rinse position” the position of the bowl
can be saved, if powered.
• Hold button “SAVE” for at least 2 seconds to activate memory mode.
The system beeps and the relevant icon ( A ) appears on the console
display to signal save mode has been activated.
NOTE: Hold down button "SAVE" for at least 2 seconds to quit
without saving the changes made.
• Press buttons “AUTOMATIC RETURN” or “RINSE POSITION” to assign
the position to the button.
The icon ( B ) for the selected program will appear on the console display

to confirm the data have been saved.
NOTE: The seat height cannot be changed when in the “RINSE

POSITION”.
NOTE: The “RINSE POSITION” button brings the backrest and

seat into the rinse position.
When button “RINSE POSITION” is pressed again, the backrest and seat
return to the previous position.
EN 31
5.1.3. Programming the chair positions A, B, C and D
This setting is specific for each operator.

Perform the following operations from the main screen:
• Bring the dental chair into the desired position with the manual movements
buttons.
NOTE: the position of the bowl can be saved, if powered.

• Hold button “SAVE” for at least 2 seconds to activate memory mode.
NOTE: Storage mode activation is signalled by a short beep and
by the dedicated icon ( A ) on the TOUCH DISPLAY.
• Push the A, B, C or D keys to associate the relevant position to the key

(e.g. C).
NOTE: The icon ( B ) referring to the program selected (e.g. C)

will appear on the TOUCH DISPLAY to confirm that it has been stored.
NOTE: To call up a set position simply briefly press the button
assigned to the relative position.
5.1.4. Emergency stop button
This button can be used in the event of an emergency to bring the patient
into the Trendelemburg position.
NOTE: The Trendelemburg position is already set and cannot be

changed.
5.1.5. SMART TOUCH screen disable button.
This button allows enabling/disabling the TOUCH DISPLAY screen so that

you can easily clean the console.
NOTE: The disabled status is indicated by a clear message on
the TOUCH DISPLAY.
32 EN
5.2. Foot control
3 types of foot controls are available:
1 "Multifunction” foot control
"Push-pedal” foot control
"Power Pedal" foot control.
NOTE: the "multifunction" and "pressure" foot controls can also be

supplied in wireless version.
5.2.1. "Multifunction” foot control
Description of the parts

1 Handle
2 Control pedal
3 Dental chair movements
4 Chip-air/patient rinsing position control.
5 Water Clean System/Automatic dental chair return control.
6 LED (not active).
7 Battery charge LED (wireless version only).
Joystick for dental chair movement (3).
With instrument removed

• Starts the instrument.
• Adjusts the rpm of rotary instruments.
• To right: operation with spray (if foreseen for selected instrument).
NOTE: At the end of work, air is automatically blown to eliminate
any drops of liquid remaining in the spray ducts.
• To left: spray-free operation
With instruments in place
• Fully right: dental chair automatic return (RA).
• Fully left: patient rinse position reached (PR).
NOTE: If the pedal is pushed fully left again, the dental chair moves
back to the work position.
WARNING!
These dental chair functions are activated by keeping the pedal at the
end of the travel for at least 2 seconds.
Controller joystick for dental chair movement ( 3 )

These buttons move the dental chair as follows:
Dental chair seat up.
Dental chair backrest up.
Dental chair seat down.
Dental chair backrest down.
To stop the chair movement, release the joystick.

NOTE: all the buttons used to move the dental chair are inoperative
when an instrument is removed and the foot control pedal is actuated.
NOTE: the joystick operating mode can be changed with the instru-
ment removed (see Paragraph 5.1.1.2.3.).
EN 33
Left-hand button operation ( 4 ).

• Key held down (at least 2 seconds) with the instrument removed:
Chip-air operation: delivers air to the turbine or micromotor.
Air is delivered by pressing the button. Air is no longer blown when the
button is released.
• Key held down (at least 2 seconds) with the instruments in place:
"Rinse position” (PR) program activated.
NOTE: Press the key again to bring the chair back to the work
position.

Right-hand button operation ( 5 )
• Key held down (at least 2 seconds) with the instrument removed:
Water Clean System operation: running water is sent to the instruments
such as the turbine, micromotor and scaler to flush the spray ducts.
Water is delivered by pressing the button. Water is no longer delivered
when the button is released and air is automatically blown to eliminate
any drops of liquid remaining in the spray ducts.
• Key held down (at least 2 seconds) with the instruments in place:
"Dental chair automatic return” program activated.
WIRLESS version.
This foot control can also be supplied in wireless version (see Paragraph
5.2.4).
Protection against liquid penetration.

The foot control is protected against liquid penetration. Degree of protection: IPX1.
Cleaning.
Clean the foot control using a suitable product (see Paragraph 1.4).
NOTE: If the foot control slips on the floor, dust the slip-proof rubber found under the base with a dry cloth.
5.2.2. "Push-pedal” foot control
Description of the parts

1 Handle

2 Control pedal
3 Dental chair movements
4 Chip-air/patient rinsing position control.
5 Water Clean System/Automatic dental chair return control.
6 Spray operation LED
7 Battery charge LED (wireless version only).

Control pedal ( 2 )
Operation:
• Remove the instrument
• Push the foot pedal to start the instrument ( a )
• Adjust the rpm/power of the instrument with the control pedal:
- to right: to increase
- to left: to decrease
NOTE: the control pedal adjusts the speed/power of the instrument

from the minimum to the maximum value set from the instrument board.
• To stop the instrument, simply release the control pedal ( a ).
NOTE: with the spray active, at the end of the operation a blast
of air is automatically activated to remove any residual drops of liquid in
the spray ducts.
WARNING!
Instrument spray is activated and deactivated by pressing the but-
tons ( 4 ) or ( 5 ).
A beep sounds to signal the operating status has been changed.
When the LED ( 6 ) is on, it indicates operation with spray.
34 EN

To stop the chair movement, release the joystick.
NOTE: All the buttons used to move the dental chair are inoperative
when an instrument is removed and the foot control pedal is actuated.

Operation:
• Holding down the button for at least 2 seconds with the instruments in
rest position:
Activation of the “Patient rinsing position” program.
NOTE: Pressing the button a second time returns the dental chair
into working position.
• Holding down the button for at least 2 seconds with instrument extracted:
Chip-air control: sends a jet of air to the turbine or the micromotor.
Air delivery is activated by pressing the button; the jet of air is interrupted

when the button is released.
NOTE: The control works only when the turbine and micromotor
are in working position.
• Briefly pressing the button with the instrument extracted:
Activation or deactivation of instrument spray.
WARNING!
A short acoustic signal warns of the switch.
Right-hand button operation ( 5 ).

Operation:
• Holding down the button for at least 2 seconds with the instruments in
rest position:
Activation of the “Automatic dental chair return” program.
Water Clean System control: sends a jet of running water to instruments
such as the turbine, the micromotor and the scaler for rinsing the spray
ducts.
Water delivery is activated by pressing the button ( 4 ); when the button is
released, the jet of water is interrupted and a blast of air is automatically
activated to remove any residual drops of liquid in the spray ducts.
WARNING!
Wireless version.
This foot control can also be supplied in wireless version (see Paragraph 5.2.4).

The foot control is protected against liquid penetration. Degree of protection: IPX1.
Cleaning.
NOTE: if the foot control slips on the floor, dust the slip-proof rubber found under the base with a dry cloth. .
EN 35
5.2.3. "Power Pedal" foot control
Description of the parts.

1 Handle.
2 Foot control.
3 Dental chair movements.
4 Chip-air control or activation/deactivation of instrument spray function.
5 Water Clean System control or activation/deactivation of instrument spray
function.
6 Automatic dental chair return or programme "B” recall activation.
7 Patient rinse position or programme "A" recall activation.
8 Spray operation LED.

Foot control operation ( 2 ).
• With instrument removed
- Pushing the pedal ( a ), the instrument is started.
The instrument's rpm (or power) can be adjusted by varying the pressure
exerted on the foot control.
NOTE: the foot control adjusts the speed/power of the instrument
from the minimum to maximum value set from the instrument board.
- Release the foot control to stop instrument operation.
NOTE: with the spray active, at the end of the operation a blast
of air is automatically activated to remove any residual drops of liquid
in the spray ducts.
• With instrument in place
When the foot control is pressed, all automatic dental chair movements
are automatically blocked.

To stop movement, release the button.

NOTE: all dental chair movements are blocked when an instrument
is being used or the BIOSTER system is running.

Chip-air control: sends a jet of air to the turbine or the micromotor.
Air delivery is activated by pressing the button; the jet of air is interrupted
when the button is released.

WARNING!

Right-hand button operation ( 5 ).
Water Clean System control: sends a jet of running water to instruments
such as the turbine, the micromotor and the scaler for rinsing the spray
ducts. Water delivery is activated by pressing the button ( 5 ); when the
button is released, the jet of water is interrupted and a blast of air is au-
tomatically activated to remove any residual drops of liquid in the spray
ducts.
WARNING!
When the LEDs ( 8 ) are on, they indicate operation with spray.
36 EN
Right lever operation ( 6 ).

NOTE: the lever functions only with the instruments in their rest
position.
For safety reasons, the selected function starts only after the switch has
been briefly actuated and then released.
• Lever pushed down:
"Dental chair automatic return” program activated.
• Lever pulled up:
Dental chair program “B" start.
Left lever operation ( 7 ).

NOTE: the lever functions only with the instruments in their rest
position.
For safety reasons, the selected function starts only after the switch has
been briefly actuated and then released.
• Lever pushed down:
"Rinse position” (PR) program activated
NOTE: when the switch is actuated the second time, the dental
chair reaches its work position.
• Lever pulled up:
Dental chair program “A" start.

The foot control is protected against liquid penetration.
Degree of protection: IPX1.
Cleaning.
NOTE: if the foot control slips on the floor, dust the slip-proof rubber found under the base with a dry cloth.
EN 37
5.2.4. Wireless foot control
The "multifunction" and "pressure" foot control can also be supplied in wireless version.
The wireless foot control contains a ZIGBEE transmitter module (module certified for Europe, Canada and the USA).
Warnings for use.
WARNING!
• Avoid keeping the wireless foot control in proximity of other RF sources, such as wireless LAN cards, other radio devices, home RF de-
vices, microwave ovens. The recommended distance is at least 2 metres in the case of microwave ovens and 1 metre in all other cases.
• Even though the electromagnetic field irradiated by the foot control is insignificant, it is advisable NOT to use it in proximity of life sup-
port equipment (e.g. pacemakers or heart stimulators) and hearing aids. Before using any electronic device in health facilities, always
ascertain that it is compatible with the other equipment present.
• Exclusively use the dental unit to charge the battery of the WIRELESS foot control.
• The internal battery may only be replaced by a qualified technician.
Warnings for first use.

It is advisable to fully charge the foot control battery before using it for the first time.
WIRELESS foot control operation.

The WIRELESS foot control operates in exactly the same way as the wired version, therefore refer to the paragraphs above paying attention to the
specific model used.
In addition, the WIRELESS foot control has a specific LED (7) that indicates the battery charge and the communication status with the dental unit.
LED ( 7 ) indications.
The colour of the LED indicates the battery charge, while the type of flashing
indicates the communication status with the dental unit.
Battery charge:
description description
colour
( cable disconnected ) ( cable connected )

GREEN Battery charge (>75%) Battery charged
ORANGE Battery charge (<50%) Battery charging
Battery needs charging
RED Battery charge error
(<25%)
Dental unit off or foot
Off Battery flat
control fault
Communication status:
flashing description
Slow Connection active in wireless mode
Fast Connection active with charging cable inserted
Double Connection search
On fixed Communication error

NOTE: this information can be shown also on the TOUCH DISPLAY
through the specially provided icons ( A ) or ( B ) (see paragraph 5.1.) or
in the specially provided control menu of the foot control (see paragraph
5.1.1.2.3.).

Battery characteristics.
The WIRELESS foot control is equipped with a rechargeable Lithium-Polymer battery ( Li-Poly, 3.7V, 5200 mAh type Guangzhou Markyn Battery
Co. Model 9051109 ).
The battery life is approximately 2 months (estimating 8 hours of consecutive daily operation) with the battery fully charged and fully efficient. The
battery efficiency reduces with age. It is estimated that the efficiency is reduced to 60% after 500 complete recharging cycles. Also in this condition,
the battery should last about 1 month.
NOTE: When the battery efficiency is so far reduced as to be deemed unsatisfactory to support the daily usage requirements, have it replaced
by a qualified technician (original spare part no. 97901336).
WARNING!
Do not attempt to replace the battery yourself.
Limited battery warranty.

The battery in the foot control is covered by a 6-month warranty from the date of installation.
38 EN
Recharging the battery.

When the batteries in the WIRELESS foot control need to be recharged,
operate as follows:
• Open the protective cap of the connector on the rear of the foot control
and connect the recharging cable.
• Connect the other end of the recharging cable to the dental unit (see
figure).
At this point, the foot control, while it remains fully operational, will start
recharging the battery ( Battery charging warning LED on ).
NOTE: The battery is fully recharged in about 6 hours.
WARNING!
Exclusively use the dental unit to charge the battery of the WIRE-
LESS foot control.
Natural battery discharge.

Should the battery not be used for long periods of time, it may slowly
discharge all the same.
After long periods of disuse, it is advisable to always fully charge the
battery before use.
Maintenance and disposal

The wireless foot control does not contain parts that can be repaired di-
rectly by the user.
In the event of a malfunction, do not attempt to carry out maintenance
operations, but directly contact the manufacturer or his local distributor at
the numbers indicated in the warranty certificate.
At the end of its lifetime, the battery must be replaced by a specialised
technician at a Service Centre.
EN 39
5.3. Syringe
Description of the instrument.

[ a ] Nozzle.
[ b ] Handpiece.
[ c ] Syringe release button.
[ d ] Air button.
[ e ] Water button.
[ f ] Hot/cold selector.
[ g ] Hot/cold indicator light.
Technical charachteristics.
• Operating time:
- 3F syringe: continuous operation,
- 6F syringe: 5 sec. operation, 10 sec. rest.
• Power supply:
- 6F syringe (CEFLA s.c. models): 24 Vac; 50/60 Hz; 2 A; 50 W.
• Classification in accordance with standard EN 60601-1:
- 6F syringe (CEFLA s.c. models): CLASS II, type B.
• Installation plan: consult the Technical Installation Manual (see Paragraph 11.).
Operation.
• Place the instrument in its work position.
• Button ( e ) = water;
Button ( d ) = air;
Buttons ( e + d ) = spray.
• 6F syringe, operation with hot water, air and spray: turn the selector [ f ]
clockwise (LED g on).
• 6F syringe, operation with cold water, air and spray: turn the selector
[ f ] anticlockwise (LED g off).
Removing the handpiece.

• The nozzle ( a ) is screwed onto the grip ( b ).
• Turn the selector switch counter-clockwise (LED g off) and press the
button ( c ) to take the grip off the syringe casing.
Removable syringe cord

The syringe has a removable cord to ease cleaning (see chapter 5).
Cleaning.
Use soft disposable paper towel dampened with detergents/disinfectants
WARNING!
• Do not soak the syringe in liquid disinfectants or detergents.
• Products not recommended: harsh products and/or products con-
taining acetone, chlorine and sodium hypochlorites.
Sterilization.
Syringe grip and spout: see paragraph 1.5.
NOTE: Bag before sterilizing.
Instructions for use.
WARNING!
• The instrument is supplied NOT STERILE and must be sterilized
before use (see paragraph 1.5.).
• It is recommended to use single-use protections and nozzles.
40 EN
5.4. Turbine
Connecting the handpiece and changing the chuck.
Refer to the specific instructions furnished with the handpiece.
Use.
WARNING!
Read the instructions for use of the various turbines.
• The cock ( f ) adjusts the water flow to the spray.
• The cock ( e ) adjusts the amount of air spray for all the instruments.
NOTE: instrument activation is indicated by the relative manage-
ment page appearing on the TOUCH DISPLAY.

• The icon buttons available on the TOUCH DISPLAY are the following:
Settable value increase
Settable value decrease
Turbine rotation speed selection
Fibre optics on/off

(only with S.H.S./S system)
Instrument spray type enable and selection
Row of general operating icons

(see paragraph 5.1.)
Quick selection of power at 1% of the maximum turbine

rotation speed

rotation speed

rotation speed.
• Use the foot control pedal to start the instrument (see paragraph 5.2).
NOTE: The turbine cord can also be used to connect the air micro-
motors equipped with 4-way connector and conform to ISO 13294 - Dental
Air Motor.
Fibre optic brightness adjustment.

• To adjust the fibre optic brightness, touch and hold (for at least 2 seconds)
the icon button .
• Adjust the brightness by touching the icon or .
• To confirm the brightness selected, exit this submenu by touching the
icon button .
NOTE: after 30 seconds of not using the instrument (foot control
lever deactivated), the fibre optics turns off.
EN 41
Turbine rotation speed change.

With the instrument in working position, select turbine speed change mode
by touching the following icon buttons:
Linear change proportional to the movement of the

the foot control lever
ON/OFF change that results in delivery of the maximum power

set upon activation of the foot control lever
The active mode icon is shown on the TOUCH DISPLAY.

NOTE: the data is automatically stored.
Instrument spray control button.

With the instrument in working position, select the type of spray delivered
by the instrument by touching the following icon buttons:
Water + air spray operation
Water-only spray operation
Operation without spray
The change is cyclic each time the button is touched and the active mode icon
is shown on the TOUCH DISPLAY.
Removable cord
The turbine has a removable cord to ease cleaning (see paragraph 5.).
Cleaning and care.

Refer to the specific instructions furnished with the instrument.
It is recommended to use Daily Oil (CEFLA s.c.) for lubrication.
Sterilization.
Only instrument handpiece: see paragraph 1.5.
WARNING!
Carefully read the operating instructions supplied with the handpiece before attempting to sterilize.
WARNING!
• The instrument is supplied NOT STERILE and must be sterilized before use (see paragraph 1.5.).
Before performing sterilization, check the instructions for use included with the device.
• Only for American and Canadian markets: instruments must be FDA-approved.
• The turbine must never be started without attaching the chuck or false chuck.
• The chuck release button must be held down during operation!
Friction between the button and micromotor rotor overheats the head and may cause burns.
• The patient’s internal tissues (tongue, cheeks, lips, etc...) must be protected against contact with the button by using suitable instruments (mirror,
etc...).
• The chucks and various instruments attached to the handpieces must comply to the standard ISO 10993-1 Biological evaluation of medical devices.
42 EN
5.5. Micromotor
Coupling the handpieces and changing the chuck.

Refer to the specific instructions furnished with the micromotor and various
handpieces.
Use.
WARNING!
Also read the instructions for use of the various motors.
The instrument is supplied non-sterile.
• Operating time: work 5 min., rest 5 min.

• The cock ( f ) adjusts the water flow to the spray.
• The cock ( e ) adjusts the amount of air spray for all the instruments.
NOTE: instrument activation is indicated by the relative manage-
ment page appearing on the TOUCH DISPLAY.

• The main icon buttons available on the TOUCH DISPLAY are the following:
Settable value increase
Settable value decrease
Reduction ratio selection
Reduction ratio selection
Speed change mode selection

Instrument spray type enable and selection
Micromotor rotation direction selection
Fibre optics on/off (see paragraph 5.1.)
Independent water supply selection/deselection Micromotor operating mode

(only with S.H.S./S system) selection ( only with i-MMs micromotor ).
Micromotor operating program

selection

the icon button .
• Adjust the brightness by touching the icon buttons or .

• To confirm the brightness selected, exit this submenu by touching the
icon button .
NOTE: after 30 seconds of not using the instrument (foot control
lever deactivated), the fibre optics turns off.
EN 43
Instrument spray control button.

With the instrument in working position, select the type of spray delivered
by the instrument by touching the following icon buttons:
Water + air spray operation
Water-only spray operation
Operation without spray
Rotation speed change mode selection.

With the instrument in working position, select rotation speed change mode
Linear change proportional to the movement of the

the foot control lever


Micromotor rotation direction inversion.

Select the micromotor rotation direction by touching the relative icon button:
Normal rotation direction
Inverted rotation direction
Inverted rotation direction is signalled by 3 beeps.
WARNING!
Subsequently, when the micromotor is extracted, 3 warning beeps
are emitted if the rotation direction is inverted.
NOTE: When the rheostat lever is activated, inversion of the
micromotor rotation direction is deactivated.
Micromotor operating mode selection ( only with i-MMs micromotor ).

The micromotor has 2 different operating modes that can be selected by
touching the relative icon button:
RESTORATIVE
(see paragraph 5.5.1.)
ENDODONTIC
(see paragraph 5.5.2.)
NOTE: the change occurs cyclically.
Micromotor operating program selection.

The micromotor has 4 operating programs identified with P1, P2, P3, P4 that
can be selected by touching the relative icon button.
Each operating program stores the following data:
- operating mode ( only with i-MMs micromotor ).
- maximum rotation speed / torque value
- fibre optics ON/OFF
- fibre optic brightness
- rotation direction inversion ON/OFF
- type of spray delivered
- Handpiece reduction ratio.
NOTE: the change occurs cyclically.
44 EN
Reduction ratio selection.

Using the icon buttons or you can select the desired reduction
ratio from those stored.
The torque value (set or current) is expressed in % or Ncm for the certified
reduction gears.
WARNING!
An icon appears next to the torque value identifying the reading
tolerance on the value indicated:
tolerance of ±10%
tolerance of ±20%.
Removable cord
The micromotor has a removable cord to ease cleaning (see paragraph 5.).
Cleaning and care.

It is recommended to use Daily Oil (CEFLA s.c.) for lubrication.
WARNING!
• Do not soak the micromotor in liquid disinfectants or detergents.
• Products not recommended: harsh products and/or products containing acetone, chlorine and sodium hypochlorites.
Sterilization.
Only instrument handpiece: see paragraph 1.5.
WARNING!
Carefully read the operating instructions supplied with the instrument before attempting to sterilize.
WARNING!
• Never put the contra angle on the micromotor while it is running.
• The chuck release button must be held down during operation!
Friction between the button and micromotor rotor overheats the head and may cause burns.
• The patient’s internal tissues (tongue, cheeks, lips, etc...) must be protected against contact with the button by using suitable instruments
(mirror, etc...).
• The chucks and various instruments attached to the handpieces must comply to the standard ISO 10993.
EN 45
5.5.1. RESTORATIVE operating mode
RESTORATIVE operation characteristics

- speed adjustable from 100 to 40000 RPM (handpiece 1:1 ),
- Rotation speed change mode settable from variable to fixed and vice versa
- Alarm signal when the maximum torque is reached
- Fast capture of the maximum speed during motor rotation.
Menu with micromotor extracted but not active.

All the icon buttons are active and each function available can be changed
(see paragraph 5.5.).
NOTE: each setting or value changed will automatically be stored
in the operating program selected (e.g. P1).
Menu with micromotor extracted and active.

The modifiable functions are the following:
• Maximum drill rotation speed using the icon buttons or ,
• Current speed freezing using the following icon button:
Sets the current rotation speed as maximum speed
• Foot control lever change mode using the following icon buttons:ù

at the same time activating a function to change
the foot control lever ON/OFF mode
Switches the foot control lever change mode from

ON/OFF to linear
5.5.2. ENDODONTIC operating mode
ENDODONTIC operation characteristics

- Speed adjustable from 100 to 600 rpm with the value always referring to the
drill irrespective of the reduction ratio
- Torque adjustable from 0.1 to 5.0 Ncm, excluding the 1:1 reduction gear (4.5
Ncm)
- Motor rotation speed change mode settable from variable to fixed and vice
versa
- Fast capture of the maximum speed during motor rotation.
Menu with micromotor extracted but not active.

All the icon buttons are active and each function available can be changed
(see paragraph 5.5.).
As well as the standard settings, in ENDODONTIC mode you can also set
“Operation when maximum torque reached” by touching the relative icon
button:
Rotation lock
Rotation lock and subsequent inversion of the rotation direction
Rotation lock, inversion of the normal rotation direction and subse-

quent return to the normal rotation direction
NOTE: each setting or value changed will automatically be stored

in the operating program selected (e.g. P1).
46 EN
Menu with micromotor extracted and active.

The modifiable functions are the following:
• Maximum drill rotation speed using the icon buttons or ,
• Current speed freezing using the following icon button:
• Foot control lever change mode using the following icon buttons:ù

at the same time activating a function to change
the foot control lever ON/OFF mode
Switches the foot control lever change mode from

ON/OFF to linear
EN 47
5.6. Scaler
Connecting the handpiece and inserts.

Refer to the specific instructions furnished with the handpiece.
WARNING!
Before attempting to connect the handpiece, make certain the contacts are perfectly dry. Blow air from the syringe, if necessary, to dry
Use.
• Operating times: see operating instructions supplied with the handpiece.
• The cock [ f ] adjusts the cooling water flow.
NOTE: instrument activation is indicated by the relative management page appearing on the TOUCH DISPLAY.
• The icon buttons available on the TOUCH DISPLAY are the following:
Scaler power increase
Scaler power decrease
Scaler power change mode selection
Fibre optics on/off

(only with S.H.S. /S system)
Cooling water enable

(see paragraph 5.1.)
Scaler operating mode selection
WARNING!
Only for the American and Canadian markets: the instruments must
be FDA-approved.

the icon button .
• Adjust the brightness by touching the icon buttons or .
• To confirm the brightness selected, exit this submenu by touching the icon
button .
NOTE: after 30 seconds of not using the instrument (foot control lever
deactivated), the fibre optics turns off.
48 EN
Scaler power change mode selection.

With the instrument in working position, select scaler power change mode
Linear change proportional to the movement of the foot control lever


Cooling water enable.

With the instrument in working position, select whether or not water should
be delivered by the instrument by touching the following icon buttons:
Operation with water
Operation without water
NOTE: during operation without water, the maximum power delivered
is 50% of the maximum power settable.
Scaler operating mode selection.

With the instrument in working position, select scaler operating mode by
touching the following icon buttons:
Normal operating mode
ENDO operating mode
NOTE: when the foot control is activated, the operating mode
cannot be changed .
EN 49
Removable cord
The scaler has a removable cord to ease cleaning (see paragraph 5.).
Cleaning and care.

WARNING!
• Do not soak the handpiece in liquid disinfectants or detergents.
Sterilization.
• Torque wrench, scaler bits and scaler handpiece: steam autoclave at 135°C (2 bar) following the instructions for use of the device.
WARNING!
Carefully read the operating instructions supplied with the instrument before attempting to sterilize.
WARNING!
• Make sure the threaded sections of the inserts and handpiece are perfectly clean.
• Do not change the shape of the inserts.
• Check wear and tear of the inserts on a regular basis, replacing them in the following cases:
- obvious wear.
- drop in performance.
- out of shape or banged.
• Notes on U-PZ7 descalers:
- Class 1 LED apparatus;
- Do not direct the light beam in anyone's eyes When cleaning or servicing the device (it is recommended to keep the fi ber optics shut
off).
• To avoid hazards or malfunctions When connecting the board, do not reverse the positions of the cords for scalers that are different
brands.
• The inserts attached to the handpiece must comply to Biocompatibility standard ISO 10993.
50 EN
5.7. T LED curing light

(not available for the American and Canadian markets)

Technical specifications.
Supply voltage: 24-36 VDC
Max. power absorbed: 6 VA
Light source: 1 5W LED
Wavelength: 430-490 nm
Acoustic signals: at cycle start, every 5 seconds, and at cycle end
Type of operation : intermittent (3 consecutive cycles - 60 sec. rest)

Programs: 6 (preset)
General description of the light

a) Light handpiece
b) Rotary end section
c) Fiber optic
d) Eye protection
e) Power cord
f) Start button
NOTE: The curing light can be used in different configurations (wand,

gun or any intermediate position) to aid the user.
NOTE: The curing light is delivered in its original packing which
should be kept for future shipment.
Description of the control pad

[ 1 ] LED 1 ( STANDARD cycle ) :
Emission of 1000 mW/cm2 for 20 seconds (this cycle is set as default
at the time of sale).
[ 2 ] LED 2 ( FAST cycle ) :
Emission of 1600 mW/cm2 for 15 seconds.
[ 3 ] LED 3 ( STRONG cycle ) :
Emission of 1800 mW/cm2 for 20 seconds.
[ 4 ] LED S :
When LED S is on, you access ramp cycle mode and at the same time
the LEDs B, R and L next to it come on:

[ LED S + LED 1 ] ramp cycle B ( BONDING ) :

Ramp cycle with emission of 500 mW/cm2 for 5 seconds, ramp from
500 to 1000 mW/cm2 for 5 seconds and 1000 mW/cm2 for 5 seconds
for a total of 15 seconds.
[ LED S + LED 2 ] ramp cycle R ( RAPID RESTORATION ) :
for a total of 15 seconds.
[ LED S + LED 3 ] ramp cycle L ( LONG RESTORATION ) :
for a total of 20 seconds. Total Total
Cycle LED Ø8 mm
[ 5 ] Malfunction signalling LED: time energy
This red LED comes on only if there is a malfunction.
standard 1 20" 1.000 mW/cm2 20.000 mJ
[ 6 ] START button:
Pressing the START button starts the cycle selected at that moment fast 2 15" 1.600 mW/cm 2
24.000 mJ
(the cycle indication LED will come on).
If it is pressed again at any time during the cycle, light beam emission strong 3 20" 1.800 mW/cm 2
36.000 mJ
will immediately be interrupted.
[ 7 ] MODE button: bonding S+1 15" ramp cycle 11.250 mJ
This button is used to select the cycle to be run. It allows changing
rapid rest. S+2 15" ramp cycle 20.250 mJ
from the cycle you are in at that moment to the immediately following
cycle. long rest. S+3 20" ramp cycle 26.250 mJ
The first three cycles (1, 2 and 3) are at constant power and the LEDs
come on individually.
When LED S is on, you access ramp cycle mode and at the same time
the LEDs B, R and L next to it come on.
Once the LED of the cycle you intend to use has come on, the lamp
is ready for use. Pressing the START button, light beam emission is
activated according to the cycle selected .
NOTE: the cycle can be selected and the button is operative
only when the curing light is not emitting any light. If the button is
accidentally pressed while light is being emitted, nothing will happen.
Operation.
WARNING!
Before use, disinfect the lamp grip. The optical fibre and the eye pro-
tection can be sterilized in a steam autoclave at 135°C.
• Put the fiber optic ( c ) in its housing until it clicks.
• Attach the curing light handpiece to the end of its power cord and tighten
the ring ( e ).
EN 51
• Take the light out of its housing on the assistant’s board or instrument
board.
NOTE: instrument activation is indicated by the relative management
page appearing on the TOUCH DISPLAY.
• Turn the front of the light and/or fiber optic to the position most suitable
for curing (wand, gun or intermediate position).
• Use the MODE button to select the desired cycle as previously directed
(the selected cycle is always indicated by the illuminated LED).
NOTE: The curing light has a permanent memory therefore the

last cycle used will always be present the next time it is used.
• Place the fiber optic in the position required for curing.
NOTE: The fiber optic should be placed as close to the material
to be cured as possible without touching it.
• Press button START to start the cycle.
WARNING!
Operation: runs 2 consecutive cycles, rests 60 seconds.
NOTE: When a programmed cycle is activated, the LEDs (1, 2,
3, B, R, L) indicate the time that elapses (in multiples of 5 seconds) and
turn off every 5 seconds of operation.
The curing light comes with a beep that BEEPS when the cycle starts,
BEEPS every 5 seconds of operation and lastly BEEPS twice at the end
of the work cycle.
• Allow light emission to stop by itself. However, it can be stopped at any
time by simply pressing the START button again.
WARNING!
• The curing light is equipped with a system that signals malfun-
ctions by illuminating the LEDS in different combinations (see next
paragraph).
• The curing light is equipped with a cut-out.
Indicators.
The following indicators are provided on the control console to signal
curing light failure:
• LED 5 and LED 1, green, constantly on.
Lamp does not emit any light. Contact technical service department.
Instrument start up controller failure.
Contact technical service department.
Power supply too low.
Contact technical service department.
• LED 5 and LED 4 flash continuously.
Handpiece cut-out tripped. These LEDS will continue to flash until the light has cooled down enough (about 5 minutes) for it to be used again.
If the problems persists, contact the technical service department.
Maximum curable thickness.

The maximum curing thickness with single cycles is 3 millimeters (refer to the instructions of the composite material used as well).
WARNING!
This thickness must not be exceeded as the layer may not be completely cured.
52 EN
Safety guidelines.
WARNING!
• The LED is a Class 2 light source in accordance with IEC 62471. DO NOT FIX THE BEAM.
The light emitted may cause eye damage in the event of direct radiation without eye protection.
Eye protection must always be worn when using the curing lamp and do not direct the light beam in eyes.
The light emitted may damage soft tissues (oral cavity mucous, gums, skin).
Be extremely careful to direct the light precisely on the material to be cured.
• People with eye diseases, such as those who have had cataracts removed or retina diseases must be adequately protected when the
curing lamp is used, for example with s uitable protective eyewear.
• The rotary end can turn 180° counter-clockwise in relation to the handpiece to change over from wand to gun configuration.
To go back to wand configuration, turn clockwise.
A click is heard when the two positions are reached. Do not turn any more once the click is heard.
The intermediate positions can be used even if a click is not heard.
Put the fiber optic back into the correct position after turning the end section.
• Do not pull the power cord.
• Do not expose the handpiece to excessive vibrations.
• Do not drop the handpiece and in particular the fiber optic. The lamp may break if accidentally banged.
Check the condition of the handpiece if it has been banged or dropped before using the curing light. Try to turn on the light and check operation
first without using it on the patient.
If cracked, broken or if there are any other faults, do not use the curing light on the patient and contact the technical service department.
The fiber optic is rather delicate and may crack or break if banged, affecting the final amount of light emitted. If dropped, carefully inspect the fiber
optic to verify if it is cracked or broken. If cracked, a strong light appears in the spot in which the fiber is cracked. In all these cases, the fiber optic
must be replaced.
• The curing light handpiece (sold separately) can be connected only to dental units with connections for this curing lamp. Connection to
any other equipment may damage the circuits inside the lamp and seriously injure the user and patient.
• The curing lamp handpiece is not protected against liquid penetration (IP20).
• The curing lamp handpiece is not suitable for use in the presence of flammable anaesthetic gas mixed with air, oxygen or nitrous oxide (N2O).
Cleaning.
The curing lamp may be a vehicle for cross contamination between patients. The most contaminated parts are the fiber optic and eye protection.
Before sterilizing them, make sure there are no residues of curing products: if necessary, clean with alcohol or a plastic spatula.
Exclusively sterilize the optical fibre and the eye protection in an autoclave at a sterilization temperature of at least 134°C.
WARNING!
• The fiber optic is able to support 500 autoclave cycles after which it tends to become opaque and therefore emit less light.
• The eye protection must also be replaced after 500 cycles.
• Contact the manufacturer to purchase original spare parts (fiber optic + eye protection: code 97660404).
The handpiece cannot be put in autoclave; disinfect it on the outside with suitable products and cover it with disposable plastic wrap. Use soft dispo-
sable paper towels to disinfect the handpiece. Do not use harsh products or soak in liquids.
WARNING!
• The curing light handpiece is NOT suitable for autoclave.
• The curing light handpiece is not protected against penetration of liquids therefore it CANNOT be soaked in solution to be sterilized.
• The outside of the lamp should be disinfected with the fiber optic on. Do not use any type of disinfectant on the exposed optical surface
of the handpiece when the fiber is removed. The surface will become irreparably opaque if it comes into contact with disinfectant.
Maintenance.
This equipment does not require any particular type of maintenance. Only technicians authorized by the manufacturer can replace and/or repair the
handpiece and dental unit. The handpiece has been purposely constructed in a manner that requires specific tools to open it and therefore it cannot
be removed by the user. The warranty is automatically void if the handpiece is altered in any way.
Troubleshooting.
• When the lamp is removed, the light does not come on (no leds on control console illuminated).
Make sure the Midwest connection is correctly attached to the power cord.
Carefully screw the ring, try to turn on the lamp and then take it off again.
If the problem persists, contact the technical service department.
• Less light emitted
- Make certain the fiber optic is not cracked or damaged in any way: replace it if it is.
Contact the manufacturer to purchase original spare parts.
- Make sure there are no residues of curing products on the end of the fiber optic: if necessary, wipe off with alcohol or a plastic spatula.
If the handpiece has to be sent back, please disinfect it.
Ship it back in its original packing.
In addition, please enclose a description of the fault with the shipping note.
EN 53
5.8. C-U2 dental camera
The C-U2 dental camera system, complete with an extremely lightweight ergonomic handpiece, is specially designed for simple and well-conceived usability
in examining the oral cavity. Auto-exposure and fi xed focus features provide easy operation. This system is designed to allow the dentist to more effi ciently
show and explain to patients all oral conditions and reasons for planned treatment. The C-U2 system allows fi lming and taking high-defi nition (1280x720)
live images of the section in question to be taken through a touch of a fi ngertip on the touch-sensitive area of the handpiece. The live intraoral images are
displayed on the monitor or Personal Computer.
WARNING!
The camera may be used as a diagnostic tool however the results are to be compared to direct observation and/or other diagnostic means. Diagnosis
based solely on the image obtained by the camera may result in poor evaluation as the electronically processed colors and shapes, may
not correspond to those truly present.
WARNING!
• The external PC and the external monitor must be of medical grade, namely they have to be certifi ed and comply with the standard IEC 60601-1 3rd Ed.
They have to be able to ensure a double insulation level for both patient (2 MOPP) and operator (2 MOOP):
- with respect to the power mains;
- to all the I/O ports (USB, LAN) supplied with Safety Extra Low Voltage (SELV).
• Even though the electromagnetic fi eld irradiated by the device is insignifi cant, it is advisable not to use it in proximity of life support equipment (e.g. pacemakers
or heart stimulators) according to the specifi cations included in the user manual of such equipment.
• The disposable infection control sheaths must be used with the device. Change the sheath for each new patient.
• After putting on a new disposable infection control sheath, check it over before using the camera, making sure it is not torn anywhere. If it is, take it off and
put on a new one.
• Do not place the handpiece in liquids or in autoclave under any circumstances.
• Store the handpiece in a clean dry area.
• Do not bend the connecting cable excessively.
• Be extremely careful not to drop the handpiece and do not expose it to excessive vibrations.
• Never use a damaged handpiece. Make sure the camera is in good condition and has no sharp edges before attempting to use it. If in doubt, do not use
the handpiece, carefully put it away, and contact technical assistance.
• Before starting the equipment, check the condition of the lens protection.
• Do not aim the light beam at the operator’s or patient’s eyes during operation.
• During continuous use (example, more than 10 consecutive minutes), the temperature of the camera’s tip usually increases signifi cantly; if this is uncomfortable,
put the handpiece in its holder for a few minutes to allow the light source to cool down. When the camera needs to be used for a prolonged time,
reduce light brightness.
• If left running for extended periods, make sure the temperature of the tip is acceptable before attempting to use the camera. Briefl y touch the clear plastic
part with your fi ngertip being careful not to touch the lens
Connecting the handpiece.

Attach the handpiece of camera C-U2 ( a ) to the end of the cord and tighten
the ring nut ( b ).
WARNING!
Make sure the cord is firmly screwed onto the handpiece.
Camera system usage.

• Put the instrument in its work position.
At this point the camera is on and may be in LIVE mode (the monitor shows
“live” images) or FREEZE mode (the last images frozen appear on the mo-
nitor), more precisely:
1- LIVE status in multi image mode
2 - FREEZE status in multi image mode
3 - LIVE status in single image mode
4 - FREEZE status in single image mode.
NOTE: If the camera is in LIVE mode, the main screen is displayed
when the instrument is put back in place.
If the camera is in FREEZE mode, the relative menu remains on the monitor
when the instrument is put back into place.

• The main icon buttons available on the TOUCH DISPLAY are the following:
Camera LED on/off
MIRROR function activation/deactivation

Multiple image or single image operating mode

selection
OSD control panel access
Image storage page selection

(only with multiple image operation)
Frozen image display

NOTE: for an explanation of the other icon buttons viewable, refer
to the paragraphs relating to the various operating modes.
54 EN
• Briefly press the foot control to stop from 1 to 16 images divided in 4 pages
on the monitor.
NOTE: The images shown on the monitor by the camera are only
temporarily saved. To permanently save the images, connect the camera
to a PC that complies to standard IEC 60950 which has a USB 2.0 HIGH
SPEED port and image software program.
Camera LED on.

Touching the icon button you can turn the camera LED on and off.
The active mode icon is shown on the TOUCH DISPLAY:
LED off
LED on
If necessary, access brightness adjustment by touching and holding (for at

least 2 seconds) the icon button and then adjust the brightness using
the icon buttons or .
To confirm the brightness selected, exit this submenu by touching the icon
button .
MIRROR function.
By touching the icon button it is possible to move from the real image
view to the mirror one.
Real image
Mirror image
NOTE: This function can only be used in LIVE mode.
Setting operation in single image or multiple image mode.

With the camera activated and in LIVE mode, touching the icon button
you can switch between single image and multiple image mode.
Single image mode active
Multiple image mode active
NOTE: activation of multiple image mode is also indicated on the

display by a dedicated icon in the top right corner.
“FREEZE” function.
This camera allows images to be frozen on the monitor.
This function can be activated in different ways:
• With the foot control ( see paragraph 5.2.).
• By tapping the touch button [ g ] on the camera’s handpiece.
In order to go back to the “live” image, simply tap the button again or
actuate the foot control.
These images can be displayed in two different ways: single image or
multi image.
In the latter mode, the screen is divided into four parts and 4 frozen images
are displayed simultaneously.
EN 55
Operation in single image mode.

Take out the camera in LIVE mode and set to single image mode, the “live”
image appears on the monitor:
• Tap the touch button [ g ] on the camera’s handpiece (or actuate the
foot control) to freeze the image which is immediately displayed on the
monitor, deleting any previous images.
• Touching the icon button the last frozen image is displayed.
NOTE: The last image frozen remains on the monitor even if the
camera is put back in place.

Operation in multiple image mode

Extracting the camera in LIVE mode and in multiple image mode, a “moving”
image is shown on the display, and in the top right corner the icon with the
number of the active storage page appears (e.g. 1):
• Touch the icon button to move from one to the next of the 4 storage
pages available.
• Touch the icon button to view the 4 images already stored on the
storage page selected.
NOTE: the number of the page selected is shown in the centre
of the monitor.
• Image storage: pressing the touch-activated button [ g ] on the camera
handpiece (or activating the pedal control), the image is frozen and
shown directly on the monitor putting it in the first free box (e.g. A) of
the page active at that moment.
Each subsequent frozen image is put in the next box going clockwise.

NOTE: once the 4 available boxes have been filled, each subse-
quent frozen image will replace the existing ones again going clockwise.

NOTE: to store other images without deleting the previous ones,
touch the button and to move to the next active storage page.
• During display (FREEZE status):
- Touching the icon button the 4 available pages are displayed in
succession,
- Touching the icon buttons or you can select one of the 4 images
on the page displayed,
- Touching the icon button the selected image is displayed full-screen.
NOTE: touching the icon button again, you go back to display
of 4 images.
- Touching the icon button the selected image is deleted.
NOTE: Touch the icon button for 3 seconds to delete all 4 images
on the page displayed.
56 EN
Handpiece status.
An optical guide, illuminated by a multicolour LED indicator, found in the

area near the control button (h), shows handpiece status as per the table
given below:
Color Situation
Blue light fl ashes, very slowly Handpiece in standby
Handpiece activated, live images

Light blue steady light
displayed
Blue/ light blue fl ashing light Handpiece in image freeze mode
Internal error: contact Customer Ser-

Brief red fl ashes
vice
MyRay Capture
This program allows the C-U2 camera to be set up when it is connected
to a PC/WORKSTATION.
For a full description on how the MyRay iCapture program works, refer to
the instructions, in electronic format, supplied with the C-U2 handpiece.
Disposable infection control sheaths

The camera can be a vehicle of cross-contamination between patients.
For this reason always use it with a disposable infection control sheath
(code 97901590) and disinfect it on the outside after use everyday .
The sheath (with white paper backing) is enclosed in two protective layers:
a transparent one with blue tab at the front and a paper one at the back.
Follow the directions below to install a new infection control sheath:
1. Insert the camera handpiece tip between the layer with white tab and
the rear paper backing. The lens, surrounded by the LEDS, must face
downwards towards the rear paper layer. Gently push the handpiece
to the end of the sheath.
2. Pull the blue tab removing the protective covers.
3. The dental camera is now protected and ready for use.
WARNING!
• Always make certain the handpiece is correctly inserted inside the
infection control sheath.
• To assure hygienic conditions for the users and patients, the disposable
infection control sheaths must be changed after each use.
• Disposal: the disposable infection control sheaths are to be treated
as special waste materials (like surgical gloves).
Cleaning and disinfecting

Clean the handpiece with a suitable product after each use: refer to Pa-
ragraph 1.4.
WARNING!
• The intraoral camera is not designed for cold disinfection by being soaked, for example in solutions such as glutharaldeide or hydrogen
peroxide.
• All products must be used as directed by the manufacturer.
• All material used to clean and disinfect must be thrown away.
Maintenance and repairs

The C-U2 camera system does not require any particular maintenance.
In the event of malfunctions, please send back the complete handpiece.
WARNING!
There are no parts that can be repaired on site. In the event of a malfunction, please contact an authorized dealer.
Returning parts.
• Please send back any defective devices in their original packaging. Do not reuse damaged boxes.
• The device must be disinfected before being shipped to prevent cross-contamination. Handpieces that have not been adequately cleaned and
disinfected will not be accepted
WARNING!
The sender shall be held responsible for any equipment damaged incurred during shipment regardless of whether or not the devices are
under warranty.
EN 57
5.9. ZEN-Xi integrated sensor
Integrated sensor ZEN-Xi is a medical device employed to acquire intraoral

x-rays in an electronic format with a Personal Computer interface device.
When used together with dental practice management software, the x-ray
pictures can be saved in the patient's folder and viewed on the desktop pc
monitor at a later time.
WARNING!
Do not use the system for any other purpose different from acquisition
of intraoral x-rays and do not use it if you are not a professional in
the dental and radiology fields.
Use.
Use and care instructions for integrated sensor ZEN-Xi are enclosed with
the apparatus.
NOTE: Integrated sensor ZEN-Xi does not interact with the dental unit
from an electric point of view.
58 EN
6. Assistant’s board operation

Main features:
• Two articulated arms secure the board (a) to the hydrogroup (b) allowing
it to be placed in the most convenient work position.
The fixed arm (c) can turn 120° around the bowl.
The pantograph arm (e) allows the assistant’s board to be moved 335
mm vertically through 6 work positions.
NOTE: to completely lower the assistant’s board, simply move it all
the way up and then lower it.
• The assistant’s board (a) comes with a control console (d) with buttons
used to operate the dental chair and hydrogroup.
• The assistant’s module may be equipped with 2 suction cannulae and
2 instruments.
• The assistant’s board comes with sliding rollers (f) that guide and hold
up the suction tubes.
NOTE: the assistant’s board is equipped with a safety device that
locks out dental chair movement when the board’s arms are obstructed.

Cleaning the sliding rollers.
Push down and take off the sliding rollers ( f ).
Clean the sliding rollers using a suitable product: refer to Paragraph 1.4.
6.1. Assistant’s touchpad
Operatory light on/off button.
Water to cup button.
Water to bowl button.
Automatic return position recall button.
Rinse position button.
Chair seat up.
Chair back up.
Chair seat down.
Chair back down.
EN 59
6.2. Syringe on assistant’s board
For detailed information regarding operation of this instrument see para-

graph 5.3.
6.3. Curing lamp on assistant’s board

graph 5.7.
6.4. Intraoral camera on assistant’s board

graph 5.8.
60 EN
6.5. Suction tubes
Suction starts by taking the tube off the board. To adjust suction, use the
slider ( a ) located on the tube handpiece.
NOTE: When the tube is put back in place, suction stops approxi-
mately 2 seconds later.
This is done to dry the suction tubes.
Cleaning the suction tubes.

As the dental units may be equipped with different suction systems (liquid
ring or wet, air) carefully follow the instructions provided by the suction
system manufacturer when disinfecting the system regarding the product
to be used, times and directions for use.
WARNING!
For cleaning of the suction system, it is recommended to use STER
3 PLUS (CEFLA s.c.) diluted in a 6% solution (equivalent to 60 ml of
product in 1 litre of water).
Removing the suction tubes.

WARNING!
Always wear gloves to prevent contact with infected material when
removing the suction tubes.
Remove the suction tubes from the conveyor fittings by turning and twisting
the tube fitting.
Detach the suction tubes from the holders by turning and twisting the tube
fitting.
WARNING!
Never directly grasp the suction tube.
Sterilization.
• Cannula holder terminals: can be sterilized in a steam autoclave (see
paragraph 1.5.).
• Suction tubes: soak to cold sterilize.
WARNING!
Never use procedures in which the temperature goes over 55 °C with
the tubes.
Maintenance.
Periodically lubricate the O-rings of the cannula holder terminals (see
Paragraph 9.4.) using S1-Protective Lubricant for O-Rings (CEFLA s.c.).
Note about biocompatibility.

Only suction tubes supplied with the dental unit and there after original
replacement tubes can be used.
The suction tubes must comply to the standard EN 10993-1 Biological
evaluation of medical devices.
ISOLITE suction tube.

For ISOLITE suction tube operation, please refer to the specific use in-
structions given by the manufacturer.
EN 61
6.6. Hydraulic saliva ejector
The hydraulic saliva ejector starts running when the tube is removed from
the support.
Cleaning after each use.

Aspirate about ½ litre of STER 3 PLUS (CEFLA s.c.) diluted in a 6% solution
(equivalent to 60 ml of product in 1 litre of water).
Cleaning the saliva ejector filter

This operation must be carried out at the end of each work day.
WARNING!
Put on gloves before attempting to perform this operation!
• Aspirate about ½ litre of STER 3 PLUS diluted in a 6% solution (equivalent
to 60 ml of product in 1 litre of water).
• In order to prevent possible dripping of liquids and secretions from the
filter ( b ) to be extracted, aspirate only air for about 5 seconds.
• Take off the cap ( a ) by turning and twisting at the same time.
• Remove the filter ( b ).
• Clean/replace the filter (code 97290060).
• Put the filter and cap back in place.
Routine maintenance
Lubricate the o-rings ( c ) with S1 – Protection for o-rings lubricant.
62 EN
7. Hydrogroup operation
7.1. Fill cup and bowl
The bowl can freely move 305° on the hydrogroup. The bowl may be po-
wered (optional) or can be turned by hand.
The bowl and water to cup spout can be removed to ease cleaning.
Control buttons.
Water to cup button.
Bowl flush button.
Cup sensor.
You can have an optical sensor fitted at the base of the cup fountain, which
detects the cup and automatically activates filling.
The sensor operates as follows:
• 2 seconds after positioning the cup under the fountain, it is filled with
water for 2 seconds (this time is not modifiable)
• Once the cup has been removed, the filling cycle can be repeated only
after 3 seconds
• During the filling cycle, removing the cup and/or pressing the “CUP
WATER DELIVERY” button, the water delivery cycle will immediately be
interrupted.
NOTE: to disable the cup sensor see paragraph 5.1.1.2.2.2.
Adjusting the amount of water used to fill the cup.

See paragraph 5.1.1.2.2.2.
Adjusting the temperature of the water sent to the cup.

See paragraph 5.1.1.2.2.2.
Setting bowl flushing.

Water can be delivered to the bowl either in manual (with the ON/OFF
button) or timed.
See paragraph 5.1.1.2.2.1. to set the desired mode of operation and water
delivery time.
Setting automatic bowl flushing.

The bowl is automatically flushed in the following cases:
• when button “Water to cup” is pressed,
• when button “Dental chair automatic return” is pressed,
• when button ‘Rinse position” is pressed.
To change operation see paragraph 5.1.1.2.2.1.
Powered bowl movement.
Bowl counter-clockwise button.
Bowl clockwise button.
NOTE: the bowl can also be moved directly by hand.
Automatic bowl motion (only with powered bowl).

The bowl moves automatically in the following cases:
• press button “Dental chair rinse position”,
NOTE: in this case, the position of the bowl can also be set (see
paragraph 5.1.2.).
• by pressing button “Dental chair reset position”.
See paragraph 5.1.1.2.2.3.for information on how to modify operation.
EN 63
Taking off the bowl filter and rinse spout.

• Pull up the spout ( l ) and take it off.
• Pull up the filter ( q ) and its cover ( p ) to remove them.

• Turn the bowl ( m ) counter-clockwise to release it and then pull it up to
take it out.
Disinfecting and cleaning.
WARNING!
cleaning the bowl and bowl filter.
The parts are to be cleaned daily at the end of each work day.
• Spouts and bowl: thoroughly wash with a specially formulated cleaner
(for example MD 550 Orotol DÜRR).
• Bowl filter: clean with running water and commercially-available cleaning
products.

WARNING!
Do not use acids or harsh products.
64 EN
7.2 S.H.S./S system ( Semplified Hygienization Sistem )
Models R7 CONTINENTAL, R7 INTERNATIONAL and R7 CART.
Description of the system

The system S.H.S. /S is equipped with a distilled water tank ( a ).
The tank can hold 1.8 liters.
Distilled water is delivered to:
• the sprays of all the instruments found on the instrument and assistant’s
board.
• the syringe on the assistant’s board.
• to fill the cup
• water quick-connect coupler (if present)
The icon button on the TOUCH DISPLAY (see paragraph 5.1.1.2.8.)

allows activating/deactivating the SHS/S system.

NOTE: the distilled water delivery status is shown by the icon ( A )
on the control panel display.
Tank reserve level.

When the liquid in the tank falls below the reserve level, the relative icon
( B ) appears on the instrument board’s console.
Filling the tank.

When the water level in the tank is low (about 500 cc), fill it as directed below:
• Deactivate the S.H.S. /S system by tapping the icon button .
Check that the icon ( B ) on the console display disappears.
NOTE: during this operation, the pressurized air contained
in the tank will automatically be discharged to the outside.
• Turn the tank counter-clockwise ( a ) and remove it.
• Pour distilled water into the tank until the maximum level is reached.
WARNING!
Use only distilled water. For a higher guarantee of hygiene you can
add 600 parts per million (ppm) of hydrogen peroxide using 20 ml of
Peroxy Ag+ (not available for the American and Canadian markets) per
litre of distilled water, or oxygenated water (20 ml of 3% oxygenated
water per litre of distilled water).
• Put the tank back in place turning it clockwise.
WARNING!
Make sure that the tank is properly tightened.
• Touch the icon button to re-enable the S.H.S. /S system and
confirm that filling is complete.
Check that the icon ( A ) appears on the console display.
WARNING!
If you are going to be absent from the surgery for long periods of time
(holidays), completely empty out the tank ( a ) before leaving.
Cleaning the tank.

We suggest cold-sterilizing periodically (at least once a month) only the tank
with peracetic acid-based products (for American and Canadian markets
we recommend using an EPA-approved product) in the following manner:
• take the tank out of the dental unit and empty it;
• prepare the solution of peracetic acid based product following the instruc-
tions provided by the manufacturer;
• fill the tank up to the rim with the peracetic acid based product;
• let the peracetic acid solution soak in the tank for the time stated by the
manufacturer;
• empty the peracetic acid solution from the tank;
• rinse the tank with distilled water;
• fill the tank with distilled water and, if necessary, add hydrogen peroxide
or oxygenated water as described above;
• put the tank back in place in the dental unit.
EN 65
7.3. Manual SHS system
Models R7 IDRICO SINGOLO, R7 M CONTINENTAL, R7 M INTERNATIO-

NAL, R7 M CART and R7 P.
Description of the system

The system comes with a canister (a), placed on the instrument board support
arm, that contains distilled water.
The tank can hold 1.8 liters.
The tank feeds:
• the sprays of all the instruments found on the instrument and assistant’s
board.

• The syringe on the assistant’s board.
• to fill the cup
• water quick-connect coupler (if present)
A by-pass lever (b), placed on the side of the canister, is used to shut off the
system if municipal water is to be supplied to the instruments.
WARNING!
With the manual SHS system, the tank reserve ( a ) and SHS system
active/inactive warning icons are not shown on the TOUCH DISPLAY.
This system allows running a disinfection cycle for the instrument spray ducts
(see paragraph 7.3.1.).
WARNING!
Perform a disinfecting cycle at the end of each work day.
Filling the tank.

When the water level in the tank is low (about 500 cc), fill it as directed below:
• Turn the switch ( c ) to "CLOSE AIR PRESSURE”.
• Turn the tank counter-clockwise and remove the tank ( a ).

NOTE: while this operation is being performed, the pressurised

air in the tank is automatically released outside.

• Pour distilled water into the tank until the maximum level is reached.
WARNING!
Use only distilled water. For a higher guarantee of hygiene you can
add 600 parts per million (ppm) of hydrogen peroxide using 20 ml of
Peroxy Ag+ (not available for the American and Canadian markets) per
litre of distilled water, or oxygenated water (20 ml of 3% oxygenated
water per litre of distilled water).
• Put the tank back in place turning it clockwise.
• Turn the toggle ( c ) to position "OPEN AIR PRESSURE”.
WARNING!
• Assure the tank is firmly secured in place before switching the toggle
(c) to position "OPEN AIR PRESSURE”.
• When you are going to be away from the office for an extended
period of time (holiday), always empty the hydrogen peroxide tank
( a ) before leaving.
BY-PASS function
The system can be shut off if municipal water is to be delivered to the
instruments.
This function is obtained by turning switch (b), beside the canister, to position
“LINE”.
Turn the toggle ( b ) to position "TANK” to go back to working with distilled
water.
Cleaning the tank.

We suggest cold-sterilizing periodically (at least once a month) only the tank
with peracetic acid-based products (for American and Canadian markets
we recommend using an EPA-approved product) in the following manner:
• take the tank out of the dental unit and empty it,
• fill the tank with disinfectant liquid up to the rim,
• leave the disinfectant liquid to dwell in the tank for at least 10 minutes,
• completely empty out the tank,
• rinse the tank with distilled water,
• fill the tank with distilled water and, if necessary, add hydrogen peroxide
or oxygenated water as described above,
• put the tank back in place in the dental unit.
66 EN
7.3.1. Disinfection cycle with oxygenated water
With the S.H.S. system, you can execute a manual disinfection cycle of
the water ducts of all the instruments on the dentist’s instrument board
and the syringe on the assistant’s board using oxygenated water (hydro-
gen peroxide).
To disinfect, proceed as directed below:
A) Prepare the disinfectant:

• Pour undiluted PEROXY Ag+ (not available for the American and
Canadian markets) (or 3% oxygenated water) into the tank marked
with an orange band.
NOTE: make sure that the tank is completely filled.
B) Putting in the disinfectant:

• Check that the spray tap of each dynamic instrument is completely

open (if not, no or too little water will come out).
• Make sure the spray cocks ( c ) found towards the bottom of the

board, are open (if they are not, either very little or no water at all
will flow out).
• Take out the bottle of distilled water ( a ) turning it clockwise.
• Replace the bottle of distilled water ( a ) with the one containing

disinfectant.
• Remove the syringe and empty the duct with the water button.
NOTE: when emptying is complete, no water will come out
of the duct.
• Repeat the same procedure for the syringe on the assistant’s board
(with the water key). Use the Water clean system with the foot control
for the remaining dynamic instruments (see paragraph 5.2).
• Remove the instruments and fill the ducts with the hydrogen peroxide
solution. Use the Water clean system with the foot control for the
dynamic instruments and the water button for the syringes.
NOTE: let the disinfectant flow from the instruments for about
6-7 seconds.
• Put the instruments back in place.
NOTE: at this point, the ducts contain the disinfectant.

C) Putting in disinfectant
WARNING!
The disinfectant must be left to dwell in the ducts for at least 10
minutes, but not more than 30 minutes.
D) Rinsing the ducts:

• Turn the toggle ( c ) to position "CLOSE AIR PRESSURE”.
• Unscrew the bottle ( a ) containing the disinfectant turning it clockwise.
• Put in the bottle containing distilled water.
• Remove the syringe and empty the water duct.
NOTE: when emptying is complete, no water will come out of the duct.
• Repeat the same procedure to drain the hydrogen peroxide from the ducts for the various instruments.
• Remove the instruments and wait for distilled water to flow out. Use the Water clean system (see paragraph 5.2) with the foot control for the
dynamic instruments and the water button for the syringes.
NOTE: allow water to flow out approximately 6-7 seconds.

• At this point, the ducts contain distilled water again and the dental unit is ready to be used.
WARNING!
• After disinfection, make sure that you close the tank containing the disinfectant (exposed to air, it loses its effectiveness).
• It is good practice to perform a disinfection cycle at least once a day, preferably at the end of the day.
PEROXY Ag+ storage.

For proper storage of PEROXY Ag+ follow the manufacturer’s instructions printed on the package.
It is important to keep the package tightly closed and store it in a cool place at a temperature not exceeding 25°C.
WARNING!
Never leave PEROXY Ag+ or oxygenated water in the tank marked with an orange band for more than one month.
In case of long absences from the studio (holidays), completely empty out the tank marked with an orange band before leaving.
EN 67
7.4. BIOSTER/S automatic disinfection system
Models R7 CONTINENTAL, R7 INTERNATIONAL and R7 CART.
Description of the system.

The BIOSTER S system allows running a disinfection cycle of the water
ducts of all the instruments on the dentist’s instrument board, of a dynamic
instrument on the assistant's board and of the cup water delivery ducts.
To run the disinfection cycle, operate as follows:

A) Preparing the disinfectant solution:
• Pour undiluted PEROXY Ag+ (not available for the American and Ca-
nadian markets) (or 3% oxygenated water) into the tank marked with
an orange band.
NOTE: Make sure that the tank is completely filled.

B) Setting the BIOSTER S cycle:
• Replace the tank ( a ) with the tank containing the disinfectant and
activate the S.H.S./S system ( see paragraph 7.2. ).
NOTE: the BIOSTER/ S cycle can only be activated if the
SHS/S system is enabled (icon A on).
• Using the TOUCH DISPLAY, access the “BIOSTER disinfection cycle
setting” menu (see paragraph 5.1.1.2.1.1.).
• Place the container ( d ) of the instruments to be disinfected over the
bowl.
• Put the cords of the instruments to be disinfected in the container.
WARNING!
Use the adapter ( f ) provided for the syringe. The heater should be
turned off.
The syringe on the assistant's board cannot be disinfected using the
BIOSTER S cycle.
The micromotor cord must be completed with motor body.
Turbine and scaler cords must be inserted without the handpiece.
• If the water to cup ducts need to be disinfected, place the container
( e ) provided under the cup spout.
• Make sure the spray cocks ( g ) found under the instrument board are
open.
C) Executing the BIOSTER S cycle:
• Start the flushing cycle by touching the icon button on the TOUCH
DISPLAY
• The first automatic phase consists of filling the water ducts with disin-
fectant.
NOTE: in the first 5 seconds the disinfectant is also delivered
by the cup water fountain.
• The time remaining to the end of the filling phase (duration: 30 seconds)
• At the end of the water duct filling phase, 1 beep is emitted and a timer
appears on the TOUCH DISPLAY, which indicates the disinfectant
contact time.
D) Disinfectant contact time:

• The contact time is fixed and cannot be modified: 600 seconds.
• At the end of the disinfectant contact phase, an acoustic signal is emitted
for 1 minute (1 beep every second).
E) Duct rinsing phase

• If you want to rinse the ducts with distilled water, replace the tank (
a ) containing the disinfectant liquid with the original tank containing
distilled water and activate the SHS/S system by tapping the icon
button .
• Start the duct rinsing phase by tapping the icon button on the
TOUCH DISPLAY.
• The time remaining to the end of the rinsing phase (duration: 120 seconds)
NOTE: in the first 20 seconds the liquid is also delivered by
the cup water fountain.
• At the end of the rinsing phase (the TOUCH DISPLAY shows the
message “End of cycle: replace instrument”) it is sufficient to replace
the extracted instruments to go back to the working condition.
68 EN
Interrupting the disinfection cycle.

The syringe on the assistant's board cannot be disinfected using the BIOSTER S cycle. .
NOTE: once the cycle has been activated, it CANNOT be interrupted.
PEROXY Ag+ storage.

For proper storage of PEROXY Ag+ follow the manufacturer’s instructions printed on the package.
It is important to keep the package tightly closed and store it in a cool place at a temperature not exceeding 25°C.
WARNING!
Never leave PEROXY Ag+ or oxygenated water in the tank ( a ) for longer than one month.
If you are going to be absent from the surgery for long periods of time (holidays), completely empty out the tank ( a ) before leaving.
NOTE: to empty the tank, it is advisable to use a suction cannula.
Error messages shown on the console display.

If the system detects a malfunction, a fault message appears on the display screen (see paragraph 10.).
WARNING!
If the disinfecting cycle is incorrectly interrupted, the equipment will shutdown until either the disinfecting cycle is performed again or
the washing cycle is carried out.
EN 69
7.5. Automatic instrument FLUSHING CYCLE (FLUSHING)

The automatic FLUSHING cycle allows to carry out an automatic flushing
cycle to renew water present in the water ducts of the instruments on the
dentist’s and the assistant’s boards and the water-to-cup duct.
Flushing may be carried out with mains water, treated water or distilled water
(if the S.H.S. system is present).
The cycle duration can be set up from 1 to 5 minutes.
WARNING!
It is advisable to carry out a FLUSHING cycle at the beginning of each
working day and between two patients.
Setting the FLUSHING cycle.

• If the S.H.S./S system is present and you want to execute the flushing cycle
with distilled water, check that the relative icon ( A ) on the console display
is on ( see paragraph 7.2. ).
If the manual SHS system is present and you want to run the flushing cycle
with distilled water, check that the bypass lever is in TANK position (see
paragraph 7.3.).
NOTE: it is advisable to execute the flushing cycle with a full tank

of distilled water.
• By using the TOUCH DISPLAY, enter the “FLUSHING cycle setting” menu
and set the cycle duration (see paragraph 5.1.1.2.1.2.).
• Position the container ( d ) for the instruments to be disinfected on the bowl.
• Insert the tubings of the instruments to be disinfected in the container.
WARNING!
Use the adapter [ f ] provided for the syringe. The heater should be
turned off.
The micromotor should be put in without the handpiece.
Turbine and scaler cords must be inserted without the handpiece.
• Make sure that the spray taps ( g ) in the lower part of the dentist’s instru-
ment board are open.
• Insert the special supplied container ( e ) under the cup spout.
FLUSHING cycle setting.

• Start the flushing cycle by touching the icon button on the TOUCH
DISPLAY (see paragraph 5.1.1.2.1.2.).
• At the end of the flushing cycle (the display shows the message “End of
cycle: put back instruments”), put the instruments extracted back into place
to return to the working condition.
Interruption of the FLUSHING cycle.

You can interrupt the flushing cycle at any time by touching the icon
button and return to the initial cycle setting menu.
Error messages shown on the console display.

If the system detects a malfunction, a fault message appears on the display
screen (see paragraph 10.).
70 EN
7.6. ACVS system (Automatic Cleaning Vacuum System)

This system allows cleaning the surgical suction system.
The system comes with a tank ( c ) that contains the liquid disinfectant and
two fittings ( d ) used to wash the suction tubes.
The detergent liquid tank has a total capacity of 250 cc.
The washing cycle is automatically carried out and should usually be
performed at the end of each surgical procedure and whenever the dental
unit is cleaned and disinfected.
WARNING!
It is recommended to use STER 3 PLUS (CEFLA s.c.) as detergent liquid,
diluted in a 6% solution (equivalent to 60 ml of product in 1 litre of water).
How to start the washing cycle.
To start the washing cycle, follow the directions given below:
• Check that the tank ( c ) contains the detergent liquid.
• Remove both suction tube terminals from the assistant’s board, making
sure the suction motor starts running.
• Open the mechanical closing of the suction tube terminals.
• Insert the terminals in the fittings ( d ) found under the manifold.
The vacuum created by the Venutri meters triggers the washing cycle.
• Washing cycle stages:
- deliver municipal water for 50 sec. using intermittent operation (2 sec.
ON - 1 sec. OFF):
- stop the water flow and let in 10 cc of liquid disinfectant;
- stop letting in liquid disinfectant and continue sucking for 10 sec.
• The washing cycle ends when the suction flow is interrupted and the
motor stops running.
“Put the suction tubes back in place” appears on the display.
• At this point, put the ends of the suction tubes in the supports on the
assistant’s board to go back to the work conditions.
Filling the tank.
If the detergent liquid in the tank ( c ) is below the minimum level, act as
follows:
• Position the dental chair at maximum height.
• Remove the tank by turning it anticlockwise.
• Pour the detergent liquid into the tank until it is full.
• Refit the tank by turning it clockwise.
Stopping the washing cycle.

If the system detects a malfunction, a fault message appears on the display
screen (see paragraph 10.).
NOTE: Once the problem has been solved, the washing cycle
automatically restarts.
Warnings for use.
WARNING: FOOT CRUSHING HAZARD

Pay attention to the patient and the staff during dental chair descent.
EN 71
7.7. Opening/closing the side hydrogroup cover
Opening the cover.

• Open the cover on the side of the hydrogroup (a) after pushing up and releasing the lock lever (b).
Closing the cover.

• Put on the cover making sure the two locks are inserted in the notches in the hydrogroup.
• Lastly, bring the bottom of the cover near the hydrogroup frame to engage the lock lever again.
72 EN
8. Accessories
8.1. Operating lamp
The operating lamp comes in 3 models:
1 Lamp with halogen light source – model VENUS.
Lamp with halogen light source – model VENUS PLUS.
Lamp with LED light source – model VENUS PLUS-L.
The instructions for use and maintenance of the lamps are available in

PDF format and can be downloaded from the download area of the website
www.anthos.com.
NOTE: During the automatic movements of the dental chair, the

lamp automatically turns off to prevent blinding the patient.
8.2. Monitor on lamp pole
The instructions for use and maintenance of the monitor are provided with
the device.
8.3. Negatoscope for panoramas
An x-ray film viewer for panoramic x-rays can be mounted on all INTER-
NATIONAL version instrument boards.
The screen dimensions are as follows: H=210mm, L=300mm.
Per accendere il negatoscopio è sufficiente agire sull'apposito interruttore ( a ):
= negatoscope on
= negatoscope off
8.4. Air/water/230V quick-connect couplers
The air/water/230V quick-connect couplers are placed to the side of the

electrical box.
WARNING!
Shut off the equipment before attempting to connect or disconnect
the air/water outlets.
Technical specifications.
• Power outlet: 230VAC 2A in accordance with IEC/EN 60320-2-2/F (only
on dental units with 230 VAC power supply).
• Air quick-connect coupler pressure: 6 Bar.
• Water quick-connect coupler pressure:
- municipal water, 2.5 Bar
- with S.H.S. system, 1,8 Bar
• Water quick-connect coupler delivery rate:
- municipal water, 1800 ml/min
- with S.H.S. system, 950 ml/min
NOTE: with S.H.S. system: to use the quick-coupling with mains
water, disable the distilled water tank (see Paragraph 7.2 - 7.3).
EN 73
8.5. Auxiliary tray holder
Models R7 CART, R7 M CART, and R7 P.
The instrument tray holder can hold two standard size trays.
Turn the knob ( b ) to adjust vertical movement according to the weight.
• turn clockwise to increase resistance (heavy loads).
• turn counter-clockwise to decrease resistance (light loads).
WARNING!
Maximum allowable load on tray 3.5 Kg (no x-ray film viewer) or 2.5
Kg (with x-ray film viewer)
74 EN
9. Maintenance
Preventive maintenance
CEFLA s.c., the manufacturer of the dental units, in accordance with applicable standards IEC 60601-1 3.a Ed. - 2007, IEC 62353 and directive MDD
93/42, and subsequent changes, for medial devices underlines that the preventive maintenance checks for the dental unit specified in the Technical
care manual and Maintenance and warranty handbook are to be carried out by authorised personnel at least once every 12 months.
ATTENZIONE!
The warranty is void if the equipment is serviced, repaired, altered or modified in any way by personnel who have not been duly authorized
by CEFLA s.c..
Safety checks.
In accordance with standard IEC 62353, the safety checks specified in the Technical care manual and Maintenance and warranty handbook supplied
with the dental unit are to be carried out at the intervals required by current local regulations. If no precise indications are given, CEFLA s.c., the
manufacturer of the dental units, recommends checking them at least every 24 months at the time of installation and whenever electrical parts that
are live are repaired/updated.
WARNING!
The manufacturer shall not be held liable for any personal injury or equipment damage if the precautions given above are not observed.
9.1. Instrument maintenance
Maintenance instructions for the instruments are enclosed with each

instrument.
WARNING!
Maintenance of the instruments should be carried out with the
equipment shut off.

9.2. Draining condensate
This operation should be done daily before starting work.

Proceed as follows:
• put a container under the cock ( a ) found below the hydrogroup,
• loosen the cock’s knob,
• after the tank has been emptied, fully close the cock.
9.3. Cleaning the surgical suction filter

This operation should be done daily at the end of work.
WARNING!
cleaning the suction filters.
Proceed as follows:
• Take out the filter ( d ).
• Clean/replace the filter (code 97461845).
• Put the filter back in place being careful to removing any amalgam still
present at the filter housing’s entrance.
NOTE: To prevent liquids and matter from dripping from the filter
taken out, perform the operations given above with the suction tube running.

EN 75
9.4. Surgical suction
The surgical suction system must be sanitized using a product suitable for
this purpose.
WARNING!
For cleaning of the suction system, it is recommended to use STER
3 PLUS (CEFLA s.c.) diluted in a 6% solution (equivalent to 60 ml of
product in 1 litre of water).
At the end of each surgical procedure.

• Execute an automatic flushing cycle or aspirate about ½ litre of sanitizing
solution with each of the cannulas used.
• Sterilize the cannula holder terminals in steam autoclave (see paragraph
1.5.).
At the end of each work day.

• Draw in 1 liter of water with each suction tube, alternating water and air
(keep the suction tube alternately in and out of the water).
• After rinsing with water, execute an automatic flushing cycle or aspirate
about ½ litre of sanitizing solution with each of the cannulas used.
WARNING!
Whatever sanitizing product you use, follow the instructions given
by the manufacturer.

NOTE: After these operations, it is advisable to aspirate only air in
order to dry the entire suction system (5 minutes).
Once a week.
Remove the cannula body from its cord attachment and lubricate the O-rings
( o ) using S1-Protective Lubricant for O-Rings (CEFLA s.c.).
Once a year.
Replace the suction tubes and ends of the tube holder.
76 EN
9.5. CATTANI surgical separator
At the beginning of each work day.

Insert inside filter ( d ) a tablet ( v ) of VF CONTROL PLUS (CEFLA s.c.)

WARNING!
carrying out this operation.
At the end of each surgical procedure.

• Execute an automatic flushing cycle or aspirate about ½ litre of sanitizing
solution with each of the cannulas used.
• Sterilize the cannula holder terminals in steam autoclave (see paragraph
1.5.).
At the end of each work day.

• Draw in 1 liter of water with each suction tube, alternating water and air
(keep the suction tube alternately in and out of the water).
• After rinsing with water, execute an automatic flushing cycle or aspirate
about ½ litre of sanitizing solution with each of the cannulas used.
NOTE: After these operations, it is advisable to aspirate only air in
order to dry the entire suction system (5 minutes).
Every 15 days.
• Clean the separator container and probes with a soft sponge and neutral
detergent.
• Clean the drain valve for the separator’s container with the device provided
for this purpose.
Once a year.
• By technician: check the siphons and drains, check all the internal tubes and
plastic and rubber parts subject to wear.
Before leaving the surgery empty for a few days.

• Start the aspirator and run it 20 - 30 minutes without sucking in liquids.
The aspirator will dry itself completely. As a result, salt caused by moisture
and basic substances will not form, salt that may cause fan seizure and motor
blockage.

How to remove the separator’s container.
WARNING!
Gloves must be worn when carrying out the following operation to prevent
contact with infected material.
• Move the dental chair fully up.
• Open the side hydrogroup cover (see paragraph 7.7.).

• Turn the electrical box.
• Completely empty the separator bowl, pressing the timed button ( c ) located
on the cover.
• If present, remove the valve ( s ) for central systems.
• Turn and raise the container ( d ) until it is detached from the drain pump ( k ).
• Detach the bowl ( d ) from the cover ( f ) pulling up the two side rubber bands
( e ).
• After the cleaning operations, refit the vessel ( d ) after lubricating the
O-rings with S1-Protective Lubricant for O-Rings (CEFLA s.c.) O-ring
before hand with silicon spray.
• Lastly, close the side hydrogroup cover.
Drain pump locked warning.

A dedicated icon ( A ) on the TOUCH DISPLAY will indicate if the drain
pump below the separator vessel locks.
At this point, shut off the equipment and empty the separator bowl by hand.
If the icon appears again, call technical service.
EN 77
9.6 Cleaning the turbine return air filter
Monthly check the oil container filter ( g ) present in the turbine’s return
air line.
If necessary, replace the filter element (code 97290014).
9.7. METASYS amalgam separator

The maintenance instructions for the METASYS amalgam separator are en-
closed with the equipment if the equipment comes with this type of separator.
The separator’s control device is located in the hydrogroup.
WARNING!
Always wear gloves to prevent contact with infected material when cleaning the separator.
WARNING!
When disposing one-time use containers full of amalgam, observe current local and national laws.
9.8. DÜRR amalgam separator
The maintenance instructions for the DÜRR amalgam separator are enclosed with the equipment if the equipment comes with this type of separator.
The separator’s control device is located in the hydrogroup.
WARNING!
Always wear gloves to prevent contact with infected material when cleaning the separator.
WARNING!
When disposing one-time use containers full of amalgam, observe current local and national laws.
9.9. Dental chair
The dental chair does not require any particular maintenance.

It is nevertheless advisable to once a year have an authorised ANTHOS technician check overall functioning.
78 EN
10. Fault messages
M = Message shown on console display

C = Cause
R = Remedy
M: “H2O level low, fill tank” M: “Lower dental chair”

C: The water in the independent water system's tank has dropped below C: The bowl does not move because the dental chair is in its way.
the minimum acceptable level. R: Lower the dental chair so that it is no longer in the way.
R: Fill the tank (see paragraph 7.2.).
M: “Check operating light fuses”
M: “Put instruments back in place” C: The operating light does not turn on because electric power is not
C: The system detected an instrument was already withdrawn while the supplied.
disinfecting cycle was being set. R: Call technical support.
R: Make sure all the instruments are in place and then set the cycle again.
If the fault message appears again, call technical support. M: “Maintenance required"
C: Scheduled maintenance required.
M: “Check instruments, repeat cycle” R: Call technical support to schedule the maintenance work.
C: The system detected the withdrawn instruments were altered during
the flushing or disinfecting cycle. M: “Footboard emergency device activated”
R: Check the selected instruments and repeat the disinfecting (see C: The dental chair encountered an obstacle.
paragraph 7.4.) or flushing (see paragraph 7.5.) cycle. R: Press the "seat up" button and clear the obstacle.
M: “H2O2 level low, fill tank” M: “Backrest emergency device activated”

C: The hydrogen peroxide in the relative tank has dropped below the C: The dental chair backrest encountered an obstacle.
minimum acceptable level. R: Press the "seat up" button and clear the obstacle.
R: Fill the hydrogen peroxide tank (see paragraph 7.4.).
M: “Move bowl”
M: “Open H2O spray cocks” C: The dental chair does not move because the bowl is in the way.
C: The system is not able to fill the lines with hydrogen peroxide during R: Move the bowl so that it is no longer in the way of the dental chair.
the disinfecting cycle.
R: Open the water spray cocks and repeat the disinfecting cycle (see M: “Seat emergency device activated”
paragraph 7.4.). If the message appears again, call technical support. C: The dental chair encountered an obstacle.
R: Press the "seat up" button and clear the obstacle.
M: “Remove all instruments”
C: The system detected an internal malfunction during the disinfecting M: “Delivery emergency device activated”
cycle. C: The side delivery board encountered an obstacle.
R: Repeat the disinfecting cycle, selecting all the instruments. If the R: Press the dental chair "seat up" button and clear the obstacle.
message appears again, call technical support.
M: “Dental chair blocked, put instrument back in place”
M: “Empty WHE system” C: An attempt was made to move the dental chair with an instrument
C: WHE system malfunction. withdrawn.
R: Empty the tank inside the WHE system and restart the system (see R: Put instrument back in place and repeat dental chair movement.
paragraph 5.1.1.2.1.3.). If the message appears again, call technical
support. M: “Dental chair blocked”
C: An attempt was made to move the dental chair while it was blocked
M: “Turn on WHE” R: Remove dental chair blockage (see paragraph 4.).
C: The system is attempting to perform a task which requires that the
WHE system is turned on.
R: Turn on the WHE system (see paragraph 7.3.). IMPORTANT INFORMATION!
M: “XXXX, call technical support” (where XXXX represents a nume-
M: “Check suction tubes, repeat cycle” rical code)
C: The system has detected that the suction tubes are not connected to C: This type of message indicated a serious internal error.
the relative fittings during the flushing or disinfecting cycle. R: Call technical support quoting the number of the error.
R: Make sure the suction tubes are properly connected and repeat the
disinfecting (see paragraph 7.4.) or flushing (see paragraph 7.5.) cycle.
If the message appears again, call technical support.
M: “Withdraw at least one instrument”

C: An attempt has been made to start a disinfecting cycle without selecting
any instruments or the cup.
R: Repeat the disinfecting cycle selecting at least one instrument or the
cup. If the message appears again, call technical support.
M: “Instrument configured”
C: The instrument in the indicated position on the board has been auto-
matically configured with the factory settings.
R: If the message appears again, call technical support.
M: “Put suction tubes back in place”

C: Suction tubes extracted when dental unit is turned on.
R: Make sure the suction tubes are correctly placed in their housings. If
the message appears again, call technical support.
M: “Put instrument back in place”

C: Instrument extracted when dental unit is turned on.
R: Make sure all the instruments are correctly placed in their housings.
M: “Check suction tube filter”

C: Suction tube flushing cycle malfunction.
R: Make sure the filters are clean, the suction tubes are not closed and
that the suction unit works correctly and then repeat the flushing cycle.
M: “Hydrogroup emergency device activated”

C: While performing an automatic movement, the assistant's board
encountered an obstacle.
R: Clear the obstacle and press the button for the desired program again.
EN 79
11. Specifications
Installation plan: 97042064 Water usage: 2 l/min.
Technical manual: 97071158 Water hardness: < 25 °f ( 14 °d )
Dental unit spare parts catalogue: 97023117 Drain connection: ø40 mm.
Dental chair spare parts catalogue: 97023117 Drainage rate: 10 l/min.
Maximum dental unit weight: 110 Kg. Drain duct inclination: 10 mm/m.
Maximum dental chair weight: 140 Kg. Aspirator connection: ø40 mm.
Maximum dental chair capacity: 160 Kg. Vacuum (minimum): 65 mbar.
Voltage: 230V~ / 115V~ Vacuum delivery rate: 450 l/min.
Frequency: 50/60 Hz. Mark of approval: CE 0051
R7 1200 W (230V~)
Electrical work in compliance with: IEC 60364-7-710
R7 M 1000 W (115V~)
Power absorbed:
1000 W (230V~)
R7 P Dental unit packaging dimensions: 1570 x 780 x 1130(h)
700 W (115V~)
Air supply pressure: 6-8 bar. Dental chair packaging dimensions: 1510 x 730 x 1000(h)
R7 140 Kg
Air delivery rate: 82 l/min.
Dental unit packaging weight: R7 M 110 Kg
Water connection: R7 P 70 Kg
1/2 Gas.
Dental chair packaging weight: 160 Kg.

Water supply pressure: 3-5 bar.
Water delivery rate: 10 l/min
FUSES
Identification Value Protection Position
Dental unit.
Fuse F2 T8A 230 V~ : Dental unit power supply line. Electrical box.
T 10 A 115 V~ : Dental unit power supply line. Electrical box.
Fuse F4 T 6,3 A Secondary protection: Hydrogroup. Electrical box.
Fuse F5 T 6,3 A Secondary protection: Dental unit. Electrical box.
Fuse F6 T 6,3 A Secondary protection: Operatory light.
Dental chair.
Fuse F1 T4A 230 V~ : Dental chair power supply line. Electrical box.
Quick-connect couplers.
Fuse T2A 230 V~ : Electrical outlet power supply line. Electrical box.
MONITOR power sup-
ply.
Fuse T4A 21 V~: MULTIMEDIA power line. Dental chair card area.
80 EN
11.1. Overall dimensions: R7 CONTINENTAL

EN 81
11.2. Overall dimensions: R7 INTERNATIONAL

82 EN
11.3. Overall dimensions: R7 CART

EN 83
11.4. Overall dimensions: R7 M CONTINENTAL

84 EN
11.5. Overall dimensions: R7 M INTERNATIONAL

EN 85
11.6. Overall dimensions: R7 M CART

86 EN
11.7. Overall dimensions: R7 P

EN 87
11.8. Overall dimensions: R7 SINGLE HYDRO GROUP

88 EN
12. Dental Unit maintenance plan

WHEN PART HOW SEE PARAGRAPH
Condensate drain. / See paragraph 9.2

Before starting work.
Insert inside each suction tube filter a tablet of
CATTANI surgical separator. See paragraph 9.5
VF CONTROL PLUS.
See documentation enclosed

Contra angle handpiece. Sterilize or disinfect the outside.
with handpiece.
Turbine. Sterilize or disinfect the outside. See paragraph 5.4
Micromotor. Disinfect outside. See paragraph 5.5
Scaler. Sterilize or disinfect outside. See paragraph 5.6
After each treatment.

Syringe. Sterilize or disinfect outside. See paragraph 5.3
Curing lamp. Sterilize fiber optic, disinfect outside. See paragraph 5.7
Disinfect outside.
C-U2 camera. See paragraph 5.8
Aspirate about ½ litre of sanitizing solution with
Surgical suction tubes. each suction tube. See paragraph 9.4
Sterilize the suction tube holder terminals.
Clean with commercial detergents formulated
Basin. for ceramic materials. See paragraph 7.1
METASYS surgical separator. See documentation enclosed with equipment. /
DURR surgical separator. See documentation enclosed with equipment. /
Operating lamp. See documentation enclosed with equipment. /
When needed.
Monitor on lamp post. See documentation enclosed with equipment. /
Clean with a suitable disinfectant carefully

following the directions for use provided by
Removable instrument tubings. See paragraph 5
the manufacturer.
Clean with a suitable disinfectant carefully
following the directions for use provided by
Coated surfaces and dental
the manufacturer. See paragraph 1.4
chair upholstery.
Spray product on disposable soft paper.
Clean filter in running water
Bowl filter. See paragraph 7.1
The content must be disposed of separately.
Check the filter and replace it if the suction rate

Surgical suction filter. See paragraph 9.3
At the end of is reduced (code 97461845).
the work day.
Surgical suction tubes. Clean the filter of the saliva ejector terminal. See paragraph 9.4
Water saliva ejector. Clean the filter of the saliva ejector terminal. See paragraph 6.6
Clean the separator’s container, drain valve

CATTANI surgical separator. See paragraph 9.5
and probes.
Weekly.
Suction tube holder terminals. Lubricate the O-rings. See paragraph 9.4
Check the filter and replace it if necessary

Monthly. Turbine return air filter. See paragraph 9.6
(code 97290014).
Contact the technical service department for

Yearly. Dental chair. /
general inspection.
EN 89

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SMART TOUCH

1.1. Symbol definition

1.2. Intended use

WARNING! (only for the American and Canadian markets)

1.2.1. Classification and reference standards

• MEDICAL DEVICES classification

1.2.2. Environmental conditions

The equipment is to be installed in rooms that satisfy the following requirements:

1.2.2.1. Transport and packaging conditions

• Temperature: from -10 to 70°C;

1.2.4. Disposing the equipment when no longer used

1.3. Safety rules

• WARNING! Moving the dental chair.

1.4. Cleaning and disinfecting

Cleaning and disinfecting instructions.

2. Description of the CLASSE R devices

Models: R7 CONTINENTAL, R7 INTERNATIONAL and R7 SINGLE

Models: R7 M CONTINENTAL and R7 M INTERNATIONAL.

Models: R7 CART and R7 M CART.

2.2. Dental units

Dental units R7 are available in the following versions:

R7 SINGLE HYDRO GROUP

2.3. Dental chair

Maximum weight capacity.

Warnings for use.

WARNING: FOOT CRUSHING HAZARD

2.4. Turning on the dental operatory

3. Warnings for models R7 CART and R7 M CART.

3.1. R7 line operating unit conversion

To convert the operating unit from the right-handed operator

• Turn the assistant’s board’s arms until they are compact in

• Start turning the hydrogroup and relative arm.

• Finish turning the hydrogroup to the left bringing it to the normal

• Turn the bowl to the new home position by hand.

• Place the pin ( c ), that stops rotation of the instrument board’s

• The operatory unit is now ready to be used by left-handed ope-

3.2. R7 M line operating unit conversion

To convert an R7 M line operating unit from the right-handed operator

4. Dental chair operation

The dental chair can be operated from the following

Dental chair movement shutdown

4.1. Safety devices

The equipment is supplied with the following safety devices:

4.2. Emergency devices

4.3. Adjustable headrest

The headrest may be of two types:

1 with manual cushion lock lever

Adjusting headrest height.

Proper positioning of the headrest.

4.4. Dental chair control panel

Description of the buttons:

Button to save dental chair functions

Button to reach home position

Button to reach rinse position

Button to raise seat

Button to raise back rest Button to retrieve programmed position “A”

Button to lower seat Button to retrieve programmed position “B”

4.5. Movable armrests (optional)

4.6. Seat rotation (optional)