Dabi Atlante Syncrus G3 User manual

2
PRESENTATION OF MANUAL
INSTRUCTIONS FOR USE
ATTENTION
Technical Name: Dental Delivery Units and Accessories
Trade Name: Dental Delivery Units
Model: Syncrus G3
Manufacturer/ Distribuitor:
Alliage S/A Indústrias Médico Odontológica
C.N.P.J. 55.979.736/0001-45 - Insc. Est. 582.002.897.114
Rod. Abrão Assed, Km 53+450m - Cx. Postal 782 CEP 14097-500
Ribeirão Preto - S.P. - Brasil
Phone [phone]
Technical Duties: Ricardo J. Ravaneli
CREA-SP: 5060714523
Registration ANVISA #: 10069210075
For greater safety:
Read and understand all the instructions contained in these instructions for use before installing
or operating this equipment.
Note: These instructions for use must be read by all the operators of this equipment.

3
INDEX
02 PRESENTATION OF MANUAL
04 IDENTIFICATION OF EQUIPMENT
04 Indication of Equipment
04 Purpose of the equipment
04 Principles and essentials for the product’s functioning
05 Description of the Equipment
07 MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CONSUMPTION
12 TECHNICAL SPECIFICATIONS
12 General features
14 Electromagnetic Emissions
18 Dimensions
19 Packing symbols
19 Product symbols
22 INFRA-STRUCTURE SPECIFICATION
22 INSTALLATION OF EQUIPMENT
22 OPERATION OF EQUIPMENT
31 PRECAUTIONS, RESTRICTIONS AND WARNINGS
31 Recommendations for preserving the equipment
31 Transportation, storage and operation
31 Sensibility to predictable environmental conditions in regular use conditions
32 Precaution and warnings “during the installation” of the equipment
32 Precautions and warnings “during the use” of equipment
33 Precautions and warnings “after” the use of equipment
33 Precautions and warnings during the “cleaning and disinfection” of equipment
33 Precautions in case of alteration in the functioning of equipment
33 Precautions to be adopted against foreseeable or uncommon risks, related to the deactivation
and abandoning of equipment
34 CORRECTIVE AND PREVENTIVE MAINTENANCE AND PRESERVATION
34 Additional procedures for reuse
34 Cleaning
34 Disinfection
36 Preventive Maintenance
36 Corrective Maintenance
37 UNFORESEEN EVENTS – SOLUTION OF PROBLEMS
39 EQUIPMENT’S WARRANTY
39 FINAL CONSIDERATIONS

4
IDENTIFICATION OF EQUIPMENT
Dear Customer
This manual is a general presentation of your product and it will give you important details to help
you to solve possible problems.
Please, read it and keep this with you.
Indication of Equipment
This equipment is for dental use use only. It must be operated and utilized by specialized professional
(certied professional, according to the legislation of the country) and following the instructions of
the manual. The operation of the equipment required, for the professional, the utilization of correct
instruments and it should to be in perfect conditions of the use, and to protect the professional,
the patients and others, in the eventual danger situation.
Purpose of the equipment
Support the working active instruments of the Surgeon, such as: triple syringe, high rotation, low
rotation, ultrasound, photopolymerizer, among others, as well as it accommodates the working material.
Principles and essentials for the product’s functioning
Delivery Unit attached to the chair, featured with hoses with connectors that take the compressed
air and the water for running the rotation instruments (high and low rotation), besides the triple
syringe.

5
Description of Equipment
Delivery Unit, for actuation and control of the syringe, rotary instruments and others, providing the
best proximity to the work area; ambidextrous (serves right and left-handed users).
Structure assembly manufactured with steel with ABS injected body provided with anti-UV protection.
Smooth paint high glossy epoxy-based, cured in an oven at 250°C, with phosphate treatment
resistant to corrosion and cleaning materials.
Smooth Hoses, rounded, light and exible, without grooves or ridges.
Automatic selection of tips through individual pneumatic valves, allowing lightness in your drive.
It has a large embedded support for instruments, allowing better accommodation of the working
hardware.
Bilateral handles.
Staggered Tips support prevents inadvertent fall of the instruments, causing damage to them.
*Auxiliary removable Tray, enabling a perfect disinfection.
*Equipped with side control panel contains a set of all commands for the chair, Delivery Unit, Water
Unit and reector.
*Flush System: Disinfection system with check valve, which provides the internal cleaning of terminals
via hoses and bactericidal liquid, preventing risk of cross contamination.
Interchangeable coupling system, adapted according to the needs of the practitioner.
Available in models *pneumatic AIR (F), mechanical (SF)*and *CART (C).
*Pneumatic Arm with travel limit stop AIR (F):
Attached to the chair, with wide horizontal and vertical movement, with pneumatic locking, powered
by button located under the handle of the equipment, providing smoothness in movements and
stop at the desired position.
*Mechanical Arm with end stop (SF):
Attached to the chair, with horizontal movements and vertical adjustment position by locking ring.
*CART (C):
Pedestal frame assembled on four casters, built in steel nished with smooth paint and rounded
corners.
To ensure safe operation of your equipment, use only the assembly congurations (Chair, Delivery
Unit, Water Unit and Light reector) provided by Reseller / Alliage Authorized Service.
*Curing Light
Product Features:
Designed to carry out curing resin material through a curing process. The wavelength of 420nm -
480nm associated with high energy emitted by Curing Light enables the multifunctionality of this
device.
It has high power LED with ecient coupling and optical distribution, providing speed and security
procedures. Ensures proper photo-activation of materials without wasting light.
The LED system of this machine has long service life, equivalent to 36 million 10-second cycles
without loss of power and eciency in the photo activation.
The reduced weight of the pen and its anatomical design ensure a more comfortable and practical
professional work.
Operation control with display and buttons on the pen itself.
Variation of choosing the operation time (5,10,15 and 20 seconds).
It has 3 application modes: Continuous, Ramp and Pulse:
• Continuous: Maximum mode and continuous light intensity (same luminosity from the beginning
to the end of the polymerization).
• Ramp: Gradual light intensity mode, increases gradually.
• Pulse: Pulse mode has cycles that oscillate at a xed frequency.
*Optional
IDENTIFICATION OF EQUIPMENT

6
- Shows the elapsed time and the end of the operation.
- No special optical lters.
- Low power consumption.
- Low cost of replacement.
The cold light does not emit heat as conventional bulbs - Low temperature light polymerizes the
resin without damaging the tooth pulp and prevents thermal expansion problems.
- The forced ventilation system, transmitting unpleasant noise is not necessary.
- High strength piece.
- Conductive light removable in ber optics, removable and autoclavable.
- Swivel eye protection - Ensures full protection without compromising the visual eld.
*Ultrasound
Product Features:
Piezoelectric Ultrasound, frequency of 30,000 Hz.
The transducer with piezoelectric system allows the insert to perform accurate movements and
linear and can be used in various dental specialties.
Fine power adjustment, suitable for each type of procedure.
For proceedings with refrigeration provides constant irrigation with ow control. It also allows the
execution of dry work (amalgam condensation, cementing inlays / on lays, etc.).
*Bicarbonate jet KIT/ Jet Hand
Product Features:
The Bicarbonate Jet (Prophylaxis) comes from the release under pressure of particles of sodium
bicarbonate, together with the water, mixing together in the nozzle of the handpiece forming jet
in the form of a concentrated spray.
Removable bicarbonate jet pen, with concentric diuser which mixes the air, water and bicarbonate
at a small distance from the handpiece.
Cover of the transducer made out of rigid and autoclavable thermoplastic resin.
Container for bicarbonate easy to access, transparent and removable.
Water register with sensitivity adjustment that allows to adapt to the need of each operation.
IDENTIFICATION OF EQUIPMENT
*Optional

7
01 - Bilateral Catcher
*02 -Triple syringe
*03 - High-speed-motor terminals
*04 - Micro motor terminal
*05 - Control panel (PAD)
*06 - X ray view
*07 - Auxiliary tray
08 - Support tools
*09 - Arm brake valve
*10 - Flush System operation
*11 - Water records for FO/MME/Ultrasound/Bicarbonate Jet
*12 - LED reversal key (Ultra Vision)
*13 - Heating water activation key in the syringe
*14 - Power (power ultrasound adjustment)
*15 - Speed (electric microengine power adjustment)
*16 - Light (electric microengine brightness adjustment)
*17 - Manometer
The contents of this page are of an informative nature, the equipment being able to dier
from that illustrated. So, upon acquiring the product check the technical compatibilty
between equipment, coupling and accessories.
MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CON-
SUMPTION
side view b
17
16
15
14
08
03
06
07
08
04
01
02
a
13
12
09
11
bottom view
}
10
b
05
a
*Optional

8
01
11
06
09
12
1513 14
10
07
05
08
04
0302
MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CON-
SUMPTION

9
*01 - Terminals:
Borden
Midwest
Fiber Optic
Electric micro motor
*02 - Curing Light
*03 - Control panel Kit
• Available in two versions (11/17 keys)
*04 - Triple syringe with fully hermoplastic injected body
*05 - Triple syringe with fully metallic ody or with the thermoplastic injected knob
*06 - Auxiliary Tray / support tools
*07 - Stainless steel cover
*08 - Bicarbonate jet kit (model with terminal and reservoir coupled to the Delivery Unit)
*09 - Bicarbonate jet kit (Jet Hand model)
• Description, application, operation and more information, see the product manual
available on the site for viewing and download.
*10 - CART coupling
*11 - Coupling pneumatic AIR
*12 - Coupling mechanical
*13 - Integrated Pedal "Chip Blower"
*14 - Progressive Pedal
*15 - Progressive pedal with drive "Chip Blower" / water cut
*16 - Heating kit for triple syringe
*17 - Negatoscope Kit
*18 - Manometer
17 18
16
19 20
*Optional
MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CON-
SUMPTION

10
*19 - Ultrasound Kit
• Available in versions with either xed or detachable transducer with or
without illumination.
*20 - Kit MME
Attention
- The drawings (page 08 and 09) illustrates all optional items; therefore, your equipment
will consist only of items selected during your purchase option.
- The use of any part, accessory or material not specied or foreseen in these instructions
for use is entirely the user’s responsibility.
*Optional
MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CON-
SUMPTION

11
Identification label "field
responsible for identifying
product’s settings".
The Delivery Unit may comprise:
Optional Initials
Borden terminal TB
Midwest Terminal TM
Fiber Optic Terminal FO
Electric micro motor Terminal MME
Curing Light OPTI
Control panel PAD
Bicarbonate Jet JET
CART coupling (C) C
Coupling pneumatic AIR (F) AIR (F)
Coupling mechanical SF
Ultrasound SONIC
Full equipment FULL◊
Note
Equipment conguration
Equipment designated "FULL◊" may contain some options in the set, such as: FO/MME/
OPTI/SONIC/PAD/JET, etc...
MODULES, ACCESSORIES, OPTIONS AND MATERIALS OF CON-
SUMPTION

12
Power Supply Voltage (coming from dental chair)
127 or 220 V~ 50/60 Hz (selectable internally)
Protection against Electric Shock
Type B and Class I Equipment
Operation mode
Continuous
Input fuse (coming from dental chair)
2x10A (110/127v) or 2x5A (220v)
Voltage in equipment (coming from dental chair)
12 and 24 V~
Inlet air pressure
60 to 80 PSI ±2
Capacity of reservoir - Water / Flush System*
1000 ml
Maximum capacity of load applied to trays
2Kgf
Net weight of Delivery Unit with “pneumatic AIR” coupling (with all the options)
22,5 Kg
Net weight of Delivery Unit with “mechanical” coupling (with all the options)
17 Kg
Net weight of Delivery Unit with “CART” coupling (with all the options)
15,10 Kg
Specications of Curring Light
Power
5,2VA
Light source
1 LED
Power of Light
1200 mW/cm2 ± 200 mW/cm2
Semicondutor LED (InGaN)
TECHNICAL SPECIFICATIONS
General features
*Optional

13
Wavelength
420nm - 480nm
Timer
5,10,15 and 20 seconds
Timer alarm
Sound alarm with beep every 05 seconds and 02 beeps at the end of the cycle
Activation
Through the hand-piece button
Light conductor
Optic ber 100% coherent that ensures the light passage without losses
Weight
0,8kg
Specications of Ultrasound
Transducer protective cover, removable and autoclavable
Autoclavable tool to replace the inserts
Frequency of Vibrations of Ultrasound
30.000Hz
Consumption of irrigating liquid
28 ml/min
Power consumed
15VA ±10%
Transducer system
Piezoelectric ceramic
Electronic circuit with frequency stabilizer
Keeps the vibration even when there is network voltage oscillation
ATTENTION
The materials used to produce the equipment are Biocompatible.
WARNING
Pay attention while using this equipment together with other movable equipment, in order
to avoid collisions.
TECHNICAL SPECIFICATIONS

14
Electromagnetic Emissions
TECHNICAL SPECIFICATIONS
Electromagnetic Emissions
The Syncrus G3 Delivery Unit is made to be used in the electromagnetic environments specied
below. The client or the user of the Syncrus G3 Delivery Unit must be sure that it is used in
such environment.
Emission test Compliance Eletromagnetic environment - Guide
RF emissions
ABNT NBR IEC CISPR 11
Group 1 This Syncrus G3 Delivery Unit uses
RF energy only for internal functions.
However, its emissions are too low and
it's unlikely to cause any interference in
the equipments next to it.
RF emissions
ABNT NBR IEC CISPR 11
Class B
Emissions of harmonics
IEC 61000-3-2
Class A This Syncrus G3 Delivery Unit is proper
to be used in all establishments; including
domestic settings and those directly
connect to a public low voltage distribution
which feeds domestic buildings.
Fluctuation of Voltage /
Emissions of icker
IEC 61000-3-3
As per

15
TECHNICAL SPECIFICATIONS
Guidelines and manufacturer's declaration - electromagnetic immunity
The Syncrus G3 Delivery Unit is made to be used in the electromagnetic environments specied
below. The client or the user of the Syncrus G3 Delivery Unit must be sure that it is used in
such environment.
Immunity
test
ABNT Test level
NBR IEC 60601
Level of
compliance
Electromagnetic
environment Directives
Electrostatic
discharge (ESD)
IEC 6100-4-2
± 6 kV Contact
± 8 kV Air
± 6 kV Contact
± 8 kV Air
Floors should be wooden,
concrete or ceramic. If
the floor is covered with
synthetic material, the
relative humidity should be
at least 30%.
Quick electric
transitory phases
/ train of pulses
(”Burst”)
IEC 61000-4-4
± 2 kV in power
supply lines
± 1 kV in input /
output lines
± 2 kV in power
supply lines
± 1 kV in input /
output lines
It is advisable that the
quality of the power supply
should be that of hospital
or typical commercial
environment.
Surges
IEC 61000-4-5
± 1 kV lines (s) to
lines (s)
± 2kV lines (s) to
ground
± 1 kV lines (s) to
lines (s)
± 2kV lines (s) to
ground
It is advisable that the
quality of the power supply
should be that of hospital
or typical commercial
environment.
Reduction,
interruption
and variance of
voltage in power
supply input lines
IEC 61000-4-11
< 5% Ut
(>95% drop in Ut)
for 0,5 cycle
40% Ut
(60% drop in Ut)
for 5 cycles
70% Ut
(30% drop in Ut )
for 25 cycles
< 5%Ut
(>95% drop in Ut )
for 5s
< 5% Ut
(>95% drop in Ut )
for 0,5 cycles
40% Ut
(60% drop in Ut)
for 5 cycles
70% Ut
(30% drop in Ut )
for 25 cycles
< 5% Ut
(>95% drop in Ut )
for 5s
The recommended power
supply quality is the same
as used for commercial or
hospital environment. If
is required a continuous
use during energy supply
outages, it is recommended
that the Syncrus G3
Delivery Unit be feed by
an uninterruptible power
supply or a battery.
Magnetic eld in
frequency of
power supply
(50/60Hz)
IEC 61000-4-8
3 A/m 3 A/m If an image distortion occurs,
may be necessary place
the equioment far from
the supply frequency or to
installa magnetic armour.
The frequency magnetic
eld shall be measured at
the installment place to
assure that it is low enough.
NOTE Ut is the a.c. power supply voltage before the application of the test level

16
TECHNICAL SPECIFICATIONS
Guidelines and manufacturer's declaration - electromagnetic immunity
The Syncrus G3 Delivery Unit is made to be used in the electromagnetic environments specied
below. The client or the user of the Syncrus G3 Delivery Unit must be sure that it is used in
such environment.
Immunity
test
ABNT test level
NBR IEC 60601
Level of
compliance
Electromagnetic Environment
Directives
RF conducted
IEC 61000-4-6
RF radiated
IEC 61000-4-3
3 vrms
150 kHz up to
80 MHz
3 V/m
88 MHz up to
2,5 GHz
3 Vrms
3 V/m
It is advisable that portable and mobile RF
communication equipment is not used near any
part of the Syncrus G3 Delivery Unit, including
cables, with a separation distance less than the
one recommended, calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance:
d = 1,2√P
d = 1,2√P 80 MHz thru 800MHz
d = 2,3√P 800 MHz thru 2,5MHz
Where P is the nominal maximum power of
output of the transmitter in watts (W), as per
the manufacturer of the transmitter, and d is the
recommended separation distance in meters (m).
It is advisable that the el intensity from the RF,
transmitter as determined by means of electric
inspection on-sitea,is less than the level of
compliance in each frequancy rangeb.
There may be interference near the equipment
marked with the following symbol:
NOTE 1 At 80MHz and 800MHz, the highest frequency range applies.
NOTE 2 These directives may not be applicable in every situation. The electromagnetic
transmission is aected by the absorption and reection of structures, objects and people.
a - The eld intensities set by the xed transmitters, such as radio base stations, telephones
(mobile phone, wireless) land mobile radio, amateur radio, AM and FM radio transmissions and TV
transmissions can not be predicted with accuracy. Due to the RF xed transmitters is recommended
to install an electromagnetic inspection at the local in order to evaluate the electromagnetic
environment. If at the place where the Syncrus G3 Delivery Unit is be using the eld intensity
level exceeds the conformity level for the RF above, is recommended to observe if the operations
are normal. Whether abnormal operations are observed, additional procedures shall be necessary
such as reorientation or replace the Syncrus G3 Delivery Unit.
b - Whether above the frequency range of 150kHz to 80 MHz is recommended a eld intensity
below than 3 V/m.

17
TECHNICAL SPECIFICATIONS
Recommended distances between portable and mobile RF communication equipments and the
Syncrus G3 Delivery Unit
The Syncrus G3 Delivery Unit is made to be used in an electromagnetic environment in which
RF disturbances are controlled. The client or the user of the Syncrus G3 Delivery Unit may
help preventing electromagnetic interference by keeping a minimal distance between mobile
and portable RF communication equipment (transmitters) and the Syncrus G3 Delivery Unit,
as recommended below, in accordance with the maximal voltage output of the communication
equipment.
Transmitter Maximum
Output (W)
Separation distance according to transmitter frequency (M)
150 kHz to 80 MHz
d= 1,2√p
80 kHz to 800 MHz
d= 1,2√p
800 kHz to 2,5 GHz
d= 2,3√p
0,01 0,12 0,12 0,23
0,1 0,38 0,38 0,73
1 1,2 1,2 2,3
10 3,8 3,8 7,3
100 12 12 23
For transmitters with a maximum nominal output power not listed above, the recommended d
separation distance in meters (M) can be determined using an equation applicable to the frequency
of the transmitter, where Pis the transmitter maximum nominal output in watts (W) according
to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, is applied the separation distance for the higher frequency range.
NOTE 2 These guidelines may not apply to all situations. The absorption and reection from
structures, objects and people aect the electromagnetic propagation.

18
Delivery Unit with CART coupling
Delivery Unit with pneumatic coupling
Delivery Unit with Mechanical coupling
Dimensions (mm)
TECHNICAL SPECIFICATIONS

19
Packing symbols
Product symbols
It determines the maximum
quantity of boxes which can be
stacked during transportation and
storage “as per packaging”.
Packing to be transported and /
or stored avoiding humidity, rains
and wet oor.
Packing to be transported and /
or stored with the harrows up.
The packing must be stored and
transported away from direct sun
light exposure.
Packing to be transported and / or
stored with care (should not suer
drop and neither receive impact).
Temperature limit for the packing
to be stored or transported.
Applied part type B.
Grounding (at several points of the
equipment) indicates the condition
of being grounded.
Attention:
Check the working instructions.
Note:
It indicates useful information for
operation of the product.
Refer to the instruction manual. Authorized representative in the
European Community.
TECHNICAL SPECIFICATIONS

20
Product symbols
General sign for mandatory action
General warning::
If the instructions are not properly
followed, the use can lead to
damage to the product, user or
patient
High-speed with FO Curring Light
Lift seat Lower seat
Lift backrest Lower backrest
It determines the initial position Dental Light
It determines the work position “1” It determines the work position “2”
It determines the work position “3” It determines the work position “4”
TECHNICAL SPECIFICATIONS