Technical Manaual Mocom M10

97071268
Rev. 02
2021-05
EN
Dental units M10 2019 - TECHNICAL MANUAL
Contents
1. GENERAL WARNINGS ............................................................................................................................................ 3
1.1. FOREWORD ......................................................................................................................................................... 3
1.2. SAFETY INSTRUCTIONS .................................................................................................................................... 4
2. PACKING AND TRANSPORT .................................................................................................................................. 6
2.1. TRANSPORT AND STORAGE ............................................................................................................................ 6
2.2. DAMAGE DURING SHIPMENT ........................................................................................................................... 7
3. PREINSTALLATION ................................................................................................................................................. 8
3.1. DENTAL UNIT POSITION .................................................................................................................................... 8
3.2. ELECTRICAL HOOK-UP ...................................................................................................................................... 8
3.3. HYDRAULIC AND PNEUMATIC CONNECTIONS (AIR - WATER - DRAINAGE - SUCTION) ........................... 9
4. DEVICE INSTALLATION AND SETTING............................................................................................................... 11
5. ACCESSORIES AND MULTIMEDIA INSTALLATION ........................................................................................... 12
6. GUIDELINES - SAFETY TEST ............................................................................................................................... 13
6.1. CHECKS REQUIRED FOR THE DRAFTING OF CONFORMITY REPORT .....................................................13
6.2. CONFORMITY REPORT ....................................................................................................................................14
6.3. APPLICATION EXAMPLE WITH INSTRUMENT ESA 620 ON DENTAL UNIT AND/OR DENTAL CHAIR ......15
6.4. INDICATIONS FOR THE SOLUTION OF NON-CONFORMITIES DETECTED IN THE TEST .........................22
7. FUNCTIONING ....................................................................................................................................................... 24
8. KEYPADS AND DISPLAY SYMBOLS .................................................................................................................... 25
9. SERVICE MENU ..................................................................................................................................................... 26
10. HOW TO QUIT SHUTDOWN / FAULT CONDITIONS DURING DISINFECTING CYCLE .................................... 35
11. ALARMS / ERRORS / WARNINGS / TROUBLESHOOTING ................................................................................ 37
12. SCHEDULED MAINTENANCE AND TECHNICAL SERVICE ............................................................................... 38
13. SYSTEM RESET .................................................................................................................................................... 39
14. ELECTRONIC BOARDS......................................................................................................................................... 40
14.1. DENTAL CHAIR-CONNECTIONS BOX BASIC BOARD ...............................................................................40
14.2. BASIC HYDROGROUP BOARD ....................................................................................................................48
14.3. BASIC INSTRUMENT’S TABLE BOARD .......................................................................................................53
14.4. HYGIENE BOARD ..........................................................................................................................................58
14.5. ASSISTANT’S MODULE BOARD ..................................................................................................................61
14.6. MULTI-FUNCTION FOOT CONTROL BOARD .............................................................................................63
14.7. POWER FOOT CONTROL BOARD ...............................................................................................................66
14.8. VENUS PLUS L MCT LAMP CONTROL BOARD ..........................................................................................68
2 CONTENTS EN
1. GENERAL WARNINGS
1.1. FOREWORD
The device described in this manual is manufactured by CEFLA s.c. - via Selice Provinciale 23/A - 40026 Imola (BO)
Italia, which is the manufacturer, in compliance with the applicable European Directives detailed in the declaration of
conformity.
These technical instructions are addressed to the personnel in charge of repair and/or maintenance operations of
CEFLA s.c. equipment and contain all the necessary information.
CEFLA s.c. shall be responsible for the safety, reliability and efficiency of the equipment provided that:
 installation, any modifications, settings or repairs are made by authorised technical personnel using CEFLA s.c.
original spare parts
 In case of installation in medical locations: the electrical installation of the relevant location complies with IEC
60364-7-710:2002 Standards (Standards on electrical installations of medical locations) or with the equivalent
Standards in force in the country of installation
 the equipment is used as outlined in User Manual
 in case of installation of an X-ray unit: The room where the X-ray unit is installed complies with the official Directives
on protection from radiation in the country of use
EN GENERAL WARNINGS 3
1.2. SAFETY INSTRUCTIONS

Information that draws the user’s attention to the need of preventing dangerous situations and ensuring the correct
and safe use of the device is reported in the text according to the following layout:
SYMBOL DESCRIPTION
WARNING: General obligation
WARNING: It is mandatory to wear safety gloves
WARNING: It is mandatory to wear safety shoes
WARNING: Use eye protections
WARNING: Use protective clothing
WARNING: It is mandatory to ensure that there is an earth connection
WARNING: See the instruction manual
WARNING: Disconnect the device from the power mains
WARNING: See the technical manual
DANGER: It indicates a situation in which the failure to follow the instructions may lead to a fault of the
equipment or injuries to the user
DANGER: High voltage
DANGER: Crushing of hands
DANGER: Crushing of feet
DANGER: X-ray emission
DANGER: Moving parts
DANGER: Class 1 LASER radiation
4 GENERAL WARNINGS EN
SYMBOL DESCRIPTION
DANGER: Class 2 light source.
DANGER: Hot surface
DANGER: Biological risk
DANGER: Sharp objects
DANGER: Corrosive substances
DANGER: Flammable materials
DANGER: Tipping over
DANGER: Heavy object. Two persons are required
WARNING!
ALWAYS DISCONNECT power supply before performing any maintenance or cleaning operation.
The packed device must be handled using, where possible, suitable mechanical means (forklift, pallet
truck, etc.) and following the indications on the package.
In case of manual handling, the device must be lifted by several persons using the suitable available
means and, if possible, it must be moved with a truck or similar means.
Wear the proper protections.
EN GENERAL WARNINGS 5
2. PACKING AND TRANSPORT

2.1. TRANSPORT AND STORAGE
Instructions on how to handle, store and open the package are given on the outside of the cardboard box.
These instructions must be carefully followed.
1) Transport and store only in the direction indicated by the

arrows
2) Do not overlap more than two units
3) Avoid collisions
4) Protect against humidity
5) Do not use hooks to handle
6) The required storage conditions are indicated:

a) temperature from - -10° to +70° C
b) relative humidity from 10 to 90%
c) atmospheric pressure from 50 to 106 kPa
It is recommended to transport and store the device at a temperature not lower than that indicated on
the packing. A prolonged exposure to a low temperature can damage the device.
The packed device must be handled using, where possible,

suitable mechanical means (forklift, pallet truck, etc.) and
following the indications on the package.
In case of manual handling, it must be lifted by two or more

persons using the suitable available means.
6 PACKING AND TRANSPORT EN

Packaging Procedure PRECAUTION
Box 1 - remove the metal staples - do not handle the dental chair by
fastening the cardboard to the its backrest
wooden base and lift up - pay attention not to lift the dental
- loosen the two screws fixing the chair from its white plastic parts
dental chair to the wooden base
Box 2 - remove the metal staples - only remove the dental unit from
fastening the cardboard to the the wooden base when you
wooden base and lift up decide to attach it to the dental
chair
2.2. DAMAGE DURING SHIPMENT

When the device is received, check the packing container for any damage suffered.
If the packages are found to be damaged on delivery, accept them with reserve by signing the delivery note and
indicating that the “CONTENTS ARE ACCEPTED BUT THEY NEED TO BE CHECKED”.
If the contents are actually damaged, notify the shipping agent and request insurance compensation for damage
within five work days. The claim is to be made by the person who commissioned the shipping agent. I.e.:
 if the goods are delivered “carriage forward”, the receiver shall notify the shipping agent
 if the goods are shipped “carriage free” or “free delivered”, the consigner shall notify the shipping agent and file a
claim for damages. In this case, CEFLA s.c. shall be informed as soon as possible.
The damaged parts returned to CEFLA s.c. for replacement shall be placed inside the same damaged package.
Return to CEFLA s.c. shall be “carriage free” (at the expense of the consigner), while shipment back to the customer
shall be at the expense of CEFLA s.c. (carriage free).
EN PACKING AND TRANSPORT 7

3. PREINSTALLATION
3.1. DENTAL UNIT POSITION
Before installing the dental unit and dental chair, prepare the surgery considering the overall dimensions (see the
installation layout available on EXTRANET).
In addition, take all the required internal and external electrical and water connections close to the connections box.
To perform this operation correctly, it is essential to refer to the 1:1 scale installation layout (available on
EXTRANET).
WARNING!
- Installation must always be permanent with anchoring to the floor (Standard IEC EN 60601).
- the (continuous) floor should meet the load-bearing capacity set forth by "DIN 1055". The total weight
of the dental unit with a 190 Kg patient is approximately 395 kg
3.2. ELECTRICAL HOOK-UP

WARNING!
The system must have an effective earth ground that conforms to local regulations.
In particular, in Italy, this is to be done in compliance with the IEC 60364-7-710:2002 specifications that require the
installation upstream the system of a differential switch with the following characteristics:
If the voltage is = 230V (+/- 10V) - 50HZ

- rated current: 10A (D TURN)
- differential sensitivity: 0.03A
If the voltage is = 100/115V (+/- 10V) - 60HZ

- rated current: 16A (D TURN)
- differential sensitivity: 0.03A
Power supply:
- normally, the equipment is supplied for 230V - 50Hz. Different power supply voltage values (e.g. 115V / 60Hz) are
available on request
- absorbed power: 1500W
- power supply: 3x1.5mm type H05 RRF
WARNING!
The colour of the 3 wires must be as set forth by the standards.
- auxiliary control: 2x0.5mm type H05 RRF
- suction system control: 3x1mm type H05 RRF
8 PREINSTALLATION EN
3.3. HYDRAULIC AND PNEUMATIC CONNECTIONS (AIR - WATER - DRAINAGE -

SUCTION)
It is recommended to fit a cock, to stop both water and air delivery, so as to disconnect the dental unit from the other
appliances of the dental surgery. Should this not be possible, disconnect the unit using two cocks inside the
connections box.
Air:
- inlet pressure between 6-8 Bar
- actual flow rate: 82 litres/minute
- free of impurities
- dry
- free of oil
- if needed, install a heavy duty filter before the air supply: 40-50 micron
- connection at floor level: 1/2 Gas female fitting
- before installing, drain the duct
Water:
- inlet pressure between 3-5 Bar
(IF THE PRESSURE EXCEEDS 5 BAR, INSTALL A PRESSURE REDUCER AT THE INLET OF THE DENTAL
UNIT)
- actual flow rate of approx. 10 litres/minute
- free of impurities
- untreated potable water hardness no greater than the values indicated in the following table (where the water
shows higher values the installation of a water treatment unit is advised):
PRECAUTION:
If “ion exchange resin water softeners” are used the treated water hardness rating must not be less than
15°f in order to protect certain machine components.
There are treatments, such as ”reverse osmosis”, that reduce water hardness by removing the mineral
salts present in the water without any softening process; with this method treated water with hardness
ratings of less than 15°f does not cause damage to the machine.
Other “carbon” or “magnetic” devices do not alter water hardness.
in mg/L
in °T (°dH) (CaCO3 = in mg/L (CaO =
WATER HARDNESS in °f (French in °I (English
(German calcium calcium oxide
CLASSIFICATION degrees) degrees)
degrees) carbonate concentration)
concentration)
VERY SOFT <7 < 3.92 < 4.9 < 70 < 39.2
SOFT 7 < 14 3.92 < 7.84 4.9 < 9.8 70 < 140 39.2 < 78.4
QUITE HARD 14 < 22 7.84 < 12.32 9.8 < 15.4 140 < 220 78.4 < 123.2
MILDLY HARD 22 < 32 12.32 < 17.92 15.4 < 22.4 220 < 320 123.2 < 179.2
HARD 32 < 54 17.92 < 30.24 22.4 < 37.8 320 < 540 179.2 < 302.4
VERY HARD > 54 > 30.24 > 37.8 > 540 > 302.4
EN PREINSTALLATION 9
WATER HARDNESS UNIT OF MEASURE CONVERSION TABLE
UNIT OF MEASURE UNIT OF MEASURE CONVERSION COEFFICIENTS
°f
- x 0.56 x 0.7 x 10 x 5.6
(French degrees)
°T (°dH)
x 1.79 - x 1.25 x 17.9 x 10
(German degrees)
°I
x 1.43 x 0.8 - x 14.3 x8
(English degrees)
mg/L (CaCO3 = calcium
carbonate x 0.1 x 0.056 x 0.069 - x 0.56
concentration)
mg/L (CaO = calcium
x 0.179 x 0.1 x 0.125 x 1.79 -
oxide concentration)
= mg/L = mg/L
= °f = °T (°dH) = °I
(CaCO3) (CaO)
- connection at floor level: 1/2 Gas female fitting

- before installing, drain the duct
Drainage:
- minimum flow rate of 10 litres per minute
- pipe internal diameter of 40mm, with outlet at floor level
- min. inclination: 1cm/m.
Suction:
- flow rate no less than 450 litres/minute
- pipe internal diameter of 40mm, with outlet at floor level
PRECAUTION
A good suction system should have 45° and not 90° bends.
10 PREINSTALLATION EN
4. DEVICE INSTALLATION AND SETTING

See the installation manual of the concerned device, available on EXTRANET.
EN DEVICE INSTALLATION AND SETTING 11

5. ACCESSORIES AND MULTIMEDIA INSTALLATION

See the installation manual of the concerned device, available on EXTRANET.
12 ACCESSORIES AND MULTIMEDIA INSTALLATION EN

6. GUIDELINES - SAFETY TEST

Checks to be carried out upon first installation, periodical checks (every year) and tests to be carried out after
repair/updates/settings of medical electrical equipment with reference to Standard IEC 62353
Safety standards for medical electrical equipment classified according to IEC 60601 in Class 1, Type B.
(ME equipment connected to mains power supply through a permanent connection, provided with protective earth
conductor).
NOTE If measurements cannot be carried out in compliance with Standard IEC 62353, they can be carried
out in compliance with Standard IEC 60601.
6.1. CHECKS REQUIRED FOR THE DRAFTING OF CONFORMITY REPORT

a) Visual inspection
The purpose of visual inspection is to ensure that the equipment in use still complies with the specifications
released by the manufacturer through the following checks:
• label data
• presence of documentation (e.g. updated user manual in printed or electronic format, instructions)
• conditions of warning plates
• condition of power cables and connectors
• condition of earth cables and correct tightening
• condition of machine protections, covers and casings
• condition of electrical board protections and correct value of the fuse on the power supply line
• conditions of light indications and acoustic signals (warning lights, LEDs, display, etc.)
• no liquid leaking out from ducts or on the bottom of the device
b) Electric measure test (to be carried out with special instruments)

• measurement of earth conductor resistance
• measurement of earth conductor leakage currents
• measurement of earth-leakage currents of the medical electrical equipment and patient
• measurement of insulation resistance between network and earth conductor
• measurement of insulation resistance between applied part and earth conductor
c) Functional checks
• check of movement controls from doctor’s and assistant’s console
• check of usage controls of the instruments applied
• check of light indications and/or acoustic signals
• check of emergencies
EN GUIDELINES - SAFETY TEST 13

6.2. CONFORMITY REPORT
14 GUIDELINES - SAFETY TEST EN

6.3. APPLICATION EXAMPLE WITH INSTRUMENT ESA 620 ON DENTAL UNIT

AND/OR DENTAL CHAIR
 Measurement of protective earth conductor resistance
 Measurement of leakage currents in earth conductor, casing and patient
 Measurement of insulation resistance between network and earth
 Measurement of insulation resistance between applied part and earth
Disconnect power supply cable from dental unit and connect it (Phase - Neutral - Earth) to the relevant instrument
socket (e.g.: ESA 620). Turn on the main switch of the dental unit.
NOTE It is advisable to follow the instructions below: the device under test must be on and must be pre-
heated in advance through an operating cycle of at least 30 minutes, until it reaches the operating
temperature.
From PC or tester screen, select the type of test with reference to Standard IEC 62353 (among the methods
specified for the test of earth-leakage currents, the direct method is equivalent to Standard IEC 60601).
Follow the instructions displayed with reference to the visual check and dental unit data entry (e.g.: device serial
number).
If the test also includes the applied part (instruments), insert the grippers of the “APPLIED PARTS” on the relevant
measurement points: one gripper in the metal end part of the syringe [A]; one gripper on the tip of scaler, nose of
micromotor, quick coupling of the turbine [B] (in case of turbines with integrated LED, install the turbine on the
tubing); one gripper in 0V of power supply box [C]; one gripper in the monitor chassis [D].
NOTE If the monitor is not present, apply the gripper to V-OUT connector of the multimedia board, in
the point corresponding to 0 Volt, as shown in picture [D1].
In case there are tools also on the assistant’s side [E], manage them as described above for points [A]
and [B].
INITIAL SETTING

NOTE Connections with the machine points must be kept for the tests described below.
Follow the instructions requested by the control instrument.
E.G.: ESA620 instrument connection
A: Syringe
B: Instruments
C: Secondary circuit
D: Multimedia circuit
E: Applied part
F: Equipment under test
WARNING: During measurement execution, hazardous voltage could remain in the device.
Press “Start” to start test sequences.
Depending on your instrument, you have to select all the tests indicated below:
A) measurement of earth conductor resistance
B) measurement of earth-leakage current
C) measurement of insulation resistance
A) Measurement of earth conductor resistance (to be carried out after setting the test current of 25 Amperes in the
tester)

NOTE (Only with test carried out with reference to Standard IEC 62353):
• the measurement instrument must be able to supply a current of at least 200mA and the open circuit
supply voltage must not exceed 24V
• before carrying out the measurements, it is necessary to calibrate the power supply cable between
measurement instrument and equipment under test
• the measurement is carried out via probe between the metal parts of the equipment (see indicated
points) and the protective conductor connection in the equipment
Measurement method
Connect one gripper to the main earth point (connections box).
Connect the second gripper (if any, otherwise use the main one, by repositioning it), in sequence, in the various
points indicated:
• connections box metal part [A] • auxiliary socket [B]

• dental chair base mechanical part [C] • inverter board support sheet [D]
• metal part on dental chair electric motors (seat and backrest, if any) [E] or on dental chair metal body [E]
DENTAL CHAIR WITH MOTORS
THAT
OPERATE AT MAINS VOLTAGE
E1: Motor
DENTAL CHAIR WITH MOTORS THAT

DO NOT OPERATE AT MAINS
VOLTAGE

• hydrogroup metal part [F]
• instrument’s table metal part [G].
• integrated X-ray unit [H]

B) Measurement of earth-leakage current
Select the specific test on the tester.
By performing the test with reference to standard IEC 62353, it is possible to select an alternative method, that
carries out the test without powering the device under test. Generally this test is carried out automatically by the
instrument that carries out the test.
NOTE Pay attention to properly set the test equipment for “earth conductor” earth-leakage currents
NOTE The limit of leakage current in earth conductor for permanently installed M.E. equipment is ≤ 5
mA (see notes in the manual of the instrument used to carry out this setting)
Measurement method - Alternative method
If the test is carried out with reference to standard IEC 62353, by selecting the direct method, that carries out the
test by powering the device under test, the check is comparable to the measurements carried out according to
standard IEC 60601.
NOTE The guidelines below refer to the test carried out with direct method
Measurement method - Direct method

NOTE The direct method is comparable to the
measurements carried out in accordance with
Standard IEC 60601-1, it allows detecting any
leakage of current when the equipment and its parts
(heaters, instruments, etc.) are in full operation.
• “Earth conductor”: start the test; it must be carried out both in normal use and in single failure conditions
(interruption of a network conductor at a time) - (normal tester automatism).
NOTE The limit of leakage current in earth conductor for permanently installed M.E. equipment is ≤ 5
mA (see notes in the manual of the instrument used to carry out this setting)

• “Casing”: start the test; it must be carried out both in normal use and in single failure conditions (interruption of
a network conductor at a time and interruption of the earth conductor*, ref. IEC 60601) - (normal tester
automatism).
NOTE In single failure conditions, the interruption of the earth conductor does not apply to the
protective earth conductor of permanently installed M.E. Equipment, whose disconnection is considered
unlikely (EN 60601_8.1.b_4th)
• “Patient”: start the test; it must be carried out both in normal use and in single failure conditions (interruption of
a network conductor at a time and interruption of the earth conductor, ref. IEC 60601) - (normal tester
automatism).
NOTE To measure patient leakage current in FULL OPERATION for each electrical instrument both on
dentist side and on assistant side (micromotor and scaler), it is necessary to:
• individually take out the instrument to be checked;
• set the maximum speed;
• activate the spray;
• move the pedal lever (if the scaler is available, to allow tip vibration, it is necessary to disconnect the
gripper, activate the scaler, then reconnect the gripper to the vibrating tip);
• finally, start the tester for value measurement.
• “Patient Auxiliary”
NOTE This test must be carried out only if the syringe with heater is available (dentist side or assistant
side).
Start the test; it must be carried out both in normal use and in single failure conditions (interruption of a
network conductor at a time and interruption of the earth conductor, ref. IEC 60601) - (normal tester
automatism).
NOTE To measure patient auxiliary leakage current in FULL OPERATION, it is necessary that:
• the syringe heater is activated;
• take out the scaler or the micromotor (if the scaler is not present);
• move the pedal lever (if the scaler is available, to allow tip vibration, it is necessary to disconnect the
gripper, activate the scaler, then reconnect the gripper to the vibrating tip);
• finally, start the tester for value measurement.
C) Measurement of insulation resistance
Select the specific test on the tester:
• “between network and earth”: this test does not require special wiring, the tester will perform it automatically
after your authorisation to proceed. Let all the probes connected as in the previous points.
NOTE PHASE and NEUTRAL are short-circuited with each other by the tester.
NOTE The test must last one minute.

• “between applied part and earth”: this test does not require special wiring, the tester will perform it
automatically after your authorisation to proceed. Let all the probes connected as in the previous points.
NOTE The test must last one minute.
The tester issues (where applicable) a paper report with test results.
a) Check that all the tests are passed.
b) Add the values to the conformity report only in the absence of the paper report (otherwise attach the report and
tick the tests in the report as performed).
c) If one or more tests have not been passed, see section 4 (“Indications for the solution of non-conformities
detected in the test”).
WARNING: If safety checks are not passed, the dental unit must NOT be used; before using it
again, the device must be repaired by an authorised technician
Now it is necessary to check that the dental unit is correctly operating by carrying out a complete check of dental unit
functions (see section 1.C - adding the result in the report).
File the report in the warranty and maintenance booklet of the dental unit.
6.4. INDICATIONS FOR THE SOLUTION OF NON-CONFORMITIES DETECTED IN THE

TEST
EARTH CONDUCTOR RESISTANCE
 Check the presence and continuity of the earth conductor between the measurement point and the main
earth node and in the intermediate sections
 Check correct tightening of the fasteners of earth conductors
INSULATION RESISTANCE
ANALYSIS ON DENTAL CHAIR

 Disconnect direct power supply to the dental chair and repeat the test
 If the test is passed, reconnect power supply to the dental chair and disconnect power supply of motors and
capacitors (if powered with network voltage) and repeat the test
 If the test is passed, reconnect motors and capacitors one by one and repeat the test until the non-compliant
component has been identified
ANALYSIS ON DENTAL UNIT

 Disconnect cup heater, if any, and repeat the test
 If the test is not passed, disconnect spray heater, if any, and repeat the test
 If the test is not passed, disconnect any syringes with heater (6F) and repeat the test
 If the test is not passed, replace the connections board to exclude a possible network filter failure
LEAKAGE CURRENT IN EARTH CONDUCTOR
ANALYSIS ON DENTAL CHAIR

 Disconnect direct power supply to the dental chair and repeat the test (if the test is not passed, perform
ANALYSIS ON DENTAL UNIT by reconnecting the dental chair power supply)
 If the test is passed, reconnect power supply to the dental chair and disconnect power supply of motors and
capacitors (if powered with network voltage) and repeat the test
 If the test is passed, reconnect motors and capacitors one by one and repeat the test until the non-compliant
component has been identified
ANALYSIS ON DENTAL UNIT

 Disconnect cup heater, if any, and repeat the test
 If the test is not passed, disconnect spray heater, if any, and repeat the test
 If the test is not passed, disconnect any syringes with heater (6F) and repeat the test
 If the test is not passed, replace the connections board to exclude a possible network filter failure
PATIENT LEAKAGE CURRENT
INSTRUMENT’S TABLE ANALYSIS

 Disconnect power supply to the dental chair and repeat the test (if the test is not passed, perform
HYDROGROUP ANALYSIS by reconnecting the instrument’s table power supply)
 If the test is passed, reconnect instrument’s table power supply, disconnect all the instrument board power
supplies and repeat the test
 If the test is passed, connect in sequence power supplies of instrument boards (repeat the test upon each
connection) until leakage origin has been detected
 Disconnect in sequence solenoid valves, tubing, handpiece and repeat the test until leakage origin has been
detected
HYDROGROUP ANALYSIS
 Disconnect hydrogroup board power supply and repeat the test
 If the test is passed, reconnect power supply to the hydrogroup, disconnect in sequence power supplies of
instrument boards in assistant's module (repeat the test upon each connection) until leakage origin has been
detected

7. FUNCTIONING
See the user manual of the concerned dental unit.
24 FUNCTIONING EN
8. KEYPADS AND DISPLAY SYMBOLS

See the user manual of the concerned dental unit.
EN KEYPADS AND DISPLAY SYMBOLS 25

9. SERVICE MENU
26 SERVICE MENU EN
SERVICE MENU
EN SERVICE MENU 27
INSTRUMENT MENU
28 SERVICE MENU EN
GENERAL SERVICE MENU
EN SERVICE MENU 29
CONFIGURATION MENU
(1 = Function enabled / 0 = Function disabled)
DENTAL UNIT CONFIGURATION
SIGNALS DESCRIPTION
GLASS_HEATER 1 = if the cup water heater is present.
MOTORIZED_BOWL 1 = if the motorised cuspidor is present.
GLASS_SENSOR 1 = if the cup sensor is present.
WATER_ CIRCULATION 1 = if anti-stagnation feature is present.
CANISTER_CATTANI 1 = if the Cattani separator is present.
BOWL 1 = if the basin is present.
SUCTION_WASH 1 = if suction washing is present.
CENTRAL_SUCT_VALVE 1 = if the centralized suction valve is present.
HOSE_SELECTION 1 = if the independent suction tube selection is present.
30 SERVICE MENU EN
SIGNALS DESCRIPTION
PERISTALTIC_PUMP 1 = if the peristaltic pump is present.
H20_SPRAY_HEATER 1 = if the spray water heater is present.
BRAKE_SENSOR 1 = if the arm brake electric sensor is present.
H20_BOTTLE 1 = if the bottle is present.
H2O2_DISINFECTION 1 = if the automatic intensive disinfection system is present.
H2O_HYGIEN_SYSTEM 1 = if the automatic continuous sanitising system is present.
WATER_BYPASS_EV 1 = if the bypass valve is present.
CHAIR_ROTATION_EV 1 = if the dental chair rotation is present.
THREEPHASE_CHAIR 1 = if the dental chair seat three-phase motor is present.
SLIDING 1 = if the dental chair sliding motor is present.
DOCTOR_TABLE 1 = if the instruments table board is present.
HYGIENE_BOARD 1 = if the hygiene board is present.
HYDRO_GROUP 1 = if the hydrogroup board is present.
ORTHO 1 = in case of Ortho dental unit.
SIDE_DELIVERY 1 = in case of Side Delivery ergonomics.
ASSISTANT_TABLE 1 = if the assistant's module is present.
CHAIR_EXT 1 = if the dental chair with split leg rest is present.
LAMP_IN_HYDRIC 1 = if the lamp is connected to the hydrogroup board.
LAMP_IN_CHAIR 1 = if the lamp is connected to the dental chair/connections board.
RECIPROCATING 1 = if the reciprocating mode is present.
FLUSHING 1 = if the Flushing is present.
PEDAL_TYPE Selection of the foot control type.
LAMP_TYPE Selection of the lamp type.
CONSOLE Selection of the console type.
MODEL Selection of the dental unit model.
ERGONOMICS Selection of the ergonomics type.
EN SERVICE MENU 31
SIGNALS DESCRIPTION
DOC_TABLE_TYPE Selection of the instruments table type.
DOC_TABLE_HOLDER Selection of the table arm type.
SYRINGE_POSITION Selection of the syringe position.
APEX YES = if the apex locator is present.
POWER RANGE +/- 10V automatic.
WIRELESS_PEDAL 1 = if the wireless foot control is present.
INSTRUMENT_A Selection of the instrument type in module A.
INSTRUMENT_B Selection of the instrument type in module B.
INSTRUMENT_C Selection of the instrument type in module C.
INSTRUMENT_D Selection of the instrument type in module D.
INSTRUMENT_E Selection of the instrument type in module E.
SYRINGE_TYPE Selection of the syringe type.
ASSIST_INSTRUMENT_1 Selection of the instrument type in assistant module 1.
DENTAL CHAIR CONFIGURATION
SIGNALS DESCRIPTION
BOWL_AND_ZEROPOSITION Bowl rotation with home position.
BOWL_AND_RINSEPOSITION Bowl rotation with rinsing position.
BOWL_AND_ABCD_POS Bowl rotation with ABCD programs.
0 = in case of dental chair interference, the bowl moves towards the lamp
post.
FAST_RETURN_BOWL
1 = in case of dental chair interference, the bowl moves from the fastest side.
ZEROPOS_BOTTLE_PRESS_OFF Bottle depressurisation with home position.
GLASS_AND_RINSEPOSITION Cup filling with rinsing position.
LAMPOFF_AND_
Lamp OFF with home position.
ZEROPOSITION
LAMPOFF_AND_RINSEPOSITION Lamp OFF with rinsing position.
32 SERVICE MENU EN
SIGNALS DESCRIPTION
BOWL_WATER_AND_RINSEPOSITIO
Bowl rinsing with rinsing position.
N
BOWLWATER_AND_LASTPOSITION Bowl rinsing with last dental chair position recall.
BOWLWATER_AND_ZEROPOSITION Bowl rinsing with home position.
PEDAL_LEVER_REVERSE Foot control lever MIN/MAX inversion.
JOYSTICK_EXTENDED_MODE Enabling of foot control joystick extended mode.
MONOSTABLE_BELL Monostable bell button.
1 = to use the lamp button that activates the bell relay (basic or CL version
EXTERNAL_LAMP
lamp).
POWERPEDALPROGRAM Dental chair programs available from Power foot control.
AUTOSTANDBY Automatic standby (enabled).
STDBYTIME Standby activation time (minutes).
HYDROGROUP CONFIGURATION
SIGNALS DESCRIPTION
BOWL_TIMER Bowl timer (Enabled / Disabled).
SUCTIONSTOP_DELAY Suction stop delay (Enabled / Disabled).
SUCTIONSTOP_BIG_HOSE Suction stop on big suction tube.
SUCTIONSTOP_SMALL_HOSE Suction stop on small suction tube.
WATER_BOWL_AND_GLASS Cup/bowl automatism.
GLASS_HEATER Cup heater presence.
GLASS_SENSOR Cup sensor presence.
H2O_BOTTLE_STATUS Distilled water bottle presence.
ASSISTANT_PROGRAMENABLED Enabling of assistant dental chair programs.
LAMP_SENSOR Presence of operating light sensor.
LAMP_SOFT_START Lamp light soft start.
0 = switching from standard light to composite light via sensor.

LAMP_SENSOR_MODE
1 = ON/OFF lamp via sensor.
GLASS_TIME Cup water filling time via button.
EN SERVICE MENU 33
SIGNALS DESCRIPTION
GLASS_SENSOR_TIME Cup water filling time via sensor.
BOWL_TIME Bowl water time.
GLASS_HEATER_TEMP Cup water temperature.
BOWL_SPEED Bowl rotation speed.
GLASS_SENSOR_SENS Cup sensor sensitivity.
BOWL_VALVE_DELAY Bowl drain valve switching off delay.
INSTRUMENT'S TABLE CONFIGURATION
SIGNALS DESCRIPTION
SYRINGEFO_ON Syringe fiber optic enabling.
APEXSOUNDON Apex locator ON/OFF alarm sound.
NOWARNINGL1L2 No basic console error messages.
DOCTORPROGRAMENABLED Enabling of doctor’s console dental chair (ABDC) programs.
TLEDAUTO 1 = for automatic operating lamp light change upon T-LED activation.
SURGYAUTO ALWAYS 0.
HEATER Spray water heater presence.
AUTOCHIPAIR Automatic chip air ON/OFF.
AUTOCHIPAIR_DELAY Automatic chip air delay.
AUTOCHIPAIR_TIMING Automatic chip air time.
SYRINGEFO_LEVEL Syringe fiber optic level.
ALARMAPEXLEVEL Apex locator alarm level.
CLOUD CONFIGURATION
SIGNALS DESCRIPTION
STATION_SSID WiFi network name.
STATION_PWD WiFi network password.
34 SERVICE MENU EN
10. HOW TO QUIT SHUTDOWN / FAULT CONDITIONS DURING

DISINFECTING CYCLE
WARNING!
If H2O2 is present in the ducts, wash the cords manually with the relative foot control and flush the
water to cup duct by pressing the fill key several times.
EN HOW TO QUIT SHUTDOWN / FAULT CONDITIONS DURING DISINFECTING CYCLE 35

WARNING!
If H2O2 is present in the ducts, wash the cords manually with the relative foot control and flush the
water to cup duct by pressing the fill key several times.
36 HOW TO QUIT SHUTDOWN / FAULT CONDITIONS DURING DISINFECTING CYCLE EN

11. ALARMS / ERRORS / WARNINGS / TROUBLESHOOTING

An up-to-date list of Alarms/Errors/Warnings/Troubleshooting can be found in the TECHNICAL MANUALS
section of the EXTRANET.
EN ALARMS / ERRORS / WARNINGS / TROUBLESHOOTING 37

12. SCHEDULED MAINTENANCE AND TECHNICAL SERVICE

The Manufacturer requires that periodic scheduled maintenance operations are carried out at least once every 12
months in order to maintain all the certifications related to the device and the manufacturer’s responsibility for the CE
marking of the product.
To this end, special PERIODIC MAINTENANCE KITS, which include all components that need to be replaced due to
wear, are provided based on the concerned device.
The technician who carries out scheduled maintenance operations takes care of the correct and truthful filling in of
the GUIDE SHEET PROVIDED FOR PERIODIC PREVENTIVE MAINTENANCE OPERATIONS (ANNUAL).
The GUIDE SHEET must be handed over to the owner of the device and constitutes conclusive proof of the control.
Following periodic scheduled maintenance operations, the technician must ensure that the “Electrical safety tests”
specified in chapter 6 of this manual are performed by him/her or other authorised personnel.
It also resets the “reset & maintenance” counter to set the periodic maintenance counter to zero via the easyaccess
application.
In case of operations on the device on which an easycheck licence is activated, the technician is required to update
the “Maintenance Booklet” of the device on easycheck Cloud portal.
NOTE The manufacturer requires a compulsory general service of the turbines 3 years after installation by
returning the devices to the headquarters or authorised repair centres.
This service must then be repeated every three years.
38 SCHEDULED MAINTENANCE AND TECHNICAL SERVICE EN

13. SYSTEM RESET
Use easyaccess App.
EN SYSTEM RESET 39
14. ELECTRONIC BOARDS

14.1. DENTAL CHAIR-CONNECTIONS BOX BASIC BOARD
97661871 DENTAL CHAIR-CONNECTIONS BOX BASIC BOARD
40 ELECTRONIC BOARDS EN
97661871 DENTAL CHAIR-CONNECTIONS BOX BASIC BOARD FUSES
EN ELECTRONIC BOARDS 41
97661871 DENTAL CHAIR-CONNECTIONS BOX BASIC BOARD LED
97661871 DENTAL CHAIR MOVEMENT LIMIT SWITCH SETTING (AUTOMATIC SETTING)
14.2. BASIC HYDROGROUP BOARD

97661873 BASIC HYDROGROUP BOARD
97661873 BASIC HYDROGROUP BOARD FUSES
97661873 BASIC HYDROGROUP BOARD LEDS
97661873 BASIC HYDROGROUP BOARD LEDS
97661873 SETTING BASIN ROTATION LIMIT SWITCH
14.3. BASIC INSTRUMENT’S TABLE BOARD

97661874 INSTRUMENT'S TABLE BASIC BOARD
97661874 INSTRUMENT’S TABLE BASIC BOARD FUSES
97661874 INSTRUMENT’S TABLE BASIC BOARD LEDS
14.4. HYGIENE BOARD

97661903 HYGIENE BOARD
97661903 HYGIENE BOARD LEDS
97661903 HYGIENE BOARD LEDS
14.5. ASSISTANT’S MODULE BOARD

97661907 ASSISTANT’S MODULE BOARD
97661907 ASSISTANT’S MODULE BOARD LEDS
14.6. MULTI-FUNCTION FOOT CONTROL BOARD

97661933 MULTIFUNCTION FOOT CONTROL BOARD
97661933 MULTIFUNCTION FOOT CONTROL BOARD LED
97661933 SETTING PROCEDURE
14.7. POWER FOOT CONTROL BOARD

97661934 POWER FOOT CONTROL BOARD
97661934 POWER FOOT CONTROL BOARD
14.8. VENUS PLUS L MCT LAMP CONTROL BOARD

97661955 VENUS PLUS L MCT LAMP CONTROL BOARD
97661955 VENUS PLUS L MCT LAMP CONTROL BOARD LEDS
97661955 POTENTIOMETER SETTING PROCEDURE
97661955 NO-TOUCH SENSOR SENSITIVITY SETTING
www.cefla.com

Technical Manaual Mocom M10

Uploaded by

Copyright:

Available Formats

You might also like

Technical Manaual Mocom M10

Uploaded by

Document Information

Original Description:

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Technical Manaual Mocom M10

Uploaded by

Copyright:

Available Formats

97071268

1.2. SAFETY INSTRUCTIONS

WARNING: General obligation

WARNING: It is mandatory to wear safety gloves

WARNING: It is mandatory to wear safety shoes

WARNING: Use eye protections

WARNING: Use protective clothing

WARNING: It is mandatory to ensure that there is an earth connection

WARNING: See the instruction manual

WARNING: Disconnect the device from the power mains

WARNING: See the technical manual

DANGER: High voltage

DANGER: Crushing of hands

DANGER: Crushing of feet

DANGER: X-ray emission

DANGER: Moving parts

DANGER: Class 1 LASER radiation

DANGER: Class 2 light source.

DANGER: Hot surface

DANGER: Biological risk

DANGER: Sharp objects

DANGER: Corrosive substances

DANGER: Flammable materials

DANGER: Tipping over

DANGER: Heavy object. Two persons are required

Wear the proper protections.

2. PACKING AND TRANSPORT

1) Transport and store only in the direction indicated by the

2) Do not overlap more than two units

4) Protect against humidity

5) Do not use hooks to handle

6) The required storage conditions are indicated:

b) relative humidity from 10 to 90%

c) atmospheric pressure from 50 to 106 kPa

The packed device must be handled using, where possible,

In case of manual handling, it must be lifted by two or more

6 PACKING AND TRANSPORT EN

Packaging Procedure PRECAUTION

2.2. DAMAGE DURING SHIPMENT

EN PACKING AND TRANSPORT 7

3.2. ELECTRICAL HOOK-UP

If the voltage is = 230V (+/- 10V) - 50HZ

If the voltage is = 100/115V (+/- 10V) - 60HZ

3.3. HYDRAULIC AND PNEUMATIC CONNECTIONS (AIR - WATER - DRAINAGE -

WATER HARDNESS UNIT OF MEASURE CONVERSION TABLE

UNIT OF MEASURE UNIT OF MEASURE CONVERSION COEFFICIENTS

- connection at floor level: 1/2 Gas female fitting

4. DEVICE INSTALLATION AND SETTING

EN DEVICE INSTALLATION AND SETTING 11

5. ACCESSORIES AND MULTIMEDIA INSTALLATION

12 ACCESSORIES AND MULTIMEDIA INSTALLATION EN

6. GUIDELINES - SAFETY TEST

6.1. CHECKS REQUIRED FOR THE DRAFTING OF CONFORMITY REPORT

b) Electric measure test (to be carried out with special instruments)

EN GUIDELINES - SAFETY TEST 13

6.2. CONFORMITY REPORT

14 GUIDELINES - SAFETY TEST EN

6.3. APPLICATION EXAMPLE WITH INSTRUMENT ESA 620 ON DENTAL UNIT