LM-Dental LM-ProPower CombiLED User manual

LMProPower CombiLED
User Manual

2
This manual is valid for:
LM-ProPower 1007274
LM-ProPower 1007375
LM-ProPower 1007274us
LM-ProPower 1007375us
LM-ProPower 1007274jp
LM-ProPower 1007375jp
Manufacturer, Marketing and Sales
LM-Instruments Oy
PL 88 (Norrbyn rantatie 8)
FI-21601 Parainen, Finland
Telephone: [phone]
Fax: [phone]
E-mail: [email protected]
Internet: www.lm-dental.com
Copyright
Copyright 2015 LM-Instruments Oy. All rights reserved. The contents of this manual may be changed without
notice. No part of this manual may be reproduced in any form or by any means without permission in writing
from LM-Instruments Oy.

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CONTENTS
1. Introduction.............................................................................................................................................. 5
2. Safety instructions .................................................................................................................................. 6
2.1. Safety notices ................................................................................................................................ 6
2.2. Electro magnetic compatibility ..................................................................................................... 7
2.3. Safety considerations to install, servicing and to repair the CombiLED unit.............................. 7
2.4. Intended and prohibited use ........................................................................................................ 7
2.5. Declaration of conformity .............................................................................................................. 7
2.6. EMC Guidance and manufacturer’s declaration........................................................................... 8
3. Content of delivery ................................................................................................................................ 11
3.1. Content of unit.............................................................................................................................. 11
3.2. General description...................................................................................................................... 11
3.3. CombiLED unit ............................................................................................................................. 12
3.4. Coupling and type plate............................................................................................................... 13
3.5. Control panel................................................................................................................................ 13
3.6. Medicament bottle (optional)....................................................................................................... 14
3.7. AirLED Polisher ............................................................................................................................ 14
3.8. Foot Control unit .......................................................................................................................... 15
3.9. Symbols on the equipment.......................................................................................................... 16
4. Taking CombiLED in to use .................................................................................................................. 17
4.1. How to install the unit. ................................................................................................................. 17
4.2. How to connect the unit to the air supply................................................................................... 18
4.3. How to connect the unit for tap water (optional) ....................................................................... 18
4.4. How to connect the unit to the supply current ........................................................................... 19
5. Operating instructions UltraLED Scaler.............................................................................................. 20
5.1. How to install UltraLED Scaler to use ........................................................................................ 20
5.2. Foot control functions for Scaler................................................................................................. 22
5.3. Power and working modes for Scaler ........................................................................................ 22
5.4. How to operate with the UltraLED Scaler .................................................................................. 23
5.5. After Scaler treatment.................................................................................................................. 24
6. Operating instructions AirLED Polisher ............................................................................................. 25
6.1. How to install AirLED Polisher to use ......................................................................................... 25
6.2. Foot control functions for Polisher.............................................................................................. 27
6.3. Power and working modes for Polisher...................................................................................... 27
6.4. Air purge quick cleaning function .............................................................................................. 27
6.5. How to operate with AirLED Polisher.......................................................................................... 28
6.5.1.Polishing for supragingival use ......................................................................................... 29
6.5.2.Polishing for subgingival use ............................................................................................. 29
6.6. After Polisher treatment............................................................................................................... 29
7. Cleaning and maintenance................................................................................................................... 30
7.1. Air purge quick cleaning function ............................................................................................... 30
7.2. Automatic cleaning function for the scaler and polisher ........................................................... 30
7.3. How to clean the equipment and the components .................................................................... 31
7.4. Recommended cleaning procedure............................................................................................ 32
7.5. Maintenance................................................................................................................................. 34
8. Troubleshooting CombiLED ................................................................................................................. 35
9. Technical data........................................................................................................................................ 39

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10. Warranty ................................................................................................................................................ 40
10.1. Warranty terms............................................................................................................................. 40
10.2. Delivery Information..................................................................................................................... 41
10.3. Installation check-list................................................................................................................... 42
10.4. Operational test............................................................................................................................ 43

Introduction
5
1. INTRODUCTION
Foreword
This is user manual for CombiLED product. Read and understand this manual before you use the product. If
there are any questions regarding the contents of this manual, please contact LM-Instruments Oy. Keep User
manual in place where it is easily available for all users.
General Requirements
Special precautions are necessary to this product regarding EMC (Electro Magnetic compatibility). It is necessary
to install the product and put it into servicing referred to the EMC data in chapter “2.6. EMC Guidance and
manufacturer’s declaration” on page 8.
Portable and mobile RF (Radio Frequency) communications equipment can have an unwanted effect on the
product.
Connect the product to electricity-, water- and compressed air supply which obeys the requirements in the
Technical data.
Servicing
Only approved service persons are permitted to do servicing to this product. The maintenance procedures
which are introduced in this manual are for the user. User must obey the maintenance measures to keep safe
and efficient operation of the product.

Safety instructions
6
2. SAFETY INSTRUCTIONS
2.1. Safety notices
The safety notices shown on this page are used to identify safety messages in these instructions:
WARNING
WARNING indicates a dangerous situation that, if not prevented, could cause
death or injury.
CAUTION
CAUTION indicates a dangerous situation that, if not prevented, could cause
minor or moderate injury.
NOTICE! NOTICE indicates a situation that, if not prevented, could result in material
damage.
This general hazard symbol identifies important safety messages in this manual. Carefully read,
understand and obey the messages. When you see this symbol,be alert: your and your patient
safety is involved.

Safety instructions
7
2.2. Electro magnetic compatibility
Special precautions are necessary to this product regarding EMC (Electro Magnetic compatibility). It is necessary
to install the product and put it into servicing referred to the EMC data in chapter “2.6. EMC Guidance and
manufacturer’s declaration” on page 8. Portable and mobile RF (Radio Frequency) communications
equipment can affect the product.
2.3. Safety considerations to install, servicing and to repair the
CombiLED unit
Connect the product to electricity-, water- and compressed air supply which obeys the requirements in the “9.
Technical data” on page 39. Only persons with applicable professional knowledge are permitted to connect
the unit to the air or water supply.
Only approved service persons are permitted to do servicing to this product.
In this manual are shown all the permitted maintenance procedures for the user, any other procedures are
strictly prohibited. Before you do any maintenance work, read and understand maintenance instructions.
2.4. Intended and prohibited use
LM-ProPower CombiLED is designed for removal of biofilm and calculus on teeth, cleaning discoloured teeth
and other dental work where the ultrasonic vibration and/or polishing is beneficial. The unit must only be used by
licensed dental and professionals approved in the correct operation of scaling- and polishing devices.
Do not use LM-ProPower CombiLED unit where it is not intended to. If you are unsure about your operation,
please contact your local dealer or place of purchase.
2.5. Declaration of conformity
The manufacturer hereby declares that the LM-ProPower CombiLED unit Class I, type B according to EN60601-
1 equipped with original accessories conforms to the essential requirements of the Medical Device Directive
93/42/EEC with reference to the following harmonized standards:
IEC 60601-1, Third edition 2005 EN 60601-1: 2006.
Classification: Medical products, Class IIa:
WARNING
Do not make modications to this product.

Safety instructions
8
2.6. EMC Guidance and manufacturer’s declaration
Guidance and manufacturer’s declaration - electromagnetic emissions
The LM-ProPower is intended for use in the electromagnetic environment specified below.
The customer or the user of the LM-ProPower should assure that it is used in such an environment.
Emission test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 The LM-ProPower uses RF energy only for its internal function.
Therefore, it’s RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions CISPR 11 Class B
The LM-ProPower is suitable for use in all establishments, in-
cluding domestic establishments and those directly connected
to the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not applicable
Guidance and manufacturer’s declaration - electromagnetic immunity
The LM-ProPower is intended for use in the electromagnetic environment specified below. The customer or the user of the
LM-ProPower should assure that it is used in such an environment.
Immunity test IEC 60601
test level
Compliance level Electromagnetic environment -
guidance
Electrostatic discharge
(ESD)
±6 kV contact ±6 kV contact Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
IEC 61000-4-2 ±8 kV air ±8 kV air
Electrical fast transient/
burst
±2 kV for power supply
lines
±2 kV for power sup-
ply lines
Mains power quality should be that
of a typical commercial or hospital
environment.
IEC 61000-4-4 ±1 kV for input/output lines ±1 kV for input/output
lines
Surge ±1 kV differential mode ±1 kV differential
mode
Mains power quality should be that
of a typical commercial or hospital
environment.
IEC 61000-4-5 ±2 kV common mode ±2 kV common mode
Voltage dips, short
interruptions and voltage
variations on power supply
input lines
IEC 61000-4-11
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
40 % UT
(60 % dip in UT)
for 5 cycles
70 % UT
(30 % dip in UT)
for 25 cycles
<5 % UT
(>95 % dip in UT)
for 5 sec
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
40 % UT
(60 % dip in UT)
for 5 cycles
70 % UT
(30 % dip in UT)
for 25 cycles
<5 % UT
(>95 % dip in UT)
for 5 sec
Mains power quality should be that of
a typical commercial or hospital en-
vironment. If the user of the LM-Pro-
Power requires continued operation
during power mains interruption, it is
recommended that the LM-ProPower
be powered from an uninterruptible
power supply or battery.
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields
should be at levels characteristic of a
typical location in a typical commercial
or hospital environment.
NOTE UTis the AC mains voltage prior to application of the test level.

Safety instructions
9
Guidance and manufacturer’s declaration - electromagnetic immunity
The LM-ProPower is intended for use in the electromagnetic environment specified below.
The customer or the user of the LM-ProPower should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance
level
Electromagnetic environment -
guidance
Portable and mobile RF communications
equipment should be used no closer to any
part of the LM-ProPower including cables,
than the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m
80 MHz to 2.5 GHz
3 V
3 V/m
Recommended separation distance:
d = 1.2√P
d = 1.2√P 80 MHz to 800 MHz
d = 2.3√P 800 MHz to 2.5 GHZ
where P is the maximum output power rat-
ing of the transmitter in watts (W) according
to the transmitter manufacturer and d is
the recommended separation distance in
metres (m).
Field strengths from fixed RF transmitters
as determined by an electromagnetic site
survey,ashould be less than the compliance
level in each frequency range b.
Interference may occur in the vicinity of
equipment marked with the following
symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
aField strengths from fixed transmitters, such as base stations fro radio (cellular/cordless) telephones and land
mobile radios amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic
site survey should be considered. If the measured field strength in the location in which the LM-ProPower is
used exceeds the applicable RF compliance level above, the LM-ProPower should be observed to verify normal
operation. If abnormal performance is observed additional measures may be necessary, such as reorienting or
relocating the LM-ProPower.
bOver the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Safety instructions
10
Recommended separation distances between
portable and mobile RF communications equipment and the LM-ProPower
The LM-ProPower is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled. The customer or the user of the equipment can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the LM-ProPower as
recommended below, according to the maximum output power of the communications equipment.
Rated maximum
output power of
transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d = 1.2√P
80 MHz to 800 MHz
d = 1.2√P
800 MHz 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 rated at a maximum output power not listed above, the recommended separation distance d in metres
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.

Content of delivery
11
3. CONTENT OF DELIVERY
Carefully unpack your LM-ProPower CombiLED unit and verify all accessories and components are included to
the content list below. If anything is missing contact your place of purchase.
3.1. Content of unit
6a
7
6b
8
1
3 2
12
11
9
10
4
5
1 LM-ProPower CombiLED unit 7 Air hose 6 mm (1/4”)
2 Scaler handpiece connected to unit 8 Foot control cable
3 Foot control unit 9 Power cord
4 Polisher introkit (content varies depending
on the order)
10 AirLED tubing with handpiece
5 Scaler introkit (content varies depending
on the order)
11 Powder container
6a (*) Water hose 6 mm (1/4”) 12 LM-ProPower fixer
6b (*) 500 ml medicament bottle
(*) depending of the type of the device
3.2. General description
LM-ProPower CombiLED combines an effective piezoelectric UltraLED scaler and an AirLED Polisher in one
versatile and ergonomic appliance. The device’s LED lights, advanced electronics, quality, and high-durability
LM-DuraGradeMAX tips enhance the execution of procedures which require great precision. Ergonomically
designed LM-ErgoGrip handpieces with soft silicone handles give the user a comfortable, relaxed grip as well as
an excellent feel.
LM-ProPower is highly adaptable to any procedure or user approach. It is not only an outstanding scaling
and cleaning device. It also brings power and versatility to endodontics, implantology, restorative treatments,
minimally invasive treatments and apical surgery.

Content of delivery
12
3.3. CombiLED unit
8
7
2
3
4
6
9
1
5
1 LM-ProPower CombiLED unit 7 Powder container
2 Depressurisation button 8 Polisher handpiece incl. tubing
(with an ErgoGrip and a nozzle mounted )
3 Medicament bottle 9 Control panel
4 Scaler Handpiece
(with an ErgoGrip and a tip installed)
5 Scaler water flow control ring
6 Foot control unit

Content of delivery
13
3.4. Coupling and type plate
2
1
6 5 4
3
1 Fuse holder
2 Type plate
3 Foot control connection
4 AC power input
5 Water hose coupling (optional)
6 Air hose coupling
3.5. Control panel
1
15
14
13
12
10
11
9
8
2
7
3
4
6
5
1 Cleaning key
2 Working mode 3 key
3 Working mode 2 key
4 Working mode 1 key
5 Polishing mode indicator
6 Polishing mode key
7 Standby indicator
8 Scaling mode key
9 Scaling mode indicator
10 Irrigation mode indicator (Scaler) Water-Jet mode
indicator (Polisher)
11 Working mode 1 indicator
12 Dry mode indicator (Scaler)
Air-Blow mode indicator (Polisher)
13 Working mode 2 indicator
14 Working mode 3 indicator
15 Cleaning mode indicator

Content of delivery
14
3.6. Medicament bottle (optional)
LM-ProPower has a medicament dispenser system, making the device independent of a fixed water supply
connection. The medicament bottle can be used for either medicament solutions or ordinary clean water.
Approved medicament solutions:
• Clean water
• Cetylpyridinium chloride
• Chlorhexidine
• Essential oils
• Hydrogen peroxide, 3% USP
• Povidine Iodine, 10% solution
• Saline solution
• Sangurinara extract
• Sodium hypochlorite 1% solution
The unit contains an electrically driven air compressor. When operating, the compressed air forces the fluid from
the bottle through the hose and to the handpiece and to the tip/nozzle.
1 2
3
1 Medicament bottle
2 Bottle connector
3 Depressurisation button
3.7. AirLED Polisher
1
2
4
3
1 O-ring (installed in cap)
2 AirLED tubing with handpiece
3 Water flow control
4 Powder container

Content of delivery
15
3.8. Foot Control unit
3
2
1
1 Foot control unit body
2 Foot control pedal
3 Connector for foot control cable

Content of delivery
16
3.9. Symbols on the equipment
Working mode 1
Working mode 2
F
Working mode 3
Irrigation/Water-Jet mode
Dry/Air-Blow mode
Automatic cleaning function
Scaling function
Polisher function
Example of type plate. The type plate is placed on the back side of the unit.
Medical electrical equipment classified by ETL with respect to electric shock, fire, mechanical, and
other specified hazards in accordance with the Safety Standards
ANSI/AAMI ES 60601-1 and CAN/CSA C22.2 No 60601-1:08
Caution
Consult accompanying documents
Compliance label indicating compliance with the Medical Device Directive 93/42/EEC. 0537 is the
ID-number of the Notified Body: VTT
Withstands autoclave temperature 135°C (275°F).
Type B applied part according to the degree of protection against electrical shock.
Fuse
Input
Output
Please do not throw the equipment into the domestic refuse. Please use the return and collection
systems available in your country for the disposal of this product. The equipment can also be
returned to the manufacturer for disposal.

Taking CombiLED in to use
17
4. TAKING COMBILED IN TO USE
NOTICE!
The product should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the product must be observed to verify
correct operation in the conguration in which it will be used.
NOTICE! Special skills required. Consult an approved technician to connect the unit to
the air and water supply.
NOTICE! Do not put the unit on or adjacent to a heat source. Excessive heat can damage
the electronics.
NOTICE! Product is not suitable for use in the presence of ammable gases.
4.1. How to install the unit
• Put the unit horizontally with the handpieces in the
holders and the hose hanging free.
• Put the unit where air is free to circulate on all
sides and below it. Do not put the unit on a wall or
adjacent to heat source.
• Do not put the unit in the immediate vicinity of
sources of electromagnetic radiation, for example
an electro surgery equipment.
• Connect the foot control cable to the foot control
and at rear side of the unit.
• Install the scaler tubing in the grove below the unit,
as in picture.

Taking CombiLED in to use
18
4.2. How to connect the unit to the air supply
NOTICE! Use only dry and ltered compressed air.
NOTICE! Special skills required. Consult an approved technician to connect the unit to
the air supply.
1. Set the air supply OFF.
2. Verify that the air pressure obeys to the data in the
technical data section. See instructions “9. Technical
data” on page 39
3. Use only dry and filtered compressed air.
4. Push the hose onto the quick connect coupling.
5. Connect the other end of the hose to the air supply.
6. Set the air supply ON.
7. To disconnect, push orange ring and pull tubing out
when orange ring still is pushed in.
4.3. How to connect the unit for tap water (optional)
NOTICE! Special skills required. Consult an approved technician to connect the unit to
the water supply.
1. Set the water supply OFF.
2. Verify that the water pressure obeys to the data
in the Technical data section. See instructions “9.
Technical data” on page 39
3. Verify that the water supply fulfils the medical
demands of hygiene.
4. Push the hose onto the quick connect coupling.
5. Connect the other end of the hose to the water
supply.
6. Set the water supply ON.
7. To disconnect, push orange ring and pull tubing out
when orange ring still is pushed in.

Taking CombiLED in to use
19
4.4. How to connect the unit to the supply current
WARNING
ELECTRICAL HAZARD! Connect the unit to an AC power outlet supplied with
a protective ground. USA and Canada: The power cable and plug must be
classied as “Hospital Grade”.
1. Verify that the voltage rating shown above type plate match the voltage of the AC power outlet.
2. Verify that the AC power supply is supplied with the protective ground.
3. Connect the power cable to the unit and the AC power supply. All indicator lamps illuminates for a short
period when the unit does a self check.
4. The unit is standby when the green lamp is illuminated.

Operating instructions UltraLED Scaler
20
5. OPERATING INSTRUCTIONS ULTRALED SCALER
WARNING
PERSONAL INJURY HAZARD! Do not use the scaler on patients with cardiac
pacemakers. The scaler may disturb the function of the pacemaker.
WARNING
PERSONAL INJURY HAZARD! New tips are not sterilized upon delivery. Sterilize
tips before use. Non-sterilized tip may cause infection to the patient.
WARNING
ELECTRICAL HAZARD! Do not use damaged or worn-out handpiece. Damaged
handpiece may expose the user or the patient for the electrical shock.
WARNING
PERSONAL INJURY HAZARD! Do not use a tip that is bent, altered worn more
than 2 mm. Prolonged use may cause tip breakage and injury to the patient.
Notice that ultrasonic instruments with small diameters are subject to breakage
at any time. If not used correctly or with too much power or force the instrument
will break.
CAUTION
PERSONAL INJURY HAZARD! Do not use nickel-titanium root canal les with
le holder. Nickel-titanium les breaks easily at high frequencies and may cause
injury to the patient or to the user.
5.1. How to install UltraLED Scaler to use
PREPARATIONS (BOTTLE VERSION)
1. Fill the medicament bottle with water or with approved medicament solution. Refer to the approved
medicament solutions, See instructions “3.8. Medicament bottle (optional)” on page 14.
2. Turn the bottle cap onto the bottle and push it onto the connector.
3. Make sure that the unit is connected to the compressed air supply and the power cable is connected.
Make sure that the unit is in standby mode, the green indicator lamp illuminates.