Planmeca Compact I Touch v2: User's Manual
Planmeca Compact I Touch v2: User's Manual
Planmeca Compact I Touch v2: User's Manual
™
EN
user's manual
10033022
The manufacturer, assembler and importer are responsible for the safety, reliability and
performance of the unit only if:
- installation, calibration, modification and repairs are carried out by qualified
authorised personnel
- electrical installations are carried out according to the appropriate requirements such
as IEC 60364
- equipment is used according to the operating instructions.
Planmeca pursues a policy of continual product development. Although every effort
is made to produce up-to-date product documentation this publication should not be
regarded as an infallible guide to current specifications. We reserve the right to make
changes without prior notice.
COPYRIGHT PLANMECA
Publication number 10033022 Revision 23
Released 10 January 2022
Table of contents
1 Introduction................................................................................................................................................. 1
1.1 Disclaimer.......................................................................................................................................1
2 Associated documentation..........................................................................................................................2
3 Training.......................................................................................................................................................4
4 Registering your product.............................................................................................................................5
5 Annual maintenance................................................................................................................................... 6
6 Symbols on product labels..........................................................................................................................7
7 For your safety..........................................................................................................................................10
7.1 Safety precautions........................................................................................................................10
7.2 Safety switches.............................................................................................................................15
7.3 Stopping chair movements quickly............................................................................................... 16
7.4 Reporting serious incidents.......................................................................................................... 17
8 Planmeca Compact i dental unit............................................................................................................... 18
8.1 Unit configuration..........................................................................................................................18
8.1.1 Over-the-patient delivery with balanced instrument arms............................................ 18
8.1.2 Over-the-patient delivery with hanging-tube instruments.............................................20
8.1.3 Side delivery with hanging-tube instruments................................................................21
8.1.4 Mobile cart with hanging-tube instruments...................................................................22
8.1.5 Independent cart with hanging-tube instruments......................................................... 23
8.2 Detachable parts.......................................................................................................................... 23
8.3 Applied parts.................................................................................................................................27
8.4 Bowl..............................................................................................................................................27
8.5 Monitor..........................................................................................................................................29
8.6 Mobile and independent cart........................................................................................................ 29
8.7 Tablet holder.................................................................................................................................30
8.8 USB connectivity.......................................................................................................................... 31
8.8.1 Instrument console.......................................................................................................31
8.8.2 Cuspidor.......................................................................................................................32
8.9 Water and air quick-connectors....................................................................................................32
8.10 Planmeca Romexis connection.................................................................................................... 33
8.11 Planmeca ProX X-ray unit............................................................................................................ 34
8.12 Planmeca intraoral scanner..........................................................................................................34
9 Planmeca Solanna and Planmeca Solanna Vision operating lights......................................................... 36
10 Instrument system.................................................................................................................................... 37
10.1 Delivery arms................................................................................................................................37
10.1.1 Over-the-Patient (OP) delivery arm..............................................................................37
10.1.2 Side delivery arm......................................................................................................... 38
10.2 Instrument console....................................................................................................................... 39
10.2.1 Instrument console with balanced instrument arms..................................................... 39
10.2.2 Instrument console with hanging-tube instruments......................................................41
10.3 Quick-connector hoses.................................................................................................................41
10.4 Instrument functions..................................................................................................................... 43
10.4.1 Instrument spray.......................................................................................................... 44
22.1 Language....................................................................................................................................114
22.2 Bowl rinse................................................................................................................................... 115
22.3 Cup fill.........................................................................................................................................115
22.4 Timer.......................................................................................................................................... 116
22.5 Door open / assistant call........................................................................................................... 117
22.6 Planmeca Solanna and Planmeca Solanna Vision operating light.............................................118
22.6.1 Indicator lights............................................................................................................ 118
22.6.2 Switching operating light on/off.................................................................................. 120
22.6.3 Switching composite mode on/off.............................................................................. 121
22.6.4 Adjusting intensity of operating light...........................................................................122
22.6.5 Adjusting intensity of operating light in composite mode........................................... 124
22.6.6 Changing light tone of operating light.........................................................................125
22.7 Planmeca Solanna Vision camera..............................................................................................126
22.7.1 Starting to use cameras............................................................................................. 127
22.7.2 Adjusting camera settings from dental unit................................................................ 129
22.7.3 Switching video streaming on/off............................................................................... 131
22.7.4 Recording video......................................................................................................... 132
22.7.5 Capturing image.........................................................................................................133
22.8 X-ray film viewer......................................................................................................................... 134
23 Operating instruments............................................................................................................................ 135
23.1 Instrument logic.......................................................................................................................... 135
23.2 Micromotor..................................................................................................................................136
23.2.1 Speed/power.............................................................................................................. 136
23.2.2 Reverse rotation.........................................................................................................137
23.2.3 Speed/power limit.......................................................................................................137
23.2.4 Instrument spray........................................................................................................ 137
23.2.5 Momentary spray....................................................................................................... 139
23.2.6 Automatic chip blow................................................................................................... 139
23.2.7 Manual chip blow....................................................................................................... 139
23.2.8 Instrument light...........................................................................................................140
23.3 Bien-Air MCX micromotor...........................................................................................................141
23.3.1 Torque........................................................................................................................141
23.3.2 RPM........................................................................................................................... 142
23.4 Bien-Air MX2 micromotor........................................................................................................... 142
23.4.1 Torque........................................................................................................................143
23.4.2 RPM........................................................................................................................... 144
23.4.3 Presets....................................................................................................................... 144
23.5 Bien-Air MX-i micromotor........................................................................................................... 145
23.5.1 Sterile water............................................................................................................... 146
23.5.2 Torque........................................................................................................................146
23.5.3 RPM........................................................................................................................... 146
23.5.4 Presets....................................................................................................................... 147
23.6 Morita TORX micromotor............................................................................................................147
23.6.1 Torque........................................................................................................................148
23.6.2 RPM........................................................................................................................... 149
23.6.3 Apical action...............................................................................................................150
23.6.4 Presets....................................................................................................................... 151
23.7 Apex locator................................................................................................................................154
23.7.1 Before using apex locator.......................................................................................... 154
23.7.2 Using apex locator..................................................................................................... 157
23.7.3 Testing apex locator function..................................................................................... 160
23.8 Turbine....................................................................................................................................... 162
23.8.1 Speed/power.............................................................................................................. 162
23.8.2 Quickstart................................................................................................................... 162
31.1 Overview.....................................................................................................................................267
31.2 Help messages in short form......................................................................................................268
31.3 Error messages in short form..................................................................................................... 277
31.3.1 General error messages............................................................................................ 277
31.3.2 Power supply related error messages........................................................................280
31.3.3 Control panel related error messages........................................................................281
31.3.4 Instrument related error messages............................................................................ 281
31.3.5 Instrument multiplexer related error messages..........................................................282
31.3.6 Suction holder related error messages...................................................................... 284
31.3.7 Foot control related error messages.......................................................................... 284
31.3.8 Operating light related error messages......................................................................285
31.3.9 Separator system related error messages................................................................. 286
31.3.10 Patient chair related error messages......................................................................... 286
31.3.11 Main CPU related error messages.............................................................................287
31.3.12 Headrest related error messages...............................................................................287
31.3.13 ActiveAqua related error messages........................................................................... 288
31.3.14 Water leak related error messages............................................................................ 289
31.3.15 Maintenance related errors........................................................................................ 289
31.3.16 Software upgrade error messages.............................................................................289
31.3.17 Error messages generated by control panel.............................................................. 290
31.4 Viewing help and error message history.................................................................................... 290
32 Consumables..........................................................................................................................................294
33 Disposal.................................................................................................................................................. 299
34 Technical information..............................................................................................................................300
34.1 Technical specifications..............................................................................................................300
34.2 Instrument classifications........................................................................................................... 303
34.3 Dimensions.................................................................................................................................304
34.3.1 Positioning of patient, dentist and assistant............................................................... 304
34.3.2 Patient area................................................................................................................305
34.3.3 Over-the-patient delivery with balanced instrument arms.......................................... 307
34.3.4 Over-the-patient delivery with hanging-tube instruments...........................................308
34.3.5 Side delivery with hanging-tube instruments..............................................................310
34.3.6 Cart............................................................................................................................ 312
34.4 Planmeca Compact i dental unit water consumption..................................................................313
35 Planmeca as EU importer.......................................................................................................................314
36 Certifications........................................................................................................................................... 315
36.1 CE...............................................................................................................................................315
36.2 EU Declaration of Conformity for PlanID RFID-reader............................................................... 315
36.3 EAC Declaration of Conformity for PlanID RFID-reader.............................................................315
36.4 FCC Class B Notice for wireless foot control..............................................................................315
36.5 FCC Class B Notice for PlanID RFID-reader..............................................................................315
36.6 Industry Canada (IC) Compliance Statement.............................................................................316
36.7 Industrie Canada (IC) Déclaration de conformité....................................................................... 316
36.8 RF Exposure...............................................................................................................................316
1 Introduction
The Planmeca dental unit is an electrically controlled dental device that
consists of a patient chair, cuspidor, delivery arm, dental instruments,
operating light and a foot control. The Planmeca dental unit is meant to be
used for dental treatment by dental care professionals.
This manual describes the Planmeca dental unit and how to use it.
Depending on the configuration of your dental unit, this manual may contain
parts that do not apply to your dental unit. Please read this manual carefully
before using the unit.
NOTE
The use of the Planmeca dental unit is allowed only under the supervision of
dental care professionals.
NOTE
This manual is valid for software revision 7.12.3 or later.
NOTE
In error situations, this manual is the primary source of information.
NOTE
For information on OEM products, please refer to OEM documentation.
All button illustrations indicate that the button on the control panel should be
pressed. Pressing a button will either switch a function on or off, depending
on the original setting, or change the value.
The settings and values shown in this manual are only examples and should
not be interpreted as recommended values unless otherwise stated.
1.1 Disclaimer
NOTE
IMPORTANT SAFETY NOTICE!
Planmeca Solanna Vision is equipped with a network connection. Planmeca
claims no responsibility for the end user’s data security or for any
malfunction in the system that may lead to data loss. User organisation must
take care of protecting the network by using a firewall.
NOTE
IMPORTANT DATA PRIVACY NOTICE!
Planmeca Solanna Vision is equipped with camera and microphone
functionalities. These can be used to record patient and employee
personal data. User organisation must take into account national regulations
concerning the fundamental rights and freedoms of natural persons and in
particular their right to the protection of personal data.
2 Associated documentation
This Planmeca dental unit is delivered with the following manuals and
diagrams:
• User’s manual
For dental care professionals. Describes the dental unit and its different
parts as well as instructs how to operate and clean the dental unit.
• Installation manual
For service personnel. Describes how to install the dental unit.
NOTE
Use the installation template (included in delivery) to position the unit
correctly.
• Technical manual
For service personnel. Gives instructions for service situations.
• Wiring diagrams (10030500)
• Pneumatic diagrams (30014222)
• User's manual for optional WEK water disinfection system
For dental care professionals. Gives instructions for use and
maintenance.
The intraoral X-ray unit Planmeca ProX can be installed to the Planmeca
dental unit. Planmeca ProX is delivered with the following manuals:
• User’s manual
For dental/health care professionals. Describes the intraoral X-ray unit
and its different parts as well as instructs how to operate and clean the
X-ray unit.
• Installation manual
For service personnel. Describes how to install the intraoral X-ray unit.
• Technical manual
For service personnel. Gives instructions for service situations.
3 Training
A hands-on user’s training is given in connection with the installation of this
device.
NOTE
As an alternative to navigating to the registration website as described
below, you can enter www.planmeca.com/register/ in your Internet browser.
Steps
1. Go to Planmeca's Product registration page.
1.a. Sign in to the dental unit.
1.b. Press Program.
5 Annual maintenance
To guarantee the dental unit’s proper operation, the unit must be checked
and serviced by a qualified Planmeca service technician according to the
maintenance schedule that has been set for your dental unit.
In the annual maintenance, the service technician replaces all parts
specified by the maintenance kit. These include, but are not limited to,
parts in contact with air, water and suction systems. In addition, the service
technician checks and services all dental unit parts suspect to wear and tear
in normal use. These include parts in the cuspidor, foot control, instrument
console, delivery arms, patient chair, suction arm and operating light. Also,
the mechanical stability and electrical safety inspection is performed.
The default maintenance interval is 365 days.
In the About this unit window you can check when the annual maintenance
was last performed and when it should be performed next.
A help message will remind you about the annual maintenance well in
advance.
Type BF applied part for specified dental instruments (Standard IEC 60417).
Strong magnet. Remove the tray mounting arm when treating patients who
have a cardiac pacemaker. (Standard ISO 7010.)
Note that the mains voltage is always present at the mains terminal under
the cover, when the unit is switched on. Do NOT open the cover. (Standard
IEC 60601-1.)
WARNING
No modification of this dental unit is allowed.
WARNING
Only instruments or equipment approved by Planmeca may be connected to
this dental unit.
WARNING
Do not simultaneously touch the patient and the PC.
WARNING
Do not simultaneously touch the patient and the USB ports, or any electrical
connectors of external instrument modules.
WARNING
Do not touch the patient when opening the cuspidor door or when the
cuspidor door is open.
WARNING
Applies only to Planmeca dental units without a patient chair
Do not lift the patient when the patient is placed under the delivery arm. Risk
of trapping!
WARNING
Maintenance procedures shall not be performed while equipment is in use
with a patient.
WARNING
The patient must not be in contact with instruments when the patient is
resuscitated with a defibrillator.
WARNING
The worm screw securing nut (1) in the chair lift motor must always be
attached to the worm screw and must not be removed. If the securing nut is
faulty or displaced, immediately stop using the dental unit and contact your
Planmeca dealer.
CAUTION
A faulty or broken dental unit must not be used.
CAUTION
Do not perform other maintenance procedures than those instructed in this
manual.
CAUTION
When servicing the unit, always switch the unit off.
CAUTION
Guide the patient to sit on the chair. Make sure no one sits on the legrest,
the backrest or any other part of the dental unit.
CAUTION
When the patient is in the chair, ensure that the patient’s arms and legs are
resting on the chair.
CAUTION
Do not allow the patient to grab the operating light or its arm when getting
seated or getting up from the patient chair.
CAUTION
Instrument hoses have a limited lifespan and should be replaced after 5
years of use.
CAUTION
Drops of water on the touch display might disturb the functioning of the
control panel.
CAUTION
Lock the control panel from the Maintenance window before using a table-
top instrument.
CAUTION
The dental unit must not be used simultaneously with the intraoral X-ray unit
Planmeca ProX.
CAUTION
The light source of the operating light may cause retinal injury if viewed upon
directly.
Protect the patient’s and dental treatment staff’s eyes with protective glasses
that block high-energy visible light (HEV light), or limit the direct exposure to
4 minutes.
CAUTION
Switch off the unit before using an electrosurgical knife.
CAUTION
The use of the electrosurgical knife may affect the function of an
implanted pacemaker or defibrillator. Please refer to the manufacturer’s own
documentation.
CAUTION
Do not use the scaler or the polymerisation light on patients with cardiac
pacemakers. The instrument can cause disturbance on the pacemaker’s
function.
CAUTION
Electromagnetic interference between the equipment and other devices
can occur in very extreme conditions. Do not use the equipment in close
conjunction with sensitive devices, or devices creating high electromagnetic
disturbances.
CAUTION
Do not use the equipment in close conjunction with anaesthetic gas or in
highly oxygenated environments (oxygen content >25%).
CAUTION
Before using the dental unit, ensure that the instruments have been properly
flushed and that the suction tubes as well as the dental unit’s waterlines
have been cleaned as instructed in this manual.
CAUTION
If the drain is blocked, the dental unit might overflow with contaminated
water and excessive water could flow onto the floor. Shut down the unit and
contact your property's caretaker and your Planmeca dealer.
CAUTION
When a water leak is detected, error E90 is displayed. Turn off the clinic’s
main water tap and contact your Planmeca dealer.
CAUTION
For surgical procedures, use sterile irrigating solutions, such as sterile water
or saline. Appropriate delivery devices should be used to deliver sterile
irrigating solutions during surgery. This may include a dedicated surgical
irrigation system with components including handpieces that are single-use
disposable or compatible with heat sterilisation methods used in outpatient
dental settings.
CAUTION
A power cut will shut down the software-controlled backflow prevention
system. If you are using a turbine without a built-in backflow prevention
system, contaminated water can enter into the turbine and turbine hose in
the event of a power cut.
CAUTION
In extreme operating conditions the temperature of the chair lift and backrest
motors might rise significantly. DO NOT TOUCH THE MOTORS!
CAUTION
In extreme operating conditions the surface temperature of the seat
upholstery may rise to 44°C (111°F). When applying maximum allowed load
on the patient chair in hot climate conditions, ensure sufficient time for the
seat upholstery to cool down.
NOTE
Before switching on the dental unit, make sure that the main water feed, air
pressure and suction motor are turned on.
NOTE
National regulations concerning the quality of dental water and dental air
must be followed when using the Planmeca dental unit.
NOTE
The water used by the dental unit instruments and cup fill are to be used for
rinsing only. For more information, please contact your Planmeca dealer.
NOTE
The main water feed must be turned off when the dental unit is not in use.
NOTE
If your dental unit is not equipped with an internal water/waterline cleaning
system, you must connect the dental unit to an external water/waterline
cleaning system.
NOTE
The user must monitor the microbial load of the water used by the dental
unit.
NOTE
If using air abrasives, please consult instructions for use given by the air
polisher manufacturer. Make sure that adequate flushing of dental unit is
performed immediately after using air polishers.
NOTE
The air used by the dental unit instruments must be dry, clean and oil-free.
NOTE
Never place heavy objects or containers of liquid on any part of the unit or
hang objects from the unit’s arm structures.
NOTE
Care should be taken when other movable equipment is used in conjunction
with the dental unit.
NOTE
The dental unit shall only be connected to a trusted private network (and not,
for example, the Internet).
NOTE
EMC requirements have to be considered, and the equipment must be
installed and put into service according to the specific EMC information
provided in the accompanying documents.
NOTE
Portable and mobile RF communications equipment can affect the dental
unit.
NOTE
External equipment intended for connection to signal input, signal output or
other connectors, shall comply with relevant IEC standard (e.g. IEC 60950
for IT equipment and the IEC 60601 series for medical electrical equipment).
In addition, all such combinations - systems - shall comply with the IEC
60601-1 standard. Equipment not complying to IEC 60601-1 shall be kept
outside the patient area.
Any person who connects external equipment to signal input, signal output
or other connectors has formed a system and is therefore responsible for the
system to comply with the requirements of IEC 60601-1. If in doubt, contact
a qualified technician or your local representative.
NOTE
If the wireless foot control has been idle for 2 hours and has gone to sleep
mode, you must press the handle twice to stop the chair movements. (The
first press wakes the foot control up from sleep mode and the second press
stops the movements.)
This type of dental unit configuration has the option of a shorter OP delivery
arm (340 mm). The shortened console arm (1) allows easy access to the
patient chair if the instrument console is placed on the assistant's side during
patient change. The shortened console arm is especially well suited for
dental units without bowl.
Headrest
The following detachable components are not critical to operation. The user
can perform dental treatment even if a wrong, similar part is fitted.
Hygienic membrane
HT instrument holder
Armrests
Disposable filters
Suction tubes
Foot cover
8.4 Bowl
CAUTION
Do not allow the patient to grab the bowl when getting seated or getting up
from the patient chair.
NOTE
Always place the bowl in home position.
NOTE
Make sure that the bowl is not above the patient chair when you drive the
chair upward.
1 Home position
2 To avoid a collision between the patient chair and the bowl when
driving the chair upward, position the bowl within this area.
If the bowl assembly for some reason comes off the cuspidor, you can put it
back as follows:
1. Place the ring to the underside of the bowl assembly
This is shown by item 1 in the picture below.
2. Make sure that the peg goes into the slot as shown in the picture below.
3. Push the bowl downwards at the same time making sure that no cables
are squeezed.
4. Turn the bowl assembly into place. You will know that it is in place when
you hear the clicking sound of the micro switch
8.5 Monitor
The monitor can be moved from its handle.
CAUTION
Do not allow the patient to grab the monitor handle or monitor arm when
getting seated or getting up from the patient chair.
NOTE
Never spray water on the monitor.
NOTE
When you move the cart, for example from one room to another, it must
be in the lowest position.
Connect the wired foot control to the bottom of the cart. The foot control can
be placed on the shelf.
COI3_cart.eps
1 Wheel lock
2 Handles
3 Locking mechanism for height adjustment
4 Connector for wired foot control
5 Foot control
6 Cart connection cable
Before attaching the tablet to the tablet holder, ensure that the round mount
interface is glued to the backside of the tablet.
To attach the tablet to the tablet holder, position the mount interface towards
its counterpart on the tablet holder slightly askew so that they interlock.
Then, turn the tablet 45° to either side to lock the tablet to the tablet holder.
NOTE
Ensure that the tablet is protected from splashes.
NOTE
Planmeca is not liable for damages caused to the tablet caused by
negligence, including but not limited to dropping the tablet on the floor.
The tablet can be charged from the USB port on the cuspidor, see section
"Cuspidor" on page 32.
NOTE
Connect only intraoral cameras supplied by Planmeca to the USB port.
8.8.2 Cuspidor
There are two optional USB ports on the cuspidor.
1 Water quick-connector
2 Air quick-connector
To avoid stagnant water inside the dental unit, regularly use enough water
with external devices connected to the water quick-connector, as the quick-
connector's waterline is not included in the dental unit's flushing and cleaning
programs.
The settings for the Planmeca Romexis connection can only be changed
by a qualified Planmeca service technician. If, for example, your dental unit
configuration includes the Planmeca Romexis Clinic Management module,
but the connection is disabled (no symbol displayed on control panel),
contact your Planmeca dealer.
For information on how to use Planmeca Romexis Clinic Management
software, see Planmeca Romexis user’s manual.
CAUTION
Drive the chair carefully when positioning the ProX X-ray unit.
CAUTION
Do not drive the chair during the exposure.
CAUTION
Do not touch the external PC and the patient at the same time.
CAUTION
Move the ProX X-ray unit behind the pylon when it is not being used.
For more information about Planmeca ProX, see Planmeca ProX User’s
Manual.
Before using the scanner you must connect it to the dental unit. The
connector on the scanner must be carefully attached to the port for the
scanner on the cuspidor (1).
CAUTION
Make sure that you attach the intraoral scanner connector the right way into
the port for the scanner. If the connector is turned the wrong way, it will not
go into the port. Use of unnecessary force will break the connector.
NOTE
There are two ports on the cuspidor. One is the port for the intraoral scanner,
and the other is a USB port. Make sure you attach the connector to the right
port.
NOTE
To avoid splashes on the scanner, remove it from the dental unit after use
and place it on the table stand.
For more information about the intraoral scanner, see Planmeca FIT user’s
manual.
You can operate the Planmeca Solanna operating light either from the light
itself, or from the dental unit’s control panel or foot control. It also features
a “no touch” function, which means that you can operate the light by waving
your hand in front of the sensor.
The Planmeca Solanna Vision operating light has all the features of the
Planmeca Solanna operating light and is also equipped with two cameras
and a microphone that can be used for video streaming, capturing still
images and recording videos.
You can operate the Planmeca Solanna Vision operating light either from
the light itself, from the dental unit’s control panel or foot control, or from
Planmeca Romexis software. All data is stored in Planmeca Romexis.
For information on how to operate the operating light, see section "Planmeca
Solanna and Planmeca Solanna Vision operating light" on page 118.
For information on how to operate the camera, see section "Planmeca
Solanna Vision camera" on page 126.
For instructions on how to program the operating light, see section
"Planmeca Solanna and Planmeca Solanna Vision operating lights" on page
201.
10 Instrument system
10.1 Delivery arms
CAUTION
Do not lean on the OP delivery arm.
CAUTION
Do not allow the patient to grab the OP delivery arm when getting seated or
up from the patient chair.
The instrument console can be positioned using the handles on the console.
The rotation area of the delivery arm is presented in the illustrations below.
The items do not need to be locked into position.
The following presents the OP delivery arm with balanced instrument arms.
CAUTION
Do not stand on the side delivery arm.
The rotation area of the side delivery arm is presented in the illustration
below.
1. Syringe
The instrument arms can be removed by pulling them out from their holders,
for example for cleaning or for covering with protective sleeves. The arms
are replaced simply by pushing them firmly into their places.
1. Roller
2. Hose guide
3. Instrument arm
When placing the instrument hose back in the roller, bend the hook of the
hose guide carefully and pass the hose over the roller.
The balance of the instrument arms can be changed according to the weight
of the instrument and personal preferences. Their flexibility can be adjusted
as follows:
1. Pull out the roller.
2. Adjust the balance of the instrument arm by moving the roller to a
desired position. Note that by positioning the roller higher up, the arm
is lighter to bend.
3. Push the roller back in to lock its position
NOTE
When balancing/adjusting the instrument arms, bear in mind that the
instruments shall under no circumstances fall over the patient.
The instrument holders can be removed by pulling them out from their
openings, for example for cleaning. The holders are replaced simply by
pushing them firmly into their places. The angle of the instrument holder can
be slightly adjusted.
1. Instrument hose
2. Quick-connector
Switch the unit off before opening the quick-connectors. When disconnecting
the syringe, empty the water and air from the hose before opening the
connector.
The instrument location on the instrument console can be changed simply by
removing the instrument with its hose and reconnecting it to the new place.
The old instrument settings will remain the same despite of the new location
of the instrument hose.
The instrument selection on the instrument console can also be
interchanged. The settings of the eight last used instruments are stored in
the memory, and are recalled when the instrument is reconnected.
NOTE
Make sure that the hoses are properly connected to avoid any leakage.
NOTE
Always make sure that the instrument hose is correct for the used
instrument. The control system identifies the instrument hose, not the
instrument. The control system does not recognise if an instrument has been
changed on the instrument hose.
NOTE
If the outer casing of the instrument hose is broken, the entire hose must be
replaced, although the hose itself might still be functioning.
NOTE
The instrument sealings must be correct and unbroken, and the instrument
must be attached properly to the hose connector. The leakage between the
instrument and the connector causes leakage air to drift into the hose lining.
NOTE
A scaler requires additional electronics and the scaler type can not be
changed without changing electronics.
NOTE
The instrument speed/power limit does not affect the air driven instruments
for which quickstart has been selected.
10.5 Trays
The tray mounting arm is attached to the instrument console with a quick-
connector. To remove the tray assembly from the instrument console, pull
the ring of the locking mechanism outwards (1) and then pull the tray arm
away from its position (2).
The integrated tray is located on the left side of the instrument console.
The tray is attached to the mounting arm with a magnetic connector and
can easily be attached and detached. You can rotate the table 180° to the
desired position. The maximum load on the quick-connect tray is 2 kilograms
(4.4 lbs).
10.6.1 Introduction
When the sterile water system is used, sterilised water is fed from a
disposable sterile water bag through an external disposable tube to a
surgical handpiece or scaler. The instrument must have an externally
mounted spray nozzle on which the sterile water tube is fitted.
CAUTION
Before using an instrument with sterile water, make sure water comes out
from the instrument.
CAUTION
The sterile water system can only be used with surgical handpieces that are
intended for sterile use, as well as with scalers with external sterile water
connection. If other instruments are used, the system is not sterile.
CAUTION
To ensure sterile conditions, extra precaution should be taken to make sure
that correct procedures are followed and all the components and tools used
(e.g. scissors) are sterile.
CAUTION
The sterile water bag, nozzle and tubes are disposable and intended for
single use only.
CAUTION
Inspect sterile packaging for damage. If sterile packaging is damaged, the
item must not be used.
CAUTION
The attachment of the sterile water bag, nozzle and tubes to the dental unit
is to be performed by dental personnel only.
CAUTION
Be careful not to squeeze your fingers in the water pump.
NOTE
When using sterile water, be careful not to step on the sterile water tubes or
otherwise squeeze them.
Refer also to the documentation delivered with the sterile water bag and the
sterile water tube.
2. Open the lid of the water pump and place the silicone part of the sterile
water tube in the pump.
Make sure that the sterile water tube is inserted so that water is pumped
from the sterile water bag to the instrument. The arrow on the pump
indicates the direction of the water flow, away from the bag and toward
the instrument.
7. In OP deliveries, attach the long end of the sterile water tube to the OP
delivery arm with the clips included in the sterile water tube package.
8. Enable sterile water from the instrument spray settings. See section
"Enabling/disabling sterile water mode" on page 186.
11 Suction system
11.1 Suction arms
NOTE
If the chair is equipped with a chair-mounted left/right suction arm, make
sure that the Flexy-holder does not hit the cuspidor when driving the chair
up.
NOTE
If the chair is equipped with a chair-mounted left/right suction arm, make
sure that the Flexy-holder is not above the cuspidor when driving the chair
down. If the chair does not move downward and H 03 is displayed, check
that the chair-mounted arm is not in the upmost position. This arm position
prevents the chair from moving downward.
11.2 Flexy-holder
The suction handpieces are placed in the Flexy-holder.
The Flexy-holder is a suction holder that is attached to the suction arm.
Its integrated control panels enable you to control selected functions of the
dental unit. For more information on the control panel, see section "Control
panel on Flexy-holder" on page 76.
The Flexy-holder has three openings. The two left-most openings can be
equipped with suction handpieces and the right-most with the assistant’s
syringe. In addition, one or two supplementary holders or a holder for the
intraoral scanner can be placed on either side of the Flexy-holder. The
supplementary holder can be equipped with a USB intraoral camera or a
polymerisation light.
NOTE
The intraoral scanner and the USB intraoral camera can not be
simultaneously attached to the Flexy-holder. If the intraoral scanner is
placed in the Flexy-holder, the USB intraoral camera can be placed in the
instrument console.
Removing holders
The suction tube, instrument and supplementary holders can be removed
from the Flexy-holder, for example for cleaning.
Remove the suction tube holder by pulling it downward from the Flexy-
holder. To replace it, push it firmly into its place.
Remove the roller from the suction tube holder by pulling it away from the
holder. To replace it, push it firmly into its place.
Remove the instrument holder by squeezing it from the bottom and at the
same time lifting it upward. To replace it, squeeze the holder and insert it into
its place.
Steps
1. To minimise contamination risk, perform suction cleaning.
For instructions, see section "Suction cleaning" on page 221.
2. Remove the side cover plate by pulling it out from the cuspidor.
3. Detach the securing ring (1) from the suction tube.
NOTE
You can grease the securing ring with non-toxic vaseline to make it
easier to remove.
4. Remove the suction tube (2) from the suction tube connector.
12 Patient chair
CAUTION
Make sure no one sits on the legrest or the backrest.
NOTE
The patient chair can be equipped with a fixed or an automatic legrest.
NOTE
If, for example, the patient feels sick and starts to vomit while lying in the
chair, you can raise the backrest quickly by pushing it up by hand from
behind the backrest. Note, however, that the backrest does not stay up by
itself but must be supported the whole time and lowered in a controlled
manner.
NOTE
Dark coloured clothes may cause coloured stains on the bright coloured
upholstery.
When the chair is empty, an Empty chair icon is displayed on the control
panel.
1. Automatic legrest
2. Lever
The automatic legrest can be locked approximately 18° from the horizontal
position. To lock the legrest, the lever has to be moved to the left. Support
the legrest with your other hand when locking or unlocking the lever. Notice
that the backrest will move upward and downward when the legrest is
locked.
1. Horizontal position
12.4 Armrests
The right armrest can be moved 90° outwards. Before you move the armrest
horizontally you must lift it slightly to unlock it. The armrest can be locked
into the positions 1 and 3 presented below. The armrest can be removed
when it is in position 2.
Surgical armrest
As an option, a surgical armrest is available. The patient’s arm can be
strapped to the armrest when, for example, infusing saline solution.
NOTE
Make sure that the patient does not lean on the armrest when getting in or
out of the chair.
To move the armrest horizontally you must lift it slightly to unlock it.
To replace the right standard armrest with the surgical armrest you must first
detach the standard armrest. To do so, lift the armrest slightly to unlock it
and move the armrest to a 45° position. When the armrest is in a 45° angle,
lift it straight up to remove it (1).
Once you have removed the standard armrest, place the surgical armrest
on the spindle in a 45° angle, push the armrest down and rotate in either
direction until it locks into place (2).
The surgical armrest is removed in the same way as the standard armrest.
NOTE
The headrest can only be pulled out as far as to the MAX mark.
Press the bar on the side of the headrest support to release the locking
mechanism and position the headrest at the top of the chair.
The headrest is now repositioned. To adjust the angle of the headrest, press
the locking bar. Manually set the headrest into the required position and
release the bar. When adjusting, support the headrest with your other hand.
13 Control panel
13.1 Control panel on instrument console
The control panel is located on the instrument console. You can use it to
control and program the instruments, the dental unit, and the chair. You can
also start maintenance procedures from the control panel.
You can operate the control panel by touching it with your finger or with a
soft stylus. The display is generally medical glove touch capable, but some
glove types have limited functionality.
The control panel shows information related to the current operation and
changes accordingly.
Some of the buttons have indicator lights that show the status of that specific
function. When the indicator light is lit, it means that the function is activated.
When the unit is in programming mode, the Program button is blue.
You can organise the items in the main window’s swipe menu according to
your preferences, see section "Organising items on control panel" on page
182.
The control panel is available in several languages and the language can be
changed from the control panel. For more information, see sections "Editing
language" on page 91 and "Language" on page 114.
NOTE
The touchpad function requires that the dental unit is connected to
Planmeca Romexis software. The software version must be 4.1 or later.
If there is no Planmeca Romexis connection, the function is disabled and the
Touchpad button is grey.
Move your finger on the control panel to move the cursor accordingly across
the monitor or tablet screen. Scroll a list or text with the scroll wheel to the
right and use the buttons at the bottom just like you would use the left and
right mouse buttons.
A short press of the left and right button clicks an item on the screen. When
you press the button for longer, the button stays activated until you release
the button by pressing it again. The button is blue when it is activated.
1. Scroll wheel
2. Left button
3. Right button
When you want to exit the touchpad-view, press OK.
Example: Drag-and-drop
Use your finger on the touchpad to move the cursor on the screen to the
item that you want to drag. When the cursor is on the item, press the left
button for 1 second to activate it. The button turns blue. With your finger on
the touchpad, drag the item to the correct location. Press the left button to
release it (the button turns grey).
In the the touchpad-view, press ABC to open the keyboard on the control
panel.
1. Chair buttons
2. Unit buttons
3. Flexy button
The function behind the Flexy button can be programmed by the service
technician. Depending on what has been programmed, you can do one of
the following by pressing the Flexy button:
• select the headrest mode (normal or tilt mode) for the motorised
headrest
• activate/deactivate the intraoral camera
• drive the chair to the rinsing position (default)
• lock/unlock the touch display
• turn the suction on/off
• turn the operating light’s composite mode on/off (short press) or adjust
its intensity (long press)
• activate/deactivate the apex locator
• change the light tone of the operating light
• turn Planmeca Solanna Vision video streaming on/off
• start/stop Planmeca Solanna Vision video recording
• capture an image with the Planmeca Solanna Vision camera
• open/close the Planmeca Solanna Vision window.
For more information, contact your Planmeca dealer.
14 Foot control
14.1 Introduction
The dental unit has one integrated foot control that operates the instruments,
the unit and the chair.
The foot control is available as a wireless and a standard version.
1. Handle
2. Left-side knob
3. Centre knob
4. Right-side knob
5. Pedal
CAUTION
The foot control is a precision instrument. Do not stand on or apply
unnecessary force to the foot control and its knobs.
CAUTION
Do not use the foot control in areas where liquids are likely to be present on
the floor.
NOTE
If you want to change from a standard pedal to the wide pedal, or vice versa,
contact your Planmeca dealer.
The two foot control pedals function differently. For example, to increase the
instrument speed, you must push the standard pedal horizontally, either to
the left or to the right. When you use the wide pedal, you increase the speed
with a vertical movement: the further down you push the pedal, the higher
the instrument speed is.
The functional differences between the standard pedal and the wide pedal
only apply to the operation of the micromotor, turbine and scaler. They
do not apply to the operation of the dental unit, chair or headrest. The
differences are described in the table below.
NOTE
When the functionality of the foot control pedal is different for the standard
pedal and the wide pedal, this is clearly indicated in the text and pictures of
this manual. When the text refers to the foot control pedal in general without
making this differentiation, the same functionality applies to both types of
pedal, although the illustration only presents the standard pedal.
NOTE
When the motorised headrest is activated, the centre knob activates other
features than those presented below. For more information, see section
"Operating motorised headrest" on page 110.
Action Function
Centre knob left Chair to automatic position A
Centre knob left, long activation Backrest down
Centre knob right Chair to automatic position B
Centre knob right, long activation Backrest up
Centre knob up Chair to automatic position C
Centre knob up, long activation Chair up
Centre knob down Chair to automatic position D
Centre knob down, long activation Chair down
Action Function
Pedal left Assistant call
Pedal down, short activation Cup fill and bowl rinse
Pedal down, long activation Cup fill for as long as the pedal is pressed
Pedal right & down Chair to rinsing position
Micromotor, turbine
Action Function
Pedal left / pedal right Drive instrument
Pedal down, short activation Change spray water & air / air / off
Pedal down, long activation Manual chip blow; activated for as long as the pedal is
pushed and held down
Scaler
Action Function
Pedal left / pedal right Drive instrument
Pedal down, short activation Change spray 1 / 2 / off
Action Function
Pedal left / pedal right / pedal down Start / stop instrument
Intraoral camera
Action Function
Pedal left / pedal right Freeze / unfreeze picture
Pedal down Save still picture
Intraoral scanner
Action Function
Pedal left Move upward in the list of scan type selection tools
Pedal right Move downward in the list of scan type selection tools
Pedal down, short activation Start scanning
Pedal down, long activation Take image
NOTE
The wireless foot control is an optional feature.
The standard foot control and the wireless foot control can not be used
simultaneously. Should such a situation occur, the standard foot control
overrides the wireless foot control.
When the wireless foot control has been idle for 2 hours, it goes into sleep
mode. You are notified about this with a message on the control panel. The
sleep mode is also indicated by a battery symbol on the control panel. Wake
up the foot control by pressing the foot control handle.
Before using the wireless foot control, check the power level of its battery.
The power level is indicated by a battery symbol on the control panel.
Power level Sleep mode Full < 40% full < 20% full
Symbol
You can also view detailed battery charging information on the control panel.
For instructions, see section "Viewing battery charging information" on page
209.
When the battery is less than 20% full you need to recharge the battery as
soon as possible.
To charge the foot control battery, connect the foot control to the power
outlet using the provided cable and power adapter. The LEDs on the foot
control blink green while the battery is being charged.
When the wireless foot control battery is full, and the foot control is
connected to the power outlet, the LEDs on the foot control are a steady
green.
CAUTION
Do not charge the foot control battery while treating a patient.
CAUTION
The battery charging area must be dry. Do not expose the charger to liquids.
NOTE
The power supply is marked and specified as a part of the Planmeca dental
unit.
NOTE
The batteries must be replaced only by a qualified Planmeca service
technician.
NOTE
The foot control batteries must be removed whenever the foot control is
stored for a longer period. The batteries must be removed only by a qualified
Planmeca service technician.
NOTE
The wireless foot control transmitter contains a radio device FCC: YI1002
and IC: 9050A-002, and the wireless foot control contains a radio device
FCC: YI1001 and IC: 9050A-001. See also section "FCC Class B Notice for
wireless foot control" on page 315.
When the unit is switched on, the on/off switch light is on.
NOTE
If your unit is equipped with a water heater, fill the cup once after switching
the unit on to start the heating. Notice that when using the water heater, the
water temperature can rise up to 46°C.
NOTE
If your dental unit is equipped with the optional Suction Tube Cleaning
System (STCS), make sure that the STCS box cover is closed when
switching the unit on.
NOTE
The sign in method depends on the dental unit’s configuration. For more
information on the configuration, or for changing it, contact your Planmeca
dealer.
NOTE
Before you can sign in with a PlanID card, you must assign a PlanID card
to your user profile. For instructions, see section "Assigning PlanID card to
user" on page 95.
If you have a PlanID card and the dental unit is equipped with a PlanID
reader, sign in by showing the PlanID card to the PlanID reader on the
instrument console.
CAUTION
At least 15 cm of separation distance between the PlanID reader and the
user's body must be maintained at all times.
To be able to sign in with your PlanID card, the PlanID connection must be
enabled. The connection status is shown in the Sign in in window.
PlanID is enabled.
If you do not have a PlanID card, you can sign in from the Sign in window by
pressing on your user name on the list. The list of users can be scrolled.
It is also possible to sign in to the dental unit as a guest user by pressing the
Guest user button in the Sign in window.
Once you have signed in, the treatment window opens and you can start
using the dental unit with your own personal settings.
Factory settings are loaded for guest users every time they sign in.
Steps
1. In the top left corner of the treatment window, press Sign out.
NOTE
Depending on the dental unit’s configuration, some users are not able to edit
their user settings. Also, if these users reset their instrument, operating light
or chair settings, the reset does not affect the settings that these users may
optionally have saved in Planmeca Romexis. For more information, contact
your Planmeca dealer.
NOTE
If your dental unit includes Planmeca PlanID, create the new user as
described in section "Assigning PlanID card to user" on page 95.
Steps
1. Press New user in the Sign in window.
For information on how to edit the user settings, see section "Editing
user settings" on page 89.
Steps
1. In the Sign in window, press Edit next to the user that you want to delete.
Your user name is deleted from the user list in the Sign in window.
NOTE
The user profile optionally saved in Planmeca Romexis is not deleted.
For more information, contact your Planmeca dealer.
• In the Sign in window, press Edit next to the user whose settings you
want to edit.
• Sign in to the dental unit and press Program > User settings.
NOTE
If your dental unit has been configured so that you cannot edit your user
settings, you can still edit the dental unit’s language as described in section
"Language" on page 114.
Steps
1. In the User settings window, press Edit next to First name.
Pressing Close exits the Set last name window without saving the user
name.
7. When you have edited all the user settings (including language, colour
theme and the automatic chair positions view), save them by pressing
OK in the User settings window.
NOTE
If your dental unit has been configured so that you cannot edit your user
settings, you can still edit the dental unit’s language as described in section
"Language" on page 114.
Steps
1. In the User settings window, press Edit next to Language.
When you press a language to select it, you will automatically return to
the User settings window.
Pressing Close exits the Program - Language window without making
changes to the language.
The available languages are:
• English
• Finnish
• German
• Spanish
• French
• Italian
• Swedish
• Hungarian
• Czech
• Danish
• Norwegian
• Russian
• Japanese
• Polish
• Traditional Chinese
• Simplified Chinese
• Romanian
• Arabic
• Dutch
• Portuguese
• Greek
• Turkish
• Estonian
• Latvian
• Lithuanian
3. When you have edited all the user settings (including user name, colour
theme and the automatic chair positions view), save them by pressing
OK in the User settings window.
Steps
1. In the User settings window, press Edit next to Color theme.
When you press a colour to select it, you will automatically return to the
User settings window.
Pressing Close exits the Program - Theme window without making
changes to the colour theme.
3. When you have edited all the user settings (including user name,
language and the automatic chair positions view), save them by pressing
OK in the User settings window.
NOTE
This reset only applies to settings stored in the dental unit. For more
information, contact your Planmeca dealer.
Steps
1. Open the User settings window.
There are two alternative ways to open this window:
In the Sign in window, press Edit next to the user whose settings you
want to reset.
OR
Sign in to the dental unit and press Program > User settings.
Before you assign the PlanID card to a user, we recommend that the
user has been created in the Admin module of Planmeca Romexis. This
is typically done by a Planmeca Romexis administrator.
The following information must be supplied when creating the user:
• In Add User window, User tab
• Username
This username is later entered in the Romexis username field in the
dental unit.
• Member of Groups
We recommend that you create a group for PlanID users and add all
PlanID users to that group.
• In Add User window, Personal tab
• First Name
• Last Name
These will be shown in the dental unit as your first and last name.
NOTE
If you have stored a picture of yourself in Planmeca Romexis software,
the picture will show in the dental unit’s User settings window and in the
Welcome-message that is displayed when you sign in to the dental unit.
Steps
1. Press New user in the Sign in window.
The username must be the same that you entered in the Add User
window in Planmeca Romexis.
Only letters A-Z and a-z, period (.), hyphen (-), underscore (_) and the
“at” sign (@) are allowed.
The Set Romexis username window closes.
5. Show the PlanID card to the PlanID reader on the dental unit.
The text PlanID tag detected is displayed.
6. Close the Assign PlanID tag window by pressing OK.
Results
Your PlanID card has now been assigned to you and you have been signed
in to the dental unit.
Steps
1. Press Program.
NOTE
The following is an example only and does not necessarily portray the
actual situation.
19.5 Service
Service contains information for service situations.
Press > to display the following items:
• Service contact details
• Annual maintenance
• Storage information
• GUI diagnostics
• PlanID
• Clock calibration
• Product registration
• Peripherals
• Dental unit model
• Screensaver
CAUTION
GUI diagnostics is only meant to be used by a qualified Planmeca service
technician.
19.5.5 PlanID
In the Details tab you can view details on the tag ID and the PlanID reader's
region of operation. To change the region, contact your Planmeca dealer.
CAUTION
The Configuration tab contains tools for enabling/disabling the PlanID reader
as well as for adjusting its power level, and is only meant to be used by a
qualified Planmeca service technician.
19.5.8 Peripherals
Peripherals contains information on and service tools for:
• Solanna operating light
• Capacitive patient sensor (Capsense)
• Planmeca ActiveAqua water treatment system
CAUTION
The tools for the Solanna operating light and the capacitive patient sensor
are only meant to be used by a qualified Planmeca service technician.
CAUTION
The Planmeca ActiveAqua annual maintenance counter is only to be reset
by a qualified Planmeca service technician.
19.5.10 Screensaver
It is possible to configure the dental unit so that a screensaver is displayed
when the Sign in window has been unused for 3 minutes. To take a standard
or custom screensaver into use, contact your Planmeca dealer.
CAUTION
The network settings may only be edited by a qualified Planmeca service
technician.
19.8 Bluetooth
When you press > next to Bluetooth, you are directed to a window where
you can enable or disable the Bluetooth connection.
19.9 Licences
Licences displays the licences used by the dental unit when you press >.
CAUTION
When driving the chair near the upper limit, make sure that the console arm
does not press or hit the patient.
CAUTION
When driving the backrest up, make sure that the patient’s hand or arm does
not get squeezed between the armrest and the backrest.
To drive the backrest down, press the Backrest down button until the chair
reaches the required position.
NOTE
If the chair is equipped with an optional automatic legrest, the legrest
position is adjusted simultaneously with the backrest position.
To drive the backrest up, press the Backrest up button until the chair
reaches the required position.
To drive the chair up, press the Chair up button until the chair reaches the
required position.
NOTE
Make sure that the bowl is not above the patient chair when driving the chair
up.
NOTE
If the chair is equipped with the chair-mounted left/right suction arm, make
sure that the Flexy-holder does not hit the cuspidor when driving the chair
up.
To drive the chair down, press the Chair down button until the chair reaches
the required position.
NOTE
If your chair is equipped with an optional automatic legrest, the lowest
possible position of the chair depends for safety reasons on the legrest
position.
NOTE
In case the chair is equipped with the chair-mounted left/right suction arm,
make sure the Flexy-holder is not above the cuspidor when driving the chair
down. If the chair does not move downward and H 03 is displayed, check
that the chair-mounted arm is not in the upmost position. This arm position
prevents the chair from moving downward.
Alternatively, you can adjust the position of the chair with the foot control.
Push and hold the centre knob in the desired direction (see picture below).
When the chair reaches the desired position, release the centre knob. You
can steer the chair only in one direction at a time.
20.2.1 Overview
Automatic chair positions can be stored into memory.
For more information on how to store the automatic positions, see section
"Automatic chair positions" on page 182.
When automatic positions have been stored into memory you can select an
automatic position from the control panel or the foot control and the chair
automatically drives to the selected position. When the chair has reached
its preprogrammed position, the position can be adjusted. To adjust the
position manually, use the foot control’s centre knob or the chair positioning
buttons on the control panel in a non-automatic mode (see section "Manual
operation" on page 103).
You can program the operating light and its composite mode to be on or
off in preprogrammed positions. The light goes off when the chair begins to
move to a position where the light has been programmed to be off, but goes
on only after the chair has reached the programmed position, where the light
has been programmed to be on. The operating light and composite mode
intensities can also be programmed to a certain value.
NOTE
If the chair is equipped with the chair-mounted left/right suction arm, make
sure the Flexy-holder is not above the cuspidor when driving the chair down.
If the chair does not move downward and H 3 is displayed, check that the
chair-mounted arm is not in its upmost position. This arm position prevents
the chair from moving downward.
• Extended view
Includes the automatic positions A, B, C, D and rinsing position in list-
format and allows renaming of positions A - D. For instructions, see
section "Extended view" on page 183.
To take the extended view into use, check the checkbox next to
Automatic positions extended in the User settings window.
• Traditional view
Includes the automatic positions A, B, C, D and rinsing position.
To take the traditional view into use, uncheck the checkbox next to
Automatic positions extended in the User settings window.
Extended view
Control panel: To move the chair to a preprogrammed position, first press
the Chair positions button in the main window. Then, in the list that opens,
select an automatic position by pressing it.
Foot control: A foot control symbol on the right side of the automatic position
on the list indicates in which direction you must push the right-side or centre
knob to drive the chair to the preprogrammed automatic position.
For information on how to adjust the preprogrammed automatic positions,
see section "Extended view" on page 183.
Traditional view
Control panel: To move the chair to a preprogrammed position, press briefly
the corresponding chair position button.
Foot control: Push the centre knob briefly to the position (A, B, C or D)
where the preprogrammed chair position has been stored. The chair will
move automatically to the preprogrammed position.
Extended view
When the chair moves to the rinsing position, the bowl on the Chair positions
button flashes throughout the movement. Filling the cup starts automatically
and the bowl is rinsed.
When the chair stops in the rinsing position, the bowl symbol on the Chair
positions button stops flashing.
To return to the previous working position, press Chair positions again
and select Working position from the list that opens. Bowl rinsing starts
automatically. An arrow on the button flashes throughout the movement.
When the chair stops, the operating light turns back on, if it was on initially.
Standard view
Press Rinsing position to move the chair to the preprogrammed rinsing
position. The indicator light flashes throughout the movement. Filling the cup
starts automatically and the bowl is rinsed.
When the chair stops in the rinsing position, the indicator light remains on
and an arrow appears below the indicator light.
When you press Rinsing position again, the chair will return to the previous
working position. Bowl rinsing starts automatically. The indicator light flashes
throughout the movement.
Foot control
You can drive the chair to the rinsing position by pushing the pedal to the far
right and down.
You can also drive the chair to the rinsing position with the foot control by
pushing down the right-side knob.
To return to the working position, push down the right-side knob again.
NOTE
Alternatively, the dental unit can be configured so that the chair moves to the
preprogrammed rinsing position when you press the Flexy button. Contact
your Planmeca dealer.
NOTE
The unit can be set up so that the Rinsing position indicator light goes off
and the previous position is not stored when you are driving from the rinsing
position to a preprogrammed position. Next time you press Rinsing position,
the chair will move to the rinsing position. Contact your Planmeca dealer.
NOTE
Automatic cup fill and bowl rinse functions when the dental unit reaches the
rinsing position are configurable; contact your Planmeca dealer.
NOTE
The water in the dental unit is intended for rinsing only, not for drinking.
1. Stop plate
2. Backrest
NOTE
Alternatively, the dental unit can be configured so that you change headrest
mode by pressing the Flexy button. Contact your Planmeca dealer.
NOTE
Do not leave your fingers under the headrest or between the headrest and
backrest when driving the headrest.
21.1.1 Joystick
If the headrest is in the tilt mode, press the joystick briefly to change the
headrest mode from tilt mode to normal mode.
1. Joystick
2. Lengthen
Push the joystick away from the backrest to drive the headrest away
from the backrest.
3. Shorten
Push the joystick toward the backrest to drive the headrest toward the
backrest.
4. Headrest up
Push the joystick up to drive the headrest up in accordance with the
movement of the anatomical tilt.
5. Headrest down
Push the joystick down to drive the headrest down in accordance with
the movement of the anatomical tilt.
The movement continues for as long as the joystick is pushed.
To activate the normal mode, briefly push the left-side knob up (factory
default).
The partially green headrest symbol on the control panel indicates that the
normal mode has been activated.
NOTE
When the dental unit is equipped with a motorised headrest, the factory
default is that the normal mode is activated by pushing the left-side knob
up. However, it is possible to configure the foot control so that the normal
mode is activated when you push the right-side knob up instead. Contact
your Planmeca dealer.
Drive the anatomical movement down (A) or up (B) by pushing the centre
knob.
Push the centre knob in direction C to lengthen and in direction D to shorten
the headrest.
The movement continues for as long as the centre knob is pushed.
NOTE
If the motorised headrest is not in the anatomical tilt line, the headrest will be
driven to this line before the anatomic tilt is adjusted. Therefore, the headrest
may first move away from the direction it is driven to.
21.2.1 Joystick
Press the joystick on the headrest for approximately 2 seconds to change
the headrest mode from normal mode to tilt mode.
1. Joystick
2. Tilt up
Push the joystick away from the backrest to tilt the headrest up and raise
the patient’s jaw.
3. Tilt down
Push the joystick toward the backrest to tilt the headrest down and lower
the patient’s jaw.
4. Headrest up
Push the joystick up to drive the headrest up in accordance with the
movement of the anatomical tilt.
5. Headrest down
Push the joystick down to drive the headrest down in accordance with
the movement of the anatomical tilt.
The movement continues for as long as the joystick is pushed.
To activate the tilt mode, push the left-side knob up (factory default) for
longer than two seconds.
The fully green headrest symbol on the control panel indicates that the tilt
mode has been activated.
NOTE
When the dental unit is equipped with a motorised headrest, the factory
default is that the tilt mode is activated by pushing the left-side knob up.
However, it is possible to configure the foot control so that the tilt mode
is activated when you push the right-side knob up instead. Contact your
Planmeca dealer.
Push and hold the centre knob to tilt the headrest backward (A) to raise the
patient’s jaw or forward (B) to lower the patient’s jaw.
You can also move the headrest up (C) or down (D) by pushing and holding
the centre knob.
The movement continues for as long as the centre knob is pushed.
NOTE
Users who can edit their user settings change the language as described in
section "Editing language" on page 91.
Steps
1. Press Program.
• Latvian
• Lithuanian
• Estonian
3. Select a language by pressing it.
Move up and down on the list by pressing the up/down buttons.
The list of languages closes and the language of your choice is
displayed on the control panel.
Control panel on Flexy-holder: Press Cup fill / Bowl rinse to rinse the bowl.
Bowl rinsing can be stopped before it stops automatically by pressing Cup
fill / Bowl rinse again.
The flow rate of the bowl rinse can be adjusted by turning the black knob
inside the unit, see section "Adjusting cup fill and bowl rinse flow rates" on
page 198.
The duration of bowl rinsing can be programmed, see section "Duration of
bowl rinsing" on page 199.
NOTE
By default, the cup fill is not activated unless the cup is positioned in its
place under the cup fill tube. To change this setting, contact your Planmeca
dealer.
NOTE
The water in the dental unit is intended for rinsing only, not for drinking.
Control panel on instrument console: Press Cup fill and the unit will
automatically fill the cup and then rinse the bowl. Cup filling can be stopped
before it stops automatically by pressing Cup fill again.
If Cup fill is pressed and held for longer than 1 second, water flows for as
long as the button is pressed, and the bowl is not rinsed.
Control panel on Flexy-holder: Press Cup fill / Bowl rinse twice or press
the button once until the cup filling starts (0.5 - 1 sec.) and the unit will
automatically fill the cup and then rinse the bowl. Cup filling can be stopped
before it stops automatically by pressing Cup fill / Bowl rinse again.
If Cup fill / Bowl rinse is pressed and held for longer than 1 second, water
flows for as long as the button is pressed, and the bowl is not rinsed.
Foot control: When all the instruments are in their holders you can fill the cup
either by briefly pushing the pedal down twice or by pushing down the pedal
once until the filling starts (0,5 - 1 sec.). The unit will automatically fill the cup
and then rinse the bowl. Cup filling stops automatically after a preset time.
Cup filling can be stopped before it stops automatically by pushing the pedal
briefly down.
If the pedal is pushed for longer than 1 second, water flows for as long as
the pedal is pushed, and the bowl is not rinsed.
The flow rate of the cup fill can be adjusted by turning the black knob inside
the unit, see section "Adjusting cup fill and bowl rinse flow rates" on page
198.
The duration of the cup fill can be programmed, see section "Duration of cup
filling" on page 200.
22.4 Timer
NOTE
Other functionalities can be used while the timer is running.
NOTE
The timer can not be run from the foot control.
Steps
1. Press Timer to open a list of available timers.
Results
When the timer reaches zero you will hear two signal tones and the indicator
light goes off.
The function can be cancelled by pressing Timer again.
The preset timers can be reprogrammed, see section "Timer settings" on
page 198.
NOTE
Only one of these functions can be enabled at a time. To change the
enabled function, contact your Planmeca dealer.
Control panel: Press Door open / assistant call to activate the function. You
will hear a short signal tone when the function starts.
Press Door open / assistant call for longer than 0.5 seconds to continue the
function until the button is released.
Foot control: When all the instruments are in their holders you can push
the pedal to the left to activate the Door open / assistant call function. If the
pedal is pushed for longer than 0.5 seconds, the function continues for as
long as the pedal is pushed.
NOTE
Alternatively, the foot control can be configured so that the Door open /
assistant call function is activated when you push the left-side or right-side
knob up. Contact your Planmeca dealer.
The duration of the signal can be programmed, see section "Duration of door
open / assistant call" on page 204.
CAUTION
Do not allow the patient to grab the operating light or its arm when getting
seated or getting up from the patient chair.
NOTE
The light must be moved from the handles only. Do NOT move the light from
the arm or from the light body.
NOTE
The light beam may speed up the hardening of some filling materials. Move
the light so that the light beam is not directed towards the filling material or
turn on the operating light's composite mode.
NOTE
To be able to use the operating light hands-free with the gesture sensor, the
sensor must be enabled.
NOTE
The sensor detects your hand movement at an approximate distance of 3 -
18 cm (1.2 - 7.1 in.) from the infrared sensor.
The distance can be adjusted, see section "Gesture sensor" on page 203.
Indicator lights
Colour Meaning
White The operating light is on and the colour temperature is neutral.
Light blue The operating light is on and the colour temperature is cool.
Yellow When the indicator light blinks yellow, the operating light is
not functioning properly and full luminosity can not be reached.
You can also hear a warning sound. Please contact your local
Planmeca service technician.
Control panel: Press Operating light to switch the operating light on or off.
Foot control: Push the left-side knob up to switch the operating light on/off.
This is the default factory setting.
NOTE
The foot control can also be configured so that the operating light is switched
on/off when you push the right-side knob up. Contact your Planmeca dealer.
NOTE
The dental unit can be configured so that you can switch the operating
light's composite mode on or off by pressing the Flexy button. Contact your
Planmeca dealer.
NOTE
The foot control can be configured so that the composite mode is switched
on/off when you push the left- or the right-side knob up. Contact your
Planmeca dealer.
NOTE
When the polymerisation light is taken from the holder and returned to it, the
composite mode is switched on. This feature is configurable; contact your
Planmeca dealer.
You will hear short successive clicking sounds while the intensity is being
adjusted and a long signal tone when the maximum/minimum intensity is
reached.
The operating light intensity can also be programmed, see section
"Planmeca Solanna and Planmeca Solanna Vision operating lights" on page
201.
NOTE
The operating light intensity will decrease to 30% of the maximum intensity
when the chair is moving.
NOTE
If the operating light is installed to another manufacturer’s dental unit, the
intensity adjustment can be done only from the operating light.
Control panel: Press and hold the Operating light button to adjust the
operating light intensity.
Foot control: Push and hold the left-side knob up to adjust the operating light
intensity.
NOTE
The foot control can also be configured so that the intensity is adjusted when
you push and hold the right-side knob up. Contact your Planmeca dealer.
After one second, the intensity will increase until you release the button/
knob. When you press and hold the button/knob again, the intensity will start
to decrease.
NOTE
If the operating light is installed to another manufacturer’s dental unit, the
intensity adjustment can be done only from the operating light.
Control panel: Press and hold the Composite mode button to adjust the light
intensity of the composite mode.
NOTE
The dental unit can be configured so that the operating light's intensity in the
composite mode can be adjusted when you press and hold the Flexy button.
Contact your Planmeca dealer.
NOTE
The foot control can be configured so that the intensity is adjusted when you
push and hold the left-side or the right-side knob up. Contact your Planmeca
dealer.
Alternatively, you can change the light tone by pressing the Flexy button,
if this function has been configured to the Flexy button. To configure the
function, contact your Planmeca dealer.
You can also change the light tone in the programming window, see section
"Colour temperature and brightness" on page 202.
Prerequisites
• Planmeca Romexis software version 6.0 or later must be installed. When
Planmeca Romexis is running, the camera is continuously connected to
the software.
• Planmeca Romexis and the dental unit have been paired by a Planmeca
service technician.
• The connection between Planmeca Romexis and the dental unit has
been enabled by a Planmeca service technician.
NOTE
The left/right notation is as seen from behind the camera.
Steps
1. Select a patient to open the patient file.
2. Select the 2D module.
3. To activate the camera, click the Solanna Vision button.
NOTE
Alternatively, you can click the Solanna Vision button in the File module.
Video streaming starts and the live stream can be viewed in the Solanna
Vision window in Planmeca Romexis. On the dental unit's control panel,
the Solanna Vision button indicates that video streaming is on.
NOTE
This does not open the Solanna Vision window in the dental unit.
TIP
To switch full screen mode on/off, press the f key on the Planmeca
Romexis keyboard.
To switch low latency mode on/off, press the l key on the Planmeca
Romexis keyboard
NOTE
When the Solanna Vision window is open on the dental unit, the indicator
lights on the operating light handles are blue and the operating light can not
be operated from the handle buttons. You can, however, use the operating
light hands-free with the gesture sensor, if the sensor is enabled.
Interface Action
Planmeca dental unit: Press Solanna Vision in the main window to open the
Control panel on instrument Solanna Vision window.
console
Planmeca dental unit: Planmeca Compact i: The Solanna Vision window can be configured
Control panel on Flexy- to be opened by pressing the Flexy button, contact your Planmeca
holder dealer.
Planmeca dental unit: Foot Planmeca Compact i: The Solanna Vision window can be configured
control to be opened from one of the side knobs on the foot control, contact
your Planmeca dealer.
The Solanna Vision window gives you access to the Solanna Vision controls.
When the Solanna Vision dental unit window is not open, the operating
light, instruments, dental unit and chair can be used normally, also when
streaming or recording is running in the background.
Press OK to close the Solanna Vision dental unit window.
NOTE
It is possible to select the camera also from the Planmeca Romexis
keyboard by pressing keyboard buttons 1 and 2.
Steps
1. Open the Solanna Vision window in the dental unit.
For instructions, see section "Activating camera from dental unit" on
page 128.
Steps
1. Open the Solanna Vision window in the dental unit.
For instructions, see section "Activating camera from dental unit" on
page 128.
2. In the Solanna Vision window, press Settings.
NOTE
If streaming does not start when you switch video streaming on, check if
you have selected a camera. For instructions, see section "Adjusting camera
settings from dental unit" on page 129.
NOTE
In the Solanna Vision window, both in the dental unit and Planmeca
Romexis, a blue button means that the function is on, and a grey button
that the function is off.
Interface Action
Planmeca dental unit: In the Solanna Vision window, press Video camera
Control panel on to turn video streaming on/off.
instrument console
In the Solanna Vision window, press Pause to pause
video streaming. Press Pause again to resume
streaming.
In the Solanna Vision window, press Microphone to
mute/unmute the microphone.
Planmeca dental unit: Planmeca Compact i: Video streaming can be configured to be switched
Control panel on Flexy- on/off from the Flexy button, contact your Planmeca dealer.
holder
Planmeca dental unit: Planmeca Compact i: Video streaming can be configured to be switched
Foot control on/off from one of the side knobs on the foot control, contact your
Planmeca dealer.
Planmeca Romexis In the Solanna Vision window, click Streaming to turn
video streaming on/off.
NOTE
In the Solanna Vision window, both in the dental unit and Planmeca
Romexis, a blue button means that the function is on, and a grey button
that the function is off.
Interface Action
Planmeca dental unit: In the Solanna Vision window, press Record to start/
Control panel on stop recording.
instrument console
In the Solanna Vision window, press Microphone to
turn the microphone on/off.
When the Solanna Vision window is open, press the r key on the
Planmeca Romexis keyboard to start/stop recording.
Planmeca dental unit: When recording is going on, the camera indicator
light on the Solanna Vision button in the main window blinks to indicate that
recording is going on.
Planmeca Romexis: When recording is going on, a red recording icon in the
top left corner of the Solanna Vision window indicates that recording is going
on.
Also, in the 2D module and File module windows, a red video camera icon in
the top right corner indicates that recording is going on.
Interface Action
Planmeca dental unit: In the Solanna Vision window, capture an image by
Control panel on instrument pressing Still camera.
console
Interface Action
Planmeca dental unit: Planmeca Compact i: The dental unit can be configured so that an
Control panel on Flexy- image is captured when you press the Flexy button, contact your
holder Planmeca dealer.
Planmeca dental unit: Foot Planmeca Compact i: The dental unit can be configured so that an
control image is captured when you push one of the side knobs on the foot
control, contact your Planmeca dealer.
Planmeca Solanna Vision When the Solanna Vision window is open on the dental unit's control
panel, press the handle button to capture an image. You will hear a
clicking sound when you press the button.
Planmeca Romexis In the Solanna Vision window, capture an image by
clicking Still camera.
When the Solanna Vision window is open, press the Enter or p key
on the Planmeca Romexis keyboard to capture an image.
When the display is used as an X-ray film viewer, its intensity is increased to
the maximum value.
CAUTION
The X-ray film viewer is suited for X-ray films with an optical density of ≤1.2
OD. It is not a tool for diagnosis.
When you want to close the X-ray film viewer, press OK.
23 Operating instruments
23.1 Instrument logic
NOTE
If you use similar instruments at the same time, keep them in their own
places. The memory operation does not recognise the parameters and
settings of the similar instruments if their places are changed.
The dental unit contains an instrument logic with the principles described
below. The active instrument can be operated with the foot control and its
settings are displayed on the control panel and they can be changed.
When the active instrument is operated, other instruments can be away from
the instrument console, but they can not be operated.
The syringe can be operated independently of other instruments at any time.
1. When the dentist picks up instrument 1 from the instrument console,
it becomes the active instrument. The dentist can drive it with the foot
control pedal (a short push to the right/left or down is enough).
2. While the dentist drives instrument 1, the assistant can pick up
instrument 2 for preparation. Picking up instrument 2 does not change
the active instrument.
3. The dentist returns the active instrument (instrument 1) to the instrument
console.
4. The assistant returns instrument 2 to the instrument console.
5. The dentist activates instrument 2 by picking it up from the instrument
console. After this, it can be driven with the foot control as above.
The memory operation of the logic settings makes it possible to store
parameters and settings for up to eight instruments. Changing the place of
the instrument on the console does not change the parameters and settings
of that instrument.
NOTE
Only one instrument at a time can be in the queue. If two or
three instruments are picked up while driving an instrument, only the
instrument that was picked up last will remain in the queue.
3. The dentist returns the active instrument (instrument 1) to the instrument
console and immediately the instrument in the queue (instrument 2) is
activated and handed to the dentist by the assistant. Instrument 2 can be
driven with the foot control as described above.
23.2 Micromotor
23.2.1 Speed/power
Standard pedal: To drive the instrument, push the foot control pedal to the
right or to the left.
Wide pedal: To drive the instrument, push the foot control pedal down.
Pushing the pedal further to the right/left or down will increase the speed
or power of the instrument. As you push the pedal, the power output is
displayed on the control panel.
The normal range is 10 - 100%.
To stop the instrument, allow the pedal to return to the rest position.
CAUTION
Ensure that the pedal is in rest position when you activate the instrument.
NOTE
The speed/power level depends on the instrument.
NOTE
The foot control can be configured so that the reverse rotation is activated/
deactivated when you push the left-side knob down. Contact your Planmeca
dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The foot control can be configured so that the micromotor’s speed or power
is limited when you push the left-side knob down. Contact your Planmeca
dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The speed/power limit can be programmed. See section "Instrument speed/
power limit" on page 185.
NOTE
Note that the speed/power limit depends on the instrument.
The spray flow rate can be programmed. See section "Instrument spray" on
page 185.
The amounts of water and air for the currently used spray type are displayed
on the control panel.
When sterile water is used, you can select between sterile water spray
and spray off. Sterile water is indicated by a Sterile water symbol and the
indicator light blinks green on the Instrument spray button.
For instructions on how to enable/disable the sterile mode, see section
"Enabling/disabling sterile water mode" on page 186.
Press Instrument spray once to switch on the water & air spray. You will hear
two short signal tones. Additionally, a green indicator light shows that the
water & air spray is switched on.
Press Instrument spray a second time to switch the air spray on. You will
hear one short signal tone. Additionally, a yellow indicator light shows that
the air spray is switched on.
Press Instrument spray a third time to switch off the instrument cooling
spray. You will hear one long signal tone. Additionally, the indicator light
goes out.
Alternatively, you can select the spray setting with the foot control. The
indicator lights on the control panel are lit accordingly.
Standard pedal: Push the pedal down briefly to select the spray setting.
Wide pedal: Push the pedal briefly to the left to select the spray setting.
Push the pedal once to switch on the water & air spray. You will hear two
short signal tones.
Push the pedal again to switch on the air spray. You will hear one short
signal tone.
Push the pedal a third time to switch off the instrument spray. You will hear
one long signal tone.
NOTE
The foot control can also be configured so that you push the left-side knob
down to select a different spray setting. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The spray must be switched off when using an instrument without a
waterline inside the handpiece.
NOTE
The instrument spray operated with the foot control can be disabled in the
service mode, in which case you can switch the spray on and off only from
the control panel. Contact your Planmeca dealer.
NOTE
The momentary spray can be enabled and configured in the service mode,
contact your Planmeca dealer.
NOTE
The momentary spray can not be activated with the wide foot control pedal.
NOTE
The foot control can be configured so that you push the left-side knob down
to switch the automatic chip blow on/off. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
The type of chip blow can be programmed, see section "Automatic chip
blow" on page 187.
Wide pedal: You can temporarily activate the manual chip blow by pushing
and holding the pedal to the right.
The flow of air will continue until you remove your foot from the pedal.
NOTE
The type of manual chip blow does not depend on the type of the automatic
chip blow, but is always dry. The manual chip blow can be set to be
dependent on programming; contact your Planmeca dealer.
NOTE
The foot control can be configured so that you push the left-side knob down
to switch the instrument light on/off. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
Besides the basic micromotor functions, the Bien-Air MCX micromotor has
some additional features. These are described below.
23.3.1 Torque
Press Torque to enable the torque function. The green indicator light means
that torque is enabled.
When torque is enabled, also the drive mode Auto stop is enabled. When
the torque limit is reached, the micromotor stops.
NOTE
Only the drive mode Auto stop is available for the Bien-Air MCX micromotor.
NOTE
The foot control can be configured so that you push the left-side knob down
to enable/disable the torque function. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The torque depends on the handpiece type.
Percent Ncm
10 0.3
15 0.4
Percent Ncm
20 0.5
25 0.6
30 0.8
35 0.9
40 1.0
45 1.1
50 1.3
55 1.4
60 1.5
65 1.6
70 1.8
75 1.9
80 2.0
85 2.1
90 2.3
95 2.4
100 2.5
23.3.2 RPM
Press RPM limit to reduce the micromotor’s maximum speed to a preset
level. The green indicator light means that the RPM limit is on. Press RPM
limit again to switch the rpm limit off.
Besides the basic micromotor functions, the Bien-Air MX2 micromotor has
some additional features. These are described below.
CAUTION
Before using the torque and RPM functions, please refer to the
file manufacturer’s instructions concerning torque and RPM value
recommendations for the files.
23.4.1 Torque
Press Torque to enable the torque function and access the drive modes. The
green indicator light means that torque is enabled.
When torque is enabled, you can select the drive mode by pressing Drive
mode, which always shows the current drive mode. The modes are:
Auto stop
The micromotor stops when the torque limit is reached.
Auto reverse
When the torque limit is reached the micromotor will operate
counter-clockwise.
Auto forward
When the torque limit is reached, the micromotor will operate
counter-clockwise (auto reverse) for 2 seconds and then
return to clockwise direction.
(The length of the counter-clockwise rotation can be modified,
see section "Modifying preset values" on page 189.)
NOTE
The foot control can be configured so that you push the left-side knob down
either to enable/disable the torque function or to select the drive mode.
Contact your Planmeca dealer.
NOTE
Check the indicator light and the drive mode symbol on the control panel to
verify that pushing the left-side knob down activates the correct function.
NOTE
Reverse rotation can not be enabled in the Auto reverse and Auto forward
modes.
NOTE
Torque can be disabled only in the Auto stop mode.
NOTE
The torque depends on the handpiece type.
Percent Ncm
10 0.4
Percent Ncm
15 0.5
20 0.7
25 0.9
30 1.1
35 1.2
40 1.4
45 1.6
50 1.8
55 1.9
60 2.1
65 2.3
70 2.5
75 2.6
80 2.8
85 3.0
90 3.2
95 3.3
100 3.5
23.4.2 RPM
Press RPM limit to reduce the micromotor’s maximum speed to a preset
level. The green indicator light means that the RPM limit is on. Press RPM
limit again to switch the limit off.
23.4.3 Presets
Each user has a personal set of presets for the Bien-Air MX2 micromotor.
Six different presets are available and the Preset button displays the
currently used preset.
If you want to use another preset than the current, follow the steps below.
1. Activate the micromotor.
2. Press Preset.
3. In the window that opens, select the desired preset (1 - 6). You will then
automatically be returned to the MX2 window.
The following table presents the default preset settings for the Bien-Air MX2
micromotor. These presets can be modified, see section "Modifying preset
values" on page 189.
The tolerance for RPM and torque values is +/- 5%.
CAUTION
The user must be familiar with implant procedures before using the Bien-Air
MX-i micromotor.
CAUTION
Always check the preset settings before using the micromotor.
NOTE
Sterile water is not available for preset i5.
The Sterile water symbol also indicates that the sterile water spray is
switched on.
23.5.2 Torque
Presets i1 - i3 have a fixed torque value of 50 Ncm that can not be changed.
Torque is not displayed on the control panel.
In presets i4 - i5 the torque limit is always on and can not be switched off.
The green indicator light on the button is always on.
Two values are displayed next to the Torque button: torque (1) and max
reached torque (2).
NOTE
The Ncm values displayed on the control panel are accurate only when 20:1
handpieces listed on the previous page are used.
When the instrument is not used, torque (1 in picture above) shows the
torque limit. When you drive the instrument, torque shows the current torque
value.
Max reached torque (2 in picture above) shows the highest torque value
during instrument use. The value is displayed also after you have stopped
the instrument and resets when you start driving the instrument again. The
max reached torque value also resets when the torque limit or RPM limit is
modified, or when you select another preset.
23.5.3 RPM
NOTE
The RPM values are accurate only when 20:1 handpieces are used.
The RPM limit is always on for the Bien-Air MX-i implantology micromotor
and can not be switched off. The green indicator light on the button is always
on.
23.5.4 Presets
Each user has a personal set of five presets for the Bien-Air MX-i
micromotor.
• i1 for pilot drilling
• i2 for implant drilling
• i3 for implant drilling
• i4 for implant tapping
• i5 for implant placement
The Preset button displays the currently used preset.
If you want to use another preset than the current, follow the steps below.
1. Activate the micromotor.
2. Press Preset.
3. In the window that opens, select the desired preset (i1 - i5). You will then
automatically be returned to the MX-i window.
The following table presents the default preset settings for the Bien-Air MX-i
micromotor. These presets can be modified, see section "Modifying preset
values" on page 189.
The tolerance for RPM and torque values is +/- 15%.
CAUTION
The user must be familiar with endodontic procedures before using the
Morita TORX micromotor.
When coupled with the CA-10RC-ENDO 10:1 handpiece, the Morita TORX
micromotor can be used together with the Morita Root ZX mini U apex
locator to measure the root canal.
When the CA-10RC-ENDO 10:1 handpiece is used, an optimum torque
reverse (OTR) function is available when the OTR preset is selected.
Besides the basic micromotor functions, the Morita TORX micromotor has
some additional features. These are described below.
23.6.1 Torque
Torque is available for presets a1 - a3, OTR and t1 - t3.
Press Torque to enable the torque limit. The green indicator light means that
the torque limit is enabled.
In the OTR preset, the torque limit is always on and can not be switched off.
The green indicator light on the button is always on.
Presets a1 - a3 and t1 - t3
When the torque limit is enabled, also the drive mode Autoforward is
enabled. When the torque limit is reached, the micromotor will rotate
counter-clockwise (reverse) until the torque value has decreased to 50%
of the torque limit value and then return to clockwise rotation.
NOTE
Only the drive mode Autoforward is available for the Morita TORX
micromotor.
NOTE
The foot control can be configured so that you push the left-side knob down
to enable/disable the torque function. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
Preset OTR
The OTR preset features an optimum torque reverse (OTR) function. When
the torque limit is reached, the micromotor reverses 90°, then moves forward
180° and repeats this movement until the torque limit is no longer reached.
NOTE
The OTR preset should only be used with the Morita TORX micromotor
coupled with the CA-10RC-ENDO 10:1 handpiece.
Calibrating OTR
CAUTION
It is possible to drive the micromotor without calibrating the OTR function,
but this may affect the operation of the micromotor.
When you select the OTR preset, or when the OTR preset is selected
and the OTR function has not been calibrated in the last 30 minutes, help
message H 59 is displayed on the screen. Press the Torque calibration
button on the help message to open the calibration window.
Calibration window
NOTE
Do not touch the file or let the file touch anything during calibration as this
will result in a failed calibration.
You can cancel the calibration by pressing Close in the calibration window.
Activating another instrument during calibration also cancels the calibration.
When the calibration has been performed successfully, close the calibration
window by pressing OK.
23.6.2 RPM
Press RPM limit to reduce the micromotor’s maximum speed to a preset
level. The green indicator light means that the RPM limit is on. Press RPM
limit again to switch the limit off.
As default, the micromotor starts with full speed when preset a1 - a3 or OTR
is selected. This is indicated by its RPM limit button.
NOTE
In the OTR preset, the RPM limit is always on and can not be switched off.
NOTE
Reaching the torque limit can also make the micromotor to rotate counter-
clockwise.
Apical action
No apical action
When the file tip reaches the point in the root canal defined
by the flash bar, this does not induce an action in the
micromotor and the micromotor continues to rotate forward.
Auto stop
The micromotor stops when the file tip reaches the point in
the root canal defined by the flash bar.
When the micromotor has stopped, a thin file can simply
be pulled out from the root canal by hand. If a thicker file
is used, the micromotor's reverse function must be used to
safely remove the file from the root canal.
Auto forward
When the file tip reaches the point in the root canal
defined by the flash bar, the micromotor will rotate
counter-clockwise (auto reverse) until it has reversed three
segments on the apex meter and then return to clockwise
direction.
-movement until the torque value has decreased below the set torque limit
and then returns to clockwise rotation.
Apical action defines the micromotor's rotation when the file tip reaches the
limit depth in the root canal (marked by a flash bar in the window). When
the apical action autoforward is selected and the limit depth is reached, the
micromotor will rotate counter-clockwise (reverse) until it has reversed three
segments on the apex meter and then return to clockwise rotation.
1 Torque action
Torque-based transition from reverse to forward rotation
2 Apical action
Apical depth-based transition from reverse to forward rotation
(when apical action autofoward is selected)
23.6.4 Presets
Each user has a personal set of presets for the Morita TORX micromotor.
Ten different presets are available and the Preset button displays the
currently used preset.
If you want to use another preset than the current, follow the steps below.
1. Activate the micromotor.
2. Press Preset.
3. In the window that opens, select the desired preset. You will then
automatically be returned to the main window.
the torque limit and rpm limit are always on, and presets t1 - t3 are torque
presets where the torque limit can be enabled.
Presets a1 - a3 and OTR can only be used with the Morita CA-10RC-ENDO
10:1 endo-contra handpiece. This handpiece must not be used with other
presets than a1 - a3 and OTR.
CAUTION
Endodontic treatment must only be performed using the Morita TORX
micromotor's a1 - a3 and OTR presets and the Morita CA-10RC-ENDO 10:1
handpiece.
CAUTION
Always check the preset settings before using the micromotor.
The table below lists the factory presets for the Morita TORX micromotor.
These presets can be modified, see section "Modifying preset values" on
page 195.
The tolerance for RPM and torque values is +/- 5%.
NOTE
The torque limit value depends on the handpiece type.
WARNING
Do not simultaneously touch the patient and the USB ports, or any electrical
connectors of external instrument modules.
WARNING
Do not use this apex locator on patients who have a pacemaker or ICD.
WARNING
Do not use this apex locator in conjunction with an electric scalpel.
CAUTION
The Morita Root ZX mini U is not recommended for use with children under
12 years of age.
CAUTION
Always check the measurement with an X-ray. In some cases, an accurate
measurement cannot be made, for example, because of the canal shape.
NOTE
When the file is in the root canal and apex measurement is going on (>2
bars on the meter scale are blinking), the control panel is locked.
CAUTION
Before performing endodontic treatments with the Morita TORX micromotor
and the CA-10RC-ENDO 10:1 handpiece, read the documentation provided
by Morita.
CAUTION
Before using the Morita Root ZX mini U apex locator, read the
documentation provided by Morita.
1. Probe cord The probe cord is plugged into the jack on the
back of the instrument console.
2. File holder If you are using a hand file with the apex locator,
insert the file holder's grey male plug into the grey
female connector on the probe cord.
If you are using the Morita TORX micromotor and
the CA-10RC-ENDO 10:1 handpiece with the apex
locator, do not use the file holder. Leave the grey
female connector on the probe cord hanging.
3. Contrary electrode Insert the contrary electrode into the white female
connector on the probe cord.
NOTE
Always grip the connector to connect/disconnect the probe cord. Never pull
or yank on the cord itself.
• Check that the file holder and contrary electrode are properly connected
to the probe cord.
• If you are using a hand file with the apex locator, touch the metal part
of the file holder with the contrary electrode. Check that all the meter
indicator bars in the Apex locator window light up.
If the indicator bars do not appear normally, stop using the device and
contact your Planmeca dealer.
• If you are using the Morita TORX micromotor and the CA-10RC-ENDO
10:1 handpiece with the apex locator, touch the file with the contrary
electrode. Check that all the meter indicator bars in the Apex locator
window light up.
If the indicator bars do not appear normally, stop using the device and
contact your Planmeca dealer.
NOTE
If the Apex locator button is not visible in your control panel's swipe menu,
you must add it. See section "Organising items on control panel" on page
182.
If you are using the Morita TORX micromotor and the CA-10RC-ENDO
10:1 handpiece, the Apex locator window automatically opens on the control
panel when you select one of the apical presets a1 - a3 or the OTR preset.
button.
3 Press to minimise the window.
When the window is minimised, press the equivalent button to
maximise the window.
4 Indicates the number of bars between the file tip and the flash
bar.
5 Flash bar
6 Handle for dragging flash bar to desired location
7 Sound button for turning off/on the sound of the apex locator.
The Sound button only turns off the sound of the apex locator. It
has no effect on the beep signals of the torque function.
We recommend that you keep the sound on at all times.
The flash bar is a reference for measurement and should be set between 2
and apex. Set the flash bar by dragging the handle to the desired location.
When you insert the file into the root canal, the flash bar starts blinking.
When the file tip reaches the point in the root canal designated by the flash
bar, the flash bar stops blinking and stays on.
As you progress down the root canal, a beep signal starts to sound when
the file tip goes below 2 on the meter scale. For the 5 first bars, the beep
signal is slow, after which the beep signal becomes fast, and finally becomes
continuous when it reaches the flash bar.
If the flash bar has been set at 2 on the meter scale, the only signal that is
heard is the continuous signal when the file tip reaches the flash bar.
1. Continuous signal
NOTE
While the test is going on, the control panel is locked.
Steps
1. Open the Apex locator window either by pressing the Apex locator button
or by activating the Morita TORX micromotor and selecting one of the
apex presets (a1 - a3).
2. Insert the tester into the jack on the back of the instrument console.
Instrument console with hanging-tube instruments
1 3 bars above 1
2 3 bars below 1
23.8 Turbine
CAUTION
A power cut will shut down the software-controlled backflow prevention
system. If you are using a turbine without a built-in backflow prevention
system, contaminated water can enter into the turbine and turbine hose in
the event of a power cut.
23.8.1 Speed/power
Standard pedal: To drive the instrument, push the foot control pedal to the
right or to the left.
Wide pedal: To drive the instrument, push the foot control pedal down.
Pushing the pedal further to the right/left or down will increase the speed
or power of the instrument. As you push the pedal, the power output is
displayed on the control panel. The normal range is 5 - 100%.
To stop the instrument, allow the pedal to return to the rest position.
CAUTION
Ensure that the pedal is in rest position when you activate the instrument.
NOTE
The speed/power level depends on the instrument.
23.8.2 Quickstart
The turbine will start with maximum speed if the quickstart is enabled.
When quickstart is enabled, the indicator light on the control panel button is
green.
Control panel: When the instrument is active, but not operated, press
Quickstart to enable/disable the quickstart.
NOTE
The foot control can be configured so that you push the left-side knob down
to enable/disable the quickstart. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
The amounts of water and air for the currently used spray type are displayed
on the control panel.
When sterile water is used, you can select between sterile water spray
and spray off. Sterile water is indicated by a Sterile water symbol and the
indicator light blinks green on the Instrument spray button.
Sterile water is meant to be used together with an air scaler.
For instructions on how to activate/deactivate the sterile mode, see section
"Enabling/disabling sterile water mode" on page 186.
Press Instrument spray once to switch on the water & air spray. You will hear
two short signal tones. Additionally, a green indicator light shows that the
water&air spray is switched on.
Press Instrument spray a second time to switch the air spray on. You will
hear one short signal tone. Additionally, a yellow indicator light shows that
the air spray is switched on.
Press Instrument spray a third time to switch off the instrument cooling
spray. You will hear one long signal tone. Additionally, the indicator light
goes out.
Alternatively, you can select the spray setting with the foot control. The
indicator lights on the control panel are lit accordingly.
Standard pedal: Push the pedal down briefly to select the spray setting.
Wide pedal: Push the pedal briefly to the left to select the spray setting.
Push the pedal once to switch on the water & air spray. You will hear two
short signal tones.
Push the pedal again to switch on the air spray. You will hear one short
signal tone.
Push the pedal a third time to switch off the instrument spray. You will hear
one long signal tone.
NOTE
The foot control can also be configured so that you push the left-side knob
down to select a different spray setting. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The spray must be switched off when using an instrument without a
waterline inside the handpiece.
NOTE
The instrument spray operated with the foot control can be disabled in the
service mode, in which case you can switch the spray on and off only from
the control panel. Contact your Planmeca dealer.
NOTE
The foot control can be configured so that the turbine's speed or power is
limited to a preset level when you push the left-side knob down. Contact your
Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The speed/power limit can be programmed. See section "Instrument speed/
power limit" on page 185.
NOTE
The turbine speed/power limit does not affect the air driven instruments for
which quickstart has been selected.
NOTE
Note that the speed/power limit depends on the instrument.
NOTE
The momentary spray can be enabled and configured in the service mode,
contact your Planmeca dealer.
NOTE
The momentary spray can not be activated with the wide foot control pedal.
NOTE
The foot control can be configured so that you push the left-side knob down
to switch the automatic chip blow on/off. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
The type of chip blow can be programmed, see section "Automatic chip
blow" on page 187.
The flow of air will continue until you remove your foot from the pedal.
NOTE
The type of manual chip blow does not depend on the type of the automatic
chip blow, but is always dry. The manual chip blow can be set to be
dependent on programming; contact your Planmeca dealer.
NOTE
The foot control can be configured so that you push the left-side knob down
to switch the instrument light on/off. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
23.9 Scaler
CAUTION
Do not use the scaler on patients with cardiac pacemakers. The scaler can
cause disturbance on the pacemaker’s function.
NOTE
A scaler requires additional electronics and the scaler type can not be
changed without changing electronics.
23.9.1 Speed/power
Standard pedal: To drive the instrument, push the foot control pedal to the
right or to the left.
Wide pedal: To drive the instrument, push the foot control pedal down.
Pushing the pedal further to the right/left or down will increase the speed
or power of the instrument. As you push the pedal, the power output is
displayed on the control panel.
To stop the instrument, allow the pedal to return to the rest position.
CAUTION
Ensure that the pedal is in rest position when you activate the instrument.
NOTE
The speed/power level depends on the instrument.
The amount of water and the spray water number (1 or 2) are displayed on
the control panel.
When sterile water is used, you can select between sterile water spray
and spray off. Sterile water is indicated by a Sterile water symbol and the
indicator light blinks green on the Instrument spray button.
For instructions on how to enable/disable the sterile mode, see section
"Enabling/disabling sterile water mode" on page 186.
Press Instrument spray once to switch on water 1. You will hear two short
signal tones. Additionally, a green indicator light shows that water 1 is
switched on.
Press Instrument spray a second time to switch on water 2. You will hear
one short signal tone. Additionally, a yellow indicator light shows that water 2
is switched on.
Press Instrument spray a third time to switch off the instrument spray. You
will hear one long signal tone. Additionally, the indicator light goes out.
Alternatively, you can select the spray setting with the foot control. The
indicator lights on the control panel are lit accordingly.
Standard pedal: Push the pedal down briefly to select the spray setting.
Wide pedal: Push the pedal briefly to the left to select the spray setting.
Push the pedal once to switch on water 1. You will hear two short signal
tones.
Push the pedal again to switch on water 2. You will hear one short signal
tone.
Push the pedal a third time to switch off the instrument spray. You will hear
one long signal tone.
NOTE
The foot control can also be configured so that you push the left-side knob
down to select a different spray setting. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The instrument spray operated with the foot control can be disabled in the
service mode, in which case you can switch the spray on and off only from
the control panel. Contact your Planmeca dealer.
NOTE
The momentary spray can be enabled and configured in the service mode,
contact your Planmeca dealer.
NOTE
The momentary spray can not be activated with the wide foot control pedal.
A coloured band at the base of the scaler tip helps you choose the proper
scaler mode on the dental unit:
• Green - periodontics
• Yellow - endodontics
• Blue - scaling
• Orange - conservative dentistry (restoration)
When the scaler is the active instrument, the scaler mode can be changed
by pressing Power.
NOTE
The foot control can be configured so that you push the left-side knob down
to change the scaler mode. Contact your Planmeca dealer.
NOTE
Check the scaler mode symbol on the control panel to verify that pushing the
left-side knob down activates the correct function.
23.9.5 LM scaler
CAUTION
Keep the patient's lips, cheeks and tongue out of the way of the activated
scaler tip, as contact may cause burns.
When the scaler is the active instrument, the scaler mode can be changed
by pressing Power.
NOTE
The foot control can be configured so that you push the left-side knob down
to change the scaler mode. Contact your Planmeca dealer.
NOTE
Check the scaler mode symbol on the control panel to verify that pushing the
left-side knob down activates the correct function.
When the scaler is the active instrument, the scaler mode can be changed
by pressing Power.
NOTE
The foot control can be configured so that you push the left-side knob down
to change the scaler mode. Contact your Planmeca dealer.
NOTE
Check the scaler mode symbol on the control panel to verify that pushing the
left-side knob down activates the correct function.
NOTE
The foot control can be configured so that you push the left-side knob down
to switch the instrument light on/off. Contact your Planmeca dealer.
NOTE
Check the indicator light on the control panel to verify that pushing the
left-side knob down activates the correct function.
CAUTION
The polymerisation light generates optical radiation and proper safety
measures should be taken when using the instrument. For detailed
information, please refer to OEM documentation.
CAUTION
Do not use the polymerisation light on patients with cardiac pacemakers.
The polymerisation light can cause disturbance on the pacemaker’s function.
NOTE
When the polymerisation light is taken from the holder in the instrument
console and returned to it, the operating light's composite mode is switched
on. This feature is configurable; contact your Planmeca dealer.
To start the polymerisation cycle, first select the desired curing mode
by pressing the navigation button on the handpiece. Then, start the
polymerisation cycle by pressing the start button on the handpiece.
The polymerisation cycle can be interrupted by pressing the start button
again.
To start the polymerisation cycle with the foot control, first select the desired
curing mode by pressing the navigation button on the handpiece. Then,
push the foot control pedal to the right or to the left or down to start the
polymerisation cycle.
The polymerisation cycle can be interrupted by pushing the foot control
pedal to the right or to the left or down.
The length of the cycle is programmable, see section "Planmeca Lumion
Plus polymerisation light" on page 197.
When the polymerisation light is activated, the length of the polymerisation
cycle is displayed on the control panel. When you start the cycle, you will
hear a signal tone. This signal tone is repeated every 10 seconds, and also
at 5 seconds. The progress of the polymerisation cycle is displayed on the
control panel.
Independent mode
The Planmeca Lumion Plus polymerisation light can also be operated in
the independent mode. The independent mode is typically used when the
Planmeca Lumion Plus polymerisation light is attached to the assistant
element, but the independent mode can also be configured to be used
on the dentist side (the configuration is performed by a Planmeca service
technician).
When the Planmeca Lumion Plus polymerisation light is in the independent
mode, it can only be controlled by the buttons on the instrument itself, not
over the control panel or the foot control.
To start the polymerisation cycle in the independent mode, first select the
desired curing mode by pressing the navigation button on the handpiece.
Then, briefly press the start button on the handpiece to start a 10-second
exposure, or press and hold the start button for 2 seconds to start a 20-
second exposure. The polymerisation cycle can be interrupted by pressing
the start button.
In the 10-second cycle, a signal tone is heard at the beginning and the end
of the cycle. In the 20-second cycle, a signal tone is heard as the cycle
starts, after 2 seconds to confirm the start of the 20-second cycle, after 10
seconds and at the end of the cycle.
NOTE
When the Planmeca Lumion Plus polymerisation light is in the independent
mode, it can not be controlled over the foot control.
Handpiece
Prerequisites
• The intraoral camera must be connected to the USB port.
When the intraoral camera is placed in the instrument console, it is
connected to the USB port on the underside of the instrument console.
When the intraoral camera is placed in the suction holder, it is connected
to the USB port on the cuspidor.
• Planmeca Romexis software must be installed and the connection
between it and the dental unit must be enabled. When Planmeca
Romexis is running, the intraoral camera is continuously connected to
the software.
NOTE
If you turn on the intraoral camera from the buttons on the handpiece, the
camera can not be operated from the dental unit's foot control.
Macro on/off
A short sound signal indicates that the macro mode is turned on/off. When
the macro mode is on, autofocus is off and the indicator light on the
handpiece is lilac.
Interface Action
Handpiece Press the Power/macro button to turn the macro
mode on/off.
Freezing/unfreezing image
A short sound signal indicates the freeze/unfreeze of an image. When the
image is frozen, the indicator light on the handpiece is green. When you
unfreeze the image, the camera goes back to live stream (indicated by the
blue indicator light on the handpiece).
Interface Action
Foot control In Planmeca Compact i dental units, push the foot
control pedal to the left or right to freeze/unfreeze the
image.
Handpiece There are two ways to freeze/unfreeze the image
from the handpiece.
• Press the Image control button halfway and hold
it to freeze the image. When you release the
button, the image unfreezes.
• Press the Image control button all the way down
and release it to freeze the image. To unfreeze
the frozen image, either press the Image control
button halfway and then release it, or press the
button all the way down and release it.
Interface Action
Planmeca Romexis Press the Freeze button to freeze the image. Press
the Resume button to unfreeze the image. The
buttons are located at the bottom of the intraoral
camera window.
Saving image
A frozen image can be saved from the dental unit, the handpiece and
Planmeca Romexis. From the handpiece you can save an image also
without freezing the image first.
A long sound signal indicates that an image is saved. When the image is
being saved, the indicator light on the handpiece blinks orange. After the
image is saved, the camera goes back to live stream (indicated by the blue
indicator light on the handpiece).
Interface Action
Foot control In Planmeca Compact i dental units, when the image
is frozen, briefly push the foot control pedal down to
save the image.
Handpiece Press the Image control button for two seconds.
Note! When saving an image from the handpiece,
you can, but do not have to freeze the image first.
Planmeca Romexis When the image is frozen, press the Save button at
the bottom of the intraoral camera window.
Macro on/off
A short sound signal indicates that the macro mode is turned on/off. When
the macro mode is on, autofocus is off and the indicator light on the
handpiece is lilac.
Interface Action
Handpiece Press the Power/macro button to turn the macro
mode on/off.
Freezing/unfreezing image
A short sound signal indicates the freeze/unfreeze of an image. When the
image is frozen, the indicator light on the handpiece is green. When you
unfreeze the image, the camera goes back to live stream (indicated by the
blue indicator light on the handpiece).
Interface Action
Foot control In Planmeca Compact i dental units, push the foot
control pedal to the left or right to freeze/unfreeze the
image.
Handpiece There are two ways to freeze/unfreeze the image
from the handpiece.
• Press the Image control button halfway and hold
it to freeze the image. When you release the
button, the image unfreezes.
• Press the Image control button all the way down
and release it to freeze the image. To unfreeze
the frozen image, either press the Image control
button halfway and then release it, or press the
button all the way down and release it.
Planmeca Romexis Press the Freeze button to freeze the image. Press
the Resume button to unfreeze the image. The
buttons are located at the bottom of the intraoral
camera window.
Saving image
A frozen image can be saved from the dental unit, the handpiece and
Planmeca Romexis. From the handpiece you can save an image also
without freezing the image first.
A long sound signal indicates that an image is saved. When the image is
being saved, the indicator light on the handpiece blinks orange. After the
image is saved, the camera goes back to live stream (indicated by the blue
indicator light on the handpiece).
Interface Action
Foot control In Planmeca Compact i dental units, when the image
is frozen, briefly push the foot control pedal down to
save the image.
Handpiece Press the Image control button for two seconds.
Note! When saving an image from the handpiece,
you can, but do not have to freeze the image first.
Planmeca Romexis When the image is frozen, press the Save button at
the bottom of the intraoral camera window.
CAUTION
Make sure that you attach the intraoral scanner connector the right way into
the USB 3.0 port for the scanner on the cuspidor. If the connector is turned
the wrong way, it will not go into the port. Use of unnecessary force will
break the connector.
NOTE
There are three USB ports on the cuspidor. Make sure you attach the
connector to the right port, see section "Cuspidor" on page 32.
NOTE
To avoid splashes on the scanner, remove it from the dental unit after use
and place it on the table stand.
Generating model
Push the left-side knob down to generate a model of the scanned area.
Starting scanning
Briefly push the foot control pedal down to start the scanning.
Taking image
Push and hold down the foot control pedal to take an image.
NOTE
In addition to the instructions below, the suction can also be configured so
that it is started/stopped by pushing the foot control’s left-side or right-side
knob up, or by pressing the Flexy button. Contact your Planmeca dealer.
NOTE
If you have stopped the suction from the foot control or the Flexy button
while the suction handpiece was in your hand, the suction will start for a
while when you return the handpiece to the suction holder. The duration of
this post-suction delay is configurable, contact your Planmeca dealer. This
feature is not available for the tilting high-volume suction handpiece.
25 Programming
25.1 Introduction
Automatic chair positions, operating light and instrument settings are saved
to the user’s personal settings. Before you start programming, make sure
that you have signed in to the dental unit with your own user name.
NOTE
If the instrument is operated during programming, the changes in settings
are seen immediately.
NOTE
The air/water flow of the syringe can not be programmed.
NOTE
To check a function setting (other than automatic position) without
programming it, press Program and the button of the desired function. The
setting is displayed on the control panel. Press OK to close the window
without changing the setting.
NOTE
Alternatively, you can change the settings with the foot control. To
increase the parameter value, push the pedal to the right. To decrease
the parameter value, push the pedal to the left. When the pedal is
pushed halfway (right or left) the parameter changes slowly. When the
pedal is pushed to its extreme position (right or left) the parameter
changes quickly.
When you press Program, you will also see the following symbols on the
control panel:
service mode
user settings
clock
software update
The Service mode and Software update buttons are reserved for service
situations only.
Steps
1. Press Program.
NOTE
The chair height cannot be programmed near the upper limit. The help code
H 8 is displayed if the chair position is not allowed. When needed, the upper
limit can be altered. Contact your Planmeca dealer.
NOTE
If you only want to rename the automatic position or adjust its position on the
list, start programming from step 4.
Steps
1. Move the chair to the required position by using the chair movement
buttons on the control panel or by using the foot control.
2. If you want the operating light or its composite mode to be on (off) in this
position, turn them on (off).
3. Adjust the intensity of the operating light and/or its composite mode as
described in section "Intensity" on page 201.
4. Press Program.
The field of the position that you have selected from the list (position C in
picture) turns blue.
Steps
1. Move the chair to the required position by using the chair movement
buttons on the control panel or by using the foot control.
For instructions, see section "Manual operation" on page 103.
2. If you want the operating light or its composite mode to be on (off) in this
position, turn it on (off).
3. Adjust the intensity of the operating light and/or its composite mode as
described in section "Intensity" on page 201.
4. Press Program.
5. Press the desired chair position where to store the chair’s position
(rinsing position, A, B, C or D).
NOTE
The instrument speed/power limit does not affect the air driven instruments
for which quickstart has been selected.
Steps
1. Activate the instrument.
2. Press Program.
Steps
1. Activate the instrument.
2. Press Program.
The pop-up window closes and the new values are displayed on the
control panel.
NOTE
The flow rates for sterile water can not be adjusted by the user.
Steps
1. Activate the instrument.
2. Press Program.
A grey button means that the sterile water mode is disabled, and a blue
button that it is enabled.
NOTE
If you disable the sterile water mode for an instrument that uses sterile
water, the flow rate for sterile water 1 and 2 automatically changes to
0%.
5. Press OK.
NOTE
The type of manual chip blow does not depend on the type of the automatic
chip blow, but is dry as a factory default. The manual chip blow can be set to
be dependent on programming, contact your Planmeca dealer.
Steps
1. Activate the instrument.
2. Press Program.
The pop-up window closes and the new values are displayed on the
control panel.
Steps
1. Activate the instrument.
2. Press Program.
The pop-up window closes and the new values are displayed on the
control panel.
Steps
1. Activate the micromotor.
2. Press Torque.
The pop-up window closes and the new value is displayed on the
control panel.
4. Optional: Adjust the torque limit.
4.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
CAUTION
Before modifying the torque and RPM functions, please refer to
the file manufacturer’s instructions concerning torque and RPM value
recommendations for the files.
Steps
1. Activate the micromotor.
2. Press Torque.
Auto reverse
When the torque limit is reached the micromotor will
operate counter-clockwise.
Auto forward
When the torque limit is reached, the micromotor
will operate counter-clockwise (auto reverse) for 2
seconds and then return to clockwise direction.
The length of the counter-clockwise rotation is
adjusted in step 13.
4. Optional: Adjust the micromotor speed rate (RPM).
4.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
5. Optional: Adjust the torque limit.
5.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
6. Optional: Adjust the counter-clockwise rotation time of the micromotor in
the Auto forward mode.
6.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
7. Optional: Press Instrument spray to toggle between water & air, air and
no spray. The amount of water and air can also be programmed.
8. Optional: Press Chip blow to switch the automatic chip blow on or off.
The amount of water and air can also be programmed.
Results
NOTE
Changing the instrument spray, chip blow and instrument light values
follows the normal programming pattern. For more information, see sections
"Instrument spray" on page 185, "Automatic chip blow" on page 187 and
"Instrument light" on page 187.
When you have modified the settings of a preset, but have not saved them,
a dash (–) replaces the preset number on the control panel.
The procedure for saving the modified preset settings is explained in section
"Saving modified preset values" on page 192.
Steps
1. Press Program.
3. Press the preset under which you want to store the modified settings.
The preset window is closed. The settings are stored in the dental unit
when you return the instrument to its holder.
CAUTION
Before modifying the torque and RPM functions, please refer to the
implant manufacturer’s instructions concerning torque and RPM value
recommendations for the implants.
NOTE
When using the Bien-Air MX-i micromotor the torque and rpm limits are
always on and can not be switched off.
Steps
1. Activate the micromotor.
2. Optional: Adjust the torque limit.
2.a. Press Program.
NOTE
Torque can only be adjusted for presets i4 - i5. Presets i1 - i3 have
a fixed torque value of 50 Ncm.
The pop-up window closes and the new value is displayed on the
control panel.
3. Optional: Adjust the micromotor speed rate (RPM).
3.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
NOTE
If you have signed in to the dental unit with a PlanID card, Planmeca
Romexis software version 6.2 or later must be installed to be able to save
the modified Bien-Air MX-i settings to your personal settings. If Planmeca
Romexis 6.2 is not installed, default preset settings are loaded when you
sign in to the dental unit.
Steps
1. Press Program.
2. Press Preset.
Steps
1. Activate the micromotor.
2. All presets: Adjust the RPM limit.
2.a. Press Program.
The pop-up window closes and the new value is displayed on the
control panel.
3. All presets except OTR: Press RPM limit to switch the RPM limit on or
off.
The pop-up window closes and the new value is displayed on the
control panel.
5. Presets a1 - a3 and t1 - t3 only: Press Torque to switch the torque limit
on or off.
6. All presets except OTR: Press Reverse to switch the reverse rotation on
or off.
10. Presets a1 - a3 and OTR only: Press Apical action to toggle between the
apical actions auto stop, auto forward, and no action.
NOTE
The button looks different depending on which apical action is currently
in use.
11. Presets a1 - a3 and OTR only: Press Sound to turn off/on the sound of
the apex locator.
This only turns off the sound of the apex locator. It has no effect on the
beep signals of the torque function. We recommend that you keep the
sound on at all times.
Results
NOTE
Changing the instrument spray, chip blow and instrument light values
follows the normal programming pattern. For more information, see sections
"Instrument spray" on page 185, "Automatic chip blow" on page 187 and
"Instrument light" on page 187.
When you have modified the settings of a preset, but have not saved them,
an asterisk can be seen on the Preset button.
The procedure for saving the modified preset settings is explained in section
"Saving modified preset values" on page 197.
NOTE
Any changes you make to the the OTR preset are saved locally to the dental
unit only until you sign out from the dental unit. The next time you sign in to
the dental unit, default OTR preset settings are taken into use.
Steps
1. Press Program.
2. Press Preset.
NOTE
The duration of the polymerisation cycle can be programmed only for the
Planmeca Lumion Plus polymerisation light.
Steps
1. Activate the instrument.
2. Press Program.
The pop-up window closes and the new values are displayed on the
control panel.
Steps
1. Press Program.
2. Press Timer.
Steps
1. Press Program.
NOTE
By default, the cup fill is not activated unless the cup is positioned in its
place under the cup fill tube. To change this setting, contact your Planmeca
dealer.
NOTE
The water in the dental unit is intended for rinsing only, not for drinking.
Steps
1. Press Program.
What to do next
The duration of the cup filling can also be programmed as follows:
1. Place an empty cup to the cup holder.
2. Press Program.
4. Push the foot control pedal down. The cup filling time will first be set to 2
seconds and will start to increase after pushing the foot control pedal for
2 seconds. The pedal can be released and then pushed again, and the
time continues to increase. Continue until the cup is filled to the desired
level.
5. Press Program.
25.7.1 Intensity
NOTE
The light intensity can also be adjusted from the operating light, see sections
"Adjusting intensity of operating light" on page 122 and "Adjusting intensity
of operating light in composite mode" on page 124.
When you have signed in to the dental unit with your own user name, all
changes you make to the light mode settings and then save, are saved to
your user profile. This means that whenever you sign in to the dental unit,
you will use your last saved light mode settings.
Steps
1. Press Program.
2. Press Operating light or Composite mode. Both buttons open the same
pop-up window.
The pop-up window closes and the new values are displayed on the
control panel.
NOTE
The colour temperature can also be adjusted from the operating light, see
section "Changing light tone of operating light" on page 125.
Steps
1. Press Program.
2. Press Operating light or Composite mode. Both buttons open the same
pop-up window.
Steps
1. Press Program.
2. Press Operating light or Composite mode. Both buttons open the same
pop-up window.
A grey button means that the function is disabled, and a blue button that
the function is enabled.
5. Adjust the distance at which the gesture sensor on the operating light
reads your hand movements by dragging the handles to a suitable
position.
6. Press OK.
Steps
1. Press Program.
25.9 Clock
NOTE
If Planmeca Romexis Clinic Management software is used together with
this dental unit, you do not need to adjust the clock settings. The dental
unit clock is synchronised with the Planmeca Romexis clock every time the
dental unit is booted up.
Steps
1. Press Program.
2. Press Clock.
The pop-up window closes and the new time is displayed on the control
panel.
25.10 Date
Steps
1. Press Program.
2. Press Clock.
When the date is not visible on the control panel, the items in the
programming window are grey. This means that they are disabled.
To show the date on the control panel and to enable programming, press
the Date button at the top of the programming window.
The button will turn blue and all items in the window will turn black (which
means that programming is enabled).
4. Select the date format.
The pop-up window closes and the new date is displayed on the control
panel.
Steps
1. Press Program.
4. The Foot control serial no field displays the current foot control’s serial
number. If you want to change the foot control, press Edit.
NOTE
On the foot control, the serial number can be found on its underside.
5. Press and hold down the handle of the foot control that you want to pair
your dental unit with to select it.
The selected foot control is shown with a black font on the list (marked
with arrow in the picture below).
The foot control that is highlighted in blue is the currently paired foot
control.
NOTE
For information on the different markings in the Bind foot control window,
press Questionmark.
6. While holding the handle down, start pairing by touching the name of the
selected foot control (black font) on the list.
A confirmation message is displayed on the dental unit’s control panel.
7. Press OK to confirm the start of the pairing process.
Steps
1. Press Program.
The Battery field shows the current charging level of the battery.
4. Press Battery to open the battery’s charging history log.
Steps
1. Press Program.
NOTE
If the Foot control channel and Transmitter power fields are inactive, you
must press the foot control handle to enable the adjusting of the settings.
4. Select the foot control channel.
You can freely choose between the channels 1 and 16, but, to minimise
radio signal interference, no two foot controls within 10 meters of each
other should have the same channel.
5. Adjust the transmitter power.
Select the lowest power level and increase it, if needed. The value range
is 1 (lowest) to 6 (highest).
6. Press OK to confirm your selections and exit the programming mode.
26 Calibrating clock
Steps
1. Press Program.
3. Select Service.
A new window opens.
4. Select Clock calibration.
A new window opens.
5. The dental unit asks you to set the current time. Press Calibrate.
6. Set the current time by changing the hour, minute and second values
with the plus (+) and minus (-) buttons. It is recommended that you
check the current time from an NTP server.
7. Press OK to exit the calibration window.
8. Wait for a minimum period of 7 days for the clock to calibrate. However,
a calibration period of 2-3 weeks is recommended.
9. Press Program to complete the calibration sequence after the minimum
calibration period.
If you at this point want to reset the calibration (the clock resumes the
time it had before you started the calibration process), press the Reset
button. You will be asked to confirm the reset in a new window.
14. Adjust the time to match the correct time by changing the hour, minute
and second values with the plus (+) and minus (-) buttons. When you
adjust the time, it is recommended that you check the correct time from
an NTP server.
15. Press OK to close the window.
The calibration can also be reset at this point, if you, for example, notice
that an error has been made during the calibration process.
NOTE
Always feed cold water to the dental unit.
NOTE
The water in the dental unit is intended for rinsing only, not for drinking.
NOTE
The water tap must be closed when the dental unit is not in use.
NOTE
If disinfectant is splashed on the surfaces of the dental unit, remove the
splashes instantly with water and mild soap to avoid stains.
The time stamp under the cleaning program name is an easy way to check
when the cleaning program was last started. However, it does not tell
whether the cleaning program was successfully completed.
While performing the flushing/cleaning, follow the instructions displayed on
the control panel. When the cleaning program runs without problems, the
messages only show briefly, but all messages can be viewed in the message
history log.
To view the message history log, see section "Viewing help and error
message history" on page 290.
Some control panel buttons are common for all cleaning programs, see the
following table.
Button Function
Displays additional information about the cleaning program
when you press the button during the cleaning cycle.
Button Function
Closes the pop-up window.
NOTE
Alternatively, the dental unit can be configured so that the touch display is
locked/unlocked when you press the Flexy button. Contact your Planmeca
dealer.
NOTE
The duration of the short flushing cycle is configurable. Contact your
Planmeca dealer.
NOTE
You can interrupt the flushing cycle by pressing Close. After the interruption,
the dental unit can be used normally.
Steps
1. Press Maintenance to go into maintenance mode.
2. Remove the cup from the cup holder. Turn the bowl away from above
the flushing holder as shown in the figure. Turn also the cup fill tube
above the bowl as shown in the figure. Press the outer edge of the
flushing holder cover (1) and remove the cover.
3. Remove the instrument handpieces from the instruments and clean them
according to the manufacturer’s instructions.
4. Place all water consuming instruments (including syringes) into the
openings in the instrument flushing holder.
Optionally, in dental units with balanced instrument arms, you can
remove the hoses of the instruments to be flushed from the instrument
arms / instrument holders before placing the instruments in the flushing
holder.
In dental units with hanging-tube instruments, the instruments to be
flushed must be removed from the instrument holders before placing
them in the flushing holder.
If water flow was not detected for all water consuming instruments,
H 36.1 is displayed. Run instruments for a while with spray water to
ensure that the flushing of instruments is sufficient.
NOTE
The duration of the long flushing cycle is configurable. Contact your
Planmeca dealer.
NOTE
In units equipped with a water heater, the long flushing fills the waterlines
and water heater with cool water and switches the water heater off. The
water heater switches automatically back on the next time instrument water
spray is used.
NOTE
You can interrupt the flushing cycle by pressing Close. After the interruption,
the dental unit can be used normally.
Steps
1. Press Maintenance to go into maintenance mode.
2. Remove the cup from the cup holder. Turn the bowl away from above
the flushing holder as shown in the figure. Turn also the cup fill tube
above the bowl as shown in the figure. Press the outer edge of the
flushing holder cover (1) and remove the cover.
3. Remove the instrument handpieces from the instruments and clean them
according to the manufacturer’s instructions.
4. Place all water consuming instruments (including syringes) into the
openings in the instrument flushing holder.
Optionally, in dental units with balanced instrument arms, you can
remove the hoses of the instruments to be flushed from the instrument
arms / instrument holders before placing the instruments in the flushing
holder.
In dental units with hanging-tube instruments, the instruments to be
flushed must be removed from the instrument holders before placing
them in the flushing holder.
NOTE
Adjust the water flow of the cup fill tube so that the water does not splash
into the bowl.
6. Release the instrument arms (if your dental unit is equipped with
balanced instrument arms).
7. Once the flushing cycle is finished, H 36 is displayed. Remove the
instruments from the flushing holder and return them to the instrument
console. Place the flushing holder cover back to its position.
If H 36 is still displayed after returning the instruments, activate the
syringe and then return it to the instrument console.
If water flow was not detected for all water consuming instruments,
H 36.1 is displayed. Run instruments for a while with spray water to
ensure that the flushing of instruments is sufficient.
What to do next
NOTE
After the flushing cycle, the unit should immediately be switched off. This
procedure ensures that cool water remains in the pipelines of the unit, thus
minimising the growth of biofilm.
NOTE
The dental unit can be configured to display help message H 99 if the unit
has been switched off without performing long flushing after water has been
used. When H 99 has been enabled, it can be displayed as a reminder only,
or it can be set to disappear only after you have performed long flushing. To
take help message H 99 into use, contact your Planmeca dealer.
NOTE
The Suction Tube Cleaning System (STCS) is an optional feature. If your
dental unit does not have this feature, clean the suction tubes with OroCup
as instructed in section "OroCup" on page 248.
Steps
1. Remove the suction handpieces from the suction tubes and clean them
according to the manufacturer’s instructions.
2. Press Maintenance to go into maintenance mode.
NOTE
Make sure that the suction tube cleaning holder itself is in place (i.e.
pushed to the bottom of the suction cleaning unit. See step 8 for a
picture of the unit).
NOTE
Make sure that a plug is inserted into each empty suction tube holder in
the suction tube cleaning holder to prevent the concentrate from spilling.
6. Lift the dosing cubic from the suction cleaning unit and fill it with
Planmeca approved suction disinfectant.
The dosing scale indicates the required amount for 1 or 2 suction tubes.
1. Dosing cubic
2. Suction tube cleaning holder
3. Start button (green)
4. Cancel button (yellow)
Results
The dental unit is now ready for normal operation.
NOTE
Before attaching the handpieces back on the suction tubes, wipe the
identification bushings (1) with Planmeca approved surface disinfectant.
27.6.1 Introduction
Waterlines are a breeding ground for biofilm. Biofilm may contain bacteria
that are harmful to the patient and to the dental team. This is why the
waterlines of the dental unit should be cleaned once a week with a
disinfectant. The solution is left in the unit overnight and the waterlines of
the unit are flushed with water the next morning. The disinfectant should not
be left in the waterlines for longer than one night.
After installation, or if the dental unit has not been used for a long time,
the waterlines of the dental unit must be treated with a disinfectant for three
consecutive cycles.
If you have several dental units with Waterline Cleaning System (WCS), you
may use the same container in all of them.
WARNING
Even though every effort has been taken to ensure patient safety, even in
case of malfunction or misuse, always make sure that the unit is properly
flushed before taking it into use.
CAUTION
Only Planmeca Planosil, Planmeca PlanPure or Alpro Bilpron disinfectant
must be used. Planmeca does not guarantee the suitability of and is not
liable for damages caused by other disinfectants.
NOTE
If you are using the Clean Water System (CWS), clean the waterlines
according to the instructions in section "Waterline cleaning" on page 262.
NOTE
Waterline Cleaning System is not available for dental units equipped with the
Planmeca ActiveAqua water treatment system.
NOTE
The dental unit waterlines should be cleaned once a week; the Maintenance
main window displays when cleaning programs were started. If Planmeca
Romexis Clinic Management software is used, detailed information on
cleaning cycles can be retrieved. For more information, see the Planmeca
Romexis user’s manual.
NOTE
Do not let the Waterline Cleaning System run over the weekend.
NOTE
The water must flow properly through the cup fill line, otherwise the unit will
not be flushed. Make sure that the cup fill line is not totally closed. The flow
through the cup fill line is recommended to be approximately 1 dl / 5 sec.
NOTE
The waterline cleaning program can be cancelled by pressing Cancel. If
the cleaning cycle is cancelled after the disinfectant container has been
attached to the dental unit, flushing is required. Help message H 35 guides
you through the flushing.
NOTE
The pop-up windows can be minimised by pressing Minimise.
Steps
1. Press Maintenance to go into maintenance mode.
2. Remove the cup from the cup holder. Turn the bowl away from above
the flushing holder as shown in the figure. Turn also the cup fill tube
above the bowl as shown in the figure. Press the outer edge of the
flushing holder cover (1) and remove the cover.
3. Remove the instrument handpieces from the instruments and clean them
according to the manufacturer’s instructions.
4. Place all water consuming instruments (including syringes) into the
openings in the flushing holder.
Optionally, in dental units with balanced instrument arms, you can
remove the hoses of the instruments to be flushed from the instrument
arms / instrument holders before placing the instruments in the flushing
holder.
NOTE
The container can not be attached to the unit if the tap is not properly
closed.
9. Fill the container with disinfectant up to the groove (marked with arrow in
figure below) and attach the lid. If you need to place the container on the
table, place it horizontally.
NOTE
Make sure that the container is properly closed before attaching it to the
unit.
NOTE
Do not press the release button (marked with arrow in picture) while
attaching the container to the unit.
Automatic feeding begins and the instrument waterlines, the cup fill line
and the bowl waterlines are filled. The Waterline cleaning window on the
control panel informs you about the progress of the cleaning cycle.
11. When the disinfectant has been fed, help message H 31 is displayed
(you will hear a signal tone).
This means that you should now turn off the unit’s power.
Let the disinfectant stay in the unit overnight (min 8h). After the waiting
period you may proceed to section "Waterline flushing" on page 231.
NOTE
The disinfectant must not be left in the unit for longer than one night (not,
for example, over the weekend).
NOTE
If you do not start waterline cleaning as described in this section, but
instead start it simply by attaching the disinfectant container to the dental
unit, help message H 55 is displayed.
To proceed with the cleaning cycle, you must select the instruments and
insert them into the flushing holder as described in steps 1 - 4 in this
section and then press the Waterline cleaning button as instructed on the
control panel.
To cancel the cleaning cycle, press Close. A help message instructs you
how to proceed:
- If the cleaning cycle is cancelled after the container has been attached
to the unit, help message H 35.1 is displayed.
- If help message H 35 is displayed, you must open the water tap, select
the instruments, put them in the flushing holder and press the Instrument
flushing button to flush the instruments.
After flushing, ensure that the water coming from the instruments is clear
before you resume working on the dental unit.
Steps
1. Switch the unit on.
Help message H 31.1 is displayed.
2. Press the release button (marked with arrow in picture) for some
seconds to release the pressure and then remove the container.
3. Open the lid, rinse the container and fill it with clean water. Attach the lid
to the container.
4. Attach the container to the unit.
NOTE
Do not press the release button while attaching the container to the unit.
When the container flushing is ready, you will hear a signal tone.
5. Help message H 32 is now displayed.
It means that the pre-rinsing cycle is completed and the container should
be removed. Remove possible excess water from the container into the
sink. Close the container by attaching the lid. Place the container on a
table or in a cabinet to wait for the next use.
6. Help message H 33 is displayed, meaning that the unit is waiting for the
water to be turned on.
A long instrument flushing cycle using the water from the dental unit
waterlines is automatically started after opening the tap. The long
flushing takes 4 minutes by default in a dental unit with cup fill and bowl
rinse functions.
To extend the duration, contact your Planmeca dealer.
7. After the long flushing cycle, make sure that the water coming from the
instruments and cup fill line is clear.
If the water is blue, run water through all water consuming instruments
and the cup fill line until the water is clear, and increase the flushing
time.
NOTE
To extend the duration, contact your Planmeca dealer.
27.6.4 Maintenance
Change the waterline disinfectant container once a year.
1. Lid
2. Collar
3. Container, code 10040749
4. Standing support
NOTE
Do not use cleaning agents in aerosol or spray form directly on any surfaces.
NOTE
All parts must be cleaned before disinfecting or autoclaving them.
NOTE
If disinfectant or cleaning solution is splashed on the surfaces of the dental
unit, remove the splashes instantly with water and mild soap to avoid stains.
NOTE
Before starting the cleaning procedures in the evening, hang the foot control
on the hook under the patient chair and make sure no cables lie on the floor.
Instrument console
Before cleaning the instrument console, lock the touch display by pressing
the Lock button in the Maintenance window.
When the touch display is locked, the Lock button is blue. Press the button
for 1 second to unlock the touch display. A progress bar is displayed while
you press the button.
Alternatively, the dental unit can be configured so that you can lock/unlock
the touch display by pressing the Flexy button. Contact your Planmeca
dealer.
NOTE
When the dental unit is equipped with hanging-tube instruments, dry the
instrument holders properly after cleaning. Wet surfaces might disturb
instrument recognition.
NOTE
The instrument console and control panel must be completely dry before
covering them with a protective cover.
28.3 Instruments
Clean and service the instruments according to the information supplied with
the instrument.
NOTE
After cleaning the instrument, let the oil run from it for at least 10 minutes
before replacing it on the console.
Do not use lubricating oil on the Morita TORX micromotor (with the exception
of its O-rings).
Throw away the intraoral camera’s disposable hygiene sleeve after use.
To remove the oil collector from the instrument console, unscrew the oil
collector attachment knob and carefully pull the collector out.
28.5 Cuspidor
28.5.1 Bowl
NOTE
Do not pour anything into the bowl unless the unit is switched on and has air
and water (that is, the compressor is switched on and the air- and waterlines
are opened).
NOTE
Do not pour anything else than water and a suction line cleaning agent into
the bowl. The water must be poured slowly into the bowl. The flow may not
exceed 5 l/min.
NOTE
Do not empty the bowl filter to the drain!
NOTE
The bowl can be removed and washed in the dishwasher. The maximum
washing temperature is 65°C. At higher temperatures the bowl may break.
Avoid rapid temperature changes in the dishwasher and when the bowl is in
use. When positioning the bowl into the dishwasher, make sure that the bowl
does not press other objects in the machine.
Clean the bowl after every patient by pouring a few drops of Planmeca
approved suction disinfectant into the bowl and using a soft brush. Rinse the
bowl by pressing Bowl rinse. The outside of the bowl can be wiped clean
with a damp cloth.
The bowl can also be removed and washed in the dishwasher if required. To
remove the bowl, do as follows:
1. Turn the bowl and the cup fill tube away from above the cuspidor.
2. Remove the bowl filter parts and empty the bowl filter.
3. Push the bowl fastening clip carefully down and
4. rotate the bowl counter-clockwise.
5. Lift the bowl slightly upward and remove it by pulling it horizontally.
NOTE
The cover cap of the filter makes the removal of the filter easier, but the filter
can also be used without the cover cap.
NOTE
When you place the suction tube cleaning holder back in the cuspidor after
cleaning, make sure it is pushed firmly into its position in the cuspidor.
NOTE
The disposable filters must be emptied/disposed into a separate amalgam
container.
NOTE
Before emptying the spittoon valve coarse filter you must empty the bowl
(spittoon) valve of any excess water by pressing the Program button for
about 5 seconds until the suction starts. The valve will close automatically
after about 15 seconds.
NOTE
The spittoon valve coarse filter must be emptied into a separate amalgam
container.
When you have emptied the filter, make sure you place it properly back in its
holder to prevent the water from leaking onto the floor.
When the filter is clogged, the dental unit will instruct you to empty the filter.
In some error situations, the dental unit may also restrict the water flow to
prevent leakage.
CAUTION
Switch the unit off before removing the amalgam collector from the dental
unit.
1 Amalgam collector
CAUTION
Switch the unit off before removing the deposit cup from the dental unit.
1 Deposit cup
NOTE
Dry the suction tube holders and the tube bushings properly after cleaning.
Wet surfaces might disturb suction tube recognition.
Steps
1. Rinse each suction tube with 0.5 litres of water by slowly aspirating water
and air through the suction handpieces.
Steps
1. Remove the used aspirating tips.
2. For hygienic and operational reasons, empty one glass of water (100 -
200 ml) with each suction tube by aspirating water and air through the
suction handpiece. Do this even if only the saliva suction tube has been
used.
3. Wipe the suction handpieces with Planmeca approved surface
disinfectant.
4. Wipe the suction holder / Flexy-holder, including the tablet holder, with
Planmeca approved surface disinfectant.
Results
NOTE
Do not use a spray disinfection solution for the suction arms and holders.
NOTE
Clean the tablet according to the instructions given by the manufacturer.
Steps
1. Disinfect the suction system either by running the suction cleaning
program or by using OroCup. For information on the suction cleaning
program, see section "Suction cleaning" on page 221.
2. When the suction system has been rinsed, disinfect the suction
handpieces in a washer-disinfector at 93°C, then optionally autoclave
them at 134°C.
3. Flexy-holder: Disinfect the supplementary holders, suction tube holders
(including rollers) and instrument holder in a washer-disinfector at 93°C.
4. Flexy-holder: Wipe the holder for the intraoral scanner with Planmeca
approved surface disinfectant.
28.6.3.1 OroCup
Steps
1. Mix the cleaning solution:
Pour 20 ml Planmeca approved suction disinfectant into the rinsing
bottle. Add 1 l water and shake well.
NOTE
Do not use dish washing detergents.
2. Place the rinsing bottle (for example OroCup) on a flat surface (table or
floor).
3. Remove the suction handpieces from their holders and push them onto
the inserts inside the cap of the rinsing bottle. Allow the bottle to empty.
4. Return the suction tubes back to the holder right after OroCup has been
emptied. Do not use suction only for air.
5. Replace the exchangeable parts (filters etc.) the next morning.
Steps
1. Pour 50 ml of Dürr MD 555 cleaner into a rinsing bottle (for example
OroCup). Add 1 l water and mix well.
2. Place the rinsing bottle on a flat surface (table or floor).
3. Remove the suction handpieces from their holders and push them onto
the inserts inside the cap of the rinsing bottle.
4. Remove the suction handpieces from the rinsing bottle when there is 250
ml of the solution left in the bottle.
7. When the valve has closed, pour the 250 ml that is left of the solution
into the bowl.
8. Let the solution affect for 30 - 120 minutes.
9. Rinse the bowl by pressing Bowl rinse.
10. Rinse the suction tubes by manually aspirating water through the suction
handpieces.
Steps
1. Mix 5 ml of Planmeca approved suction disinfectant with 250 ml water
and stir well.
2. Open the bowl valve to remove any excess water by pressing the
Program button for about 5 seconds until the suction starts. The valve
will close automatically after about 15 seconds.
3. When the valve has closed, pour the suction disinfectant solution into the
bowl.
4. Let the solution affect overnight. Rinse the suction system the next
morning with 2 l of water.
5. Rinse the bowl with water the next morning by pressing Bowl rinse.
NOTE
We recommend that the suction handpieces be replaced once a year.
28.10 External PC
The external PC together with its mouse and keyboard can be wiped with a
dry cloth, or according to the manufacturer’s instructions.
CAUTION
When cleaning the external PC, always disconnect the PC from the mains
electricity supply.
29 Planmeca ActiveAqua
29.1 Introduction
CAUTION
No chemicals must be added to the Planmeca ActiveAqua water treatment
system.
1 Prefilter
Steps
1. Use the syringe to fill half a cup with water.
2. Immerse a test strip in the water and carefully swirl the test strip around
for 30 seconds.
3. Take out the test strip and compare its colour with the colour chart on the
test strip bottle.
4. On help message H90.1 on the control panel, select the chlorine level
according to the measurement and press OK.
The chlorine level alternatives are < 0.2 (low), 0.2 - 0.8 (optimal), and >
0.8 (high).
Based on these measurements, a help message is displayed and the
dental unit automatically adjusts the electrolysis strength in normal use,
which in turn affects the chlorine level.
Results
If the water does not contain enough chlorine (value < 0.2), perform long
instrument flushing and measure the free chlorine concentration again.
For instructions on how to perform long instrument flushing, see section
"Long instrument flushing" on page 219.
If the chlorine level is continuously too low, raise the value of Electrolysis
strength in normal use in the ActiveAqua maintenance window. If raising the
value does not help, contact service.
For information on functions performed in the ActiveAqua maintenance
window, see section "Adjusting Planmeca ActiveAqua settings" on page 258.
A counter keeps track of the change period. Change the prefilter when the
dental unit displays help message H90.2.
CAUTION
To ensure the proper operation of the dental unit, it is important that you
change the prefilter when help message H90.2 is displayed and do not reset
the prefilter change period counter until the prefilter has been replaced.
NOTE
If you for some reason need to delay the prefilter change, press the Close
button on help message H90.2 and change the prefilter as soon as possible.
Depending on the dental unit's settings, H90.2 is displayed again when you
sign in to the dental unit or when the dental unit is switched on.
NOTE
If help message H91.1 is displayed often, the prefilter may be clogged and
should be changed.
NOTE
It is very important that the water hardness value has been set correctly
in the Planmeca ActiveAqua settings to ensure proper operation of the
Planmeca ActiveAqua water treatment system and to prevent calcification
of the Planmeca ActiveAqua electrolysis chamber.
Steps
1. Switch off the dental unit.
2. Open the cuspidor door.
3. Lift (1) the ActiveAqua module and then turn it out from the cuspidor (2)
to access the prefilter.
NOTE
Hold a plastic bag around the prefilter at removal, as some water will
drop from the filter head.
Detach the prefilter by first rotating it in the direction shown below and
then pulling it downward.
5. Attach the new prefilter by first placing it into position and then rotating it
in the opposite direction until it locks into position.
6. Turn the ActiveAqua module back into the cuspidor and press it down so
that it locks into position.
7. Close the cuspidor door.
8. Switch on the dental unit.
9. Confirm the prefilter change by pressing Reset on help message H90.2.
11. Wait for 90 s while ActiveAqua circulates water to bleed the prefilter.
Steps
1. Press Program.
NOTE
It is very important that the water hardness value is correct to ensure
proper operation of the Planmeca ActiveAqua water treatment system and to
prevent calcification of the Planmeca ActiveAqua electrolysis chamber.
Steps
1. Press Program.
4. Press Edit next to Water hardness (dH) to adjust the water hardness
value.
NOTE
Adjusting this setting resets the free chlorine 7-day counter.
8. Press Edit next to Electrolysis strength, Instrument flushing to adjust the
electrolysis strength when instruments are flushed.
1. Clean-water bottle
2. Pressure monitor
The switches on the clean-water bottle assembly let you control the water
supply.
1. Water supply
Lets you select the water supply for your dental unit. Turn the switch
toward ‘CITY’ to select domestic water, and toward ‘BOTTLE’ to select
the clean-water bottle.
NOTE
If your dental unit is installed so that it has no domestic water, this switch
is missing and the water supply for the dental unit is clean-water bottle
only.
2. Water bottle pressure control
The pressure in the water bottle can be adjusted by turning the knob.
The pressure can be checked from the pressure monitor and should be
between 2.5 and 2.8 bar.
3. Water bottle
When the clean-water bottle is used (water supply -switch turned toward
‘BOTTLE’), the water bottle -switch lets you turn the bottle on or off.
When the switch is toward ‘ON’, the pressure is maintained in the bottle,
and the bottle can be used.
When the switch is toward ‘OFF’, you can detach the bottle, for example,
for cleaning. Allow a few seconds for the pressure to drop before
unscrewing the bottle.
CAUTION
Only Planmeca Planosil, Planmeca PlanPure or Alpro Bilpron disinfectant
must be used. Planmeca does not guarantee the suitability of and is not
liable for damages caused by other disinfectants.
NOTE
To avoid stains, possible disinfectant splashes should be wiped away
immediately.
NOTE
You can interrupt the flushing cycle by pressing Close. After the interruption,
the dental unit can be used normally.
Steps
1. Open the dental unit door.
NOTE
Ensure that the water supply switch is turned toward ‘BOTTLE’ and that
the water bottle switch is turned toward ‘ON’.
6. Press Maintenance to go into maintenance mode.
7. Remove the instrument handpieces from the instruments and clean them
according to the manufacturer’s instructions.
8. Place all water consuming instruments (including syringes) into the
openings in the instrument flushing holder.
Optionally, in dental units with balanced instrument arms, you can
remove the hoses of the instruments to be flushed from the instrument
arms / instrument holders before placing the instruments in the flushing
holder.
In dental units with hanging-tube instruments, the instruments to be
flushed must be removed from the instrument holders before placing
them in the flushing holder.
NOTE
Leave the instruments in the flushing holder overnight.
Steps
1. Open the dental unit door.
2. Remove the clean-water bottle.
First, turn the Water bottle switch toward 'OFF'. Then, take a hold of the
bottom of the bottle, turn the bottle slightly so that the pin moves along
the groove and pull the bottle downwards.
The system will first identify the instruments and then each instrument
hose is flushed with air and water for 30 seconds in its turn.
6. Release the instrument arms (if your dental unit is equipped with
balanced instrument arms).
7. Repeat the flushing sequence in steps 5 and 6 at least three more times,
or until the water is clean. If the clean-water bottle runs out of water, refill
it.
If the water quality of the domestic water is good, you can also use the
domestic water mode when performing the flushing.
8. Balanced instrument arms: Place the instrument hoses back in the
instrument arms, and the instruments back in the instrument console.
Hanging-tube instruments: Place the instruments back in the instrument
holders.
Results
The dental unit is now ready for use.
Some help messages have a Close button that allow you to close the
message before it is automatically closed.
Error messages warn of a fault in the dental unit and require actions from
the user. To correct the error situation, and thus to close the error message,
follow the instructions in the message. Some error messages contain a
question mark that you can press to receive more information about the
error.
NOTE
The level of detail displayed in the error messages is configurable. Contact
your Planmeca dealer.
When you press the hyperlink Contact service in the help or error message,
the service contact details are displayed. The details are only to be changed
by a qualified Planmeca service technician.
The Minimise button allows you to minimise the help or error message to a
help or error bar.
NOTE
The WCS related help messages can be disabled. Contact your Planmeca
dealer.
NOTE
The list may contain help messages related to features that are not part of
your unit configuration.
Help messages
Help messages
Help messages
Help messages
Help messages
Help messages
Help messages
Help messages
Help messages
Help messages
NOTE
The lists may contain error messages related to features that are not part of
your unit configuration.
ERROR EXPLANATION
CODE
E1.01 Main water valve short circuit.
Disconnect valve and check if error disappears.
E1.02 Main air valve short circuit.
Disconnect valve and check if error disappears.
E1.03 Bowl rinse valve short circuit.
Disconnect valve and check if error disappears.
E1.04 Cup filling valve short circuit.
Disconnect valve and check if error disappears.
E1.05 Water flush valve short circuit.
Disconnect valve and check if error disappears.
E1.06 Separator pulse valve short circuit.
Disconnect valve and check if error disappears.
ERROR EXPLANATION
CODE
E1.07 Ejector valve short circuit.
Disconnect valve and check if error disappears.
E1.08 Extra out 1 short circuit.
Disconnect output and check if error disappears.
E1.09 Extra out 2 short circuit.
Disconnect output and check if error disappears.
E1.10 Extra out 3 short circuit.
Disconnect output and check if error disappears.
E1.11 Separator start signal / Microvac's start valve short circuit.
E1.12 Assistant syringe water valve short circuit.
Disconnect valve and check if error disappears.
E1.13 Separator alarm reset signal short circuit.
Disconnect output and check if error disappears.
E1.14 PLANET output (ELMP) short circuit.
Disconnect output and check if error disappears.
E2.01 Incoming water valve open circuit.
Error can be detected when circuit is dead.
E2.02 Incoming air valve open circuit.
Error can be detected when circuit is dead.
E2.03 Bowl rinse valve open circuit.
Error can be detected when circuit is dead.
E2.04 Cup filling valve open circuit.
Error can be detected when circuit is dead.
E2.05 Main Control PCB output open circuit warning.
E2.06 Separator pulse valve open circuit.
Error can be detected when circuit is dead.
E2.07 Main Control PCB output open circuit warning.
E2.08 Main Control PCB output open circuit warning.
E2.09 Main Control PCB output open circuit warning.
E2.10 Main Control PCB output open circuit warning.
E2.11 Separator start signal open circuit / Microvac valve open
circuit.
E2.12 Assistant syringe water valve open circuit.
Error can be detected when circuit is dead.
E2.13 Separator alarm reset signal open circuit.
Error can be detected when circuit is dead.
E2.14 Main Control PCB output open circuit warning.
E2.15 Not used or not in the manuals.
ERROR EXPLANATION
CODE
E3.1 Incoming air pressure compared to water pressure is too low.
Ensure that air pressure main switch is on. If problem persists,
contact service.
E3.2 Internal water pressure too low.
Check dental unit's incoming water pressure. Ensure that
dental unit inlet water tap is open.
E3.4 Internal air pressure (after regulator) is too low.
Ensure that air pressure main switch is on. If problem persists,
contact service.
E3.5 Internal air pressure (after pres. regulator) is too high.
Check pressure regulator, pressure sensor and pressure block
connector.
E3.6 Waterline cleaning feed pressure too low.
Check and adjust waterline cleaning feed pressure. Replace
waterline cleaning feed regulator if problem still exists.
E3.7 Waterline cleaning flush pressure too low.
Check dental unit's incoming water pressure. Ensure that
dental unit inlet water tap is open.
E4.1 Short circuit in cable from MCB to control panel / suction
holder in branch 1.
E4.2 Short circuit in cable from MCB to control panel / suction
holder in branch 2.
E4.3 Communication bus (CAN) is not operational or CAN devices
are disconnected (foot control, operating light, motorised
headrest, uWmc).
E4.4 Communication bus (Console CAN) is not operational.
E5 Unsupported device attached.
Detach the device or contact service.
E6.01 Cuspidor up -safety circuit error.
E6.02 Cuspidor down -safety circuit error.
E6.03 Chair down -safety circuit error.
E6.04 Bowl up -safety circuit error.
E6.05 Bowl down -safety circuit error.
E6.07 Console up -safety circuit error.
E6.08 Console down -safety circuit error.
E6.09 Emergency stop -safety circuit error.
WARNING
If a fuse has blown, contact your Planmeca dealer. Fuses must be changed
only by a qualified Planmeca service technician.
ERROR EXPLANATION
CODE
E7 Power supply related error messages. IPS voltage failure on
MCB.
E7.01 Instrument power supply overcurrent shutdown.
Instrument power supply may be shortcircuited or selected
instrument hose may be faulty.
E9 Internal operating voltage too low. Unit functionality may be
limited.
E10 Internal operating voltage too high.
E11.1 OP-light fuse (F5) and/or Water heater fuse (F7) has blown on
the MCB.
E11.2 Separator fuse (F6) and/or Syringe heater fuse (F8) has blown
on the MCB.
E11.3 Either of the +24V electronics fuses (F9 or F10) has blown on
the MCB.
E11.4 Rectifier D5 or D1 short circuit or either of the 24V electronics
fuses (F3 or F4) has blown on the MCB. Chair, instrument and
headrest control not allowed.
E11.5 Separator fuse (F5) has blown on the MCB.
E11.6 Water heater fuse (F6) has blown on the MCB.
E11.7 Syringe heater fuse (F7) has blown on the MCB.
E11.8 Polymerisation light fuse (F8) has blown on the MCB.
E12.1 SELV voltage too low. Unit functionality may be limited.
E12.2 SELV voltage too high.
E13 Mains frequency outside acceptable range.
E14 IPS temperature measurement sensor error.
E15 IPS heatsink is running too hot on MCB.
E16 Attached scaler electronics is of new type.
E16.1 New type of scaler electronics is attached to MCB.
Update MCB software.
E16.2 New type of scaler electronics is attached to IMUX.
Update MCB software.
E16.3 Scaler electronics slot does not match with scaler hose
connection.
Check scaler electronics connection.
ERROR EXPLANATION
CODE
E16.4 Other instrument than scaler is connected to slot where scaler
electronics is.
Check scaler electronics connection.
E17 Power Supply related error messages.
E18 Power Supply related error messages.
ERROR EXPLANATION
CODE
E19.1 Control panel in branch 1 is of new type.
Update MCB software.
E19.2 Control panel in branch 2 is of new type.
Update MCB software.
E20.1 Control panel 1 button stuck.
Control panel button is stuck during self test.
E20.2 Control panel 2 button stuck.
Control panel button is stuck during self test.
E21 Control panel related error messages.
E22 Control panel related error messages.
ERROR EXPLANATION
CODE
E23 Polymerisation light bulb has blown or is not properly attached
to socket.
E23.1 Instrument overtemperature error.
Check the instrument handpiece and let the instrument cool
down.
E23.2 Micromotor error; phase missing.
Check that the micromotor and hose are connected properly.
E23.3 Instrument undervoltage error.
E23.4 Instrument power protection error.
E23.5 Instrument EEPROM error.
E23.6 Instrument overvoltage error.
ERROR EXPLANATION
CODE
E23.7 Instrument data communication error.
Check that instrument hose is properly connected. Do not
unmount hose when instrument is selected.
E23.8 Apex locator / Morita micromotor PCB failure.
E23.9 Unable to save instrument settings to selected preset.
E25 Satelec mini LED polymerisation light requires newer IMUX
PCB version.
ERROR EXPLANATION
CODE
E28.1 Reference resistor signal out of bounds when unit is switched
on.
E28.2 Active instrument signal out of bounds.
Error in hose identifcation system in IMUX. Ensure that the
instrument's quick connector is properly attached.
E28.3 Syringe signal out of bounds.
Error in hose identifcation system in IMUX. Ensure that the
instrument's quick connector is properly attached.
E28.4 Reference resistor signal out of bounds when instrument is
activated.
Ensure that the instrument's quick connector is properly
attached.
E28.5 Syringe signal changes during use (blinking).
Error in hose identifcation system in IMUX. Ensure that the
instrument's quick connector is properly attached.
E29 Voltage error in instrument light power supply in IMUX.
If there is a problem with one instrument only, replace the
hose. If the problem is with several instruments or the hose is
ok, contact service.
E32.1 IMUX is not responding. IMUX cable disconnected or failure in
cable or IMUX.
E32.2 IMUX software is not compatible (IMUX is of new type) with
MCB software.
Update MCB software.
E32.3 IMUX data error (cable short circuit).
E32.4 IMUX communication error.
E32.5 Wrong IMUX type or wrong unit type.
E33.1 Syringe select valve short circuit.
E33.2 Instrument 1 select valve short circuit.
ERROR EXPLANATION
CODE
E33.3 Instrument 2 select valve short circuit.
E33.4 Instrument 3 select valve short circuit.
E33.5 Instrument 4 select valve short circuit.
E33.6 Instrument multiplexer related error messages.
E33.7 Drive/Cooling air valve short circuit.
E33.8 Air coolant valve short circuit.
E33.9 Water coolant valve short circuit.
E34.1 Syringe select valve open circuit.
E34.2 Instrument 1 select valve open circuit.
E34.3 Instrument 2 select valve open circuit.
E34.4 Instrument 3 select valve open circuit.
E34.5 Instrument 4 select valve open circuit.
E34.6 Instrument multiplexer related error messages.
E34.7 Drive/Cooling air valve open circuit.
E34.8 Air coolant valve circuit.
E34.9 Water coolant valve circuit.
E35.1 Drive/Cooling air pressure sensor output below 0.2 V.
E35.2 Air coolant pressure sensor output below 0.2 V.
E35.3 Water coolant pressure sensor output below 0.2 V.
E35.4 Differential pressure sensor output below 0.2 V.
E36.1 Drive/Cooling air measurement over range.
Check if micromotor handpiece has air- and waterlines. Check
if instrument, handpiece or hose is blocked.
E36.2 Spray air measurement over range.
Check if micromotor handpiece has air- and waterlines. Switch
off spray water and air if there are no air- and waterlines in
instrument or handpiece.
E36.3 Spray water measurement over range.
Check if micromotor handpiece has air- and waterlines. Switch
off spray water and air if there are no air- and waterlines in
instrument or handpiece.
E36.4 Differential pressure sensor output above 5 V.
E37 Pressure sensor cable not properly attached to IMUX.
E39 Drive (cooling) air valve control servo cannot maintain
pressure to instrument.
E42 Air coolant (spray air) control servo cannot maintain required
pressure.
E45 Water coolant (spray water) control servo cannot maintain
required pressure.
ERROR EXPLANATION
CODE
E47 Suction holder is of new type.
E47.1 Suction holder in branch 1 is of new type.
Update MCB software.
E47.2 Suction holder in branch 2 is of new type.
Update MCB software.
E48.1 No suction holders detected.
Either the holder is missing or faulty, or the cable to the holder
is loose or faulty.
E48.2 Suction holder related error messages.
E48.3 Suction holder related error messages.
E48.4 Suction holder related error messages.
E49.1 Suction holder PCB or its cable is faulty in branch 1.
Either the holder is missing or faulty, or the cable to the holder
is loose or faulty.
E49.2 Suction holder PCB or its cable is faulty in branch 2.
Either the holder is missing or faulty, or the cable to the holder
is loose or faulty.
E50 Unidentified STCS jumper configuration.
E50.1 Water management system (WMS) must be set to Bottle
water off -mode when starting suction cleaning.
E50.2 Suction disinfectant pump is not running.
ERROR EXPLANATION
CODE
E51.1 Cable from foot control is loose or connected into wrong
connector on MCB.
E51.2 Foot control is not responding.
Ensure that the foot control cable is properly attached to the
unit. If it is, contact service.
E51.3 Foot control pedal was pressed down when dental unit was
switched on.
Restart the unit without touching the foot control.
E51.4 Foot control pedal was not in home position when dental unit
was switched on.
Restart the unit without touching the foot control.
ERROR EXPLANATION
CODE
E51.5 Foot control's chair control knob was not in home position
when dental unit was switched on.
Restart the unit without touching the foot control.
E51.6 Foot control left knob is either stuck or active at power-up or
after pedal use.
E51.7 Foot control right knob is either stuck or active at power-up or
after pedal use.
E52 Foot control is of new type, update MCB software.
MCB software must be updated.
E52.1 Incompatible wireless foot control receiver software.
E52.2 Incompatible wireless foot control software.
E52.3 Incompatible foot control software.
E53 Foot control data error (cable short circuit).
E54.0 Foot control error.
E54.1 Foot control EEPROM write failure.
E54.2 Foot control EEPROM read failure.
E54.3 Pedal too far from sensors, channel A.
E54.4 Pedal too far from sensors, channel B.
E54.5 Sensor plate is tilted too much to either side, checksum error.
E54.6 Sensor plate is too close to PCB, channel A.
E54.7 Sensor plate is too close to PCB, channel B.
E54.8 Foot control re-trigger error.
E54.9 Foot control calibration error.
E55 Wireless foot control connection lost.
ERROR EXPLANATION
CODE
E56 Operating light erroneously connected or short circuit in push
button.
E57 Incompatible SingLED software.
E58 Operating light bulb burned out.
Replace bulb.
ERROR EXPLANATION
CODE
E59.1 Separator reports functional error.
Refer to Metasys separator documentation.
E59.2 Separator reports functional error.
Refer to Dürr separator documentation.
E60 Separator is not responding or separator cable is faulty.
E61 Separator is flooded with too much water.
E62 Newly attached separator is of new type and cannot be
controlled by MCB.
E63.1 Water management system (WMS) seems to be installed,
although it should not be (according to service mode).
E63.2 No Water management system (WMS) is installed, although it
should be according to service mode.
ERROR EXPLANATION
CODE
E64 Lift motor position potentiometer or its cable is faulty or
disconnected.
E65 Lift motor does not run or no signal from position
potentiometer.
E65.1 Lift motor does not run. EmeStop relay PCB/cables or position
sensor/cable may be faulty.
E66 Lift motor or its position potentiometer cable has a wrong
connection.
E67 Backrest position potentiometer or its cable is faulty or
disconnected.
E68 Backrest motor does not run or no signal from position
potentiometer.
E68.1 Backrest motor does not run. EmeStop relay PCB/ cables or
position sensor/ cable may be faulty.
E69 Backrest motor or its position potentiometer cable has a wrong
connection.
E70.1 Lift motor error.
E70.2 Backrest motor error.
ERROR EXPLANATION
CODE
E72.1 Program (Flash-EPROM) error. Main software is corrupted.
Replace Flash- EPROM.
E72.2 Program (Flash-EPROM) error. Boot software is corrupted.
Replace Flash- EPROM.
E72.3 Program (Flash-EPROM) error.
Update MCB software.
E72.4 Data transfer error while updating main PCB SW from control
panel memory device.
E73.1 EEPROM error, CPU EEPROM erase/program failure, replace
CPU.
E73.2 CPU configuration register contents are wrong, replace CPU.
E73.3 CPU EEPROM checksum error.
E73.4 CPU EEPROM checksum programmed. Replace CPU if error
occurs often.
E75.1 CPU error, WD reset.
E75.2 Illegal OP-code.
E75.3 Illegal vector.
E75.6 Mains voltage failure.
E75.7 Clock monitor reset.
E76 Main PCB hardware test failed.
E76.1 Unknown PCB version. Software upgrade required.
E79 IMUX water pressure cannot be released during waterline
cleaning cycle.
E79.1 IMUX water pressure rose during waterline cleaning cycle
when pressure rise was not expected.
ERROR EXPLANATION
CODE
E80.1 Motorised headrest is not found (according to service mode
configuration).
E80.2 Motorised headrest is found, but is not set in service mode
configuration.
E80.3 Headrest joystick (dentist side) stuck or cable broken.
E80.4 Headrest joystick (assistant side) stuck or cable broken.
E80.5 Motorised headrest motor A potentiometer or cable is faulty or
disconnected.
ERROR EXPLANATION
CODE
E80.6 Motorised headrest motor B potentiometer or cable is faulty or
disconnected.
E80.7 Motorised headrest length potentiometer or cable is faulty or
disconnected.
E81 Motorised headrest communication error (may be too old or
wrong software or loose cables or short circuit).
E81.1 Motorised headrest communication error.
E82 Headrest software is incompatible with MCB software.
Headrest or MCB software should be upgraded.
E82.1 Headrest software is incompatible with MCB software.
Headrest or MCB software should be upgraded.
E82.2 Incompatible headrest software.
ERROR EXPLANATION
CODE
E83 ActiveAqua connection loss
E83.1 ActiveAqua and main PCB settings vary.
Check and set water hardness (dH) and electrolysis settings
in service modes (n.181 and n.182) or in the ActiveAqua
view. Reset the counters for prefilter replacement and annual
maintenance.
E83.2 ActiveAqua electrolysis chamber asymmetrical current error.
E83.3 ActiveAqua electrolysis chamber high current error.
E83.4 ActiveAqua electrolysis chamber low current error.
E83.5 ActiveAqua RT clock malfunction.
E83.6 ActiveAqua water flow high.
Water flow too high due to faulty water flow sensor or leakage
in the system.
E83.7 ActiveAqua level sensors missing.
Level sensors are not connected.
E83.8 ActiveAqua electrolysis chamber very high current.
E83.9 ActiveAqua water container fill timeout.
ActiveAqua can not fill the water container. Ensure that
nothing blocks the inlet water (stuck inlet water filter or flow
reducer inside the main water block) and that the water
container does not leak.
E84.1 ActiveAqua water container fill self-test fail.
ActiveAqua can not fill the water container. Ensure that
nothing blocks the inlet water.
ERROR EXPLANATION
CODE
E84.2 ActiveAqua electrolysis chamber self-test fail.
Electrolysis chamber current not detected in ActiveAqua self-
test. Check the chamber connection.
E84.3 ActiveAqua water flow self-test fail.
Water flow not detected in ActiveAqua self-test. Check the
flow meter, circulation valve and pump.
E84.4 ActiveAqua pressure switch selft-test fail.
ActiveAqua pressure switch short circuit detected.
E84.5 ActiveAqua container recirculation flow self-test fail.
ActiveAqua water flow detected even if there should not be
any.
E84.9 ActiveAqua software is incompatible with dental unit software.
Perform dental unit software upgrade.
ERROR EXPLANATION
CODE
E90 Water leak detected.
Main water valve is closed.
E90.1 Water leak detected. Water use allowed temporarily.
ERROR EXPLANATION
CODE
E91 Annual maintenance overdue.
Annual maintenance should have been performed <x> days
ago.
ERROR EXPLANATION
CODE
E99 Software upgrade failure.
Retry upgrade.
E99.1 MCB software upgrade failure.
Retry upgrade.
ERROR EXPLANATION
CODE
E99.2 IMUX software upgrade failure.
Retry upgrade.
E99.3 Control panel software upgrade failure.
Retry upgrade.
E99.4 Operating light software upgrade failure.
Retry upgrade.
E99.5 Motorised headrest software upgrade failure.
Retry upgrade.
E99.6 Foot control software upgrade failure.
Retry upgrade.
E99.7 Wireless foot control software upgrade failure.
Retry upgrade.
E99.8 Wireless foot control receiver software upgrade failure.
Retry upgrade.
E99.9 PlanID reader software upgrade failure.
Retry upgrade.
ERROR EXPLANATION
CODE
EP19.3 Control panel version mismatch.
EP19.5 Control panel software upgrade has failed or memory card is
faulty.
EP21.1 Control panel display is faulty.
EP21.2 Control panel data error.
EP21.5 Unable to read Main PCB software version.
EP21.6 Control panel software not installed or software error.
Insert software update SD-card or contact service.
EP21.7 Touch panel is not working.
Steps
1. Press Program.
NOTE
The following is an example only and does not necessarily portray the
actual situation.
Help messages
Error messages
A grey button means that the message type is not listed, and a blue
button that it is listed.
NOTE
Carefully consider when the deletion of message history is appropriate
as it contains information that is valuable to the Planmeca service
technician.
6. Press OK to close the window.
NOTE
The Save message history to USB -option is meant to be used only by a
qualified Planmeca service technician.
32 Consumables
Consumables are detachable parts of the dental unit that the user can
change.
Suction handpieces
Disinfectants
33 Disposal
In order to reduce the environmental load over the product’s entire lifecycle,
Planmeca products are designed to be as safe as possible to dispose of.
Planmeca products fulfil the requirements of Directives 2011/65/EU (RoHS)
and 2012/19/EU (WEEE).
Disposal of obsolete units is the responsibility of the waste possessor. The
risks involved and the necessary precautions must be taken into account
when handling waste products.
Parts which can be recycled should always be taken to the appropriate
processing centres, after hazardous waste has been removed. All parts
and components containing hazardous materials must be disposed of in
accordance with waste legislation and instructions issued by the local
environmental authorities.
The following parts contain hazardous waste:
• Amalgam separators in dental units, including filters and amalgam
collector /deposit cup (amalgam)
Batteries must be disposed of following the requirements of Directive
2006/66/EEC and in accordance with waste legislation and instructions
issued by the local environmental authorities.
The following parts contain batteries:
• Dental unit wireless foot control
• Circuit boards (may contain)
34 Technical information
34.1 Technical specifications
Original manufacturer
PLANMECA Oy, Asentajankatu 6, 00880 Helsinki, FINLAND
Phone: +358 20 7795 500, fax: +358 20 7795 555, www.planmeca.com
Colours
Painted parts: RAL-9016
Upholstery colours: Please consult your dealer for availability
Mechanical dimensions
Installed: (H x D x W) 1210 mm x 963 mm x 1990 mm
(see template for details)
Weight
150 kg (331 lbs)
Maximum allowed load on patient seat
Maximum allowed patient weight 185 kg (407 lbs) and accessories load of
15 kg (33 lbs)
Environmental conditions
Transportation conditions
Temperatures: -20°C to +60°C (-4°F to +140°F)
Relative humidity: 5% RH to 95% RH; non-condensing humidity
Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi)
Storage conditions
Temperatures: -5°C to +60°C (+23°F to +140°F)
Relative humidity: 5% RH to 95% RH; non-condensing humidity
Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi)
If the unit has been stored at temperatures below +10 °C (+50 °F) for
more than a few hours, time must be allowed for the unit to reach room
temperature in the original packing before connecting the unit to the mains
voltage.
Operating conditions
Temperatures: +15°C to +35°C (+59°F to +95°F)
Relative humidity: 5% RH to 95% RH; non-condensing humidity
Air pressure: 800 hPa to 1060 hPa (12 psi to 15 psi)
Altitude: < 2000 m (less than 1.25 miles)
Mains voltage and frequency
Mains voltage setting: 100V~
115V~
220-240V~
Mains frequency: 50 or 60 Hz
Fuse rating and type
Output pressure: water 2.8 bar, air 5.5 bar (regulated internal water
and air pressure)
Foot control power supply (optional)
Type: MENB1010A0903F01
Wireless foot control (optional)
Battery size: AA, HR6
Battery type: NiMH 1.2V, min 2000mAh, low self-discharge,
UL-listed (USA, Canada only)
Planmeca ProSensor power supply (optional)
Phihong Single Port Injector
Type: PSA16U-480 (POE)
Input voltage: 100-240 VAC (50-60 Hz)
Output voltage: 48VDC
Max. output current: 0.35 A
Insulation voltage
Primary-secondary 3000VDC
Planmeca approved disinfectants for the suction system are Dürr Orotol
Plus and ORBI-Sept Evacuation System Disinfection Concentrate. For
more information on these disinfectants, please refer to the manufacturer’s
documentation.
Type BF
The following lists the instruments that are available for the Planmeca dental
unit and their electrical classification type.
Instrument classifications
Instrument Type
DCI autoclavable 3-way syringe B
Luzzani Ergo 3-way syringe B
Luzzani Minibright 6-way syringe B
Luzzani Minibright 6-way syringe with LED B
PM fibre optic turbine hose S B
Bien-Air MCX brushless micromotor with LED B
Bien-Air MX2 brushless micromotor with LED B
Bien-Air MX-i LED implantology micromotor B
SycoTec SLM-E Typ 810 brushless micromotor with LED B
Morita TORX micromotor B
EMS No Pain scaler B
EMS No Pain LED scaler B
LM-ProPower Ultra scaler B
LM-ProPower UltraLED scaler B
Satelec Newtron scaler B
Satelec Newtron LED scaler B
Planmeca Lumion Plus LED polymerisation light B
Planmeca Somia USB intraoral camera BF
Planmeca Emerald intraoral scanner B
34.3 Dimensions
NOTE
The following picture is an example only and presents one possible
scenario. The actual positioning of dentist and assistant depends on the
used working method, treatment situation, region etc. and can therefore not
be explicitly stated in this manual.
1. Dentist’s area
2. Assistant’s area
CAUTION
Use only Planmeca specified devices inside the patient area.
CAUTION
The floor of the patient area must be dry.
NOTE
Connect only Planmeca specified devices to the dental unit.
NOTE
The external PC must be protectively earthed and IEC 60950 -approved (CE
marked).
NOTE
The monitor must fulfil IEC 60601-1 ed.3 requirements.
34.3.6 Cart
35 Planmeca as EU importer
Planmeca is the EU importer for the following manufacturers:
EU authorised representative:
EMS France SARL
Route de Pontarlier 32, 39460 Foncine le Haut, France
EU authorised representative:
Medical Technology Promedt Consulting GmbH
Altenhofstrasse 80, 66386 St. Ingbert, Germany
EU authorised representative:
Dental Components Europe (DCE)
56 Bis Avenue de la Lanterne, 06200 Nice, France
36 Certifications
36.1 CE
Hereby, Planmeca Oy declares that the radio equipment type PlanID™ is in
compliance with Directive 2014/53/EU.
The full text of the EU declaration of conformity is available upon request.
36.8 RF Exposure
This device has been tested for compliance with FCC RF exposure limits
in a portable configuration. At least 15 cm of separation distance between
the PlanID device and the user's body must be maintained at all times. This
device must not be used with any other antenna or transmitter that has not
been approved to operate in conjunction with this device.