Instructions for use

ESTETICA E50 Life

Distributed by: Manufacturer:
KaVo Dental GmbH Kaltenbach & Voigt GmbH
Bismarckring 39 Bismarckring 39
D-88400 Biberach D-88400 Biberach
Phone +49 (0) 7351 56-0 www.kavo.com
Fax +49 (0) 7351 56-1488
 Instructions for use ESTETICA E50 Life
Table of contents

Table of contents
1 User instructions............................................................................................................................................... 7
1.1 User guide................................................................................................................................................ 7
1.1.1 Abbreviations............................................................................................................................... 7
1.1.2 Symbols....................................................................................................................................... 7
1.1.3 Target group................................................................................................................................ 7
1.2 Service...................................................................................................................................................... 7
1.3 Terms and conditions of warranty............................................................................................................. 8
1.4 Transportation and storage....................................................................................................................... 8
1.4.1 Currently valid packaging regulations......................................................................................... 8
1.4.2 Damage in transit........................................................................................................................ 8
1.4.3 Information on the packaging: Storage and transportation......................................................... 9

2 Safety............................................................................................................................................................. 11
2.1 Description of safety instructions............................................................................................................ 11
2.1.1 Warning symbol......................................................................................................................... 11
2.1.2 Structure.................................................................................................................................... 11
2.1.3 Description of hazard levels...................................................................................................... 11
2.2 Purpose – Proper use............................................................................................................................. 11
2.2.1 General...................................................................................................................................... 11
2.2.2 Product-specific......................................................................................................................... 14
2.3 Safety instructions.................................................................................................................................. 15
2.3.1 General information................................................................................................................... 15
2.3.2 Product-specific......................................................................................................................... 17

3 Product description......................................................................................................................................... 20
3.1 Treatment unit versions.......................................................................................................................... 20
3.1.1 KaVo ESTETICA E50 Life TM................................................................................................... 20
3.1.2 KaVo ESTETICA E50 Life S...................................................................................................... 20
3.2 Patient chair Standard and COMPACTchair.......................................................................................... 21
3.3 Device body with patient unit.................................................................................................................. 22
3.4 Dentist unit versions............................................................................................................................... 24
3.4.1 TM table..................................................................................................................................... 24
3.4.2 S table....................................................................................................................................... 25
3.5 Assistant element – Versions ................................................................................................................. 26
3.5.1 Standard assistant unit.............................................................................................................. 26
3.5.2 Assistant element right, left (optional)....................................................................................... 27
3.6 Three function handpiece (3F handpiece).............................................................................................. 28
3.7 Multifunctional handpiece (MF handpiece)............................................................................................. 28
3.8 Controls.................................................................................................................................................. 29
3.8.1 Dentist's unit TM table............................................................................................................... 29
3.8.2 Dentist's unit S table.................................................................................................................. 29
3.8.3 Assistant unit............................................................................................................................. 30
3.8.4 Groups of keys.......................................................................................................................... 30
3.8.5 Foot control................................................................................................................................ 33
3.9 Rating plate and identification plate........................................................................................................ 34
3.10 Technical data........................................................................................................................................ 38

4 Operation........................................................................................................................................................ 44
4.1 Switching the device on and off.............................................................................................................. 44

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4.2 Adjusting the dental chair....................................................................................................................... 44

4.2.1 Adjusting the arm rest (optional)................................................................................................ 44
4.2.2 Adjust head rest......................................................................................................................... 45
4.2.3 Positioning the dental chair manually........................................................................................ 47
4.2.4 Automatic positioning of dental chair......................................................................................... 48
4.2.5 Safety shut-off........................................................................................................................... 53
4.3 Moving the patient chair.......................................................................................................................... 57
4.4 Moving the dentist unit............................................................................................................................ 57
4.4.1 Moving the dentist unit TM........................................................................................................ 58
4.4.2 Moving the dentist unit S........................................................................................................... 58
4.5 Moving the patient unit............................................................................................................................ 59
4.5.1 Swinging the patient unit by hand............................................................................................. 59
4.6 Moving the assistant element................................................................................................................. 60
4.6.1 Adjusting the height of the standard assistant element............................................................. 60
4.6.2 Moving the assistant element right, left (optional)..................................................................... 60
4.7 Using functions through the menu.......................................................................................................... 62
4.7.1 Using the user menu................................................................................................................. 62
4.7.2 Standby menu........................................................................................................................... 67
4.7.3 Using the MEMOdent menu...................................................................................................... 70
4.7.4 Changing the turbine settings in the MEMOdent menu............................................................. 70
4.7.5 Changing the settings for INTRA LUX motors KL 703 LED / KL 701 and COMFORTdrive...... 71
4.7.6 Changing PiezoLED settings in the MEMOdent menu.............................................................. 72
4.7.7 Changing settings for the multifunctional handpiece in the MEMOdent menu.......................... 74
4.7.8 Use the Timer............................................................................................................................ 75
4.7.9 Using the CONEXIOcom menu................................................................................................. 76
4.8 Using function through the dentist or assistant unit................................................................................ 78
4.8.1 Using the hygiene functions...................................................................................................... 78
4.8.2 Using the light functions............................................................................................................ 79
4.8.3 Using the timer.......................................................................................................................... 85
4.9 Operating the foot switch........................................................................................................................ 86
4.9.1 General functions...................................................................................................................... 86
4.9.2 Special functions of the wireless foot control............................................................................ 86
4.9.3 Establishing a connection between the wireless foot control and the treatment unit................ 88
4.9.4 Positioning the patient chair with the foot control...................................................................... 90
4.9.5 Preset level................................................................................................................................ 90
4.9.6 Preselect dentist........................................................................................................................ 90
4.9.7 Start and regulate instruments.................................................................................................. 90
4.9.8 Setting the cooling condition..................................................................................................... 91
4.9.9 Actuate blown air....................................................................................................................... 91
4.9.10 Preselect counterclockwise motor rotation................................................................................ 91
4.9.11 Adjusting the instrument light.................................................................................................... 92
4.9.12 Use physiological saline solution (optional accessory)............................................................. 92
4.9.13 Using CONEXIOcom (fee-based additional option).................................................................. 92
4.9.14 Charging the wireless foot control............................................................................................. 93
4.10 Using instruments................................................................................................................................... 94
4.10.1 Holder logic................................................................................................................................ 94
4.10.2 Using suction hoses.................................................................................................................. 94
4.10.3 Using the three function handpiece........................................................................................... 96
4.10.4 Using the multifunctional handpiece.......................................................................................... 97
4.10.5 Using the PiezoLED................................................................................................................ 101

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4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)................................................. 101
4.11.1 General information................................................................................................................. 101
4.11.2 Open ENDO mode.................................................................................................................. 102
4.11.3 Change settings in the option menu........................................................................................ 103
4.11.4 Set parameters........................................................................................................................ 104
4.11.5 Leaving ENDO Mode............................................................................................................... 107
4.12 Use pump for physiological saline solution (optional accessory).......................................................... 107
4.12.1 General information................................................................................................................. 108
4.12.2 Connecting the coolant............................................................................................................ 108
4.12.3 Activating the pump for the respective holder (enabling) and regulating the pump................ 109
4.12.4 Change salt bag...................................................................................................................... 109
4.12.5 Attaching and etaching the pump............................................................................................ 110
4.12.6 Exchange the pump hose........................................................................................................ 111
4.13 Using the COMFORTdrive 200 XD/COMFORTbase (optional accessory).......................................... 114
4.13.1 General use............................................................................................................................. 114
4.13.2 Fitting the motor hose on the dentist's element....................................................................... 114
4.13.3 Replacing the high-pressure bulb of the COMFORTbase....................................................... 114
4.13.4 Replace O-rings....................................................................................................................... 115
4.14 Using the USB interface....................................................................................................................... 115
4.15 Using the camera.................................................................................................................................. 116

5 Preparation methods DIN EN ISO 17664..................................................................................................... 117

6 Accessories and kits..................................................................................................................................... 118

6.1 Device................................................................................................................................................... 118
6.2 Dental chair........................................................................................................................................... 118
6.3 Assistant unit........................................................................................................................................ 118
6.4 Dentist unit............................................................................................................................................ 119

7 Safety checks - testing instructions.............................................................................................................. 120

7.1 Introduction........................................................................................................................................... 120
7.1.1 General instructions................................................................................................................. 120
7.1.2 Notes for medical electrical systems....................................................................................... 121
7.1.3 Essential parts of the safety check.......................................................................................... 122
7.1.4 Testing intervals...................................................................................................................... 123
7.1.5 Notes on the test method in accordance with IEC 62353....................................................... 123
7.1.6 Notes on repeat testing........................................................................................................... 123
7.2 Instructions for safety checks............................................................................................................... 123
7.2.1 Preparatory measures to be undertaken on the device.......................................................... 123
7.2.2 Visual inspection (inspection by examination)......................................................................... 125
7.2.3 Safety measurement............................................................................................................... 128
7.2.4 Functional test......................................................................................................................... 137
7.2.5 Assessment and documentation ............................................................................................ 140

8 Appendix - Additional measuring sites......................................................................................................... 142

8.1 Additional scanning sites SL X in the protective conductor measurement........................................... 142
8.2 Additional measuring sites AP X for EUL/EPL measurement............................................................... 143
8.3 Additional connection sites ACP X (additional earth connections)....................................................... 144

9 Troubleshooting............................................................................................................................................ 145

10 Data on electromagnetic compatibility according to EN 60601-1-2.............................................................. 149

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10.1 Electromagnetic Transmissions............................................................................................................ 149

10.2 Resistance to electromagnetic interference.......................................................................................... 149
10.3 Recommended safe distance between portable and mobile HF telecommunications equipment and the
treatment unit........................................................................................................................................ 150
10.4 Immunity to electromagnetic interference............................................................................................. 151

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 Instructions for use ESTETICA E50 Life
1 User instructions | 1.1 User guide

1 User instructions

1.1 User guide

Requirement
Read these instructions prior to first use to avoid misuse and prevent damage.

1.1.1 Abbreviations
Abbre‐ Explanation
viation
IfU Instructions for use
CI Care instructions
AI Assembly instructions
TI Technician's instructions
SC Safety checks
IEC International Electrotechnical Commission
RI Repair instructions
RK Retrofitting kit
AS Assembly set
EP Enclosed parts
EMC Electromagnetic compatibility
PI Processing instructions

1.1.2 Symbols
See the Safety/Warning Symbols section

Important information for users and technicians

CE mark according to EC Directive 93/42 for medical devices

Action required

1.1.3 Target group

This document is for dentists and dental office staff.

1.2 Service
KaVo Customer Service:
+49 (0) 7351 56-1000
[email protected]
Please refer to the serial number of the product in all inquiries!
For further information, please visit: www.kavo.com

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Instructions for use ESTETICA E50 Life
1 User instructions | 1.3 Terms and conditions of warranty

1.3 Terms and conditions of warranty

KaVo provides the final customer with a warranty that the product cited in the hand‐
over certificate will function properly and guarantees zero defects in the material or
processing for a period of 12 months from data of purchase, subject to the following
conditions:
Upon justified complaints of flaws or a short delivery, KaVo will make good its warran‐
ty by replacing the product free of cost or repairing it according to the customer's wish‐
es. Other claims of any nature whatsoever, in particular with respect to compensation,
are excluded. In the event of default and gross negligence or intent, this shall only ap‐
ply in the absence of mandatory legal regulations to the contrary.
KaVo cannot be held liable for defects and their consequences due to natural wear,
improper cleaning or servicing, non-compliance with operating, servicing or connection
instructions, calcification or corrosion, contaminated air or water supplies or chemical
or electrical factors deemed abnormal or impermissible in accordance with factory
specifications.
The warranty does not usually cover bulbs, glassware, rubber parts and the colour‐
fastness of plastics.
Defects or their consequences that can be attributed to interventions on or changes
made to the product by the customer or a third party are excluded from the warranty.
Defects or their consequences that can be attributed to interventions on or changes
made to the product by the customer or a third party are excluded from the warranty.

1.4 Transportation and storage

1.4.1 Currently valid packaging regulations

Note
Only valid for the Federal Republic of Germany.
Dispose of and recycle the sales packaging appropriately in accordance with current
packaging regulations, employing waste management or recycling companies. Com‐
ply with the comprehensive return system. KaVo has had its sales packaging licensed
for this purpose. Please comply with the regional public waste-disposal system.

1.4.2 Damage in transit

In Germany
If the packaging is visibly damaged on delivery, please proceed as follows:
1. The recipient of the package must record the loss or damage on the delivery re‐
ceipt. The recipient and the representative of the shipping company must sign this
delivery receipt.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use the product.
4. Report the damage to the shipping company.
5. Report the damage to KaVo.
6. Consult with KaVo first, before returning a damaged product.
7. Send the signed delivery receipt to KaVo.

If the product is damaged but there was no discernable damage to the packaging
upon delivery, proceed as follows:

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 Instructions for use ESTETICA E50 Life
1 User instructions | 1.4 Transportation and storage

1. Report the damage to the shipping company immediately and no later than 7 days
after delivery.
2. Report the damage to KaVo.
3. Leave the product and packaging in the condition in which you received it.
4. Do not use a damaged product.

Note
If the recipient fails to comply with any of the above-mentioned obligations, the
damage will be considered to have arisen after delivery
(in accordance with the General German Freight Forwarders´ Terms and Conditions, Art. 28)
.

Outside Germany

Note
KaVo shall not be held liable for damage arising from transportation.
The shipment must be checked on arrival.

If the packaging is visibly damaged on delivery, please proceed as follows:

1. The recipient of the package must record the loss or damage on the delivery re‐
ceipt. The recipient and the representative of the shipping company must sign this
delivery receipt.
Without this evidence, the recipient will not be able to assert a claim for damages
against the shipping company.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use the product.

If the product is damaged but there was no discernable damage to the packaging
upon delivery, proceed as follows:
1. Report any damage to the shipping company either immediately or no later than 7
days after delivery.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use a damaged product.

Note
If the recipient fails to comply with any of the above-mentioned obligations, the
damage will be considered to have arisen after delivery
(in accordance with CMR law, Chapter 5, Art. 30).

1.4.3 Information on the packaging: Storage and transportation

Note
Please keep the packaging in case you need to return the product for servicing or
repair.
The symbols printed on the outside are for transportation and storage, and have the
following meaning:

Transport upright with the arrows pointing upwards!

Fragile - protect against impact!

Protect from moisture!

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Instructions for use ESTETICA E50 Life
1 User instructions | 1.4 Transportation and storage

Permissible stacking load

Temperature range

Humidity

Air pressure

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 Instructions for use ESTETICA E50 Life
2 Safety | 2.1 Description of safety instructions

2 Safety

2.1 Description of safety instructions

2.1.1 Warning symbol

Warning symbol

2.1.2 Structure

DANGER
The introduction describes the type and source of the hazard.
This section describes potential consequences of non-compliance.
▶ The optional step includes necessary measures for hazard prevention.

2.1.3 Description of hazard levels

The safety instructions listed here, together with the three levels of danger will help
avert property damage and injury.

CAUTION
CAUTION
indicates a hazardous situation that can cause damage to property or mild to moder‐
ate injuries.

WARNING
WARNING
indicates a hazardous situation that can lead to serious or fatal injury.

DANGER
DANGER
indicates a maximal hazard due to a situation that can directly cause death or fatal
injury.

2.2 Purpose – Proper use

2.2.1 General
The user must ensure that the unit works properly and is in satisfactory condition be‐
fore each use.
The KaVo equipment system is a dental treatment unit in accordance with ISO 7494
with a dental chair in accordance with ISO 6875. This KaVo product is designed for
use in dentistry only and may only be used by trained medical personnel. Any other
type of use is not permitted.
"Proper use" includes following all the instructions for use and ensuring that all inspec‐
tions and service tasks are performed.

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Instructions for use ESTETICA E50 Life
2 Safety | 2.2 Purpose – Proper use

The overarching guidelines and/or national laws, national regulations and the rules of
technology applicable to medical devices for start-up and use of the KaVo product for
the intended purpose must be applied and followed.

KaVo accepts liability for the safety, reliability, and performance of components sup‐
plied by KaVo, provided:
▪ installation, instructions, expansions, adjustments, changes or repairs were carried
out by technicians trained by KaVo or third parties authorised by KaVo, or by the
personnel of authorised distributors.
▪ the unit was operated in accordance with the instructions for use, care and instal‐
lation.
▪ the IT components supplied by the operator meet the technical requirements in
these instruction for use for hardware and software, and they are installed and set
up according to the descriptions of these components.
▪ in the case of repairs, the requirements of IEC 62353 (DIN VDE 0751-1) "Repeat
tests and tests before start-up of electrical items of medical equipment and sys‐
tems - general regulations" are met in full.

It is a responsibility of the user:

▪ only use equipment that is operating correctly,
▪ protect him or herself, the patient and third parties from danger, and
▪ avoid contamination from the product..

The applicable national legal regulations must be observed during the use of the de‐
vice, in particular the following:
▪ Applicable regulations governing the connection and start-up of medical devices.
▪ Current occupational safety regulations.
▪ Current accident prevention regulations.
Regular performance of maintenance and safety checks is essential for the permanent
assurance of the operating and functional safety of the KaVo product and for the pre‐
vention of damage and hazards.
Testing and maintenance intervals: Maintenance must be performed once a year, the
safety check (STK) at intervals of 2 years. Shorter intervals for the safety check may
be specified by the tester if necessary.

The following persons are authorised to repair and service the KaVo product:
▪ Technicians of KaVo branch offices after appropriate product training.
▪ Specifically KaVo-trained technicians of KaVo franchised dealers.
In Germany, operators, equipment managers and users are obliged to operate their
equipment in accordance with the MPG regulations.
The services encompass all the test tasks required in accordance with § 6 of the medi‐
cal devices operator ordinance (Medizinprodukte-Betreiberverordnung, MPBetreibV).

Note
The product must be cleaned and serviced according to instructions if it is not to be
used for an extended period of time.

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 Instructions for use ESTETICA E50 Life
2 Safety | 2.2 Purpose – Proper use

Note
The MULTIflex couplings, the current K/KL motors, and the ultrasonic scaler hoses
of KaVo are equipped as standard with a protective device to prevent treatment wa‐
ter from being drawn back into the treatment centre via the handpieces. If products
from other manufacturers are used at the standardised interfaces, it must be ensur‐
ed that they are equipped with an appropriate protective device! If this is not the
case, they may not be used!

Information about electromagnetic compatibility

Note
Based on IEC 60601-1-2 (DIN EN 60601-1-2) concerning the electromagnetic com‐
patibility of electrical medical devices, we must draw your attention to the following
points:
• Medical electrical devices are subject to special precautions concerning the elec‐
tromagnetic compatibility and must be installed and operated in accordance with the
KaVo assembly instructions.
• High-frequency communications devices may interfere with electrical medical de‐
vices.

See also:
2 10 Information about electromagnetic compatibility in accordance with
EN60601-1-2, Page 149

Note
KaVo cannot guarantee the compliance of accessories, cables, and other compo‐
nents not supplied by KaVo with the EMC requirements of IEC 60601-1-2 (DIN EN
60601-1-2).

Disposal

Note
Any waste which is generated must be recycled or disposed of in strict compliance
with all applicable national regulations in a manner which is safe both for people
and the environment.
If you have any questions regarding proper disposal of the KaVo product, please
contact the KaVo branch.

Disposal of electronic and electrical devices

Note
According to EC directive 2002/96 concerning used electrical and electronic devi‐
ces, this product is subject to the cited directive and must be disposed of according‐
ly within Europe.
For more information, please visit www.kavo.com or contact your specialised dental
supplier.
For final disposal, please contact:

In Germany

To return an electrical device, you need to proceed as follows:

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Instructions for use ESTETICA E50 Life
2 Safety | 2.2 Purpose – Proper use

1. On the homepage www.enretec.de of enretec GmbH, you can download a form for
a disposal order under the menu item eom. Download the disposal order or com‐
plete it as an online order.
2. Enter the corresponding information to complete the order, and submit it as an on‐
line order or by fax +49 (0) 3304 3919-590 to enretec GmbH.
The following contact options are also available for questions and for initiating a
disposal order:
Phone: +49 (0) 3304 3919-500
Email: [email protected] and
Postal address: enretec GmbH, Geschäftsbereich eomRECYCLING®
Kanalstraße 17
D-16727 Velten
3. A unit that is not permanently installed will be picked up at the office.
A permanently installed unit will be picked up at the curb at your address on the
agreed date.
The owner or user of the device will have to bear the cost of disassembly, trans‐
portation and packaging.

International
For country-specific information on disposal, contact your dental supplier.

2.2.2 Product-specific

Designated use and target group

KaVo is designed for dental treatment of children and adults.
The KaVo equipment system is a dental treatment unit in accordance with ISO 7494
equipped with a dental chair in accordance with ISO 6875. KaVo three-way and multi‐
function handpieces are dental instruments in accordance with EN 1639. They support
the dental application in the mouth of the patient by supplying air, water or spray. In
addition, the multifunctional handpiece supplies light and heated media. This KaVo
product is designed for use in dentistry only and may only be used by trained medical
personnel.

Connecting devices
KaVo-approved accessories for patient communication. These accessories must be
used exclusively.

Accessories Use Name Material code

Monitors Monitor 19“ KaVo Screen HD 1.011.0302
Monitor 22“ KaVo Screen One 1.011.0300
Cameras Intraoral camera ERGOcam One 130 1.011.2130
ERGOcam One 160 1.011.2129
Caries diagnostic DIAGNOcam 2170 1.011.0400
device U
Cables between unit USB extension cord USB extension cord 1.004.6953
and PC - 5 meters 5m with 1:1 hub
USB extension cord USB extension cord 1.011.3745
- 10 meters 2x5m with 1:1 hub
Display port cable - LTG Display port 5m 1.011.3583
5 metres Standard
Display port cable - LTG Display port 1.011.0298
10 metres 10m Standard

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 Instructions for use ESTETICA E50 Life
2 Safety | 2.3 Safety instructions

Note
The USB interfaces of the system may only be connected to IT devices approved
by KaVo.

Note
When connecting IT equipment to the the medial electrical system, observe EN
60601-1.

Note
Charge the wireless foot control with the charger supplied by KaVo only.

Note
The foot control charger may only be used indoors and must be protected from
moisture.

2.3 Safety instructions

2.3.1 General information

Note
The safety and reliability of the system can only be ensured when the described
procedure is followed.

DANGER
Explosion hazard.
Risk of fatal injury.
▶ Do not use KaVo product in areas subject an explosion hazard.

WARNING
Inappropriate operating conditions.
Impairment of the electrical safety of the device.
▶ It is essential to comply with the operating conditions specified in the "Technical
Specifications" chapter.

WARNING
Use of un-authorised accessories or un-authorised modifications of the product.
Accessories that have not been approved and/or inadmissible modifications of the
product could lead to hazards and/or personal injury or material damage.
▶ Only use accessories that have been approved for the combination with the prod‐
uct by the manufacturer or are equipped with standardised interfaces (e. g. MUL‐
TIflex couplings, INTRAmatic).
▶ Do not make any modifications to the device unless these have been approved by
the manufacturer of the product.

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Instructions for use ESTETICA E50 Life
2 Safety | 2.3 Safety instructions

WARNING
Injury or damage from damaged functional parts.
Damage to functional parts can cause further damage or personal injury.
▶ Check the device, electrical cables and any accessories for possible damage to
the insulation and replace if necessary.
▶ If functional parts are damaged: discontinue your work and repair the damage or
notify a service technician!

WARNING
Disposal of the product in the appropriate manner.
Infection hazard.
▶ Before disposal, reprocess and sterilise the product and accessories accordingly.

CAUTION
Health hazard and property damage due to non-compliance with servicing schedule.
Infection hazard to users and patients.
Product damage.
▶ Comply with servicing schedule.

CAUTION
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶ Perform regular proper care and maintenance!

CAUTION
Risks from electromagnetic fields.
Electromagnetic fields might interfere with the functions of implanted systems (such
as pacemakers).
▶ Ask patients if they have a cardiac pacemaker or other system implanted before
you start the treatment!

CAUTION
Malfunctions due to electromagnetic fields.
The product meets the applicable requirements regarding electromagnetic fields. Giv‐
en the complex interactions between equipment and cell phones, the product may be
influenced by a cell phone that is in use.
▶ Do not use cell phones in medical offices, hospitals or laboratories!
▶ Put electronic devices such as e.g. computer storage media, hearing aids etc.
down during operation!

CAUTION
Damage from liquids.
Residual liquids of any type can cause stains on or damage to cushions and parts of
the housing.
▶ Remove any residual liquids without delay.

Note
The operator may only carry out repair work if the device is switched off and no pa‐
tient is being treated.

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 Instructions for use ESTETICA E50 Life
2 Safety | 2.3 Safety instructions

2.3.2 Product-specific

WARNING
Injury or infection hazard from laid down instruments.
Given the arrangement of the instruments, injury or infections in the hand and under‐
arm can arise when reaching for the tray holder or operating device. Increased risk of
infection from diseased patients.
▶ Be aware of the arrangement of the instruments when accessing the tray holder
or operating device.

WARNING
Health impairment due to reverse suction via the instruments.
Infection hazard.
Products from other manufacturers, which are not equipped with a protective device
to prevent the drawing of treatment water into the treatment unit via the instruments,
may be used at standard interfaces
▶ If you are using products from other manufacturers at the standardised interfaces,
ensure that the products are equipped with the corresponding protective devices.
▶ Do not use products without a protective device.

CAUTION
Sitting down on a dental chair that is in horizontal orientation is associated with a risk
of injury.

▶ Do not sit on the head or foot end of the patient chair when it is in a horizontal
position.

CAUTION
The swinging arm may fall and cause injury.
If the swinging arm is overloaded, it can become damaged and injure the patient or
user.
▶ Never load the swinging arm, spring arm or dentist's unit by using it as a support.

CAUTION
Risk of injury by suspended instruments (S table).
Patients may get injured by sharp instrument tips.
▶ When you move the dentist's unit, make sure that nobody is injured.
▶ Alert patients and care providers to the risk of injury.

CAUTION
Risk of injury during cleaning of the treatment unit.
Lack of instructions to the cleaning staff and lack of preparation of the treatment unit
can lead to the cleaning personnel sustaining injuries.
▶ Only trained professionals and instructed cleaning personnel may be present in
the treatment rooms.
▶ Position the chair for cleaning and turn the device off.

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Instructions for use ESTETICA E50 Life
2 Safety | 2.3 Safety instructions

CAUTION
Electrical power.
Electrical shock.
▶ Set up the external PC outside of the patient environment keeping a minimal dis‐
tance of 1.5 m.
▶ Connect the PC and equipment connected to the PC in accordance with IEC
60601-1 / 60950.

CAUTION
Electrical power.
Electrical shock from incorrectly connecting a non-medical system to the USB interfa‐
ces of the device.
▶ Connect any IT device to the medical system in accordance with IEC 60601-1.
▶ Use USB devices with no additional power supply (USB-powered) only.
▶ Applied parts connected to the USB interface of the dentist element must comply
with the requisite insulation.
▶ USB-powered devices failing to meet the requisite insulation for applied parts
must be placed appropriately such that direct contact of the USB device and the
patient is excluded.
▶ It is not permissible to touch USB-powered devices failing to meet the requisite
insulation for applied parts and the patient at the same time.

CAUTION
Health damage due to germ formation.
Infection hazard.
▶ Before starting, rinse all the water drain lines without instruments.
▶ Before start-up and after the device has not been used for a while (weekends,
holidays, vacations, etc.), rinse or purge with air the air and water lines.
▶ Option: perform intensive germ reduction (if assembly kit is available).
▶ Actuate the tumbler filler several times.

CAUTION
Third party device connection kit (optional): Hazard of reinfection from standing water.
Infections.
When a water-using unit is connected to the third-party connection kit, always perform
the following tasks on the device:
▶ Before starting, rinse all the water drain lines without instruments (if applicable).
▶ Before startup and after the device has not been used for a while (weekends, holi‐
days, vacations, etc.), rinse or purge the air and water lines.
▶ Make sure that the water-using unit is resistant to H2O2 since the water is steri‐
lised with OXYGENAL 6 (at a concentration up to 0.02%).

CAUTION
Long stay in the patient chair.
Decubitus formation.
▶ Take precautions against the formation of decubitus in long treatments.

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 Instructions for use ESTETICA E50 Life
2 Safety | 2.3 Safety instructions

CAUTION
Risk of injury and material damage from incorrect use of the charger for the wireless
foot control.
Personal injuries, damage to the wireless foot control or the charger.
▶ Do not use the treatment unit during the charging process!
▶ Do not use the wireless foot control charger supplied to charge non-rechargeable
batteries.
▶ Charge the wireless foot control with the charger supplied only.

CAUTION
Risk of injury when the dental chair or headrest is moved.
Hair of the patient or practice personnel may get caught when the headrest of the
dental chair is moved.
▶ Mind the hair of the patient or practice personnel when moving the dental chair or
the headrest.

CAUTION
Risk of injury when moving the patient or patient chair.
The patient or treatment personnel can be pinched or crushed.
▶ Position all moving parts, such as dentist element, assistant element, operating
light, screens, etc., outside the collision range when you move the patient or pa‐
tient chair.

CAUTION
Damage to the handpiece hoses from stickers.
Handpiece hoses can burst.
▶ Do not affix stickers or adhesive tape.

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Instructions for use ESTETICA E50 Life
3 Product description | 3.1 Treatment unit versions

3 Product description

3.1 Treatment unit versions

3.1.1 KaVo ESTETICA E50 Life TM

3.1.2 KaVo ESTETICA E50 Life S

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.2 Patient chair Standard and COMPACTchair

3.2 Patient chair Standard and COMPACTchair

① Headrest ② Backrest
③ Chair base ④ Seat
⑤ Arm rest (optional)

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Instructions for use ESTETICA E50 Life
3 Product description | 3.3 Device body with patient unit

3.3 Device body with patient unit

① Patient element ② Unit body

The central control is housed in the
unit body.
③ Pressurised water bottle ④ Spittoon bowl
(supplementary equipment)
⑤ Tumbler filler ⑥ Supply element
Customer connection of power, water,
compressed air, wastewater, and suc‐
tion air
⑦ Foot control

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.3 Device body with patient unit

E50 Life with Centramat

① Patient element ② Unit body

The central control is housed in the
unit body.
③ Centramat ④ Spittoon bowl
(supplementary equipment)
⑤ Tumbler filler ⑥ Supply element
Customer connection of power, water,
compressed air, wastewater, and suc‐
tion air
⑦ Foot control

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Instructions for use ESTETICA E50 Life
3 Product description | 3.4 Dentist unit versions

3.4 Dentist unit versions

3.4.1 TM table

① Handle ② Three-function handpiece or multi‐

functional handpiece
③ Turbine (multiflex coupling) ④ INTRA LUX motor KL 703 or
INTRA LUX motor KL 701
⑤ Ultrasonic Scaler PiezoLED ⑥ ERGOcam One
⑦ Tray support ⑧ Site for affixing the USB interface (op‐
tional accessory)
⑨ Control element

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.4 Dentist unit versions

3.4.2 S table

Note
The holder assignment and arrangement of the instruments can be changed as
needed and does not have to follow the picture.

① Small X-ray image viewer ② Three-function handpiece or multi‐

functional handpiece
③ Turbine (multiflex coupling) ④ INTRAlux motor KL 703 LED or IN‐
TRA LUX motor KL 701
⑤ Ultrasonic Scaler PiezoLED ⑥ Control element
⑦ Site for affixing the USB interface (op‐
tional accessory)

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Instructions for use ESTETICA E50 Life
3 Product description | 3.5 Assistant element – Versions

3.5 Assistant element – Versions

3.5.1 Standard assistant unit

① Three-function or multifunctional ② Spray mist suction

handpiece
③ Control element ④ Saliva ejector
⑤ Satelec Mini LED ⑥ Tray holder for dental assistant
(polymerisation handpiece)

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.5 Assistant element – Versions

3.5.2 Assistant element right, left (optional)

Assistant element right, left with height adjustment (optional)

① Three-function handpiece ② Spray mist suction

③ Control element ④ Saliva ejector
⑤ Satelec Mini LED
(polymerisation handpiece)

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Instructions for use ESTETICA E50 Life
3 Product description | 3.6 Three function handpiece (3F handpiece)

3.6 Three function handpiece (3F handpiece)

① MF handpiece hose ② Gripping sleeve

③ Media buttons (air/water) ④ Labelled blue: Three-function hand‐
piece (3F handpiece)
⑤ Cannula

3.7 Multifunctional handpiece (MF handpiece)

① MF handpiece hose ② Gripping sleeve

③ Media buttons (air/water) ④ Labelled gold: Multifunctional hand‐
piece (MF handpiece)
⑤ Cannula

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.8 Controls

3.8 Controls

3.8.1 Dentist's unit TM table

Dentist's unit

A Group of keys for the dental chair B Group of keys for illumination
C Group of keys for hygiene D Group of keys for menu selection
(MEMOdent menu)
E Group of keys for the timer

3.8.2 Dentist's unit S table

A Group of keys for menu selection B Group of keys for illumination

(MEMOdent-menu)
C Group of keys for hygiene D Group of keys for the timer
E Group of keys for the dental chair

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Instructions for use ESTETICA E50 Life
3 Product description | 3.8 Controls

3.8.3 Assistant unit

A Group of keys for hygiene B Group of keys for illumination

C Group of keys for the timer D Group of keys for the dental chair

3.8.4 Groups of keys

Group of keys for the dental chair

The keys of the assistant unit each have two functions and show two symbols.

Assistant element key Dentist element key Name

"Chair up" key

"AP 0" key

(automatic position 0)

"Chair down" key

"SP" key
(rinsing position)

"LP" key
(last position)

"AP" key
(activate automatic posi‐
tion)
"Backrest down" key

"AP 1" key

(automatic position 1)

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.8 Controls

Assistant element key Dentist element key Name

"Backrest up" key

"AP 2" key

(automatic position 2)

"Collapsed position" key

Group of keys for illumination

Key Name Control element
"Operating light" key dentist element only
"Operating light dimming" Dentist element and
key assistant element
"X-ray image viewer" key dentist element only

Group of keys for hygiene

Key Name Control element
"Tumbler filler" key Dentist element and assis‐
tant element

"Bowl rinsing" key Dentist element and

assistant element

"Bell" key dentist element only

"Intensive germ reduction" assistant element only

key

"HYDROclean" key assistant element only

Group of keys for menu selection (MEMOdent menu)

Group of keys for menu selection

① Selection keys for menu functions ② Display

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Instructions for use ESTETICA E50 Life
3 Product description | 3.8 Controls

Group of keys for the timer

Key Name Control element
"Additional motor drives" Dentist element only
key

"Remote Control" key Dentist element only

"Timer 1" key Dentist element and

assistant element

"Timer 2" key Dentist element only

"Timer 3" key Dentist element only

"Timer 4" key Dentist element only

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.8 Controls

3.8.5 Foot control

The footswitches of the foot control have two functions. The functions of the foot‐
switches depend on if an instrument is mounted or removed.

Foot control Premium and wireless foot control | Foot control Standard

Item Name Function with handpiece Function with handpiece

mounted taken out
① U-shaped switch Switches the footswitch‐
es to the "Chair motion"
function.
② "LP/preselected spray" Drives dental chair to Sets the spray preselec‐
footswitch previous position. tion.
③ "Chair position/direction Changes the position of Selects the direction of
of motor rotation" 4-way the dental chair. motor rotation (for mo‐
switch tors KL 701 / KL 703
LED / COMFORTdrive
200XD).
④ "SP/blown air" footswitch Drives dental chair to Activates blown air (chip
rinsing position. blower) on the instru‐
ment (does not apply to
PiezoLED).
⑤ "Preselection of level/ Preselection of level Starts the motor/hand‐
handpieces" foot-pedal pieces and controls the
speed/intensity of the
handpieces.

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Instructions for use ESTETICA E50 Life
3 Product description | 3.9 Rating plate and identification plate

3.9 Rating plate and identification plate

Rating plate

Rating plates inside and outside

Internal attachment site for rating plate

25s

400s

Outside attachment site for rating plate

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.9 Rating plate and identification plate

SN Serial number
Read and take note of the content of accompanying documents

Please note the instructions for use

Follow the instructions for use!

Type B applied part

Type BF applied part

Operating mode:
Operating time of the patient chair: 25 seconds
Pause time of the patient chair: 400 seconds
(The permissible operating times correspond to common dental procedure.)
Fuse ratings:
The "?????" depend on the mains voltage and are either T10 H or T6.3H.
100 V~ ,110 V~, 120 V~, 130 V~ = T10H
220 V~ , 230 V~, 240 V~ = T6.3H
For disposal information, see also: Purpose – Intended use

CE mark according to Medical Devices Directive EC 93/42

VDE mark

DVGW certification
DVGW CERT registration number AS-0630BT0111

Identification plates

ESTETICA E50 Life nameplate

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Instructions for use ESTETICA E50 Life
3 Product description | 3.9 Rating plate and identification plate

Rating plate and dentist element ID

Site of attachment of nameplate and type BF applied parts ID on dentist element

Nameplate dentist element (e.g. table TM) / marking of the application parts of type BF

Type Device type

SN Year of manufacture - serial number
REF Material number

Miscellaneous signs

Attachment site back-side of wireless foot control

Follow the instructions for use!

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.9 Rating plate and identification plate

Labelling and marking of the three-function handpiece and

multifunctional handpiece

Company logo of the manufacturer

SN Serial number
CE mark according to 93/42/EEC medical devices

Sterilisable up to 135 oC

Disposal instructions according to Directive WEEE 2002/96/EG Annex N

Follow instructions for use

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Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

3.10 Technical data

Drilling template and setup plan

Installation plan (Mat. no. 3.002.4533) 2 sheets each right-handed and 2 sheets
left-handed
Installation plan with COMPACTchair 2 sheets each right-handed and 2 sheets
(Mat. no. 1.003.6767) left-handed

Electrical system
2
Electrical lead 3 x 2.5 mm
Free end above the floor 1 000 mm
Input voltages 100/110/120/130/220/230/240 V AC
Frequency 50/60 Hz
Input voltage set by the manufacturer See rating plate
Power consumption at 100 to 240 V 100 to 600 VA – with appropriate device
configuration, deviations in this range are
possible!
Customer-provided fuse protection Automat C 16 or screw-plug fuse 10 A
Protective conductor above floor See DIN VDE 0100-710, 1000 mm
Heat emission 360 to 3,240 kJ/h
Heat emission Ø 900 kJ/h
Mark of approval CE / DVGW / VDE
Foot control IPX1: Protection against water drips

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

Wireless foot control

Frequency band ISM 2.4 GHz
Radiated output max. 0 dBm e.i.r.p. (max. 1 mW)
Supply rechargeable battery
Type Varta PoLiFlex PLF503759
Number of cells 1
Charging time 2h
Rated capacity 1100 mAh, 1140 mAh type
Charger 1.005.4229
Type of charger FW7574S 1.005.4229 (Euro), 1.007.3208
(UK), 1.007.3207 (USA/Japan)
Input voltage 100 - 240 V AC / 50 - 60 Hz / 0.15 A
Output voltage 4.2 V DC / 1 A
Operating time At least one month – The indicated operat‐
(charge cycle) ing time assumes normal handling of the
treatment unit and wireless foot control.
This may vary according to the treatment
approach.

Triple-function handpiece and multifunctional handpiece

Flush the water and air passages for 20 to 30 seconds before working at the begin‐
ning of the day.

Water pressure 1.5 ± 0.3 bar; Flow pressure; 4 x manom‐

eter
Max. static pressure water 2.5 ± 0.3 bar
Water flow 80 ± 10 ml/min
Air pressure 3.3 ± 0.1 bar; Flow pressure; 4 x manom‐
eter
Max. dynamic pressure air 4 + 0.5 bar
Air flow at least 16 Nl/min
Operating time (multifunctional handpiece 1 minute
only)
Interval (multifunctional handpiece only) 3 minutes

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Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

Electrical multifunctional handpiece

Safety extra-low voltage according to DIN 24 V AC ± 10% (non-grounded voltage)
EN 60601-1:
Frequency 50/60 Hz
Type of use BF
Heat output for water approx. 90 W
Heat output for air approx. 20 W
Lamp voltage max. 3.2 V ± 0.15 V
High-pressure lamp power max. 2.5 W

Water supply

Note
If the water is very hard (above 12 °dH), a water softening device must be fitted in
the ion-exchange process.
Insufficient water hardness (below 8.4 °dH) can promote the formation of algae.

Note

The "water inlet block" assembly kit does not include a separation between the
treatment water and water supplied by the local mains. The operator must observe
and adhere to relevant national directives concerning the prevention of backflow. If
these rules are not adhered to, the manufacturer can assume no liability for the
quality of the treatment water and the microbial re-contamination of the public drink‐
ing water network.

Note

In conjunction with the "DVGW water block with integrated water disinfection" a wa‐
ter disinfection unit is installed in dental units from KaVo. The disinfectant OXY‐
GENAL 6 is continually added to the water in a concentration which is harmless for
persons, but hygienically effective to maintain the quality of the treatment water.
The handling is described in the care instructions for the treatment units. Supple‐
mentary measures such as the rinsing of water conducting lines and intensive disin‐
fection must be carried out according to the instructions of the manufacturer.

WARNING
Danger of infection if the national guidelines are not observed.
Contamination of the treatment water or the drinking water network.
▶ Observe and adhere to the national guidelines concerning the quality of water for
human consumption (potable water) – if available.
▶ Observe and adhere to the national guidelines concerning the prevent of reflux
(flow of water from the treatment unit to the public water network) – if relevant.

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

WARNING
Risk of infection if the "Water block, compact" is used without additional safeguards.
Contamination of the treatment water and/or drinking water supply with germs.
▶ With regard to the "Water block, compact" assembly kit, please note that no disin‐
fection facility is installed in the unit, and take appropriate safeguards. KaVo rec‐
ommends to use the "Water block DVGW with integrated water disinfection facility
in combination with KaVo OXYGENAL 6 (Mat. no. 04893451).
▶ If the Water bottle kit is used with the enclosed dosing attachment (Mat. no.
10020287), add the proper amount of KaVo OXYGENAL 6 (Mat. no. 04893451)
with each filling. For the correct amount, please refer to the Instructions of the
dosing attachment for water disinfection.
According to DIN EN 1717, each unit that is not listed by DVGW must be provided
with an upstream type AA, AB or AD safety device. (The DVGW water bottle kit is cer‐
tified; see the following list.)
When establishing a water connection, prevent brackish water pools with standing wa‐
ter (also in the house plumbing).
For further information, please refer to www.dvgw.de

Free drainage according to DIN EN 1717 - Water block DVGW, water bottle DVGW,
DVGW certified register no.: AS-0630BT0111
Water quality Tap water, cold water connection
Water hardness 1.5 to 2.14 mmol/l ≙ 8.4 to 12 °dH
pH 7.2 to 7.8
Customer water filtering 80 µm
Water connection Shut-off valve with brass cone compres‐
sion screw connection 3/8" to Ø 10 mm
provided
Above-floor water connection min. 50 mm, max. 105 mm with valve
opened
Water inlet pressure 2.0 to 6.0 bar
Water inlet pressure 4 l/min
Diameter of the drain connection 40 mm
Above-floor drain connection 20 mm
Outflow quantity max. 4 l/min
Slope of water drain pipe downstream from device: at least 10 mm
per metre

Air supply

WARNING
Non-adherence to national guidelines on the quality of the dental air.
Infection hazard.
▶ Observe and adhere to the national guidelines on the quality of the dental air - if
existent.
▶ Blow through the air line prior to commissioning.

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Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

Air inlet pressure 5.2 to 7 bar

Air consumption max. 80 Nl/min.
Pressure dew point < -30 ºC (compressor with dry air system)
3
Oil content < 0.1 mg/m (oil-free compressor)
3
Contamination < 100 particle/cm with particle sizes of 1
to 5 µm
Customer air filtration 50 µm
Air connection Shut-off valve with brass cone compres‐
sion screw connection 3/8" to Ø 10 mm
provided
Air connection above floor level min. 50 mm, max. 105 mm with valve
opened

Suction
Suction vacuum at device intake
Suction air quantity at spray with wet suction with dry suction
mist cannula
minimal V~250 Nl/min > 60 mbar > 85 mbar
recommended V~300 > 80 mbar > 120 mbar
Nl/min
Suction vacuum static max. < 180 mbar < 180 mbar

Note

If the negative dynamic pressure is > 180 mbar, the unit must be equipped with the
negative pressure regulating valve assembly kit.

Diameter of the suction connection 40 mm

Above-floor suction connection 20 mm
The values apply to the KaVo measuring set (Mat. no. 0.411.8500).

Central Dekaseptol supply (optional)

P 2 - 5 bar by means of ball valve, to be pro‐
vided by customer (John Guest
PPMSV040808W)
V 0.005 - 0.15 l/min
Material of supply hoses Polyethylene (LLDPE), John Guest, di‐
mensions dependent on object (building,
number of units)
Supply hoses must be routed to be frost-protected, not above 25 °C and not exposed
to direct sunlight.

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 Instructions for use ESTETICA E50 Life
3 Product description | 3.10 Technical data

Operating environment

WARNING
Inappropriate operating conditions.
Impairment of the electrical safety of the device.
▶ It is essential to comply with the operating conditions specified in the "Technical
Specifications" chapter.

Floor quality The quality of the flooring must meet the

load bearing ability for buildings
DIN 1055 page 3 and have a pressure re‐
sistance in accordance with DIN 18560 T
1.
o
Ambient temperature +10 to +40 C
Relative humidity 30 to 75%
Air pressure 700 hPa - 1,060 hPa
Max. elevation for operation up to 3,000 m

Maximum loads
Max. patient weight load on patient chair 185 kg
Standard
Max. patient weight load COMPACTchair 135 kg
Tray holder of the dentist element - loada‐ 2 kg
ble up to
Assistant unit tray holder - loadable up to 1 kg
Dentist element - loadable up to 2 kg

Transportation and storage conditions

o
Ambient temperature -20 to +55 C
Relative humidity 5% to 95% non-condensing
Air pressure 700 to 1,060 hPa

Weight
Treatment unit with patient chair Standard 279 kg gross, 224 kg net
Includes steel setup plate and patient 344 kg gross, 289 kg net
communication
Treatment unit with COMPACTchair 255 kg gross, 200 kg net
With steel set-up plate and patient com‐ 320 kg gross, 265 kg net
munication
For more information about the packages, please refer to Assembly Instructions

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Instructions for use ESTETICA E50 Life
4 Operation | 4.1 Switching the device on and off

4 Operation

4.1 Switching the device on and off

Note
Always switch the machine off before leaving the office.

E50 Life without/with Centramat

▶ Switch on the device using the main switch.
ð The display of the dentist unit ① shows the preselected basic menu.
ð The green LED "Device turned on" lights up on the assistant unit ②.

4.2 Adjusting the dental chair

4.2.1 Adjusting the arm rest (optional)

Armrest for the standard dental chair

To make it easier for the patient to sit in the chair, the armrest can be swung up.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

CAUTION
The patient's hands are in a bad position when the chair is rising
Danger of crushing fingers between the backrest and armrest.
▶ Make sure that the patient is sitting in the right position (especially children).

Arm rest for patient chair COMPACTchair

To make it easier for the patient to sit in the chair, the arm rest of the patient chair can
be swiveled forward.

▶ Swivel the arm rest forward

▶ Then swivel the arm rest back into place.

4.2.2 Adjust head rest

Setting locking dial of 2-joint headrest (standard)

CAUTION
Adjusting the headrest.
Injury of neck muscles.
▶ Make sure that the patient is aware of the headrest setting.
▶ Patients need to raise their head slightly during adjustment.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

▶ Push in or pull out the headrest depending on the patient's size.

▶ To swing the headrest, turn the locking dial to the left, move the headrest into po‐
sition, and turn the dial to the right to lock it.

▶ To remove the headrest cushion, remove the screw ②, pull the cushion ① up
slightly, and remove it to the front.

Setting locking dial of 2-joint headrest (optional)

CAUTION
Adjusting the headrest.
Injury of neck muscles.
▶ Make sure that the patient is aware of the headrest setting.
▶ Patients need to raise their head slightly during adjustment.
The bar length and angle of the headrest can be adjusted.
▶ Press the lock button and push in or pull out the headrest depending on the pa‐
tient's height.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

Note
The service technician can adjust the braking force.

▶ Press the lock button and swing the headrest into the desired position.
When swinging the headrest back into position, make sure that there is nothing
between the area A and head cushion.

4.2.3 Positioning the dental chair manually

CAUTION
Danger of injury from overload or dynamic load.
Patient chair may be damaged by overloading it.
▶ Do not subject the patient chair to a load exceeding its limit (185 kg).
▶ Do not subject the patient chair to dynamic loads.

CAUTION
Motorised movement of the chair
The patient or treatment personnel can be clamped or crushed.
▶ Monitor the patient and treatment personnel when changing the patient's position.

CAUTION
Risk of injury when moving the patient or patient chair.
The patient or treatment personnel can be pinched or crushed.
▶ Position all moving parts, such as dentist element, assistant element, operating
light, screens, etc., outside the collision range when you move the patient or pa‐
tient chair.

Positioning the chair and backrest manually using the dentist or

assistant unit

Use the following buttons to adjust the chair height and position of the backrest:

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Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

Key Function
The chair moves up.

The chair moves down.

The backrest moves upward.

The backrest moves downward.

▶ Press the related key.

ð The chair or backrest moves in the desired direction.
Positioning the chair and backrest manually using the foot control
The 4-way switch of the foot control assumes the function of the button wheel on the
dentist unit when manually positioning the dental chair.

Requirement
All instruments are in their holder.
▶ Chair up: Move the cross switch on the foot control in direction ①.
▶ Chair down : Move the cross switch on the foot control in direction ③.
▶ Backrest up: Move the cross switch on the foot control in direction ②.
▶ Backrest down: Move the cross switch on the foot control in direction ④.

4.2.4 Automatic positioning of dental chair

CAUTION
Danger of injury from overload or dynamic load.
Patient chair may be damaged by overloading it.
▶ Do not subject the patient chair to a load exceeding its limit (185 kg).
▶ Do not subject the patient chair to dynamic loads.

CAUTION
Danger of crushing during automatic chair movement.
The patient or treatment personnel can be clamped.
▶ Monitor the patient and treatment personnel when changing the chair position.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

CAUTION
Risk of injury when moving the patient or patient chair.
The patient or treatment personnel can be pinched or crushed.
▶ Position all moving parts, such as dentist element, assistant element, operating
light, screens, etc., outside the collision range when you move the patient or pa‐
tient chair.
The chair position can be adjusted continuously.
Automatic positions can be saved, and the saved positions can be recalled by the
push of a button.
The chair and backrest movements are simultaneous in the automatic program.
Exception: When the operating voltage for the standard patient chair is below 200 V,
the movements in the automatic program or sequential. In this case, a service techni‐
cian must change the program.

Gradually adjust the chair position

The standard patient char and COMPACTchair are adjusted in the same manner.

Special features of the COMPACTchair

Note
If the backrest is moved, the foldable foot piece also moves. The foot section can‐
not be moved separately.
The backrest can be moved vertically up to 85o to make it easier for patients to get in
and out.
When the backrest is horizontal, the chair can be moved lower than when the backrest
is vertical.

Save chair positions

The chair positions can be saved and retrieved at any time by the press of a button.
Win the position is retrieved, the chair automatically moves to the saved position (the
so-called "automatic position," or "AP" for short).
The four chair positions can be saved on the control panels. Two of these four posi‐
tions can be saved with the foot control.
It is for example recommendable to save the sitting down and getting up position using
the "AP 0" key and the rinsing position with the "SP" key.
▶ Move the chair into the position that is to be saved.

Save on the Comfort dentist or assistant unit

▶ Briefly press the "LP/AP" button.

ð The LEDs of the buttons, "AP 0", "AP 1", "AP 2" and "SP", flash for approximately
four seconds.
▶ During these four seconds, press the "AP 0", "AP 1", "AP 2" or "SP" button, until a
signal sound is issued.
ð The chair position is saved on the button.
Note
The automatic position "Last position" is saved on the "LP" button. Press the "LP"
button for the chair to automatically move to the last position before the rinsing posi‐
tion. The "LP" button cannot be assigned to another automatic position.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.2 Adjusting the dental chair

Recalling automatic positions with the dentist unit

The following keys can be used to recall saved chair positions.

Key Operation
Move to the rinsing position.

The last position before actuating the SP is assumed.

Move to automatic position 0.

Move to automatic position 1.

Move to automatic position 2.

Move to the collapsed position.

▶ Briefly press the desired button.

ð Chair automatically moves to the stored position.
ð Upon arrival at the stored position, the display diode on the button is turned on.
Saving automatic positions with the dentist unit
Recommended assignment of buttons:
"SP" button: rinsing position
"AP 0" button: entry and exit position
"AP 1" button: treatment position, e.g. for lower jaw treatment
"AP 2" button: treatment position, e.g. for upper jaw treatment
"Collape position" button: collapse position
▶ Move the chair to the desired position.
▶ To save the chair position, press "AP 0", "AP 1", "AP 2", "SP" or "Collapsed posi‐
tion" button until you hear an acoustic signal.
ð The display diode of the pressed button is turned on. The chair position is saved.
Last position
After the "LP" button is pressed, the chair moves into its position before the "SP" but‐
ton was pressed.

Note
The memory is erased when you turn off the device. After turning on the device
again (for example in the morning or after lunch), the chair does not execute a spe‐
cific movement when you press the "LP" button.

Recalling automatic positions with the assistant unit

▶ Briefly press the "AP" key.

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ð The LEDs of the "AP 0", " AP 1", " AP 2", "SP", and "LP" keys flash for approxi‐
mately four seconds.

▶ During these four seconds, briefly press the "AP 0", " AP 1", " AP 2", "SP" or "LP"
key.

ð The chair moves into the selected automatic position.

Saving automatic positions with the assistant unit

Note
The automatic position "Last position" is saved on the "LP" button. Press the "LP"
button for the chair to automatically move to the last position before the rinsing posi‐
tion. The "LP" button cannot be assigned to another automatic position.

▶ Move the chair to the desired position.

▶ Briefly press the "AP" key.

ð The LEDs of the "AP 0", " AP 1", " AP 2", "SP", and "LP" keys flash for approxi‐
mately four seconds.

▶ During these four seconds, press the "AP 0", "AP 1", "AP 2" or "SP" button, until
an acoustic signal is issued.

ð LED of the pressed button lights up. The chair position is saved.
Recalling automatic positions with the foot control

Note
If an instrument is removed, the chair functions of the foot control are blocked. The
blocking can be removed by briefly pressing the stirrup switch. The functions are
then available.

① Spray preselection/AP footswitch ② Blown air/AP footswitch

③ Foot pedal

The chair positions can be recalled with two foot switches; the standard setting is as
follows:
▪ "Spray selection" foot switch: automatic position "LP" (last position)

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▪ "Blown air" foot switch: automatic position "SP" (rinsing position)

Move the chair when the instrument is mounted

▶ Press the "SP" foot switch.

or

▶ Press the "LP" foot switch.

ð The chair moves into the selected automatic position.

Move the chair when the instrument is removed

Note
If an instrument is removed, the chair functions of the foot control are blocked. The
blocking can be removed by briefly pressing the stirrup switch. The functions are
then available.

▶ Press the stirrup switch and then the "Preselected spray" or "Blown air" foot
switch.

ð The chair moves into the selected automatic position.

Saving an automatic position with the foot control

① Spray preselection/AP footswitch ② Blown air/AP footswitch

③ Foot pedal

The chair positions can be saved on two footswitches; the standard setting is as fol‐
lows:
▪ "Spray default" footswitch: "LP" automatic position (last position)
▪ "Blown air" footswitch: "SP" automatic position (rinsing position)

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▶ Hold down the foot pedal and foot-operated button "SP", and simultaneously
press any button for an automatic position ("AP 0", "AP 1", "AP 2" or "SP") on the
dentist or assistant unit until you hear a beep.

ð The automatic position is saved for the foot-operated button.

or

▶ Hold down the foot pedal and foot-operated button "LP", and simultaneously press
any button for an automatic position ("AP 0", "AP 1", "AP 2" or "SP") on the dentist
or assistant unit until you hear a beep.

ð The automatic position is saved for the foot-operated button.

4.2.5 Safety shut-off

To prevent collisions arising from the movement of the patient chair, safety shutoff
switches are installed to protect the patient and practice personnel from injury and the
treatment unit from damage.

CAUTION
Damage to the assistant element and dental chair.
Despite some safety shut-downs being present, certain positions of the assistant unit
may collide with the dental chair.
▶ Keep the assistant unit out of the range of motion of the patient chair.
▶ Always monitor the chair movement.

CAUTION
Pinching from the treatment chair.
The safety shutoff of the treatment chair is activated by lifting the respective compo‐
nent. Depending on the patient's body weight and the leverage, more force can be
exerted on the object to be triggered than is necessary to trigger the switching func‐
tion.
▶ The treatment personnel must move outside of the chair's swinging range when‐
ever the chair moves.

CAUTION
Risk of injury when moving the patient or patient chair.
The patient or treatment personnel can be pinched or crushed.
▶ Position all moving parts, such as dentist element, assistant element, operating
light, screens, etc., outside the collision range when you move the patient or pa‐
tient chair.

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Patient chair Standard

NOTICE
Overheating of the drives.
Material damage to the patient chair.
▶ Note the maximal on-time of 2 minutes without interruption (10 %).
▶ After 2 minutes of on-time, keep a pause of 18 minutes.

Safety shutoff for the standard patient chair

Item Safety switch-off actu‐ LED on assistant ele‐ LED on dentist element
No. ated ment
① Patient unit swung over
the patient chair

② Assistant element

③ Backrest

④ Bracket on the foot con‐

trol

⑤ Kick plate

⑥ Seat

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Patient chair COMPACTchair

Safety shutoff for the COMPACTchair patient chair

① Patient element pivoted over dental ② Assistant element

chair
③ Backrest ④ Bracket on the foot control
⑤ Seat ⑥ Foldable part of the seat

Display LED Safety shut-down

Assistant element

Seat, backrest, lower chair programme

Bendable part of seat (only COMPACTchair)

Foot control

Patient element

Note
The chair's position cannot be changed with the key wheels when a safety shutoff is
activated.
Exception: The patient unit safety switch only stops the upward and downward
movement of the patient chair. The backrest can be moved up and down.
The safety shutoff occurs went a movement angle has been exceeded, or part of the
treatment unit collides with an object.
If a person or object actuates a safety shutoff, the chair immediately stops moving.
The fact that the safety shutoff has been activated is displayed by the corresponding
display flashing on the dentist or assistant unit.

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Note
The chair's position cannot be changed with the key wheels when a safety shutoff is
activated.
▶ To deactivate an activated safety shutoff, remove the triggers from the to the
range of movement of the stool.

CAUTION
Changing the chair's position when the safety circuit is on.
Personal injury.
Damage to the device.
▶ When changing position, do not move the chair against the active safety circuit
when actively shutting off the safety circuit.

CAUTION
Pinching from the treatment chair.
The safety shutoff of the treatment chair is activated by lifting the respective compo‐
nent. Depending on the patient's body weight and the leverage, more force can be
exerted on the object to be triggered than is necessary to trigger the switching func‐
tion.
▶ The treatment personnel must move outside of the chair's swinging range when‐
ever the chair moves.
To allow the chair to move freely, it can also be moved when the safety circuit is on.
Use this function for repair purposes only.

▶ Press and hold down the "SP" and "LP" simultaneously.

▶ Move the chair using the button wheel buttons.

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4.3 Moving the patient chair

Patient chair Standard

Patient chair COMPACTchair

4.4 Moving the dentist unit

CAUTION
Damage from overloading the dentist element.
Exceeding the maximum weight of more than 2 kg by adding handpieces, accesso‐
ries, etc., can cause damage.
▶ Do not overload the dentist element!

CAUTION
Risk of injury when the dentist or assistant element is moved.
The patient or office staff may be injured or bruised.
▶ Monitor the patient and office staff when moving the dentist or assistant element.
The swinging range of the dentist unit is limited by stops.

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Note
Do not pull the dentist unit by the instrument hose.
▶ To adjust the height of the dentist unit, release the brake, adjust the height, and
reset the brake.

4.4.1 Moving the dentist unit TM

CAUTION
Excessive load on the support system
The patient or treatment personnel may be injured.
The support system may be damaged.
▶ Do not exceed the permissible maximum weight (generated e.g. by instruments
and accessories).
▶ Do not use the swinging arm for a support!

CAUTION
Damage from overloading the dentist element.
Exceeding the maximum weight of more than 2 kg by adding handpieces, accesso‐
ries, etc., can cause damage.
▶ Do not overload the dentist element!

Dentist unit TM

4.4.2 Moving the dentist unit S

CAUTION
Risk of injury by suspended instruments (S table).
Patients may get injured by sharp instrument tips.
▶ When you move the dentist's unit, make sure that nobody is injured.
▶ Alert patients and care providers to the risk of injury.

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CAUTION
Damage from overloading the dentist element.
Exceeding the maximum weight of more than 2 kg by adding handpieces, accesso‐
ries, etc., can cause damage.
▶ Do not overload the dentist element!

Dentist unit S

4.5 Moving the patient unit

4.5.1 Swinging the patient unit by hand

The swinging range is about 250o.

Note
When the patient unit is swung over the patient chair, the safety shutoff is activated.

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4.6 Moving the assistant element

4.6.1 Adjusting the height of the standard assistant element

The assistant unit can be vertically positioned in four levels.

▶ To set a higher level, pull the assistant unit upward gently until it audibly locks in
place.
▶ To set a lower level, pull the assistant unit all the way up until the lock releases,
and then lower the assistant unit.

Mounting the tray holder

▶ Mount the tray holder on the assistant's unit.

① Tray holder ② Holder

The support ② for the tray holder ①is an optional accessory.

4.6.2 Moving the assistant element right, left (optional)

CAUTION
Pinching from the treatment chair.
The treatment staff can get pinched or crushed.
▶ The treatment personnel must move outside of the chair's swinging range when‐
ever the chair moves.

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CAUTION
Material damage caused by overloading.

▶ Do not rest your foot near the pivot point and/or transverse arm of the assistant
element.

Pivoting range of assistant element r, l (optional)

▶ Move the backrest up before swinging the assistant element.
▶ Move the assistant element to the desired position in its swinging range.

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Adjusting the height of the assistant element right, left (optional)

Note

Handpieces may drop out of the holders while the assistant element is being
moved, especially during adjustment of the height. In order to prevent handpieces
from being damaged, make sure that no handpiece drops down while you move the
assistant element.

▶ Undo the clamping screw and push the assistant element into the desired posi‐
tion.
▶ Re-tighten the clamping screw.

4.7 Using functions through the menu

4.7.1 Using the user menu

The following options can be opened in the user menu:

Option Function Description

1 User Set number of users.
2 Tumbler Set tumbler filling time.
3 Bowl Set bowl rinsing time.
4 Handpiece light Set cold light afterglow period.
5 ENDO Set ENDO holder.
Available only if an ENDO dongle is
present.

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Option Function Description

6 Equipment profile ▪ Save equipment profile from treat‐
ment unit to SD card.
▪ Save equipment profile from SD
card to treatment unit.
7 Time of day Set time of day.
8 Date Set date.
9 Time / date display mode Set display mode for time of day and
date:
▪ Time of day only
▪ Time of day without seconds
▪ Time of day and date
▪ Date only
10 LCD Set contrast of LCD display.
11 Language Set menu language:
▪ Deutsch
▪ English
▪ Italiano
▪ Français
▪ Castellano
12 LED lamp DIM mode Set dimming mode for LED lamp.
Available only if an LED lamp is
present.
13 Colour temp. of LED lamp Set color temperature of LED lamp.
Available only if an LED lamp is
present.
14 Firmware Display current firmware version.

Starting and closing the user menu

▶ Press the "Next" key (S6) to switch to the user menu.

ð Option 1 "Number of users" or most recently used option is displayed.

▶ Press the "Enter" key (S6) to exit from the option menu.

ð The changed settings are saved.

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Navigation in the user menu

Function keys Description

S1 Switch option to "Return"
S2 Switch option to "Forwards"
S3 Move cursor (if possible)
S4 Reduce set value
S5 Increase set value
S6 Exit the user menu and save the settings.

▶ Press the "Next" key (S6) to switch to the user menu.

ð Option 1 "Number of users" or most recently used option is displayed.

▶ Press the "Back" and "Forward" keys to select the desired option (1 through 14).

▶ Press the "Enter" key (S6) to exit from the option menu.

ð The changed settings are saved.

Option 1: Set number of users

▶ Press the "increase value" or "reduce value" key to select in the number of users
from 1 to 6.

Option 2: Set tumbler filling time

▶ Press the "reduce value" or "increase value" key to select a tumbler filling time
from 0 - 51 seconds.

Option 3: Set bowl rinsing time

▶ Press the "reduce value" or "increase value" key to select a bowl rinsing time from
0 - 51 seconds.

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Option 4: Set LUX afterglow period

▶ Press the "increase value" or "reduce value" key to set the LUX afterglow period
between 0 to 10 seconds. The default value is 3 seconds.

Option 5: Set ENDO holder

Note

The "ENDO holder" option is only displayed if the EBS torque control (ENDO) is in‐
stalled.

▶ Press the "increase value" or "reduce value" keys to set the selected holder.

Option 7: Set the time of day

▶ Press the "increase value" or "reduce value" keys to set the clock time.

▶ Press the"move cursor" (S3) button to switch between minutes and hours.

Option 8: Set the date

▶ Press the "Increase value" or "Decrease value" keys to set the date.

▶ Press the"Move cursor" (S3) key to switch between day, month, and year.

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Option 9: Set display mode for time of day and date

Option "Display mode for time of day / Date", "Time of day only" setting

Option "Display mode for time of day / Date", "Time of day only <no sec>" setting

Option "Display mode for time of day / Date", "Time of day and date" setting

Option "Display mode for time of day / Date", "Date only" setting
▶ Press the "Increase value" and "Decrease value" keys to select a setting for the
display mode for date and time of day.

Option 10: Setting the display contrast

▶ Press the "increase value" or "reduce value" keys to set the contrast of the dis‐
play.

Option 11: Setting the menu language

▶ Press the "increase value" or "reduce value" keys to set the desired language.

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Option 12: Setting dimming mode for the LED lamp.

Note

The "Set dimming mode for LED lamp" option is only indicated if an LED lamp is
installed on the treatment centre and has been activated by the technician in serv‐
ice mode.

Note

The COMPOsave mode switches on. when the "Dim operating light" button is acti‐
vated. The light can be dimmed in COMPOsave mode.
COMPOsave is a dimmer mode. In the COMPOsave mode the hardening of the of the
composite is greatly reduced by filtering the blue parts of the light spectrum.
The COMPOsave mode can be recognised by the yellow light.

▶ Press the buttons to "Increase value" or "Reduce value" to select whether the the
LED lamp should be dimmed via the "Dim button" on the dentist element or
switched to the COMPOsave mode.

Option 13: Setting the colour temperature of the LED lamp

Note

The "Set colour temperature for LED lamp" option is only indicated if an LED lamp
is installed on the treatment centre and has been activated by the technician in
service mode.

▶ Press the "Increase value" or "Reduce value" buttons keys to set the colour tem‐
perature for the LED lamp. The factory setting is 5500 K.

Option 14: Displaying the firmware version

The firmware version is displayed

4.7.2 Standby menu

Standby menu as the standard setting

The devices starts in the Standby menu.

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The unit automatically switches to the Standby menu when the Instrument menu and
Multimedia menu are closed.

Select function
The display shows display fields with symbols for the operating functions.
Below each display field, there is a key for selecting the displayed operating function.

Example standby menu with selection buttons

Permitting level switching

Level switching is deactivated in the basic state.
The level switching symbol displays the current dentist.

Note
The device acts like on level E when level switching is deactivated.
This means: centring of the foot pedal is not activated.

▶ To switch between levels, keep the "Bell" and the "Bowl flushing" keys and the
foot pedal depressed, until a signal sound can be heard.

After activating level switching, the level switching symbol shows the level (E, 1 2 or 3
- in this example level 2 is selected). The pre-selected dentist is only displayed very
small in the level switching symbol.

Note
The device automatically saves the activation of level switching for the current den‐
tist.

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Note
Level switching is deactivated using the same key combination as activation.

▶ To select a level, briefly press the selection button for "Preselect level".

Selecting the dentist

Dentist selection level when switching is deactivated

▶ Press the “Dentist” key.

ð The display changes to the settings menu.

▶ Press the key for the desired dentist (dentist 1 to dentist 6).
The number of dentists can be set in the user menu.
Two dentists are set as the default.

Dentist selection when level switching is activated

▶ Hold the “Select level” key for 4 seconds.

ð The display changes to the settings menu.

▶ Press the key for the desired dentist (dentist 1 to dentist 6).
The number of dentists can be set in the user menu.
Two dentists are set as the default.

Status display in the Standby menu

If a status message is available, the standby menu shows an exclamation mark on se‐
lection key "S2" ①.

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▶ Press the "S2" selection key ① to display status messages.

▶ Press the selection keys "+" ② and "-" ① to switch between multiple status mes‐
sages.
▶ Press the "OK" selection key ③ to exit from the display of status messages.

Error messages in the status display

See also:
2 9 Troubleshooting, Page 145

4.7.3 Using the MEMOdent menu

Instrument-specific values are displayed and adjusted in the MEMOdent menu.
The display depends on which instrument was withdrawn.
To save the instrument-specific values, there are 3 memory levels (1, 2, 3) each avail‐
able for six dentists (dentist 1 through dentist 6).
In level E, the centring of the foot pedal is deactivated, and no preferential speed can
be programmed.

4.7.4 Changing the turbine settings in the MEMOdent menu

Note
Following instructions for use, service instructions and installation instructions in the
instrument packaging.

The following settings can be changed in the MEMOdent menu:

▪ Speed
▪ Cooling status
▪ Cold light intensity
▶ Remove the turbine from the holder.
▶ To select a level, briefly press the selection button for "Preselect level".

▶ Press "Preselect level" button for 4 seconds in order to change settings.

ð The display switches to the turbine setting menu.

▶ Press the "Save" key to save the values. You can save after setting each value, or
after setting all values.
ð Saving is acknowledged with a tone.

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Setting the speed

▶ Press the key for "Decrease value" to decrease the speed.

or

▶ Press the "Increase value" key to increase the speed.

ð The speed is shown in the display.

Setting the cooling level

▶ Adjust the cooling with the selection button for "Cooling status".

Symbol Feature
No cooling

Spray air cooling status

Spray cooling status

NaCl cooling status (optional accessory)

Requirement:
NaCl is preselected through foot control.
Activation through cross switch.

See also:
2 3.8.5 Foot control , Page 33

Setting the cold light

The cold light can be set in 9 levels.

▶ Briefly press the "Cold light" key.

ð The cold light intensity changes one level.

If the cold light is unselected, a dash appears in the display.

4.7.5 Changing the settings for INTRA LUX motors KL 703 LED / KL
701 and COMFORTdrive

Note
Following instructions for use, service instructions and installation instructions in the
motor packaging.

The following settings can be changed in the MEMOdent menu:

▪ Direction of motor rotation
▪ Speed (only if switch between levels is activated)
▪ Cooling status
▪ Cold light intensity

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The settings for the speed, cooling and cold light are made in the same manner as
with the turbine.

See also:
2 Changing the turbine settings in the MEMOdent menu, Page 0
▶ Take motor off the holder.

▶ Briefly press "Preselect level" button to select the level.

▶ Press "Preselect level" button for 4 seconds in order to change settings.

ð The display switches to the motor settings menu.

▶ Press the "Save" key to save the values. You can save after setting each value, or
after setting all values.
ð Saving is acknowledged with a tone.

Setting the rotational direction of the motor

Note
The direction of motor rotation can only be changed when the motor is at rest.
▶ Choose clockwise or counterclockwise rotation using the "Motor rotational direc‐
tion" button.

Symbol Function
Clockwise rotation

CCW rotation

4.7.6 Changing PiezoLED settings in the MEMOdent menu

Note
Please comply with the enclosed "PiezoLED" Instructions for Use.

The following settings can be changed in the MEMOdent menu:

▪ Output intensity
▪ Operating mode (P1 / P2 / P3 / E)
▪ Cooling status (no cooling / spray water cooling)
▪ Light On/Off (intensity cannot be set)
▶ Take PiezoLED from the holder.

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ð The following is shown on the display.

▶ Briefly press "Preselect level" button to select the level.

▶ Press "Preselect level" button for 4 seconds.

ð The display switches to the settings menu of the PiezoLED.

▶ Press the "Save" key to save the values. You can save after setting each value, or
after setting all values.
ð Saving is acknowledged with a tone.

Setting the intensity

▶ Press the button for "Decrease value" to decrease the intensity.

or

▶ Press the button for "Increase value" to increase the intensity.

ð The intensity is shown on the display.

Define operating mode (PiezoLED only)

Note
The selection of the mode depends on the treatment method and the tip used. For
information about the selection of an operating mode, please refer to the "Operating
modes P1 / P2 / P3 and E" section of the "PiezoLED Instructions for Use".

▶ Press the "Mode" key to select the operating mode.

Modes P1 / P2 / P3 / E are available for selection.

Setting the cooling level

▶ Adjust the cooling with the selection button for "Cooling status".

Symbol Function
No cooling

Spray water cooling

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Dosing the amount of spray water

CAUTION
Lack of working tip cooling.
Heat damage to tooth or handpiece.
▶ Never work under dry conditions, except in case of tips designed for these condi‐
tions.
▶ Set a minimum flow rate of 6 ml/min. For this purpose, adjust the flow rate such
the water is just between dripping and flowing during irrigation.
▶ For the amount of spray water for each tip, please refer to the PiezoLED Instruc‐
tions for Use.

See also:
2 Instructions for Use PiezoLED
▶ Adjust the amount of spray water using the regulating ring.

Turn the light On / Off (PiezoLED only)

▶ Briefly press the "Light" button to switch between "On" and "Off".

Symbol Function
Light "Off"

9 Light "On"

4.7.7 Changing settings for the multifunctional handpiece in the

MEMOdent menu
The following settings can be changed in the MEMOdent menu:
▪ Cold light intensity
▪ Air/water heating
The cold light intensity is adjusted in the same manner as with the turbine.

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See also:
2 Changing the turbine settings in the MEMOdent menu, Page 0

▶ Briefly press "Preselect level" button to select the level.

▶ Remove the multifunction handpiece from the holder.

▶ Press "Preselect level" button for 4 seconds in order to change settings.

ð The display changes to the multifunctional handpiece settings menu.

▶ Press the "Save" key to save the values. You can save after setting each value, or
after setting all values.
ð Saving is acknowledged with a tone.

Adjusting the air/water heating

▶ Adjust the heating using the "Air/water heating" button.

Symbol Function
Air/water heating "on"

Air/water heating "off"

4.7.8 Use the Timer

Select the timer time

▶ To start a timer time, e.g. Timer 1, press the "Timer 1" button.

ð Time on the timer starts to run. A beep is issued after the timer time is elapsed.
▶ In order to stop the time on a timer, press the selected "Timer" button again.

Note
The activated timer times are also shown in the MEMOdent menu.
When several timer times are running simultaneously, they are displayed in the se‐
quence of when they elapse. Once each activated timer time elapses, a signal
sound is emitted.

Set the timer time

A maximum 59:59 minutes can be set using the timer.

▶ To set a timer time, e.g. Timer 1, press the "Timer 1" key until you hear a signal.

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ð The display switches to the settings menu for the timer time.

▶ Press the key for "Decrease value" to reduce the time.

or

▶ Press the key for "Increase value" to increase the time.

ð The set time is displayed in the display.

▶ Establish the direction of counting by pressing the "Count down/up" key.

Symbol Function
The timer counts down (for example: 0:30 to 0)

The timer counts up (for example: 0 to 0:30)

▶ Press "Save" button to save the value.

ð A signal sound confirms that the value has been saved.

or

▶ Press the "Back" button to return to the default (without saving).

4.7.9 Using the CONEXIOcom menu

Note
To start the CONEXIOcom menu, no handpiece may be removed.

Note
For all CONEXIOcom functions, the dental unit must be connected to an installation
of the KaVo "CONEXIO" software.
The function of the CONEXIOcom menu is to control the display of previously recor‐
ded and saved images and videos. In order to use the function, the unit must have ac‐
cess to the data of the KaVo Software "CONEXIO" software. For details on the config‐
uration, please refer to the "CONEXIO" installation instructions.

Opening CONEXIOcom
In order to display existing images, open the menu with the "Remote Control" button.
Select the proper patient on the corresponding PC for this purpose. It is also feasible
to automatically transfer the patient from your invoicing programme to CONEXIO. For
details on the configuration, please refer to the "CONEXIO" installation instructions.
If no patient is selected, images from the clipboard are displayed. If the clipboard is
empty, no image is displayed. The clipboard is deleted automatically when the patient
is logged off the corresponding PC.

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The CONEXIOcom menu is opened automatically for recording of images or videos as

soon as a device (DIAGNOcam U, ERGOcam One) is taken out.

To close CONEXIOcom: Replace the active device to its holder or close the CONEX‐
IOcom menu with the "Remote Control" button.

①Patient name, patient's first name or no patient

> Selected device ②
③ ④ ⑤ ⑥ ⑦ ⑧

No Icon Setting
1 - Info line
This line displays the active patient
name (if selected in CONEXIO) under
which the data obtained are stored.
If no patient is selected, images and
videos are stored in the clipboard un‐
der "unassigned patient".
2 - If a device is active, the device type is
shown. The following is implemented
at this time:
DIAGNOcam U
ERGOcam One
3 Previous image/video
To be able to communicate efficiently
with the patient, individual images can
be selected and displayed directly.
4 Next image/video
To be able to communicate efficiently
with the patient, individual images can
be selected and displayed directly.
This uses a rolling system that advan‐
ces from left to right and from top to
bottom.
5 Save image/video
Press briefly - saves the selected im‐
age/video.
Press long - all images/videos are
saved in the Swap Tray.
If no patient is selected, the images
stay in the clipboard and cannot be
saved permanently. As soon as a pa‐
tient is selected, these temporary da‐
ta in the clipboard are deleted.
When an active patient is logged off
(or a new patient is logged on) in
CONEXIO, a query is shown asking
whether the images in the shall be
deleted or saved. Data deleted at this
point cannot be restored subsequent‐
ly.

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No Icon Setting
6 Discard image/video
Press briefly - deletes the selected
image/video
Press long - all images/videos in the
clipboard are deleted
7 Full screen toggle
Toggles between full screen and split
screen mode
8 Screen display:
This button changes the display on
the monitor. The following settings
can be made:
1/2/4/6 – number of images dis‐
played.
The live image is always shown as
the last image in split view.

4.8 Using function through the dentist or assistant unit

4.8.1 Using the hygiene functions

The following buttons are available for the hygiene functions:

Key Function
The tumbler is being filled. The filling time can be
changed.

The bowl is being rinsed. The flushing time can be

changed.
Upon leaving the rinsing position (SP), the bowl is rinsed
for the full rinsing time. (The function can be deactivated
by the service technician).
HYDROclean function
Also refer to: Care instructions

Intensive germ reduction/rinsing function

Also refer to: Care instructions

The following applies to all hygiene functions except the intensive germ reduction and
rinsing function:
▶ To activate a function, press the button.
▶ Press the button again to terminate the function.

Changing the settings of the hygiene functions

The following settings can be changed:
▪ Tumbler filling time
▪ Bowl rinsing time

Adjusting the bowl rinsing and tumbler filling time

▶ Hold down the button of the hygiene function to be set until you hear a tone.

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A tone sounds for 1 second when you set the bowl rinsing and tumbler filling times.
▶ Release the button when the desired time is reached.

Note
A technician can block the setting of the time.

4.8.2 Using the light functions

The following buttons are available for the light functions:

Key Function Function

(Press briefly) (Press slowly)
Turns operating light On/ The brightness of the treat‐
Off. ment light is set in five
▪ Treatment light on: LED steps.
is on
▪ Treatment light off: LED
is not on
COMPOsave mode is The brightness of the dim‐
switched on / off. ming (treatment light) is set
in five steps.
X-ray viewer (supplementa‐ The colour temperature of
ry accessory) turned On/ the treatment light is set in
Off. five steps.
▪ X-ray image viewer on:
LED is on
▪ X-ray image viewer off:
LED is not on

Operation of the treatment light KaVoLUX 540 LED U

WARNING
Unintentional activation of the KaVo KEY Laser III and KEY Laser 3+.
Simultaneous application of the operating light KaVoLUX 540 LED and the KaVo KEY
Laser III or KEY Laser 3+ can lead to the unintentional activation of the KaVo KEY
Laser III and KEY Laser 3+.
▶ When using the KaVo KEY Laser III or the KEY Laser 3+, switch the operating
light to laser mode.
▶ Or switch off the operating light, do not use the KaVo KEY Laser III or KEY Laser
3+ and the KaVoLUX 540 LED operating light simultaneously.

WARNING
Wrong handling.
Reversible blinding (temporary sight impairment).
▶ Do not direct the light field at patients, users or/and third parties while you switch
on the light.
▶ Do not direct the light field at the patient´s eyes when you move the light head.
▶ Maintain a clearance of ca. 700 mm between the light and the mouth of the pa‐
tient.

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CAUTION
Stroboscopic effect of the rotating instrument.
A stroboscopic effect could arise in instruments rotating at a certain speed during ap‐
plication of the KaVoLUX 540 LED. This is an optical illusion, where the instrument
appears to be standing still or rotating extremely slowly.
Injury hazard.
▶ If the stroboscopic effect appears, change the speed fractionally and continue op‐
erating in the usual manner.

CAUTION
Faulty measurement in connection with KaVo DIAGNOdent.
Simultaneous application of the operating light KaVoLUX 540 LED and the KaVo DI‐
AGNOdent can lead to faulty measurements.
▶ Switch the operating light to laser mode when using the KaVo DIAGNOdent.
▶ Or switch off the operating light, do not use KaVo DIAGNOdent and operating
light KaVoLUX 540 LED simultaneously.

CAUTION
Premature hardening of composite fillings.
A light intensity that is too high can have a negative impact on the durability of the
treatment.
▶ Select the appropriate dimming level according to the processing time.

The KaVoLUX 540 LED operating light can be used in the following modes:
▪ Normal light: preset at 5,500 Kelvin and 30,000 Lux corresponding to daylight
quality
▪ COMPOsave-Modus: enables longer processing periods for composites by filter‐
ing the blue components of the light
▪ Dimmed light: approx. 4,000 Kelvin; equivalent to the light of a halogen operating
lamp
▪ Laser mode: Light mode, which has no negative influence on the KaVo KEY Laser
III, the KEY Laser 3+ or the KaVo DIAGNOdent.
When operated In dimmed mode, the LED lamp functions according to a dimmed hal‐
ogen lamp. The colour temperature is approx. 4,000 K and the composite can harden
prematurely. This can have a negative impact on the durability of the treatment.
The COMPOsave modes prevents the composite from hardening prematurely. As op‐
posed to the dimmed light, the blue components of the light are filtered in the process.
Therefore the composite can be processed longer in COMPOsave mode.

Turning the operating light On and Off

The KaVoLUX 540 LED operating light can be used in the following modes:
▪ Normal light: preset at 5,500 Kelvin and 30,000 Lux corresponding to daylight
quality
▪ COMPOsave-Modus: enables longer processing periods for composites by filter‐
ing the blue components of the light
▪ Dimmed light: approx. 4,000 Kelvin; equivalent to the light of a halogen operating
lamp
▪ Laser mode: Light mode, which has no negative influence on the KaVo KEY Laser
III, the KEY Laser 3+ or the KaVo DIAGNOdent.

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Sensor KaVoLUX 540 LED

▶ Press the "Treatment light" button.

ð
or
▶ Hold your hand just in front of the sensor.
ð Treatment light is switched on, Display LED shining.
▶ Press the "operating light" button once again.

or
▶ Hold your hand just in front of the sensor.
ð Treatment light is switched off, Display LED not shining.
Setting the brightness

Note

The maximum possible brightness of the light is set in five steps using the "Treat‐
ment light" key.

▶ Press and hold down the "Treatment light" key.

ð Signal buzzes, brightness changes from dark to bright in stages.

▶ When the desired brightness is reached, release the "Treatment light" key.

Switch on COMPOsave mode

When operated In dimmed mode, the LED lamp functions according to a dimmed hal‐
ogen lamp. The colour temperature is approx. 4,000 K and the composite can harden
prematurely. This can have a negative impact on the durability of the treatment.
The COMPOsave modes prevents the composite from hardening prematurely. As op‐
posed to the dimmed light, the blue components of the light are filtered in the process.
Therefore the composite can be processed longer in COMPOsave mode.

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Note

The COMPOsave mode switches on. when the "Dim operating light" button is acti‐
vated. The light can be dimmed in COMPOsave mode.

Sensor KaVoLUX 540 LED

▶ Press the "Dim treatment light" key.

or
▶ Hold your hand in front of the sensor for 2 sec.
ð The COMPOsave mode switches on.
ð The COMPOsave mode can be recognised by the yellow light.
▶ Press the "Dim treatment light" key.

or
▶ Hold your hand in front of the sensor for 2 sec.
ð The treatment light switches back to normal light mode.
Switching between COMPOsave mode and dimmed light and normal
light
The KaVoLUX 540 LED operating light can be used in the following modes:
▪ Normal light: preset at 5,500 Kelvin and 30,000 Lux corresponding to daylight
quality
▪ COMPOsave-Modus: enables longer processing periods for composites by filter‐
ing the blue components of the light
▪ Dimmed light: approx. 4,000 Kelvin; equivalent to the light of a halogen operating
lamp
▪ Laser mode: Light mode, which has no negative influence on the KaVo KEY Laser
III, the KEY Laser 3+ or the KaVo DIAGNOdent.
When operated In dimmed mode, the LED lamp functions according to a dimmed hal‐
ogen lamp. The colour temperature is approx. 4,000 K and the composite can harden
prematurely. This can have a negative impact on the durability of the treatment.

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The COMPOsave modes prevents the composite from hardening prematurely. As op‐
posed to the dimmed light, the blue components of the light are filtered in the process.
Therefore the composite can be processed longer in COMPOsave mode.

▶ Press and hold down the switch of the foot control and press the "Dim treatment
light" button until you hear the buzzer.

ð The treatment light switches from COMPOsave mode to dimmed normal light.

▶ Press and hold down the switch of the foot control and press the "Dim treatment
light" button until you hear the buzzer.

ð The treatment light switches back to COMPOsave mode.

ð The COMPOsave mode can be recognised by the yellow light.
Setting the brightness of the dimmer (COMPOsave mode or normal
light)

Note
The brightness of the light is set in five stages using the "Dim treatment light" key.

Note
The time it takes for composites to harden is dependent on the brightness or the
effective radiation intensity of the light: The processing time is reduced with increas‐
ing brightness / effective radiation intensity. The processing time for composites is
prolonged with reducing brightness / effective radiation intensity.

▶ Press and hold down the "operating light dimming" button.

ð Signal buzzes, brightness changes from dark to bright in stages.

▶ Once the desired brightness is reached, release the "operating light dimming" but‐
ton.

Setting the colour temperature

Note

The colour temperature of the treatment light KaVoLUX 540 LED U can be set be‐
tween five stages with the "X-ray viewer" button in operating mode "Treatment lamp
on". The visual perception of the teeth can be adapted or enhanced by changing
the colour temperature.
4.000 to 4.500 Kelvin: similarity to halogen light
5.500 Kelvin: daylight quality

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▶ Press and hold down the "X-ray viewer" button.

ð Signal buzzes, colour temperature changes.

▶ Release the button when the desired colour temperature is achieved.

Turning the laser mode On and Off

Note

The "laser mode" function is available only from the following version:
- Operating light V1.2.1
Older versions must be updated prior to download.

See also:
2 GA KaVoLUX 540 LED

Note

Falsified colour reproduction: the laser mode only possesses a restricted spectrum
output. Therefore a colour comparison should not be carried out in laser mode.
In laser mode, another light mode is generated, which has no negative influence on
the KaVo KEY Laser III, the KEY Laser 3+ or the KaVo DIAGNOdent.

Sensor KaVoLUX 540 LED

▶ Press the "operating light“ button and the "operating light dimming" button simulta‐
neously on the dentist element of the treatment unit.

ð The laser mode switches on.

ð Laser mode is activated: the operating light shines for 1 second in green and then
changes to a white light.
ð The indicator diodes of the two buttons flash alternatively.
or
▶ Hold your hand in front of the sensor for 3 sec.
ð The laser mode switches on.
ð Laser mode is activated: the operating light switches initially in COMPOsave mode
and then shines for 1 second in green and then changes to a white light.

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ð The indicator diodes of the two buttons flash alternatively.

Operation of the 3D joint

▶ Turn the switching ring to the left until it snaps into place.
ð Treatment light can be rotated 45° to the left or 45° to the right.
▶ Turn the switching ring to the right and it will spring back to its original position.
ð If the treatment light is turned to the centre position (zero position), it will automati‐
cally lock into place in the centre position.

Using the EDI operating light

▶ Press the "Operating light dimming" button to turn the operating light On/Off (as‐
sistant unit only, only if function was set by the service technician).

Note

The EDI operating light can also be turned On/Off and dimmed directly on the lamp
head.

4.8.3 Using the timer

Four timers can be selected. Set the timer on the dentist unit.

See also:
2 4.7.8 Using the timer, Page 75

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Select the timer time

▶ To start a timer time, e.g. Timer 1, press the "Timer 1" button.

ð Time on the timer starts to run. A beep is issued after the timer time is elapsed.
▶ In order to stop the time on a timer, press the selected "Timer" button again.

4.9 Operating the foot switch

4.9.1 General functions

The footswitches of the foot control have two functions. The function of the control de‐
pends on whether an instrument is in its holder or whether it has been removed.

See also:
2 3.8.5 Foot control , Page 33

4.9.2 Special functions of the wireless foot control

CAUTION
Electrical power
Personal injury or damage to the wireless foot control.
▶ The user must never touch the charger connector and the patient at the same
time!
▶ Do not touch the contacts of the charger connector!

CAUTION
Damage or malfunction due to improper servicing.
Reduced product life.
▶ Comply with the information provided in the servicing instructions to ensure cor‐
rect servicing!
The wireless foot control transmits the user activities to the treatment centre in a wire‐
less manner.

Rear of the wireless foot control

Item Labelling Function

No.
① LED display Status display / charge status display

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Item Labelling Function

No.
② On/Off switch On/off switch to prevent deep dis‐
charge during long periods of non-
use. The wireless foot control can re‐
main switched on at all times as a
matter of principle. The device must
be switched off for transport. The bat‐
tery can also be charged when it is
switched off.
③ Charge socket Charge socket for the provided charg‐
er (Mat. no. 1.005.4229).
The battery charge of the wireless foot control is indicated by the LED display and is
signaled by a tone.

Residual capacity Foot control status Status display / charge Beep

status display
< 100 % Idle state Flashes green -
Foot control is on (approx. 2 second inter‐
vals)
Active actuation Flashes green -
(approx. 200 millisecond
intervals)
< 30 % Idle state Flashes yellow A single brief beep when a
Foot control is on (approx. 2 second inter‐ button is pressed.
vals)
Active actuation Flashes yellow A single brief beep when a
(approx. 200 millisecond button is pressed.
intervals)
< 10 % Idle state Flashes yellow Two brief beeps when a
Foot control is on (approx. 2 second inter‐ button is pressed.
vals)
Active actuation Flashes yellow Two brief beeps when a
(approx. 200 millisecond button is pressed.
intervals)

See also:
2 4.9.14 Charging the wireless foot control, Page 93

CAUTION
Critical battery level
If the battery reaches a critical charge status, a signal is sounded every time a func‐
tion key is pressed.
▶ Always charge batteries when necessary.
▶ To ensure that the battery of the wireless foot control is always charged in a time‐
ly manner, note the visual and acoustic signals of the wireless foot control when
starting the treatment unit.

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4.9.3 Establishing a connection between the wireless foot control and

the treatment unit

Note
Only one wireless foot control per treatment centre can be registered to a RF re‐
ceiver. If another foot control was previously registered, the last foot control to be
registered will be deleted with every new start of the synchronisation process.

Note
Every wireless foot control and every RF receiver has a unique address, which can
be exchanged during the synchronisation procedure. This ensures unambiguous
assignment.
The different wireless foot controls operate on different channels in order to prevent
interference during the application of several wireless foot controls.

① "Confirmation" key ② "Up" key

③ "Down" key

To establish a connection between the wireless foot control and the treatment unit, the
devices need to be synchronised. Synchronisation needs to be performed once by a
service technician.
▶ Use the "Up" or "Down" keys to select the menu item "Login", and activate with
the "Confirm" key.

ð Synchronisation starts. The currently set channel is displayed.

A combination of keys must be entered on the wireless foot control in the proper se‐
quence during a countdown of 30 seconds.

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▶ Press the foot pedal, then move the cross switch toward "Chair up", and then ac‐
tuate and hold the stirrup switch until OK appears on the display.

ð If synchronisation is successful, the message "OK" appears on the display, and

the status LED of the radio-operated foot control shines green for 5 seconds.
If the keys are not pressed within the 30 second countdown period or if the keys are in
the incorrect sequence, synchronisation is terminated after the 30 second period is
over.
The display indicates if synchronisation was successful.

Display Meaning
– timeout – A radio partner was not found.
– ok – The radio partner was successfully
trained. The connection is established.
– Invalid device – An attempt was made to train a device
that was not permitted for the terminal.
The RF receiver can only be synchronised
with the wireless foot control.
▶ If synchronisation is unsuccessful, repeat the process, make sure that the se‐
quence is correct and observe the countdown time.

▶ After synchronisation on the RF receiver is successful, press the "Up" or "Down"

keys to select the menu item "Exit", and end the service mode with "OK".

ð The set values will be accepted and saved.

Note
Since there is no cable connection, the foot control and treatment centre must be
unambiguously assigned to each other. This assignment can be effected by identi‐
fying the wireless foot control through a self-selected designation (such as the num‐
ber of the treatment room) on the rating plate of the wireless foot control.

Example of the identification of the wireless foot control

CAUTION
Improper use of the wireless foot control
Damage or malfunction
▶ In case of improper use (such as cleaning), turn off the wireless foot control or the
treatment unit.

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4.9.4 Positioning the patient chair with the foot control

See also:
2 Positioning the dental chair manually
2 Position the dental chair using the button cross or 4-way switch

4.9.5 Preset level

▶ Press the footpedal.

ð The level is increased each time the foot pedal is pressed.

4.9.6 Preselect dentist

Requirement
All instruments are in their holder.

▶ Hold down the foot pedal and press the stirrup switch.

ð Each time the stirrup switch is pressed, the selection advances to the next dentist
(dentist 1 to 6).
The number of dentists can be set in the user menu.
Two dentists are set as the default.

4.9.7 Start and regulate instruments

Note
The foot pedal is equipped with a middle centring function, i.e., the foot pedal al‐
ways returns to levels 1 to 3 each time after it is moved to the left or right.

CAUTION
Centring in the middle is effected for the foot control by a positioning motor.
If the positioning motor breaks down, switching from or into the middle position using
the foot control is no longer feasible. The different levels can still be selected, but the
foot pedal does not leave the middle position and cannot switch into the middle posi‐
tion. The speed currently set on the wireless foot control is always shown on the dis‐
play of the treatment unit.
▶ Charge battery.
▶ If centring in the middle does not work despite the batteries being charged, the
positioning motor is defective. Have the positioning motor checked!

Note
Delays can arise after a function has been triggered if the wireless connection of the
wireless foot control is problematic.

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▶ Remove the handpiece (such as turbine, motor) from the holder.

ð The handpiece is active.

▶ Press the footpedal.

ð The removed instrument runs at the set speed or intensity.

▶ Changing speed or intensity with the foot pedal.

ð The left stop corresponds to the minimum speed/intensity.

ð The right stop corresponds to the maximum speed/intensity.

4.9.8 Setting the cooling condition

▶ Remove the handpiece (such as turbine, motor) from the holder
ð The handpiece is active.

▶ Press "Preselected spray" footswitch.

ð The cooling level is raised each time the footswitch is pressed: no cooling - air -
spray.
ð The cooling level is displayed on the dentist's and assistant's element.

4.9.9 Actuate blown air

▶ Remove the handpiece (such as turbine, motor) from the holder.
ð The handpiece is active.

▶ Press the "Blown air" foot button.

ð As long as the footswitch is pressed, blown air exits the removed handpiece (not
with the PiezoLED)

4.9.10 Preselect counterclockwise motor rotation

▶ Take motor from the holder.
ð The handpiece is active.

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▶ Slide the cross switch upward.

ð The direction of motor rotation is reversed each time the cross-switch is actuated:
counterclockwise rotation - clockwise rotation.
ð The direction of motor rotation is displayed on the dentist element.

4.9.11 Adjusting the instrument light

▶ Slide the cross switch to the right. (spotlight function)
ð Cold light "On" (even when Cold light: "Off" is preselected).

▶ Slide the cross switch to the left.

ð Change the cold light status: "On/Off"

4.9.12 Use physiological saline solution (optional accessory)

Requirement
Treatment centre is turned on. The handpiece is connected to the pump via the
pressure line.
▶ Remove the handpiece.

▶ Press the cross-switch of the foot control for 4 seconds until you hear the signal.

▶ After activation, select the "NaCl" cooling on the dentist control unit.

4.9.13 Using CONEXIOcom (fee-based additional option)

3
5 7

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No Setting
① U-shaped switch
Discard image/video
Press briefly - deletes the selected image/video
Press long - all images/videos in the clipboard are deleted
② Previous image/video
Select previous image/video
③ Next image/video
Select next image/video
④ Screen display
The number of displayed images (Split View) is reduced:
The live image is always shown as the last image in split view.
⑤ Screen display
The number of displayed images (Split View) is increased:

The live image is always shown as the last image in split view
⑥ Capture Mode
Toggles between the recording modes, video recording and image recording
⑦ Screen display
Toggles between full screen and normal view
⑧ Save image/video
Press briefly - freezes the live image
Press long - saves the live image directly.
If no patient is selected, the images are stored directly under "unassigned patient".

4.9.14 Charging the wireless foot control

The wireless foot control is operated by means of an installed rechargeable battery.

CAUTION
Risk of injury and material damage from incorrect use of the charger for the wireless
foot control.
Personal injuries, damage to the wireless foot control or the charger.
▶ Do not use the treatment unit during the charging process!
▶ Do not use the wireless foot control charger supplied to charge non-rechargeable
batteries.
▶ Charge the wireless foot control with the charger supplied only.

Note
Charge the wireless foot control with the charger supplied by KaVo only.

Note
The foot control charger may only be used indoors and must be protected from
moisture.
▶ Connect the charger to the wireless foot control.
The charger display communicates the following:

Display Meaning
shines green The unit is ready
shines yellow The battery is being charged
Shines weak green Battery is charged
does not shine The battery is dead, or there is a short-circuit

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Display Meaning
The battery voltage is above the tolerance range
Reversed poles
The transition from charging to full is indicated by the fluttering of the display.

4.10 Using instruments

Note
Consult the separate instructions for the installation, use and servicing of the indi‐
vidual handpieces (e.g. turbine, COMFORTdrive, ultrasonic scaler, camera, Satelec
Mini LED, etc.) for pertinent information.

4.10.1 Holder logic

All handpieces on the dentist's side are secured against simultaneous use by holder
logic. If an handpiece has been removed when the unit is switched on, the relevant
holder will not be activated until the relevant handpiece has been replaced.
Only the withdrawn handpiece is active, i.e., any handpiece that is withdrawn after‐
ward is not started. Exception: MF handpiece (parallel operation is possible here).

4.10.2 Using suction hoses

▶ Remove the spray mist suction device or saliva ejector from the holder.
ð The spray mist suction device or saliva ejector automatically turns on, and then
when it is placed in the holder, it turns off.
The suction flow of the saliva ejector or spray mist suction device can be reduced or
blocked with the slide valves integrated in the handpieces.

▶ Move the slide valve completely upward.

ð The slide valve is open: maximum suction.
▶ Move the slide valve down all the way.
ð The slide valve is closed: no suction.
Note
Connectors for the spray mist suction and the saliva ejector without slider as well as
reducing pieces for the spray mistsuction are available as accessories.
▪ Short cannula holder for the spray mist suction (Mat. no. 0.764.5783)
▪ Long cannula holder for the spray mist suction (Mat. no. 0.764.5853)
▪ Short cannula holder for the slather extractor (Mat. no. 0.764.5863)
▪ Cannula adapter for the reducing handpiece at 7 mm (Mat. no. 0.764.5873)
▪ Cannula adapter for the reducing handpiece at 11 mm (Mat. no. 0.764.5883)

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Vacuum stop

CAUTION
Danger of backflow
Swallowing or choking hazard for the patient
▶ Only actuate the vacuum stop when the suction cannula is not in the patient's
mouth.

Note

Vacu-Stop is available in combination with Venturi suction, external wet suction sys‐
tem, and suction valve.
When the base switch is actuated, the suction of the removed hose is stopped.

Note
For units with a BS selective holder, a service technician can set the vacuum stop
function to either stop all suction hoses or only stop the spray mist suction when the
saliva ejector is simultaneously activated.
This setting is not possible if a BS selective holder is not provided All sunction ho‐
ses are switched off in the case of Vacu-Stop
When delivered, the spray mist suction only stops when the vacuum stop function is
used.

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4 Operation | 4.10 Using instruments

4.10.3 Using the three function handpiece

CAUTION
Cannulas that are worn or not locked into place.
Injury from swallowing the cannula.
▶ Before each treatment, ensure that the cannula is locked into place and firmly
seated.
▶ Only use original KaVo cannulas.

CAUTION
Risk of injury from touching the cheek with the handpiece.
Irritation of the mucosa.
▶ Rotate the cannula of the handpiece into an operating position where there is no
contact of the mucosa.

① Air button (A) ② Cannula

③ Gripping sleeve ④ Water button (W)
⑤ Ring blue

Note
The cannulas can be rotated 360o..
▶ Remove the turbine from the holder.
▶ Press the air button ① and continuously increase or decrease the exiting air flow
by applying more or less pressure on the air button ①.
or
▶ Press the water button ④ and continuously increase or decrease the exiting water
jet by applying more or less pressure on the water button ④.
or
▶ Simultaneously press the air button ① and water button ④ and continuously in‐
crease or decrease the exiting spray by applying more or less pressure on the two
buttons.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.10 Using instruments

Removing the cannulas

▶ Hold the 3-way or multifunctional handpiece at the gripping sleeve and take off the
cannula with a slight twisting motion.

4.10.4 Using the multifunctional handpiece

CAUTION
Risk of injury from touching the cheek with the handpiece.
Irritation of the mucosa.
▶ Rotate the cannula of the handpiece into an operating position where there is no
contact of the mucosa.

CAUTION
Cannulas that are worn or not locked into place.
Injury from swallowing the cannula.
▶ Before each treatment, ensure that the cannula is locked into place and firmly
seated.
▶ Only use original KaVo cannulas.

CAUTION
Insufficient clearance between cannula and surface of gums or gingiva.
Injury hazard.
▶ Adhere to a minimum clearance of 10 mm between cannula and surface of gums
or gingiva.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.10 Using instruments

CAUTION
Damage due to missing media.
Air and water heating systems are destroyed.
▶ Check if the air and water are connected.
▶ Check the air and water supply!
▶ If possible, switch the heating off at the unit when putting into operation for the
first time or after servicing! Press the buttons carefully several times until the me‐
dia are available. Then activate heating and check its operation.

① Air button (A) ② Cannula

③ Grip sleeve ④ Water button (W)
⑤ Ring gold

Note
Cannulas can be rotated by 360o.
The "on" time for the handpiece with heating is 5 minutes with a resting time of 3
minutes.

Note
If only the cold light is preselected (heater: off), the multifunctional handpiece shines
when it is removed from the holder.
▶ Remove the turbine from the holder.
▶ Adjusting the air/water heating.

See also:
2 4.7.7 Changing the multi-function syringe settings in the MEMOdent menu, Page
74
▶ Check the passage for the media in the cannula ② each time before using it on a
patient.
▶ Press the air button ① and continuously increase or decrease the exiting air flow
by applying more or less pressure on the air button ①.
or
▶ Press the water button ④ and continuously increase or decrease the exiting water
jet by applying more or less pressure on the water button ④.
or

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.10 Using instruments

▶ Simultaneously press the air button ① and water button ④ and continuously in‐
crease or decrease the exiting spray by applying more or less pressure on the two
buttons.

Removing the cannulas

▶ Hold the 3-way or multifunctional handpiece at the gripping sleeve and take off the
cannula with a slight twisting motion.

Using the cold light

Requirement
The light and heating are preselected.
▶ Setting the cold light intensity.

See also:
2 4.7.7 Changing the multi-function syringe settings in the MEMOdent menu, Page
74
▶ Press the air button ① and/or the water button ②.

or

▶ Press the "Handpieces" foot pedal.

ð The light turns on.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.10 Using instruments

Replacing the lamp

CAUTION
Danger of injury from a hot valve body.
Risk of burn injury.
▶ Switch main device switch off.
▶ Allow the instrument to cool down after extended use.

▶ Pull off the grip sleeve ④ together with the cannula from the valve body ①.

Replacing the high-pressure lamp

▶ Push the holder ③ towards the front and draw and remove the defective high
pressure lamp ② from its holder.
▶ Install a new high pressure lamp (Mat. no. 1.002.2928).

Replacing the KaVo MULTI LED lamp

Note
The KaVo MULTI LED bulb is a semiconductor element and may only be operated
with direct current. To ensure proper function, the poles need to be inserted correct‐
ly.
▶ Push the holder ③ forward and pull the defective KaVo MULTI LED lamp ② out of
the socket.
▶ Insert new Kavo MULTI LED lamp (Mat. no. 1.007.5372).

The following may happen after you turn on the KaVo MULTI LED lamp:
▪ Case 1: KaVo MULTI LED lamp is on.
▪ Case 2: KaVo MULTI LED lamp is faint.
• - Increase the cold light intensity on the unit until the desired light intensity is
reached.
▪ Case 3: KaVo MULTI LED lamp is red or off.
• - Take KaVo MULTI LED lamp out of its socket as described above and re-insert it
after rotating it 180° about its axis.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

4.10.5 Using the PiezoLED

CAUTION
Handpiece inserts can be damaged from long-term use, or when dropped or bent.
They cannot be guaranteed to function properly.
Injury from insert breakage.
▶ Check the handpiece inserts before each use.

CAUTION
Sharp-edged tips.
Risk of injury.
▶ When not in use, always keep the supplied torque wrench attached to the tip!

Note
Please comply with the enclosed "PiezoLED" Instructions for Use.

Operation via the MEMOdent menu

See also:
2 4.7.6 Changing PiezoLED settings in the MEMOdent menu, Page 72

Operation with the foot control

▶ Press the "Instruments" foot pedal.

▶ To adjust the intensity, move the "Instruments" foot pedal to the side.

4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional

accessory)

4.11.1 General information

Note
The Endo drive can only be operated with the INTRA LUX KL 703 LED or INTRA
LUX KL 702 motors.

INTRA LUX KL 703 LED

INTRAmatic LUX KL 702

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Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

CAUTION
Use of impermissible filing systems.
Do not use impermissible filing systems which can damage the product or cause per‐
sonal injury.
▶ Only use approved NiTi filing system with a conicity >2% that are suitable for rota‐
ry preparation.
▶ Only use files with shafts in conformance with DIN EN ISO 1797-1, DIN EN ISO
1797-2, DIN EN ISO 3630-1 and DIN EN ISO 3630-2 having a shaft diameter of
2.334 to 2.350 mm
▶ Follow manufacturer's instructions (mode of operation, speed, torque levels, tor‐
sion resistance, etc.), and use the files according to their intended use.

CAUTION
Use of damaged files.
Injury to the patient or damage to the medical device.
▶ Before preparing each root canal, insert a dental dam for safety reasons.
▶ Before each use, the files must be checked for possible signs of material fatigue,
deformation or excessive stress and if such signs appear, they must be replaced.

CAUTION
Incorrect transmission ratio.
Damage from incorrect speed / incorrect torque.
▶ Only use KaVo 1:1 reducing shanks 20LH or 20LP with 1:1 INTRA LUX head L68
B (Mat. no. 1.008.1834) or 3:1 INTRA LUX head L66 BU (Mat. no. 1.008.1831).

CAUTION
Excessive torque.
Injury or damage to instruments.
▶ Use root canal instruments in ENDO mode only.

Technical specifications for the KL 703 LED / KL 702 in ENDO mode

Note
The technical specifications apply to the KL 703 LED / KL 702 in ENDO mode.

Speed range up to 6,000 rpm

Maximal torque 2.5 Ncm

Operating mode

Note
30 seconds operating time/9 minutes pause is the potential load threshold of the
motor (full load at maximum speed).
In practice, pulse loads lasting seconds or pause times lasting seconds or minutes are
realistic given that the maximum possible motor current is not normally reached. This
equates to the dentist's normal way of working.

4.11.2 Open ENDO mode

▶ Remove the endomotor INTRA LUX Motor KL 703 / KL 702 from the holder.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

▶ Press the "Additional motor drives" key.

ð The display switches to the "ENDO" menu.

Note
Before using the endomotor, always check the speed and transfer ratio.
The Endo mode is left as soon as the INTRA LUX KL 703 LED / KL 702 endomotor is
returned to the holder. The Endo mode is activated automatically once the endomotor
is removed, providing that the Endo mode was previously ended by putting the endo‐
motor back in place.

Note
The device does not automatically start when endo mode was left by pressing the
"Motorised auxiliary drives" button, or if endo mode has never been activated since
the last time the unit was turned on.
A service technician can deactivate the automated start.

Parameters in the display

① Direction of motor rotation ② Torque mode

③ Transmission factor ④ ENDO Mode
⑤ Speed ⑥ Parameter memory
⑦ Torque

CAUTION
Incorrectly set parameters.
Injury or property damage from incorrect input values.
▶ Check all input values before use.

4.11.3 Change settings in the option menu

▶ Press the "Next" key to switch to the option menu.

ð The last used menu is displayed.

The following settings can be changed in the option menu:

Display Function
Option: 1. Transmission factor
Set the transmission factor to 1:1 or 3:1

Option: 2. Display of torque

Set the torque display in Ncm or in %
1:1 transmission: 100% = 2.5 Ncm
3:1 transmission: 100% = 8 Ncm

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Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

Display Function
Option: 3. Autorev./Fwd. time
In Autorev./Fwd time mode, you can set
the time (1 to 10 seconds) in which the
motor automatically starts rotating to the
right which makes it unnecessary to stop
with the foot control.

Options 1, 2 or 3 can be selected by pressing the "Back" and "Forward" keys.

You can change the option parameters with the "Increase value" and "Decrease val‐
ue" keys.

▶ Press the "Enter" key to leave the option menu.

ð The changed parameters are saved.

4.11.4 Set parameters

There are six parameter memories (P1 to P6).

The following parameters can be changed:

▪ Speed
▪ Torque
▪ Torque mode

Select the parameter memory

▶ Press "Programme" button in order to call-up the desired parameter memory loca‐
tion (P1 to P6).
or

▶ Press the "SP/Blown air" foot button.

ð Each time the button is pressed, the parameter memory location advances by one
step (P1 - P2 - P3 - … - P6 - P1)

Change and save parameters

▶ Press the "Program" key to open the desired parameter memory (P1 to P6).

▶ Press the key for "Select parameters" to select the desired parameter.

ð The cursor flashes on the parameter to be changed.

▶ Press the "UP" or "DOWN" key to change the selected parameter.

Note
If you hold down the "Up" and "Down" keys repeat automatically.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

▶ To save the parameters, press the "Program" key for two seconds until you hear
the signal.
ð The changed parameters are saved in the selected parameter memory.
Note
You can save the parameters each time you set a new one, or after setting all the
parameters.

Setting the speed

The speed can be adjusted in steps of 10 from 100 rpm to 500 rpm, in steps of 50
from 500 rpm to 1000 rpm, and in steps of 100 from 1000 rpm to 6000 rpm.

▶ Press the "DOWN" key to reduce the speed.

or

▶ Press the "Up" key to increase the speed.

ð The speed is shown on the display and is effective immediately.

Save the parameters in programs 1 to 6 using the "Program" key (press for 2 sec‐
onds). You can save after setting one parameter, or after setting all parameters. Sav‐
ing is acknowledged with a tone.

Setting the torque

The torque is limited to the set value.

Note
The ENDO warning signal sounds when you reach 90% of the set torque.
1:1 transmission ratio
The torque can be set in 0.05 Ncm steps in the range from 0.15 Ncm to 2.5 Ncm, or in
2% steps in the range from 1% to 100%.
3:1 transmission ratio
The torque can be set in 0.05 Ncm steps in the range from 0.4 Ncm to 8 Ncm, or in
1% steps in the range from 1% to 100%.

See also:
2 4.11.2 Call up ENDO mode, Page 102

▶ Press the "Down" key to reduce the torque.

or

▶ Press the "Up" key to increase the torque.

ð The torque is shown on the display and is effective immediately.

Save the parameters in programs 1 to 6 using the "Program" key (press for 2 sec‐
onds). You can save after setting one parameter, or after setting all parameters. Sav‐
ing is acknowledged with a tone.

Set torque mode

Three different torque modes are available:

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Instructions for use ESTETICA E50 Life
4 Operation | 4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)

▪ Autoreverse
▪ Torque Control only
▪ Autorev / Forward

▶ Press the "Up" or "Down" key to select the desired torque mode.

ð The torque mode is shown on the display and is effective immediately.

Save the parameters in programs 1 to 6 using the "Program" key (press for 2 sec‐
onds). You can save after setting one parameter, or after setting all parameters. Sav‐
ing is acknowledged with a tone.

Torque mode Torque Control only

▶ Press the foot pedal.

ð The motor starts by rotating clockwise (if not selected otherwise).

The torque is limited to the set threshold. The speed reduces until it stops depending
on the load.
The direction of rotation is always to the right.
A tone sounds when the set torque threshold is reached.

▶ Push 4-way button on the foot control upward in order to switch to counterclock‐
wise rotation.

or

▶ Press "Motor rotational direction" button.

Torque mode Autorev / Forward

▶ Press the foot pedal.

ð The motor starts by rotating clockwise (if not selected otherwise).

When the set torque is reached, a signal sound is emitted, and the motor switches to
counterclockwise rotation. After the set time, the motor automatically reverts to clock‐
wise rotation. The time can be set in the option menu (Option 3).

See also:
2 4.11.3 Changing settings in the options menu, Page 103

Note
The motor's rotational direction can be reversed with the cross-switch on the foot‐
switch in all torque modes.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

Set Autoreverse torque mode

▶ Press the foot pedal.

ð The motor starts by rotating clockwise (if not selected otherwise).

A tone sounds when the set torque is reached. The motor rotates at a constant speed
to the left.

See also:
2 4.11.3 Changing settings in the options menu, Page 103

▶ To stop this, release the foot pedal.

▶ Press the foot pedal

ð The motor rotates to the right.

4.11.5 Leaving ENDO Mode

▶ Press the "Additional motor drives" button.

or
▶ Place the INTRA LUX KL 703 LED / KL 702 back in the holder.

Note
If the unit was switched to "Instant ENDO" mode, ENDO mode is only interrupted
when the ENDO motor is placed in the holder, and it is continued when the ENDO
motor is removed.
The function can be set by the service technician.

See also:
2 4.11.2 Call up ENDO mode, Page 102

4.12 Use pump for physiological saline solution (optional accessory)

Accessory can be used in treatment units TM and S.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

4.12.1 General information

Na C l

Dr
uc
k
Sa
ug

+
-

Overview of saline pump

① Holder ② Salt bag

③ Suction hose ④ Knurled screw
⑤ Pump ⑥ Electrical lead
⑦ Metering head ⑧ Pressure hose

4.12.2 Connecting the coolant

Note
All liquid-conducting parts are not sterile. They must be sterilised before the first
treatment. All parts conducting liquids must be kept sterile.

See also:
2 Servicing Instructions , Page 0

Connect the coolant with the standard instrument hose

▶ Attach the pressure line ① to the motor hose with the enclosed hose clips ②.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

Note
The distance from the motor to the first hose clip must be approx. 80 mm.

4.12.3 Activating the pump for the respective holder (enabling) and
regulating the pump
Requirement
Treatment centre is turned on. The handpiece is connected to the pump via the
pressure line.
▶ Remove the handpiece.

▶ Push down the cross-switch of the foot control for 4 seconds until you hear the
signal.

ð After activation, "NaCl" cooling can be selected.

Note
The first time the pump is turned on, it takes approximately 10 seconds until saline
solution exits from the handpiece.
The pump does not have any back suction.
▶ Gradually adjust the amount of saline solution using the metering head.
Rotation in "+" direction: increases the quantity
Rotation in "-" direction: reduces the quantity

Na C l

Dr
uc
k
Sa
ug

+
-

▶ Push down the cross switch for 4 seconds until the signal sounds to turn off the
saline pump.

4.12.4 Change salt bag

▶ Pull the hose with its tip out of the empty salt bag and replace with a new one.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

4.12.5 Attaching and etaching the pump

Mounting the pump

Note
Make sure that the pump is mounted insulated with the plastic plate on the table
housing or holder.

Na C l

Dr
uc
k
Sa
ug

+
-

▶ Affix the pump ⑤ to the treatment unit with the knurled screw.
▶ Insert the electrical lead ⑥ in the rear of the dentist element.
▶ Insert the bottle holder ① and secure with the knurled screw ④.

Note
Due to the weight and the provided tools, the 0.5 l NaCl bag should be used. Do not
use glass bottles!
▶ Suspend the NaCl bag ② on the bottle holder ①.
▶ Insert the tip of suction hose ③ into the NaCl bag ② and connect the other end of
the suction hose ③ to the pump outlet, "Intake".
▶ Connect the pump hose ⑧ to the pump output, "Pressure", and the other end of
the pressure hose to the instrument line.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

Remove the pump

If there is no need for cooling with saline solution for an extended period of time, the
pump can be removed.

Na C l

Dr
uc
k
Sa
ug

+
-

▶ Turn off the treatment unit.

▶ Remove pressure hose ②.
▶ Unplug electrical line ①.
▶ Unscrew the knurled screw under the pump.
▶ Removed pump and store it.

4.12.6 Exchange the pump hose

▶ Make sure that all hoses for saline solution are empty.
▶ If the hoses are not empty yet, remove the suction hose from the NaCl bag.

▶ Press down the foot pedal until the hoses are free of saline solution.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

▶ Remove the suction hose and pressure hose from the plug-in nipples for pressure
① and suction ②.Remove the suction hose and pressure hose from the plug-in
nipples for pressure 1 and suction 2.

Na C l

Dr
uc
k
Sa
ug

+
-

▶ Unlock the pump lock by turning it to the right, and remove the hose holder pro‐
ceeding in downward direction.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.12 Use pump for physiological saline solution (optional accessory)

▶ Remove the pump hose (Mat. no. 00655789) ① to be replaced from the hose
holder (Mat. no. 02362288) ② and replace it with a new one.

▶ Insert the new pump hose into the hose holder.

▶ Make sure that the flexing system is horizontal (turn manually if necessary).
▶ Insert the hose holder from below, and turn the pump hose locking to the right.

N aCl
D
ru
ck

S
au
g

+
-

Ordering information:
▪ Pump hose: obtainable as a cut section (Mat. no. 0.065.5789); must be cut to 13
cm before installation.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.13 Using the COMFORTdrive 200 XD/COMFORTbase (optional accessory)

4.13 Using the COMFORTdrive 200 XD/COMFORTbase (optional

accessory)

4.13.1 General use

CAUTION
Failure to comply with the Instructions for Use of the COMFORTdrive 200 XD
Injury to persons or property damage
▶ The use of the COMFORTdrive 200 XD is described in separate Instructions for
Use. Read these instructions before starting up the COMFORTdrive 200 XD and
the COMFORTbase!
The KaVo COMFORTdrive 200 XD is a dental instrument for the high speed range up
to 200,000 rpm. It can be attached only to the KaVo COMFORTbase coupling.
The hose of the KaVo COMFORTbase is part of the coupling and cannot be removed!
Operation and changing the settings via the control element is identical to the INTRA
LUX motor KL 703.

See also:
2 4.7.5 Changing the settings for INTRA LUX motors KL 703 LED / K 200 and COM‐
FORTdrive, Page 71

4.13.2 Fitting the motor hose on the dentist's element

▶ Connect the motor hose of the COMFORTbase to the connector for the motors
and pneumatic instruments.

4.13.3 Replacing the high-pressure bulb of the COMFORTbase

CAUTION
Danger of burns from hot high-pressure lamp.

▶ Switch main device switch off.

▶ Let the COMFORTbase cool down after long use.

Requirement
The COMFORTdrive is pulled off from the COMFORTbase.
▶ Push the accompanying lamp changer on the high-pressure lamp and pull out the
lamp axially.

▶ Insert the new lamp into the lamp changer, and introduce it into the hole in the
face of the supply hose. Carefully slide the lamp into the mount.

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 Instructions for use ESTETICA E50 Life
4 Operation | 4.14 Using the USB interface

▶ Carefully press out the lamp by activating the ejector.

4.13.4 Replace O-rings

CAUTION
Missing or damaged O-rings.
Malfunctions and premature failure.
▶ Make sure that all O-rings are on the coupling and undamaged.
Number of available O-rings: 3
▶ Press the O-ring between your fingers to form a loop.
▶ Push the O-ring to the front, and remove it.
▶ Insert new O-rings (Mat. no. 1.005.0327) into the grooves.

Note
The O-ring on the COMFORTbase may only be lubricated with cotton ball wet with
KAVOspray.

See also:
2 Care instructions for the COMFORTbase

4.14 Using the USB interface

CAUTION
Electrical power.
Electrical shock.
▶ Set up the external PC outside of the patient environment keeping a minimal dis‐
tance of 1.5 m.
▶ Connect the PC and equipment connected to the PC in accordance with IEC
60601-1 / 60950.

CAUTION
Electrical power.
Electrical shock from incorrectly connecting a non-medical system to the USB interfa‐
ces of the device.
▶ Connect any IT device to the medical system in accordance with IEC 60601-1.
▶ Use USB devices with no additional power supply (USB-powered) only.
▶ Applied parts connected to the USB interface of the dentist element must comply
with the requisite insulation.
▶ USB-powered devices failing to meet the requisite insulation for applied parts
must be placed appropriately such that direct contact of the USB device and the
patient is excluded.
▶ It is not permissible to touch USB-powered devices failing to meet the requisite
insulation for applied parts and the patient at the same time.

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Instructions for use ESTETICA E50 Life
4 Operation | 4.15 Using the camera

The treatment unit may be fitted with up to three USB ports. Camera interfaces are sit‐
uated on the underside of the dentist element (T-table) or in the dentist element (S-
table). Only the cameras approved/enclosed in the delivery by KaVo may be connec‐
ted to these interfaces.
The USB port in the back is connected directly to the back-of-the-head PC (in the
presence of the corresponding wiring). USB devices meeting the specifications listed
above can be connected to this interface. To use USB devices that have been con‐
nected, it may be necessary to install a suitable driver software on the back-of-the-
head PC.

Getting the USB ports ready for use

▶ To run an USB device, connect the USB port in the terminal box of the treatment
centre to an external back-of-the-head PC. Use one or maximally two USB exten‐
sion cables 5 m (Mat. no. 1.004.6953) according to need.
▶ USB devices connected to the dentist element must meet the USB standards,
USB 1.0, 1.1 or 2.0, and consume max. 500 mA of electrical power.

4.15 Using the camera

See also:
2 Instructions for Use ERGOcam One

See also:
2 Instructions for Use DIAGNOcam 2170 U

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 Instructions for use ESTETICA E50 Life
5 Preparation methods DIN EN ISO 17664

5 Preparation methods DIN EN ISO 17664

Note
The preparation methods can be found in the care instructions.

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Instructions for use ESTETICA E50 Life
6 Accessories and kits | 6.1 Device

6 Accessories and kits

6.1 Device
Name Description
Water block DVGW with in‐ With a DVGW permit and electronic monitoring of the fill‐
tegrated water germ reduc‐ ing level of the disinfection container.
tion system
Water block compact Without DVGW permit.
With water filter and shutoff valve.
Water bottle DVGW with With DVGW permit.
water block, compact Features a tumbler and handpiece water supply that is
independent of external water supply, includes Oxygenal
dosing attachment for manual dosing of the germ reduc‐
tion liquid into the water bottle.
Steel mounting plate For installation on the left or right.
Connecting third-party To connect or supply third-party devices such as an air‐
equipment flow through the quick couplings.
Amalgam separator DÜRR Approved amalgam separation systems with a
CAS separation > 95 %.
CS1 separation DÜRR Separation using a solids collector.
Solids collector kit Wastewater solids collector for wet suctioning.
External suction Wastewater and wet suction air are drawn from a central
location.
Water jet pump For saliva ejector.
Operating light EDI / KaVo‐ Operating light.
LUX 540 LED U
Tray support For the small handpiece tray.
Warm water heater Heats the tumbler water.
Low-pressure regulator Regulator for suction air when the suction vacuum is too
high.
Selective support kit Turns on the saliva ejector and/or spray mist suction.
Intensive germ reduction Only in combination with DVGW water block kit.
Centramat Central filling of the Dekaseptol bottle.
Dekamat Partially automatic cleaning and servicing of the suction
system.

6.2 Dental chair

Name Description
Arm rest The arm rest can be swung up to make it easier for the
patient to get in and out.

6.3 Assistant unit

Name Description
Satelec Mini LED LED polymerisation light.
Triple function handpiece Multifunctional handpiece featuring air, water, no heat‐
ing, and no cold light.

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 Instructions for use ESTETICA E50 Life
6 Accessories and kits | 6.4 Dentist unit

Name Description
Multifunctional handpiece Multifunctional handpiece featuring air, water, heating,
and cold light.
Saliva ejector, water-oper‐ With water jet pump.
ated

6.4 Dentist unit

Name Description
Multiflex LUX hose For connection of turbine and SONICflex and all hand‐
pieces fitting on the multiflex coupling.
Motor hose, For connection of INTRA LUX motor KL 701, motor KL
COMFORTbase 404L 703 LED, COMFORTdrive 200XD.
COMFORTbase 404S
Assembly kit INTRA LUX Brushless motor with light.
motor KL 703 LED
Assembly kit INTRA LUX Collector motor with light.
motor KL 701
KaVo COMFORTdrive 200 Dental handpiece for the high speed range up to 200,000
XD rpm. It can be attached only to the KaVo COMFORT‐
base coupling.
Three-function handpiece Multifunctional handpiece featuring air, water, no heat‐
ing, and no cold light.
Also available as an "upright" version.
Multifunctional handpiece Multifunctional handpiece featuring air, water, heating
and cold light.
Also available as an "upright" version.
PiezoLED Handpiece for the removal of dental calculus with the tip
sets, Scaler / Paro / Endo / Prep.
Radiograph viewer Röbi For installation on the light mounting pole.
1440
X-ray viewer 5x5 For image size of 5 x 5 cm (install on left or right side of
dentist element).
Spray heater for instru‐ Heater for spray water heating.
ments without handpieces
Tray holder for a standard Standard tray, US tray, and/or 2x-standard trays (install
tray / US tray / 2x-standard on left or right side of dentist element).
tray
Assembly kit for physiologi‐ For aseptic bur cooling during surgical work.
cal saline solution
6-outlet handpiece tray Extension of the integrated handpiece tray.
Torque control (endo) Drive for endodontic treatment.
Patient communication: Display of previously recorded and saved images and
videos.
▪ Screen One / Screen
HD
▪ DIAGNOcam 2170 U
▪ ERGOcam One

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7 Safety checks - testing instructions

7.1 Introduction

7.1.1 General instructions

Note

The safety checks may only be carried out by one or more electricians (as defined
in IEC 61140) who have received appropriate training for the device to be inspec‐
ted.

Note

The contents and specified tests in this document are based on the international
standard IEC 62353 (DIN VDE 0751-1). This standard applies to testing and inspec‐
tions of medical electrical devices or medical electrical systems, which are defined
in IEC 60601-1 (DIN EN 60601-1).

Note

In order to evaluate the safety of medical devices, systems or components of medi‐

cal devices or systems, the safety checks must be carried out at the times specified
below:
▶ Prior to first use
▶ during servicing
▶ during inspections and maintenance
▶ following service and maintenance
▶ on the occasion of repeat testing

Note

In the case of devices that have not been manufactured in accordance with IEC
60601-1, (DIN EN 60601-1) these requirements can be employed taking the man‐
datory safety standards for the production of these devices into consideration.

Note

If the unit comprises several electrical devices or electrical devices from several
manufacturers that are connected to a system in connection with the KaVo dental
unit, the manufacturer data contained in the instructions for use for all products sub‐
ject to safety controls must also be observed.

Note

Accessories to ME devices that could have an impact on the safety of the device to
be tested or the measured results must be included in the safety checks.

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Note

All tests concerning the included safety checks of accessories must be documen‐
ted.

Note

Furthermore, the manufacturer data contained in the instructions for use must be
adhered to in all products to be tested and inspected.

Note

KaVo offers a medical device book for keeping an inventory and recording essential
master data on the medical device. The medical device book is only available in
German (Mat. no. 0.789.0480).

Note

The following tests and measurements must be documented, for example in the
medical device book. We recommend using the templates at the end of the docu‐
ment

Note

The sequence of testing recommended by the manufacturer must be followed.

7.1.2 Notes for medical electrical systems

Note

An ME System is the combination of individual devices (as defined by manufactur‐

ers) that must meet the following conditions:
▶ At least one of these devices must be a medical electrical device.
▶ The devices must be functionally connected or at least they should be connec‐
ted by the application of a multiple socket outlet.

Note

With ME systems, the person responsible for putting the system together must em‐
ploy the necessary measuring parameters and measuring procedures defined in
IEC 60601-1 (DIN EN 60601-1).

Note

Each individual device in an ME system, which has a separate connection to the

power supply network, or which can be connected to or separated from the power
supply network without the aid of a tool, must be checked individually. Moreover,
the ME system must be checked as one unit to avoid the situation, in which the „ag‐
ing“ of individual devices lead to unacceptable values in sum.

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Note

An ME system that is connected to the supply network by means of a multiple sock‐

et outlet must be treated as one device during checks and testing.

Note

If the ME system or part of the system is connected to the supply network by means
of a isolating transformer, the transformer must be included in the measurements.

Note

In ME systems, in which more than one ME device are interconnected via data lines
or otherwise, e. g. via electrically conductive attachments or coolant tubes, the earth
wire resistance of every single device must be checked.

Note

If it should be impossible to check single ME devices that are functionally connected

to an ME system individually for technical reasons, the ME-System must be
checked as a whole.

7.1.3 Essential parts of the safety check

Visual inspection
Optical appraisal of the safe and usable condition of the medical device and its acces‐
sories.

Measurements
▪ Measurement of the earth wire resistance in accordance with IEC 62353 (DIN
VDE 0751-1)
▪ Measurement of the leakage current of the device EUL in accordance with IEC
62353 (DIN VDE 0751-1)
▪ Measurement of the leakage current of the user part EPL in accordance with IEC
62353 (DIN VDE 0751-1)

Note

A measurement of the isolation resistance in accordance with IEC 62353 (DIN VDE
0751-1) need not be carried out. This check is covered by the measurement of the
leakage current on application of a prescribed safety tester defined in IEC 62353
(DIN VDE 0751-1) Annex C!

Functional test
Medical device function test as well as testing of all safety shutdowns with reference to
accompanying documentation/ instructions for use.

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7.1.4 Testing intervals

▪ Testing interval every 2 years according to device type IIa (without HF surgery)

7.1.5 Notes on the test method in accordance with IEC 62353

▪ Protection class 1
▪ Type BF
▪ The device is firmly connected / threshold: SL < 0,3 Ω
▪ Measurement according to EUL / threshold: < 10mA*
▪ Measurement according to EGA / threshold: < 5 mA
*The EUL threshold is compatible with the value defined in IEC 60601 (DIN EN
60601), taking comment 2 from table 2 into consideration.

7.1.6 Notes on repeat testing

Note

The value determined in these tests must be documented and evaluated together
with the measuring processes. The measured values may not overshoot the speci‐
fied values.

Note

Comparisons with previous measurements must be carried out if the measured val‐
ues undershoot the threshold values by more than 10 %. The test intervals should
be reduced if a deterioration in values is determined!

7.2 Instructions for safety checks

7.2.1 Preparatory measures to be undertaken on the device

WARNING
Electrical power.
Death or injury from electric shock.
▶ Before servicing, pull the mains plug out of the socket or completely disconnect
the device from the power to de-energise it!
▶ After conversion, check the electrotechnical safety in accordance with IEC 62353
(DIN VDE 0751-1).
▶ Turn off the main switch before any servicing work.

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▶ Loosen the fastening screw on the bracket master switch.

Without/with Dekamat/Centramat
▶ Take off the cover ② in upward direction.
▶ Release the rear cover ① below and remove it.

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▶ Unscrew the fastening screws (see: arrows) of the cladding and take off the cov‐
ers.

Without/with Dekamat/Centramat

7.2.2 Visual inspection (inspection by examination)

Check the following points in advance:
▪ Has the equipment of the ME device or the ME system been changed since the
last inspection?
▪ Was the change documented and approved (test protocol, STK)?
▪ Are there any indications of insufficient safety?

Check the ratings of fuses that are accessible from outside

▶ Verify whether the main fuse on the main switch ② of the unit complies with the
specified nominal data ①.

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1
Visual inspection and appraisal of the medical device and accessories
The following list is an example and makes no claim of being complete.

Check the following items:

▪ Stability of the device
▪ No damage to the cladding or casing (cracks, breakage)
▪ Functioning of the carrier systems on dentist and assistant side, treatment lamp,
and display (brakes, height adjustment, etc.)
▪ Condition of the handpiece and suction hoses
▪ Condition of all installed application parts
▪ Condition of the control panels
▪ Condition of the threads for the fitting of tips to the ultrasound scaler handpiece
▪ Condition of the operating light
▪ Absence of leaks on the body of the device
▪ Condition of the power connection provided by the treatment centre
▪ Condition of air and water connections
▪ Any damage on the sight window and the casing of the camera ERGOcam
▪ Expiry date of the water bottle inserted in the BS water bottle not exceeded

Check of legibility and completeness of the safety-related labels

▶ Check if all safety-related markings (plates and labels) are present and legible.

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▶ Check if the rating plate and serial number plates are present and legible.

25s

400s

Attachment locations: nameplate, markings BF and note "Comply with the instructions for use"

Control of the availability of the necessary documents

▶ Verify whether the required instructions for use and care instructions are available
in the surgery.

Note

Any irregularities determined in the visual inspection must be recorded in the test
protocol. It is essential to determine whether defects and deficiencies could have an
adverse impact on the safe operation of the unit. If the determined irregularities
present a safety hazard and cannot be rectified directly, the unit must be closed
down until the safe operation is restored.

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7.2.3 Safety measurement

WARNING
Danger to persons due to a lack of care exercised during the safety checks and test‐
ing.

▶ Prior to connecting the treatment centre to the sight window, disconnect from the
mains supply network.
▶ Carry out all safety checks and tests in a manner that will ensure that there will be
no danger to the testing personnel, patients or other persons.

Note
The safety tester must comply with the requirements defined in IEC 62353 (DIN
VDE 0751-1), Annex C.

Note
If no other specifications have been made, all values relating to voltage and current
are effective values of alternating voltage, direct voltage or pulsating voltage res. al‐
ternating current, direct current or pulsating current.

Note
Connection cables such as data cables and cables for the functional earth could
simulate protective conductor connections. These types of supplementary but unin‐
tentional protective earth connections could lead to erroneous measurements.

Note
Cables and wires e.g. power supply cords, measuring circuits and data lines must
be arranged in such a manner that will ensure that their influence on measurements
will be restricted to a minimum.

Note

The following measuring aid can be ordered: KaVo measuring cable (Mat. no.
0.411.8811)

Using the measuring cable ① the unit is disconnected from the mains supply and con‐
nection of the treatment centre to the sight window is enabled. Hence, the customer-
provided mains supply L & N on the power input board need not be disconnected. The
adapter cable ② is included in the delivery of the KaVo measuring cable and is re‐
quired for older treatment centres that are not equipped with an X2 connector.

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Connecting the safety tester with KaVo measuring cables to the

treatment centre

▶ Remove plug X2 from the power input board and plug into the matching connector
X2 of the KaVo- measuring cable (Mat. no. 0.411.8811).
▶ Plug the second plug X2 of the KaVo measuring cable into the network card (X2).
▶ Insert the protective contact plug of the KaVo measuring cable into the sight win‐
dow.

Connecting the safety tester without the KaVo measuring cable to the
treatment centre

N
L

PE

▶ Switch L + N of the on-site power supply cord to be voltage-free.

▶ Disconnect L + N on terminals X1.1 and X1.2.
▶ Connect the safety tester directly to terminals X1.1 (L) and X1.2 (N) and protective
earth conductor terminal (PE).

Note

The main switch of the ME device / ME system must be turned on during measure‐
ment.

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Connect the application parts [AP] to the safety tester:

▶ Connect ① to ④ with the safety tester.

▶ Connect the safety tester to meauring points AP X.

Note

Additional measuring points AP X must be taken into consideration in the presence

of accessories: e.g. accessories such as PIEZO ultrasound scaler, HF surgery etc.

See also:
2 8 Annex - Additional measuring points, Page 142

Connect accessible conductive parts [ACP] with PE

ACP = accessible conductive parts

ACP
ACP

Note

Additional measuring points ACP X must be taken into consideration in the pres‐
ence of accessories: e.g. accessories such as saline pump etc.

See also:
2 8 Annex - Additional measuring points, Page 142

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ACPs on the treatment centre

No ACPs need to be connected to the protective conductor (PE) during the measure‐
ment on the treatment unit , as all relevant parts are connected to the PE and included
in the test before they leave the factory.

ACPs on treatment lamps

No ACPs need to be connected to the treatment lights during the measurement with
the protective conductor (PE) because all relevant parts have already been connected
with the protective conductor (PE) in the factory and are included in the test.

Measure protective conductor resistance

Threshold: < 0,3 Ω (maximum value!)

Note

The integrity of the power supply cable, in particular the protective earth wire of the
power cable must be ensured. As this is a fixed installation, the evaulation can be
conducted by means of a visual inspection. If damage is determined, the further
procedure to be taken is specified in the general instructions.

Note

In this measurement the resistance of the protective earth connection of the supply
network can be taken into consideration.

Note

If applicable: all removable supply connection lines, which are retained for use,
should be taken into consideration and the respective PE measured.

Protective earth measurement

The protective conductor resistance must be measured at the following parts of the
device:
▪ Treatment centre
▪ Treatment lamp
▪ Accessories

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Note
Additional measuring points SL X need to be taken into consideration in the pres‐
ence of accessories: e.g. additional devices, such as third-party connector, USB
port of the intraoral camera, etc.

See also:
2 8 Annex - Additional measuring points, Page 142

Scan the treatment centre with the test tip

Measuring points on the device base

① Main switch holding plate ② Stand cover base plate

③ Surroundings of the protective con‐
ductor terminal

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Scanning the patient chair with the test tip

2
3

① Top part of the chair ② Base plate of chair base

③ Switching power supply

COMPACTchair measuring points

① Leg rest ② Chair power supply

③ Chair base plate

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Scanning the operating elements with the test tip

① Dentist element S: table bottom ② Dentist element TM: table bottom

① Assistant element: fastening screw on

bottom side of assistant element

Scan the treatment lamp with the test tip

KaVoLUX 540 LED U operating light

① Fastening screw of the handle support

when the gripping sleeve has been re‐
moved

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Operating light EDI/MAIA

No measuring points need to be scanned on the operating lights EDI and MAIA.

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Touch monitor with test tip:

▶ Touch measuring point ① with the test tip.

or
▶ Sample the measuring point ② after removing the display cover.

Measure protective conductor resistance of accessories

See also:
2 8 Annex - Additional measuring points, Page 142

Measure equivalent unit leakage current

Threshold: < 10 mA (maximum value!)

ACP

Protection class 1

WARNING
Electrical power.
Death or injury from electric shock.
▶ Conduct test for leakage current in devices of Protection Class 1 only after the
protective earth test has been passed.

WARNING
Electrical power.
Death or injury from electric shock.
▶ Prior to connecting the treatment centre to the sight window, disconnect the treat‐
ment unit from the mains supply network.

Measure equivalent patient leakage current

Threshold: < 5 mA (maximum )

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ACP

Protection class 1

WARNING
Electrical power.
Death or injury from electric shock.
▶ Conduct test for leakage current in devices of Protection Class 1 only after the
protective earth test has been passed.

WARNING
Electrical power.
Death or injury from electric shock.
▶ Prior to connecting the treatment centre to the sight window, disconnect the treat‐
ment unit from the mains supply network.

Note

In the testing of ME devices with several application parts, the parts must be con‐
nected in succession. The measured results must be evaluated using the threshold
values. Application parts, which are not included in the measurement, remain open.

Note

An additional measurement of the leakage current from type B application parts

need only be carried out if this is specified by the manufacturer (see accompanying
documents).

Note

A separate measurement is not usually required for type B application parts. The
application parts are connected to the casing (see diagram) and included in the
measurement of the leakage current of the casing, whereby the same reliable val‐
ues are applicable.

7.2.4 Functional test

The following conditions must be fulfilled in all function tests:
▪ The basic function of the treatment centre must be guaranteed.
▪ The treatment centre must be fit for use.
▪ It must not exhibit any irregularities, noise or abrasion etc.
The following list is an example and makes no claim of being complete.
▪ Function test of the safety circuits (see diagram below)
▪ Functioning of the master switch of the device
▪ Functioning of the displays

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▪ Function test of the holder switch of the dentist and assistant element
▪ Functional test of the 3F/MF handpiece – seating of the cannula
▪ Functional test of operating light
▪ Function test of the suction hoses
▪ Function test of the foot control
▪ Function of the chair:
- Travel on all axes
- Testing of the limit switches
▪ Functional test ...

Patient chair Standard

Safety shutoff for the standard patient chair

Item Safety switch-off actu‐ LED on assistant ele‐ LED on dentist element
No. ated ment
① Patient unit swung over
the patient chair

② Assistant element

③ Backrest

④ Bracket on the foot con‐

trol

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Item Safety switch-off actu‐ LED on assistant ele‐ LED on dentist element
No. ated ment
⑤ Kick plate

⑥ Seat

Patient chair COMPACTchair

Safety shutoff for the COMPACTchair patient chair

① Patient element pivoted over dental ② Assistant element

chair
③ Backrest ④ Bracket on the foot control
⑦ Seat ⑧ Foldable part of the seat

If a person or object actuates a safety shutoff, the chair immediately stops moving.
The fact that the safety shutoff has been activated is displayed by the corresponding
display flashing on the dentist or assistant unit.

Display LED Safety shut-down

Assistant element

Seat, backrest, lower chair programme

Bendable part of seat (only COMPACTchair)

Foot control

Patient element

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7.2.5 Assessment and documentation

Note
All tests conducted must be documented comprehensively. The documents must
contain at least the following particulars:

▶ Name of the test centre

▶ Name of the test engineer
▶ Name of the tested device (e. g. type, serial number)
▶ Tests and measurements
▶ Data, type and measuring results of the visual inspections
▶ Data, type and measuring results
▶ Data, type and measuring results of function tests
▶ Measuring/test equipment including SN/test equipment number and calibration
period
▶ Final evaluation
▶ Name, date and signature of test engineer
There is a copy of a test report template at the end of chapter STK. KaVo recom‐
mends the use of this template.

Note

Following testing, repair or adjustment, it must be verified whether the ME equip‐

ment or ME system has been restored to the state that is required for the intended
usage before it is employed once again.

Note
If the safety of the tested ME equipment or ME system has not been established,
e.g. the tests have not been completed with positive results, the equipment or sys‐
tem must be marked accordingly and the potential hazard emanating from the
equipment or system must be communicated in writing to the RESPONSIBLE OR‐
GANISATION (to the operator, as a rule). This action is not required if the cause of
the malfunction could be determined and rectified. The defect must be recorded in
the protocol.

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Instructions for use ESTETICA E50 Life
8 Appendix - Additional measuring sites | 8.1 Additional scanning sites SL X in the protective conductor measurement

8 Appendix - Additional measuring sites

Note
With reference to accessories not listed here, the specifications of the relevant in‐
structions for use must be observed.

8.1 Additional scanning sites SL X in the protective conductor

measurement

ERGOcam One module

① Screw in bottom part of housing

Note

The modules are not earthed with a safety conductor. In the case of excessive PE
resistance, the electrical connection between the module and the dentist element
must be improved. This can be accomplished, for example, by means of a serrated
lock washer on the fastening screw.

Connecting third-party equipment

▶ Position the test tip on the middle contact ①.

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8 Appendix - Additional measuring sites | 8.2 Additional measuring sites AP X for EUL/EPL measurement

BS ceiling adapter operating light

① Base plate for the ceiling adapter ② Surroundings of the protective con‐
ductor connector
③ Surroundings of the protective earth
conductor terminal

8.2 Additional measuring sites AP X for EUL/EPL measurement

Scan the PIEZO ultrasonic scaler with test probe

Note

Measuring points must be connected on the following ultrasonic scalers:

- PiezoLED ultrasonic scaler

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Exemplary presentation of the measuring point on the PiezoLED ultrasonic scaler

① Test probe on ultrasonic scaler tip in

ultrasonic scaler handpiece

Note

The switch on the handpiece must be activated during the EPA measurement

Note

Additional measuring points AP X need to be taken into consideration in the pres‐

ence of accessories: e.g. if third-party devices are connected, cameral of the multi‐
media system, etc.

8.3 Additional connection sites ACP X (additional earth connections)

Touch the saline pump with the test tip

Na C l

Dr
uc
k
Sa
ug

+
-

① Test tip on bottle holder

Note

A fixed connection from ACP to the PE terminal must be established for the EUL
and EPL measurement. This can be accomplished with a measuring cable and con‐
nection terminals.

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9 Troubleshooting

9 Troubleshooting

Note
In case of malfunctions, consult the separate instructions for the use and care of the
individual instruments (such as the turbine, motor, camera, Satelec Mini LED, etc.).

Malfunction Cause Remedy

Nothing works. Main switch is off. ▶ Turn on main switch.
Main service fuse interrup‐ ▶ Unplug the unit from the mains.
ted the electric circuit. ▶ Check and replace, if required, the main service
fuse.
The main service fuse is situated next to the mas‐
ter switch.
▶ For this purpose, open the bayonet closure with a
screwdriver and replace the fine-wire fuse. (220,
230, 240 V AC: T 6,3 H Mat. no. 0.223.2783);
(100, 110, 120, 130 V AC: T 10 H Mat. no.
1.007.2529).
▶ The re-close the bayonet closure with the screw‐
driver.
The patient chair does not The safety shutoff is acti‐ ▶ Check the safety shutoff and eliminate the reason
move. vated. for the shutoff.

(The LED on the control

panel flashes.)
Display without indicator. Bus / hardware error. ▶ Turn the device off and on.
▶ Call the service technician to look into the problem
if it continues to exist.
Operating device no func‐ Bus / hardware error. ▶ Turn the device off and on.
tion. ▶ Call the service technician to look into the problem
if it continues to exist.
Several handpieces are si‐ Hardware error. ▶ Stop working and call the service technician
multaneously activated.
The LED on the "LP/AP" The data connection to the ▶ Turn wireless foot control on.
button flickers. foot control is faulty. ▶ Call a service technician.
(Assistant unit)
The LED on the "AP1" but‐ The data connection to the ▶ Turn wireless foot control on.
ton flickers. assistant unit is faulty. ▶ Call a service technician.
(Dentist unit)
The LED on the "AP2" but‐ The data connection to the ▶ Call a technician.
ton flickers. chair control is faulty.
(Assistant element)
Turbine making loud run‐ Turbine wheel faulty. ▶ Replace turbine wheels.
ning noises. Follow the operating instructions for the turbine.

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9 Troubleshooting

Malfunction Cause Remedy

The Satelec Mini LED Also refer to: Instructions ▶ Also refer to: Instructions for use for the Satelec
does not work. for use for the Satelec Mini Mini LED

LED
No cold light on the hand‐ Cold light not preselected. ▶ Preselect cold light.
pieces. The high-pressure lamp or ▶ Replace the high-pressure lamp or Multi LED.
Multi LED on the hand‐ Also refer to: Instructions for Use of the handpiece

piece is defective.
See also:
2 Instructions for Use of the handpiece
No heating function on the Spray heating not prese‐ ▶ Pre-select spray heating.
multifunctional handpiece. lected.
No cold light on the multi‐ Cold light not preselected. ▶ The heating function is preselected.
functional handpiece. ▶ Preselect cold light.
No spray in the instru‐ No spray preselected. ▶ Preselect spray.
ments. Close the ring for control‐ ▶ Open the ring for controlling the spray on the in‐
ling the spray on the instru‐ struments.

ments.
Spray at the instruments is The spray nozzles are ▶ Clean the spray nozzles according to the accom‐
insufficient. dirty/clogged. panying instrument operating instructions.

Leaks in instruments. O-rings at MULTIflex or ▶ Replace O-rings.

motor coupling, gripping
sleeve or cannula of the tri‐
ple-function handpiece are
damaged.
PiezoLED or PIEZOsoft PiezoLED or PIEZOsoft ▶ Also refer to: Instructions for Use of the PIEZOsoft/
without function. not pivoting. PiezoLED

The suction hoses do not Slides on the conical sec‐ ▶ Open the slide valve.
have any suction. tions are closed.
Sieves in suction connec‐ ▶ Replace sieves.
tor are blocked.
Foot switch for vacu-stop ▶ Release the foot switch.
has been pressed.
Suction machine not run‐ ▶ Turn on the suction machine.
ning. ▶ Check the suction machine fuse.
The amalgam separator ▶ Operating instructions of the amalgam separator.
does not work correctly.
Water in the return air fil‐ O-rings of the MULTIflex ▶ Replace all O-rings of the MULTIflex coupling.
ter. coupling are damaged.
A melody sounds. The amalgam separator ▶ Exchange the amalgam container.
CAS1 is almost full (95%).

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9 Troubleshooting

Malfunction Cause Remedy

The CAS1 amalgam sepa‐ ▶ Also refer to: Instructions for use for the CAS 1 or
rator is defective. ▶ Call a Service technician.
Ten beeps are issued. The Oxygenal container is ▶ Stop filling the Oxygenal container.
too full.
Signal sound is issued ev‐ The Oxygenal container is ▶ Refill the Oxygenal container.
ery 10 seconds. empty. Also refer to: Servicing instructions

The LED on the "Intensive

germ reduction" key flash‐
es (green).
(Assistant unit)
MEMOdent menu displays
the error.
LED on "HYDROclean" Malfunction in the amal‐ ▶ Call a service technician.
button (red) flashes. gam separator. ▶ Note the amalgam separator warning notice.
Also refer to: Operating instructions of the amal‐
gam separator

See also:
2 Operating instructions of the amalgam separator
Emergency shut off of the ▶ Call a technician.
bowl valve (only when ex‐
ternal suction is installed)
ERGOcam/DIAGNOcam PC is switched off. ▶ Turn on the computer.
does not work. USB cable too long. ▶ Make sure that the cable length does not exceed
10 m (2 x 5 m passive with repeater).
No data transmission to No or faulty ethernet con‐ ▶ Notify network administrator.
the multimedia menu of the nection between dental
unit. unit and office network.
An acoustic signal is is‐ Leaking water switch rec‐ ▶ Remove water from the unit body. If necessary,
sued every second. ognises leaking water. have a technician fixed the leak.

Malfunction Cause Remedy

Display shows: ID 33 No CAN node and/or inter‐ ▶ Call a service technician.
nal communication is faul‐
ty.
Display shows: ID 56 Wireless foor control bat‐ ▶ Charge battery.
tery is empty.
Display shows: ID 64 Water is shut off. ▶ Turn water on.
Water works leaks strong‐ ▶ Call a technician.
ly.
Water works malfunction

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Instructions for use ESTETICA E50 Life
9 Troubleshooting

Malfunction Cause Remedy

Display shows: ID 65 Safety switch of bowl suc‐ ▶ Turn external suction on.
tion has been reached. ▶ Check and clean, if required, the bowl valve.
Display shows: ID 66 Amalgam separator mal‐ ▶ Remedy the malfunction.
function Also refer to: Instructions for Use of amalgam sep‐
arator

See also:
2 Instructions for Use of amalgam separator
Display shows: ID 67 The oxygenal container is ▶ Refill the Oxygenal container.
empty. Also refer to: Servicing instructions

See also:
2 Servicing instructions
Display shows: ID 68 Call for service ▶ Have a service performed.
▶ Call a technician.
Display shows: ID 69 Intensive germ reduction ▶ Carry out an intensive disinfection.
must be carried out. Also refer to: Servicing instructions

See also:
2 Servicing instructions
Display shows: ID 70 Dekaseptol empty. ▶ Replenish Dekaseptol.
Also refer to: Servicing instructions

See also:
2 Servicing instructions
Display shows: ID 72 Dekaseptol bottle. ▶ Insert the DEKASEPTOL bottle.
Also refer to: Care instructions

See also:
2 Care instructions
Display shows: ID 74 Centramat empty. ▶ Notify the service centre.
Indicator if the DEKASEP‐
TOL bottle is not full after
600 s (10 min).
Display shows: ID 75 Centramat too full. ▶ Notify the service centre.
Display shows: ID XX This error is not described ▶ Call a technician.
in this chapter.
Display shows: CAN fail Internal communication er‐ ▶ Turn the unit off and on again, consult a service
ror. technician according to need.

Display shows: System Unit does not work. ▶ Call a service technician.
State

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 Instructions for use ESTETICA E50 Life
10 Data on electromagnetic compatibility according to EN 60601-1-2 | 10.1 Electromagnetic Transmissions

10 Data on electromagnetic compatibility according to EN 60601-1-2

10.1 Electromagnetic Transmissions

The treatment unit is designed for operation in an environment as specified below.
The customer or user of the should make sure that the device is used in an environ‐
ment of the specified type.

Measurements of emitted interfer‐ Conformance Electromagnetic environment -

ence Guidelines
HF emissions according to CISPR Group 1 The device uses HF energy for its
11 internal functions exclusively. There‐
fore, the HF emission of the device
is very low and interference with ad‐
jacent electronic devices is unlikely.
HF emissions according to CISPR Class B The device is suitable for use in all
11 facilities including residential ones,
and facilities that are directly con‐
nected to a public power supply that
also supplies residential buildings.
Emission of harmonics according to Class A The device is suitable for use in all
EN 61000-3-2 facilities including residential ones,
and facilities that are directly con‐
nected to a public power supply that
also supplies residential buildings.
Emission of voltage fluctuations/ Conforms The device is suitable for use in all
flicker according to EN 61000-3-3 facilities including residential ones,
and facilities that are directly con‐
nected to a public power supply that
also supplies residential buildings.

10.2 Resistance to electromagnetic interference

The treatment unit is designed for operation in an environment as specified below.
The customer or user of the should make sure that the device is used in an environ‐
ment of the specified type.

Interference immunity tests EN 60601 test level Compliance level Electromagnetic environ‐
ment - Guidelines
Electrostatic discharge ± 6 kV contact discharge ± 2/4/6 kV contact dis‐ Floors should be made of
(ESD) according to EN ± 8 kV atmospheric dis‐ charge wood or concrete or be fit‐
61000-4-2 charge ± 2/4/8 kV atmospheric ted with ceramic tiles. If the
discharge floor is fitted with synthetic
material, the relative hu‐
midity must be at least
30%.
Fast transient electrical in‐ ± 2 kV for power lines ± 2 kV for power lines The quality of the supply
terference / bursts accord‐ ± 1 kV for input and output voltage should correspond
ing to EN 61000-4-4 lines to that of a typical business
or hospital environment.
Surges according to EN ± 1 kV push-pull voltage ± 1 kV push-pull voltage The quality of the supply
61000-4-5 ± 2 kV common mode volt‐ ± 2 kV common mode volt‐ voltage should correspond
age age to that of a typical business
or hospital environment.

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Instructions for use ESTETICA E50 Life
10 Data on electromagnetic compatibility according to EN 60601-1-2 | 10.3 Recommended safe distance between portable
and mobile HF telecommunications equipment and the treatment unit
Interference immunity tests EN 60601 test level Compliance level Electromagnetic environ‐
ment - Guidelines
Voltage interruptions, < 5% UT < 5% UT The quality of the supply
short-term interruptions (> 95% interruption) (> 95% interruption) voltage should correspond
and fluctuations of the sup‐ for ½ period for ½ period to that of a typical business
ply voltage according to 40% UT 40% UT or hospital environment. If
EN 61000-4-11 (60% interruption) (60% interruption) the user needs the to work
for 5 periods for 5 periods even if the power supply is
70% UT 70% UT interrupted, we recom‐
(30% interruption) (30% interruption) mend supplying energy to
for 25 periods for 25 periods the from an uninterruptible
< 5% UT < 5% UT power supply or battery.
(> 95% interruption) (> 95% interruption)
for 5 s for 5 s
(250 periods) (250 periods)
Magnetic field at a supply 3 A/m 3 A/m Magnetic fields at the
frequency (50/60 Hz) ac‐ mains frequency should
cording to EN 61000-4-8 correspond to typical val‐
ues in a business and
hospital environment.
NOTE: V T is the alternating mains voltage before the test level is used.

10.3 Recommended safe distance between portable and mobile HF

telecommunications equipment and the treatment unit
The is intended for use in an electromagnetic environment in which the HF interfer‐
ence parameters are controlled. The customer or user of the can help prevent electro‐
magnetic interference by maintaining the minimum clearance between portable and
mobile HF telecommunication devices (transmitters) and the depending on the output
of the communication device as indicated below.
Safe distance depending on the transmission frequency:

Rated power P of the Safe distance depending on the transmission frequency in m

transmitter in W 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d=1.17 P d=1.20 P d=2.3 P
0.01 0.12 0.12 0.23
0.1 0.37 0.38 0.73
1 1.17 1.20 2.3
10 3.69 3.79 7.27
100 11.7 12 23
U1 = Compliance level according to 4-6: 3 Veff
E1 = Compliance level according to 4-3: 3 V/m
Factor [3.5/U1] [12/E1] [23/E1]
For transmitters whose maximum rated power is not in the above table, the recom‐
mended safe distance d in meters (m) can be calculated using the equation for the re‐
spective gap, where P is the maximum rated power of the transmitter in Watts (W) ac‐
cording to the manufacturer's information.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not be applicable in every case. The spread of electro‐
magnetic waves is absorbed and reflected by buildings, objects and people.

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 Instructions for use ESTETICA E50 Life
10 Data on electromagnetic compatibility according to EN 60601-1-2 | 10.4 Immunity to electromagnetic interference

10.4 Immunity to electromagnetic interference

The treatment unit is designed for operation in an environment as specified below.
The customer or user of the should make sure that the device is used in an environ‐
ment of the specified type.

Interference immunity EN 60601 test level Compliance level Electromagnetic environment -

tests Guidelines
Wire-based HF interfer‐ 3 Veff 3 Veff Handheld and mobile wireless devi‐
ence according to EN 150 kHz to 80 MHz 3 V/m ces should not be used at a shorter
61000-4-6 outside the ISM bandsa distance from the including cables
Wireless HF interfer‐ V/m than the recommended safe clear‐
ence according to EN 80 MHz to 2.5 GHz ance calculated using the appropri‐
61000-4-3 ate equation for the emission fre‐
quency.
Recommended safe distance:
d = 1.17 P
d= 1.17 P for 80 MHz to 800 MHz
d= 2.33 P for 800 MHz to 2.5 GHz
where P is the maximal nominal
power of the transmitter in watts
(W) as specified by the transmitter
manufacturer and d is the recom‐
mended safe clearance in metres
(m).
b
The field strength of stationary
wireless radio transmitters as meas‐
ured locallycshould be lower than
the conformance level at all fre‐
quencies.
d
Interference is possible in the vicin‐
ity of devices bearing the following
icon.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not be applicable in every case. The spread of electro‐
magnetic waves is absorbed and reflected by buildings, objects and people.
a
The ISM frequency bands (for industrial, scientific, and medical applications) between
150 kHZ and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz;
26.957 MHz to 27.283 MHz, and 40.66 MHz to 40.70 MHz.
b
The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz
and in the frequency range from 80 MHz to 2.5 GHz are intended to reduce the proba‐
bility of mobile/handheld communications facilities causing interference when they are
inadvertently introduced into the patient area. For this reason, the additional factor of
10/3 is applied in the calculation of the recommended safe clearances in these ranges
of frequencies.
c
The field strength of stationary transmitters, such as, e.g. base stations of mobile
phones and mobile terrestrial radio devices, amateur radio stations, AM and FM radio
and television transmitters, cannot be determined exactly based on theoretical consid‐
erations. A site study should be considered to determine the electromagnetic environ‐
ment in terms of stationary transmitters. If the measured field strength at the site, at
which the is used, exceeds the compliance levels shown above, the should be moni‐
tored to demonstrate proper function. If any uncommon performance characteristics
are observed, additional measures may be required, such as, e.g., changing the orien‐
tation or using a different location for the .

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10 Data on electromagnetic compatibility according to EN 60601-1-2 | 10.4 Immunity to electromagnetic interference

d
In the frequency range of 150 kHz to 80 MHz, the field strength should be less than
3V eff V/m.

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