KaVo ESTETICA E50 Life User manual

Instructions for use
ESTETICA E50 Life

Distributed by:
KaVo Dental GmbH
Bismarckring 39
88400 Biberach
Germany
Phone [phone]
Fax [phone]
Manufacturer:
KaVo Dental GmbH
Bismarckring 39
88400 Biberach
Germany
www.kavo.com

Instructions for use ESTETICA E50 Life
Table of contents
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Table of contents
1 User instructions ............................................................................................................... 6
1.1 Terms and conditions of warranty.................................................................................... 8
2 Safety................................................................................................................................. 9
2.1 Explosion hazard ........................................................................................................... 9
2.2 Infection hazard ............................................................................................................ 9
2.3 Electrical shock..............................................................................................................10
2.4 Technical condition ........................................................................................................ 10
2.5 Electromagnetic interferences ......................................................................................... 10
2.6 Use .............................................................................................................................. 11
2.7 Accessories and combination with other equipment........................................................... 12
2.8 Qualification of personnel ............................................................................................... 12
2.9 Service and repair ......................................................................................................... 12
3 Description of the product................................................................................................. 13
3.1 Treatment centre – Versions........................................................................................... 13
3.1.1 KaVo ESTETICA E50 Life TM .............................................................................. 13
3.1.2 KaVo ESTETICA E50 Life S ................................................................................ 13
3.2 Patient chair Standard and COMPACTchair ....................................................................... 14
3.3 Unit body with patient element (optional)......................................................................... 15
3.4 Dentist element – Versions.............................................................................................17
3.4.1 TM table .......................................................................................................... 17
3.4.2 S-table............................................................................................................ 17
3.5 Assistant element – Versions ..........................................................................................19
3.5.1 Assistant element – Standard/Assistant element – Short ...................................... 19
3.5.2 Assistant element right, left (optional) ................................................................ 20
3.6 Triple function handpiece (3F handpiece) ......................................................................... 21
3.7 Multifunctional handpiece (MF handpiece) ........................................................................ 21
3.8 Multifunctional handpiece Minilight 3F/G3F ....................................................................... 21
3.9 Control elements ........................................................................................................... 22
3.9.1 Dentist element TM table .................................................................................. 22
3.9.2 Dentist element S-table .................................................................................... 22
3.9.3 Assistant element............................................................................................. 23
3.9.4 Groups of keys................................................................................................. 23
3.9.5 Foot control ..................................................................................................... 25
3.10 Power and rating plates.................................................................................................. 26
3.11 Technical specifications .................................................................................................. 28
3.12 Intended use................................................................................................................. 36
4 Operation........................................................................................................................... 40
4.1 Switching the device on and off.......................................................................................41
4.2 Adjusting the patient chair.............................................................................................. 42
4.2.1 Adjusting the arm rest (optional) ....................................................................... 42
4.2.2 Adjusting the headrest...................................................................................... 44
4.2.3 Positioning the patient chair manually................................................................. 46
4.2.4 Automatic positioning of patient chair ................................................................. 47
4.2.5 Safety shutdown .............................................................................................. 51
4.3 Moving the patient chair................................................................................................. 55
4.4 Moving the dentist element.............................................................................................55
4.4.1 Moving the dentist element TM .......................................................................... 56
4.4.2 Moving the dentist element S ............................................................................ 56

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4.5 Moving the patient element (optional)..............................................................................57
4.5.1 Moving the patient element (optional) ................................................................ 57
4.6 Moving the assistant element.......................................................................................... 57
4.6.1 Adjusting the height of the Standard assistant element ........................................ 57
4.6.2 Moving the assistant element right, left (optional)................................................ 58
4.7 Using functions through the menu................................................................................... 60
4.7.1 Using the user menu......................................................................................... 60
4.7.2 Standby menu ................................................................................................. 65
4.7.3 Using the MEMOdent menu ............................................................................... 67
4.7.4 Changing the turbine handpiece settings in the MEMOdent menu .......................... 68
4.7.5 Changing the settings for INTRA LUX motors KL 703 LED / KL 701 and COM-
FORTdrive .......................................................................................................
69
4.7.6 Changing the PiezoLED settings in the MEMOdent menu....................................... 70
4.7.7 Changing the multifunctional handpiece settings in the MEMOdent menu ............... 71
4.7.8 Using the timer ................................................................................................ 72
4.7.9 Using the CONEXIO menu (from V2.1) ............................................................... 73
4.8 Using function through the dentist or assistant element..................................................... 79
4.8.1 Using the hygiene functions............................................................................... 79
4.8.2 Using the light functions.................................................................................... 80
4.8.3 Using the timer ................................................................................................ 86
4.9 Operating the foot control............................................................................................... 87
4.9.1 General functions ............................................................................................. 87
4.9.2 Positioning the patient chair with the foot control................................................. 87
4.9.3 Preselecting the level ........................................................................................ 87
4.9.4 Preselecting the dentist..................................................................................... 87
4.9.5 Starting and adjusting instruments..................................................................... 87
4.9.6 Setting the cooling status.................................................................................. 88
4.9.7 Activating blown air .......................................................................................... 88
4.9.8 Preselecting counterclockwise motor rotation....................................................... 88
4.9.9 Setting the instrument light............................................................................... 88
4.9.10 Using physiological saline (optional accessory)..................................................... 89
4.9.11 Special functions of the wireless foot control........................................................ 89
4.9.12 Establishing a connection between the wireless foot control and the treatment
centre (Bluetooth) ............................................................................................
90
4.9.13 Establishing a connection between the wireless foot control and the treatment
centre .............................................................................................................
92
4.9.14 Charging the wireless foot control ...................................................................... 94
4.10 Using handpieces...........................................................................................................95
4.10.1 Instrument priority ........................................................................................... 95
4.10.2 Using suction hoses .......................................................................................... 95
4.10.3 Using the triple function handpiece..................................................................... 97
4.10.4 Using the multifunctional handpiece ................................................................... 98
4.10.5 Use multifunctional handpiece Minilight 3F/G3F ...................................................101
4.10.6 Using the PiezoLED...........................................................................................102
4.11 Using the KL 703 LED / KL 702 in ENDO mode (optional accessory)....................................
102
4.11.1 General ...........................................................................................................102
4.11.2 Calling up ENDO mode......................................................................................104
4.11.3 Changing settings in the options menu ...............................................................104
4.11.4 Setting the parameters .....................................................................................105
4.11.5 Exiting ENDO mode ..........................................................................................107
4.12 Using the pump for physiological saline (optional accessory) ..............................................
108

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4.12.1 General ...........................................................................................................108
4.12.2 Connecting the coolant......................................................................................109
4.12.3 Activating the pump for the respective holder (enabling) and regulating the pump ..110
4.12.4 Changing the coolant container..........................................................................111
4.12.5 Attaching and detaching the pump .....................................................................111
4.12.6 Replacing the hose set sterile.............................................................................113
4.13 Using the COMFORTdrive 200 XD / COMFORTbase (optional accessory) ..............................
115
4.13.1 General use .....................................................................................................115
4.13.2 Installing the motor hose on the dentist element .................................................115
4.13.3 Replacing the high-pressure lamp of the COMFORTbase .......................................115
4.13.4 Replacing the O-rings .......................................................................................116
4.14 Using the USB interface..................................................................................................
116
4.15 Using the camera ..........................................................................................................
117
5 Reprocessing methods DIN EN ISO 17664 .......................................................................118
6 Accessories and assembly kits ..........................................................................................119
6.1 Equipment ....................................................................................................................
119
6.2 Patient chair..................................................................................................................
119
6.3 Assistant element ..........................................................................................................
119
6.4 Dentist element.............................................................................................................
120
7 Safety check – Test instructions........................................................................................122
7.1 Introduction..................................................................................................................
122
7.1.1 General notes ..................................................................................................122
7.1.2 Notes for medical electrical systems ...................................................................123
7.1.3 Components of the safety check ........................................................................123
7.1.4 Testing intervals...............................................................................................124
7.1.5 Notes on the test method in accordance with IEC 62353 ......................................124
7.1.6 Notes on recurrent testing.................................................................................124
7.2 Instructions for the safety check .....................................................................................
125
7.2.1 Preparatory measures to be undertaken on the device .........................................125
7.2.2 Visual inspection (inspection by examination)......................................................126
7.2.3 Measurements .................................................................................................128
7.2.4 Functional tests................................................................................................137
7.2.5 Assessment and documentation.........................................................................140
7.3 Test protocol for the safety check....................................................................................
141
8 Annex – Additional measuring points ...............................................................................142
8.1 Additional scan points SL X for the protective earth measurement ......................................
142
8.2 Additional measuring points AP X for the EUL/EPA measurement........................................
143
8.3 Additional connection points ACP X (additional earth connections) ......................................
144
9 Troubleshooting ................................................................................................................145
10Information concerning the electromagnetic compatibility according to EN IEC
60601-1-2..........................................................................................................................
149
10.1 Operating environment and EMC warning notes................................................................
149
10.2 Results of the electromagnetic tests ................................................................................
149

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1 User instructions
Dear user,
Congratulations on purchasing this KaVo quality product. By following the notes
below you will be able to work smoothly, economically and safely.
© Copyright by KaVo Dental GmbH
All other trademarks are property of their respective owners.
Target group
The instructions for use are intended for medical professionals, in particular
dentists and dental practice personnel.
General marks and symbols
See Chapter on User Instructions/Hazard Levels
Important information for users and service technicians
Action request
CE- mark (European Community). A product bearing this mark meets
the requirements of the applicable EC directives.
Sterilisation parameters
▪ Steriliser with Dynamic-Air-Removal (pre-vacuum) method:
– 3 minutes at 135oC (275 oF)
– Drying time: 16 min.
▪ Steriliser with gravity displacement method:
– 10 minutes at 135oC (275 oF)
– Drying time: 30 min.
Thermodisinfectable
Original language German
Information on the packaging
Material number
Serial number
Manufacturer
Note: Please note accompanying documents
Follow the electronic instructions for use

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HIBC Code
EAC conformity mark (Eurasian Conformity)
Transportation and storage conditions
(temperature range)
Transportation and storage conditions
(air pressure)
Transportation and storage conditions
(Humidity)
Protect from moisture (Keep dry)
Protect from impact
Transport upright
Permissible stacking load
Medical device, labelling of medical devices
CE mark for medical devices
UDI symbol
Hazard levels
The warning and safety notes in this document must be observed to prevent
personal injury and material damage. The warning notes are designated as
shown below:
HAZARD
In cases which – if not prevented – directly lead to death or severe injury.
WARNING
In cases which – if not prevented – can lead to death or severe injury.
CAUTION
In cases which – if not prevented – can lead to minor or moderate injury.
CAUTION
In cases which – if not prevented – can lead to material damage.

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KaVo Technical service
If you have any technical questions or complaints, please contact the KaVo
Technical service:
[phone]
[e-mail] or [e-mail]
Please refer to the serial number of the product in all inquiries! For further in-
formation, please visit: www.kavo.com
Currently applicable packaging law
Dispose of and recycle the packaging appropriately in accordance with current
packaging law, employing waste management / recycling companies. Comply
with the comprehensive return system. KaVo has had its packaging licensed for
this purpose. Please comply with the regional public waste-disposal system.
1.1 Terms and conditions of warranty
KaVo provides the final customer with a warranty that the product cited in the
transfer form will function properly and guarantees zero defects in the material
or processing for a period of 12 months from the date of purchase, subject to
the following conditions:
Upon justified complaints of flaws or a short delivery, KaVo will make good its
warranty by replacing the product free of cost or repairing it according to the
customer's wishes. Other claims of any nature whatsoever, in particular with
respect to compensation, are excluded. In the event of default and gross negli-
gence or intent, this shall only apply in the absence of mandatory legal regula-
tions 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 col-
ourfastness 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.
Claims from this warranty can only be asserted when the transfer form (copy)
belonging to the product has been sent to KaVo, and the original can be
presented by the operator or user.

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2 Safety | 2.1 Explosion hazard
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2 Safety
The instructions for use are an integral part of the product and must be read
carefully prior to use and must be accessible at all times.
The device may only be used in accordance with the intended use, any other
type of use is not permitted.
NOTE
All serious events occurring in relation to the product must be reported to the
manufacturer and the competent authority of the member state, in which the
user and/or patient resides.
Individual warning notes must be observed in the corresponding chapters.
2.1 Explosion hazard
Electrical sparks in the product can lead to explosion or fire.
4 Do not set up or operate the product in areas where there is an explosion
hazard.
The use of medical gases can lead to explosion or fire.
4Do not used medical gases in the vicinity of the product.
2.2 Infection hazard
Patients, users or third parties could be infected by contaminated medical
devices.
4Take suitable personal protective measures.
4Follow the instructions for use of the components.
4Before initial startup and after each use, reprocess the product and ac-
cessories appropriately.
4Reprocess the product and accessories appropriately before disposal.
Given the arrangement of the instruments, injury or infections may occur when
reaching for the tray holder or control panel.
4Be aware of the arrangement of the instruments when you reach for the
tray holder or operating device.
Suspended instruments (S-table) can cause injury.
4When you move the dentist element, make sure that nobody gets injured.
It is feasible to use, on standardised interfaces, products from other manufac-
turers, which are not equipped with a protective device preventing back-suction
of treatment water via the instruments into the dental treatment centre. Infec-
tion may be caused by back-suction at the instruments.
4If products from other manufacturers are used at the standardised inter-
faces, you must make sure that the products are equipped with an appro-
priate protective device.
4Do not use products with no protective device.
If a water consumer is connected to the third-party connector assembly kit (op-
tional), stagnant water may cause reverse contamination with germs.
4Before starting, rinse all water drain lines while no handpiece is attached (if
applicable).
4Before initial start-up and after downtimes (weekends, holidays, vacations,
etc.), rinse or purge the air and water lines with air.
4Mind the H2O2 resistance of the water consumer since the water is doped
with OXYGENAL 6 (concentration up to 0.02 %).
Germ formation can lead to infection.
4Carry out an intensive germ reduction.

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4Actuate the tumbler filler several times.
4Note and comply with national regulations concerning the quality of water
for human use (drinking water) - if applicable.
4Note and comply with the national guidelines concerning the quality of the
dental air - if any.
Reflux can lead to infections.
4Only use saliva ejector cannulas and connection pieces of the spray mist
suction with integrated secondary air cannulas to prevent a reflux.
2.3 Electrical shock
Improper connection of a non-medical system to the USB interfaces of the
device can lead to electrical shock and injury to patient, user and third parties.
4Connect any USB device to the medical system in accordance with IEC
60601-1 / IEC 62368-1.
4Use USB devices with no additional power supply (USB-powered) only.
4Applied parts connected to the USB interface of the treatment centre must
comply with IEC 60601-1 type BF.
4It is not permissible to touch USB devices failing to comply with IEC
60601-1 type BF for applied parts and the patient at the same time.
2.4 Technical condition
A damaged product or damaged or NOT KaVo original components could injure
patients, users or third parties.
4Only operate devices or components if they show no signs of damage on the
outside.
4Check to make sure that the device is working properly and is in satisfactory
condition before each use.
4Have parts with sites of breakage or surface changes checked by the service
personnel.
4If the following defects occur, stop working and have the service personnel
carry out repair work:
▪ Malfunctions
▪ Damage
▪ Irregular running noise
▪ Excessive vibration
▪ Overheating
The electrical safety of the device may be affected by improper operating condi-
tions.
4Comply with the operating conditions specified in the "Technical Specifica-
tions" chapter.
Instrument hoses may burst due to stickers.
4Do not affix stickers or adhesive tape to instrument hoses.
2.5 Electromagnetic interferences
Electromagnetic fields might interfere with the functions of implanted systems
(such as pacemakers).
4Ask patients if they have a cardiac pacemaker or other system implanted
and counsel them about the risks before you start the treatment.
High-frequency communications devices may interfere with medical electrical
devices.
4Do not use cell phones in medical offices, hospitals or laboratories.

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4Remove electronic devices such as e.g. computer storage media, hearing
aids etc. during operation.
4Comply with the tables of electromagnetic compatibility during installation
and commissioning.
4If the device needs to be used in the immediate vicinity of other equipment,
monitor the device or system for malfunctions.
2.6 Use
Sitting down on a dental chair that is in horizontal orientation may lead to in-
jury.
4Do not sit down or support yourself on the head or foot end or edges of the
upholstery of the patient chair when it is in a horizontal position.
4Do not support yourself or sit on the armrest.
Exposing the arm system to an overload may cause damage and ensuing in-
jury.
4Never strain the swivel arm, spring arm, assistant element and dentist ele-
ment by using it as a support.
Lack of instructions to the cleaning staff and improper preparation of the treat-
ment centre can lead to the cleaning staff sustaining injuries.
4Only trained professionals and instructed cleaning personnel may be present
in the treatment rooms.
4Position the chair for cleaning and turn the device off.
Injury and material damage may result from the improper use of the charger
for the wireless foot control.
4Do not use the treatment centre during the charging process.
4Do not use the enclosed wireless foot control's charger to charge non-re-
chargeable batteries.
4Charge the wireless foot control with the enclosed charger only.
Long stay in the patient chair can lead to decubitus (pressure sores).
4Take precautions against the formation of decubitus in long treatments.
Overload or dynamic loads can lead to injury and material damage.
4Do not subject the patient chair to a load exceeding its limit (180 kg).
4Do not subject the patient chair to dynamic loads.
Hair of the patient or practice personnel may get caught when the headrest of
the dental chair is moved.
4Mind the hair of the patient or practice personnel when moving the dental
chair or the headrest.
Manual motions of components can lead to injury and material damage.
4Monitor the patient and treatment personnel when you move components.
While entering or exiting, the patient make get entangled in instrument hoses
of the dentist element.
4Position the dentist element outside the entry and exit area.
Automatic motions of the patient chair can lead to injury and material damage.
4Monitor the patient and treatment personnel when changing the chair posi-
tion.
Components of the product may be in the walking path and may lead to injury.
4In use, mind the walking path.
4Keep entry and exit positions unobstructed.
Improper use of the cannula can lead to injury.

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4Rotate the cannula of the handpiece into an operating position where there
is no contact to the mucosa.
4Before each treatment, ensure that the cannula is locked into place and
firmly seated.
4Adhere to a minimum clearance of 10 mm between cannula and surface of
gums or gingiva.
2.7 Accessories and combination with other equipment
Use of non-authorised accessories or non-authorised modifications of the device
could lead to injury.
4Only use accessories that have been approved for combination with the
product by the manufacturer.
4Do not make any modifications to the device unless these have been ap-
proved by the manufacturer of the product.
The use of non-approved accessories as well as non-approved modifications
made to the medical device cause the conformity of the medical device accord-
ing to MDR 2017/745 to be voided. Anybody using non-approved accessories or
making non-approved modifications is deemed, according to MDR 2017/745, to
be the sole liable manufacturer of the medical device and to assume full re-
sponsibility. The new manufacturer is obliged to provide a new declaration of
conformity for the new medical device.
2.8 Qualification of personnel
Application of the product by users without the appropriate medical training
could injure patients, users or third parties.
4Make sure that the user has read and fully comprehends the instructions for
use.
4Make sure that the user has read and comprehends the national and re-
gional regulations.
4The device may be used only if the user has completed the appropriate
medical training.
The operator is responsible for making sure that the product is not used by un-
authorised persons.
2.9 Service and repair
Repairs, servicing and safety checks may only be performed by trained service
personnel. The following persons are authorised to do this:
▪ Service technicians of KaVo branches after the appropriate product training
▪ Service technicians of KaVo authorised dealers after the appropriate product
training
Observe all the following items during servicing work:
4Have the service and testing tasks carried out according to the Medical
Device Operator Ordinance.
4After servicing, interventions on and repairs of the device and before re-use,
have the service personnel perform safety checks on the device.
Improper maintenance and care may lead to premature wear and malfunction.
4Service regularly with suitable agents.
Residual liquids of any type can cause stains on or damage to cushions and
parts of the housing.
4Remove any residual liquids without delay.
The operator may only carry out repair work if the device is switched off and no
patient is being treated.

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3 Description of the product
3.1 Treatment centre – Versions
3.1.1 KaVo ESTETICA E50 Life TM
3.1.2 KaVo ESTETICA E50 Life S

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3.2 Patient chair Standard and COMPACTchair
①Headrest ②Backrest
③Chair base ④Bench
⑤Arm rest (optional)

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3.3 Unit body with patient element (optional)
①Patient element (optional) ②Unit body
The central control is housed in
the unit body.
③Pressurized water bottle
(additional equipment)
④Spittoon bowl
⑤Tumbler filler ⑥Supply element
Customer connection of electricity,
water, compressed air, wastewa-
ter and suction air
⑦Foot control

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E50 Life with Centramat
①Patient element (optional) ②Unit body
The central control is housed in
the unit body.
③Centramat
(supplementary equipment)
④Spittoon bowl
⑤Tumbler filler ⑥Supply element
Customer connection of electricity,
water, compressed air, wastewa-
ter and suction air
⑦Foot control

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3 Description of the product | 3.4 Dentist element – Versions
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3.4 Dentist element – Versions
3.4.1 TM table
①Handle ②Triple function handpiece or multi-
functional handpiece
③Turbine handpiece (MULTIflex
coupling)
④INTRA LUX Motor KL 703 or
INTRA LUX Motor KL 701
⑤Ultrasonic scaler PIEZO Soft or
PiezoLED
⑥Camera
⑦Tray holder ⑧Site for affixing the USB interface
(optional accessory)
⑨Control element
3.4.2 S-table
NOTE
The holder assignment and arrangement of the instruments can be changed
as needed and does not have to be as shown in the figure.

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3 Description of the product | 3.4 Dentist element – Versions
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①Site for affixing the USB interface
(optional accessory)
②Triple function handpiece or multi-
functional handpiece
③Turbine handpiece (MULTIflex
coupling)
④INTRAlux Motor KL 703 LED or IN-
TRA Lux Motor KL 701
⑤Ultrasonic scaler PIEZO Soft or
PiezoLED
⑥Control element

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3.5 Assistant element – Versions
3.5.1 Assistant element – Standard/Assistant element –
Short
7
①Triple function or multifunctional
handpiece
②Spray mist suction
③Control element ④Saliva ejector
⑤Satelec Mini LED
(polymerisation handpiece)
⑥Tray holder for dental assistant
⑦Standard swivel arm (50cm)
or
short swivel arm (32cm)

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3.5.2 Assistant element right, left (optional)
Assistant element right, left with height adjustment (optional)
①Triple function handpiece ②Spray mist suction
③Control element ④Saliva ejector
⑤Satelec Mini LED
(Polymerisation handpiece)