KaVo SMARTmatic S80 K User manual

Instructions for use
SMARTmatic S80 K - 1.011.6771

Distributed by:
KaVo Dental GmbH
Bismarckring 39
D-88400 Biberach
Phone [phone]
Fax [phone]
Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
D-88400 Biberach
www.kavo.com

Table of contents
1 User instructions............................................................................................................................................. 4
2 Safety ............................................................................................................................................................. 6
2.1 Infection hazard ..................................................................................................................................... 6
2.2 Technical condition ................................................................................................................................ 6
2.3 Accessories and combination with other equipment.............................................................................. 7
2.4 Qualification of personnel ...................................................................................................................... 7
2.5 Service and repair.................................................................................................................................. 7
3 Description of the product............................................................................................................................... 8
3.1 Purpose - Intended use ......................................................................................................................... 8
3.2 Technical Specifications ........................................................................................................................ 8
3.3 Transportation and storage conditions .................................................................................................. 9
4 Startup and shut down.................................................................................................................................... 10
5 Operation........................................................................................................................................................ 11
5.1 Attaching the medical device ................................................................................................................. 11
5.2 Removing the medical device................................................................................................................ 11
5.3 Inserting the milling tools or diamond grinders ...................................................................................... 11
5.4 Removing the dental burs or diamond grinders..................................................................................... 12
6 Troubleshooting.............................................................................................................................................. 13
6.1 Check for malfunctions .......................................................................................................................... 13
6.2 Troubleshooting ..................................................................................................................................... 13
6.2.1 Replacing the O-rings ............................................................................................................... 13
7 Reprocessing steps in accordance with ISO 17664 ....................................................................................... 14
7.1 Preparations at the site of use ............................................................................................................... 14
7.2 Cleaning................................................................................................................................................. 14
7.2.1 Manual external cleaning .......................................................................................................... 14
7.2.2 Automated external cleaning .................................................................................................... 14
7.2.3 Manual internal cleaning ........................................................................................................... 14
7.2.4 Automated internal cleaning ..................................................................................................... 15
7.3 Disinfection ............................................................................................................................................ 15
7.3.1 Manual external disinfection ..................................................................................................... 16
7.3.2 Manual internal disinfection ...................................................................................................... 16
7.3.3 Automated external and internal disinfection ........................................................................... 16
7.4 Drying .................................................................................................................................................... 17
7.5 Care products and systems - Servicing ................................................................................................. 17
7.5.1 Servicing with KaVo Spray........................................................................................................ 17
7.5.2 Servicing with KaVo SPRAYrotor ............................................................................................ 18
7.5.3 Servicing with KaVo QUATTROcare ....................................................................................... 18
7.5.4 Servicing with KaVo QUATTROcare PLUS ............................................................................. 18
7.6 Packaging .............................................................................................................................................. 19
7.7 Sterilisation ............................................................................................................................................ 20
7.8 Storage .................................................................................................................................................. 20
8 Tools and consumables.................................................................................................................................. 21
9 Warranty provisions........................................................................................................................................ 22
Instructions for use SMARTmatic S80 K - 1.011.6771
Table of contents
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Instructions for use SMARTmatic S80 K - 1.011.6771
1 User instructions
4 / 24
1 User instructions
Dear User
Congratulations on purchasing this KaVo quality product. By following the instructions
below you will be able to work smoothly, economically and safely.
© Copyright by KaVo Dental GmbH
KaVo Repair Service
For repairs, please contact your local dealer or the KaVo Repair Service directly:
[phone]
[email protected]
KaVo Technical Service
If you have any questions or complaints, please contact the KaVo Technical service:
[phone]
[email protected]
Target group
This document is intended for dentists and their assistants. The startup section is also
intended for service technicians.
General marks and symbols
Refer to the chapter on Safety/Warning symbol
Important information for users and service technicians
Action request
CE mark (European Community). A product bearing this mark meets the re-
quirements of the applicable EC directive.
Can be steam-sterilised at 134 oC -1 oC / +4 oC (273 oF -1.6 oF / +7.4 oF)
Thermodisinfectable
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:
DANGER
In cases which – if not prevented – directly lead to death or severe injury.
WARNING
In cases which – if not prevented – could lead to death or severe injury.

Instructions for use SMARTmatic S80 K - 1.011.6771
1 User instructions
CAUTION
In cases which – if not prevented – could lead to minor or moderate injury.
NOTICE
In cases which – if not prevented – could lead to material damage.
5 / 24

Instructions for use SMARTmatic S80 K - 1.011.6771
2 Safety | 2.1 Infection hazard
6 / 24
2 Safety
The instructions for use are a component of the product and must be read carefully
prior to use and be accessible at all times.
The device may only be used in accordance with the instructions for use, any other
type of use is not permitted.
2.1 Infection hazard
Patients, users or third parties could be infected by contaminated medical devices.
▶ Take suitable personal protective measures.
▶ Follow the instructions for using the components.
▶ Before the initial startup and after each use, prepare and sterilise the medical
device and accessories accordingly.
▶ Carry out the cleaning and sterilisation as described in the instructions for use.
The procedure has been validated by the manufacturer.
▶ It is essential to ensure the effectiveness of the cleaning and sterilisation in the
case of deviation in procedure.
▶ Prior to disposal, the product and accessories must be appropriately prepared or
sterilised.
▶ In the case of injury to soft tissue, do not continue treatment in the oral cavity with
instruments driven by compressed air.
▶ Use gloves or finger guard whenever you test, insert, and remove the tool.
2.2 Technical condition
A damaged device or components could injure patients, users and third parties.
▶ Only operate devices or components if they are undamaged on the outside.
▶ Check that the device is working properly and is in satisfactory condition before
each use.
▶ Have parts with sites of breakage or surface changes checked by the Service.
▶ If the following defects occur, stop working and have the service personnel carry
out repair work:
▪ Malfunctions
▪ Damage
▪ Irregular running noise
▪ Excessive vibration
▪ Overheating
▪ Tool is not seated firmly in the handpiece
Observe the following instructions in order to guarantee optimum functioning and pre-
vent material damage:
▶ Service the medical device with care products and systems regularly as described
in the instructions for use.
▶ The device should be cleaned, serviced and stored in a dry location, according to
instructions, if it will not be used for a longer period.
High torque of micromotors can lead to severe burn injuries.
▶ Service micromotors regularly.
▶ Do no use any damaged motors.

Instructions for use SMARTmatic S80 K - 1.011.6771
2 Safety | 2.3 Accessories and combination with other equipment
▶ Do not use motors for unauthorised purposes.
2.3 Accessories and combination with other equipment
Use of un-authorised accessories or un-authorised modifications of the device could
lead to injury.
▶ Only use accessories that have been approved for combination with the product
by the manufacturer.
▶ Only use accessories that are equipped with standardised interfaces.
▶ Do not make any modifications to the device unless these have been approved by
the manufacturer of the product.
The lack of control equipment for changing the speed range and the direction of rota-
tion can lead to injury.
▶ Control facility for changing the speed and the direction of rotation must be
present.
▶ The medical device may only be combined with a treatment centre released by
KaVo.
▶ Comply with the Instructions for Use of the treatment centre.
2.4 Qualification of personnel
Application of the product by users without the appropriate medical training could in-
jure the patients, the users or third parties.
▶ Make sure that the user has read and understood the instructions for use.
▶ Only employ the device if the user has the appropriate medical training.
▶ Observe national and regional regulations.
The improper use of the device could lead to burns or injuries.
▶ Never touch soft tissue with the handpiece head or instrument cover.
▶ After treatment, place the medical device properly in the cradle without the tool.
2.5 Service and repair
Repairs, servicing and safety checks may only be performed by trained service per-
sonnel. 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 train-
ing
Observe all the following items during servicing work:
▶ Have the service and testing tasks carried out in accordance with the Medical
Product Operator Ordinance.
▶ Following expiry of the warranty, have the tool holding system checked once a
year.
▶ KaVo recommends specifying in-house service intervals where the medical device
is brought to a professional shop for cleaning, servicing and a function check.
Defined the service interval depending on the frequency of use.
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Instructions for use SMARTmatic S80 K - 1.011.6771
3 Description of the product | 3.1 Purpose - Intended use
8 / 24
3 Description of the product
SMARTmatic S80 K (Mat. No. 1.011.6771)
3.1 Purpose - Intended use
Indications for use:
This medical device is
▪ intended for dental treatment only. All other types of use or modifications of the
product are not permitted and can be hazardous. The medical device is intended
for the following applications: Drilling, caries excavation, endodontics, processing
of tooth and restoration surfaces.
▪ A medical device according to relevant national statutory regulations.
Proper use:
According to these provisions, this medical device may only be used for the described
application by a properly trained user. You need to comply with the following:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these Instructions for use
According to these regulations, the user is required to:
▪ to only use equipment that is operating correctly,
▪ adhere to the specified intended use
▪ to protect him or herself, the patient and third parties from hazards, and
▪ to prevent contamination from the product
3.2 Technical Specifications
Drive speed max. 40,000 rpm
Speed transmission 1:1
Cooling air flow 5.5 to 9.5 Nl/min
Pushbutton chuck Ø 1.6 mm
Usable with contra-angle cutters or grinders.
The contra-angle handpiece S80 K can be mounted on INTRA Motor 181K.

Instructions for use SMARTmatic S80 K - 1.011.6771
3 Description of the product | 3.3 Transportation and storage conditions
3.3 Transportation and storage conditions
NOTICE
Startup after refrigerated storage.
Malfunction.
▶ Prior to startup, strongly refrigerated products must be allowed to warm up to a
temperature of 20 °C to 25 °C (68 °F to 77 °F).
Temperature: -20°C to +70°C (-4°F to +158°F)
Relative humidity: 5% RH to 95% RH absence of condensation
Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi)
Protect from moisture
9 / 24

Instructions for use SMARTmatic S80 K - 1.011.6771
4 Startup and shut down
10 / 24
4 Startup and shut down
WARNING
Hazard from non-sterile products.
Infection hazard for dentist and patient.
▶ Prior to initial startup and after each use, reprocess the product and accessories.
WARNING
Dispose of the product in appropriate manner.
Infection hazard.
▶ Reprocess and sterilise the product and accessories before disposal.
NOTICE
Damage from soiled and moist cooling air.
Contaminated and moist cooling air can cause malfunctions.
▶ Make sure that the supply of cooling air is dry, clean, and uncontaminated accord-
ing to EN ISO 7494-2.
NOTICE
Damage to the contra-angle handpiece caused by spray air and spray water.
Property damage
▶ Un-select spray air and water on the supply unit before startup!

Instructions for use SMARTmatic S80 K - 1.011.6771
5 Operation | 5.1 Attaching the medical device
5 Operation
5.1 Attaching the medical device
WARNING
Release of the medical device during treatment.
A medical device that is not properly locked in place can release from the motor coup-
ling and fall off.
▶ Carefully pull on it before each treatment to ensure that the medical device is se-
curely locked on the motor coupling.
NOTICE
Removing and attaching the contra-angle handpiece while the drive motor is rotating.
Damage to the driver.
▶ Never attach or remove the contra-angle handpiece while the drive motor is rotat-
ing.
NOTICE
Pressing the foot switch while attaching or detaching the medical device.
Property damage to the medical device.
▶ Do not connect or remove the medical device while pressing the foot switch.
▶ Lightly spray O-rings on motor coupling with KaVo Spray.
▶ Place the medical device on the motor coupling and lock it into place.
▶ Pull on the medical device to make sure that it is securely affixed to the coupling.
5.2 Removing the medical device
▶ Unlock the medical device from the motor coupling by twisting it slightly and then
pulling it along its axis.
5.3 Inserting the milling tools or diamond grinders
Note
Only use carbide cutters or diamond grinders that correspond to DIN EN ISO
1797-1 type 3, are made of steel or hard metal and meet the following criteria:
- Shaft diameter: Ø 1.59 to Ø 1.60 mm
- Overall length: max. 25 mm
- Shaft clamping length: min. 11 mm
- Blade diameter: max. Ø 2 mm
WARNING
Use of unauthorised dental burs or diamond grinders.
Risk of injury.
▶ Comply with the instructions for use and use the dental bur or diamond grinder
properly.
▶ Only use dental burs or diamond grinders that do not deviate from the specified
data.
11 / 24

Instructions for use SMARTmatic S80 K - 1.011.6771
5 Operation | 5.4 Removing the dental burs or diamond grinders
12 / 24
WARNING
Hazard from rotating bur or diamond grinder.
Lacerations.
▶ Do not touch the bur or diamond grinder when it is rotating!
▶ Remove the bur/diamond grinder from the medical device after treatment to avoid
injury and infection when putting it away.
CAUTION
Use of dental burs or diamond grinders with worn or damaged shafts.
Risk of injury, tool may fall out during treatment.
▶ Never use dental burs or diamond grinders with damaged or worn shafts.
CAUTION
Hazard from defective chuck system.
The tool can fall out and cause injury.
▶ Pull on the tool to check if the chucking system is functioning properly and that
the tool is firmly clamped. Wear gloves or a thimble when you check, insert, or re-
move the bits to prevent injury and infection.
NOTICE
Tool shaft slips inside the chuck due to excessive speed of the tool or abrupt engage-
ment of the tool.
Material damage to tool shaft and chuck system, reduction of the service life of tool
and chuck system.
▶ Do not operate the tool at a higher speed than recommended by the manufac-
turer.
NOTICE
Use of dental burs or diamond grinders with worn or damaged shafts.
Material damage to the chuck system, tool is difficult or impossible to remove from the
chuck system.
▶ Do not use dental burs or diamond grinders with damaged or worn shafts.
▶ Forcefully press the push button with your thumb and simultaneously insert the
dental bur or diamond grinder all the way to the stop.
▶ Check that the dental bur or diamond grinder is securely attached by pulling on it.
5.4 Removing the dental burs or diamond grinders
WARNING
Hazard from rotating bur or diamond grinder.
Lacerations and damage to the chuck system.
▶ Do not touch the bur or diamond grinder when it is rotating!
▶ Do not press the push-button while the cutter or grinder is rotating.
▶ Remove the cutter/grinder from the contra-angle handpiece after treatment to
avoid injury and infection when putting it away.
▶ After the dental bur or diamond grinder has stopped rotating, firmly press the
press-button with your thumb and simultaneously pull out the dental bur or dia-
mond grinder.

Instructions for use SMARTmatic S80 K - 1.011.6771
6 Troubleshooting | 6.1 Check for malfunctions
6 Troubleshooting
6.1 Check for malfunctions
CAUTION
Missing or damaged O-rings.
Malfunction and premature failure.
▶ Make sure that all O-rings are on the coupling and are undamaged.
CAUTION
Heating of the product.
Burns or product damage from overheating.
▶ Do not use the product if it is irregularly heated.
▶ The medical device is too hot while working:
Service the medical device.
▶ When the speed drops or is uneven:
Service the medical device.
▶ An O-ring is missing on the motor coupling:
Replace O-ring.
See also:
2Instructions for use of motor
6.2 Troubleshooting
6.2.1 Replacing the O-rings
CAUTION
Hazard from improper care of the O-rings.
Functional problem or complete failure of the medical device.
▶ Do not use Vaseline or other grease or oil.
Note
The O-rings on the coupling may only be lubricated with a cotton ball wetted with
KaVo Spray.
▶ 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 into the grooves.
13 / 24

Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.1 Preparations at the site of use
14 / 24
7 Reprocessing steps in accordance with ISO 17664
7.1 Preparations at the site of use
WARNING
Hazard from non-sterile products.
There is a risk of infection from contaminated medical devices.
▶ Take suitable personal protective measures.
▶ Remove all residual cement, composite or blood immediately.
▶ Reprocess the medical device as soon as possible after treatment.
▶ Remove the dental bur or diamond grinder from the medical device.
▶ The medical device must be dry when transported to reprocessing.
▶ Do not place in solutions or similar substance.
7.2 Cleaning
NOTICE
Never reprocess this medical device in an ultrasonic device.
Malfunction and material damage.
▶ Clean manually or in a washer disinfector only.
7.2.1 Manual external cleaning
Accessories required:
▪ Tap water 30 oC ± 5 oC (86 oF ± 10 oF)
▪ Brush, e.g. medium-hard toothbrush
▶ Brush off under flowing tap water.
7.2.2 Automated external cleaning
KaVo recommends washer disinfectors in compliance with EN ISO 15883-1 that are
operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD program, the cleaning agent
neodisher® MediClean and the neutralisation agent neodisher® Z.
▶ The program settings and cleansers and disinfectants that must be used can be
found in the instructions for use of the thermodisinfector.
▶ Directly after automated cleaning/disinfection, treat the medical device with the
KaVo care products and systems provided by KaVo.
7.2.3 Manual internal cleaning
Validated internal cleaning (removal of residual protein) can be accomplished with
KaVo CLEANspray and KaVo DRYspray.

Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.3 Disinfection
▶ Cover the medical device with the KaVo CLEANpac bag, and place it on the cor-
responding care adapter. Press the spray button three times for 2 seconds each
time. Remove the medical device from the spray attachment and let the cleanser
act for one minute.
▶ Afterwards, rinse for 3-5 seconds with KaVo DRYspray.
See also:
2KaVo CLEANspray / KaVo DRYspray Instructions for Use
Note
KaVo CLEANspray and KaVo DRYspray for manual interior cleaning are only avail-
able in the following countries:
Germany, Austria, Switzerland, Italy, Spain, Portugal, France, Luxembourg, Bel-
gium, Netherlands, United Kingdom, Denmark, Sweden, Finland and Norway.
In other countries interior cleaning can only be carried out with thermodisinfectors in
accordance with EN ISO 15883-1.
7.2.4 Automated internal cleaning
KaVo recommends washer disinfectors in compliance with EN ISO 15883-1 that are
operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD program, the cleaning agent
neodisher® MediClean and the neutralisation agent neodisher® Z.
▶ For program settings as well as cleansers and disinfectants to be used, please
refer to the Instructions for Use of the thermodisinfector.
▶ In order to prevent damage to the medical device due to residual fluid, make sure
that the inside and outside of the device is dry after the end of the cycle. Remove
any residual liquids from the interior and exterior of the medical device using com-
pressed air.
▶ Immediately after drying, lubricate the medical device with care agents from the
KaVo care system.
The drying procedure is normally part of the cleaning program of the thermodisin-
fector.
Note
Please observe the instructions for use of the thermodisinfector.
7.3 Disinfection
WARNING
Incomplete disinfection.
Infection hazard.
▶ Principally, KaVo recommends carrying out an final disinfection of the unpack-
aged item to guarantee the complete disinfection.
NOTICE
Using the disinfectant bath or chlorine-containing disinfectants.
Malfunction and material damage.
▶ Do not disinfect the device in the disinfection bath or with chlorine-containing dis-
infectants.
15 / 24

Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.3 Disinfection
16 / 24
7.3.1 Manual external disinfection
KaVo recommends the following products based on compatibility of the materials.
The microbiological efficacy must be ensured by the disinfectant manufacturer and
proven by an expert opinion.
▪ Mikrozid AF made by Schülke & Mayr (liquid or cloths)
▪ FD 322 made by Dürr
▪ CaviCide made by Metrex
Consumables required:
Cloths for wiping the medical device.
▶ Spray the disinfectant on a cloth, then wipe down the medical device and allow
the disinfectant to act according to the instructions of the
disinfectant manufacturer.
▶ Follow the instructions for use of the disinfectant.
7.3.2 Manual internal disinfection
The efficacy of manual internal disinfection must be demonstrated by the manufac-
turer of the disinfection agent. With KaVo products, use only disinfection agents that
have been released by KaVo with respect to the compatibility of materials (e.g. WL-
cid / made by ALPRO).
▶ Immediately after internal disinfection, lubricate the KaVo medical device with care
agents from the KaVo care system.
7.3.3 Automated external and internal disinfection
KaVo recommends washer disinfectors in compliance with EN ISO 15883-1 that are
operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD program, the cleaning agent
neodisher® MediClean and the neutralisation agent neodisher® Z.
▶ For program settings as well as cleansers and disinfectants to be used, please
refer to the Instructions for Use of the thermodisinfector.
▶ In order to prevent damage to the medical device due to residual fluid, make sure
that the inside and outside of the device is dry after the end of the cycle. Remove
any residual liquids from the interior and exterior of the medical device using com-
pressed air.
▶ Immediately after drying, lubricate the medical device with care agents from the
KaVo care system.
The drying procedure is normally part of the cleaning program of the thermodisin-
fector.
Note
Please observe the instructions for use of the thermodisinfector.

Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.4 Drying
7.4 Drying
Manual Drying
▶ Blow off the outside and inside with compressed air until water drops are no
longer visible.
Automatic Drying
The drying procedure is normally part of the cleaning program of the thermodisin-
fector.
▶ Follow the instructions for use of the thermodisinfector.
7.5 Care products and systems - Servicing
WARNING
Sharp dental bur or diamond grinder in the medical device.
Risk of injury from sharp and/or pointed dental bur or diamond grinder.
▶ Remove dental bur or diamond grinder.
NOTICE
Improper service and care.
Premature wear and reduced product service life.
▶ Service regularly with suitable agents.
Note
KaVo guarantees the proper function of KaVo products only if the care products lis-
ted as accessories are used, since these were tested for proper use on our
products.
7.5.1 Servicing with KaVo Spray
KaVo recommends servicing the product as part of the reprocessing after each use,
i.e. after each cleaning, disinfection, and before each sterilisation.
▶ Remove the insert.
▶ Cover the product with the Cleanpac bag.
▶ Plug the product onto the cannula, and press the spray button for one second.
Servicing the chucking system
KaVo recommends cleaning and servicing the chuck system once a week.
▶ Remove the cutter or grinder, place the spray nipple tip in the opening and spray.
▶ Carry out the servicing according to the instructions in the section, "Servicing with
KaVo Spray".
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Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.5 Care products and systems - Servicing
18 / 24
7.5.2 Servicing with KaVo SPRAYrotor
KaVo recommends servicing the product as part of the reprocessing after each use,
i.e. after each cleaning, disinfection, and before each sterilisation.
▶ Place the product on the appropriate coupling on the KaVo SPRAYrotor and cover
it with the Cleanpac bag.
▶ Service the product.
See also:
2Instructions for use KaVo SPRAYrotor
7.5.3 Servicing with KaVo QUATTROcare
Note
QUATTROcare 2104 / 2104 A is no longer included in the current delivery pro-
gramme.
Follow-up product:
▶ QUATTROcare PLUS 2124 A
Servicing and cleaning device with expansion pressure for the interior cleaning of inor-
ganic residues and optimum care.
(no validated cleaning of the interior in accordance with German RKI requirements)
KaVo recommends servicing the product as part of the reprocessing after each use,
i.e. after each cleaning, disinfection, and before each sterilisation.
▶ Remove the dental bur or diamond grinder.
▶ Service the product.
See also:
2Instructions for use KaVo QUATTROcare 2104 / 2104A
Servicing the chuck
KaVo recommends cleaning and servicing the chuck system once a week.
See also:
2Instructions for use KaVo QUATTROcare 2104 / 2104A
▶ Remove the cutter or grinder, place the spray nipple tip in the opening and spray.
▶ Subsequently treat with the specified care products and systems.
See also:
2Servicing with KaVo QUATTROcare
7.5.4 Servicing with KaVo QUATTROcare PLUS
Servicing and cleaning device with expansion pressure for the interior cleaning of inor-
ganic residues and optimum care.

Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.6 Packaging
(no validated cleaning of the interior in accordance with German RKI requirements)
KaVo recommends servicing the product as part of the reprocessing after each use,
i.e. after each cleaning, disinfection, and before each sterilisation.
▶ Remove the dental bur or diamond grinder.
▶ Service the product in the QUATTROcare PLUS.
See also:
2Instructions for use KaVo QUATTROcare PLUS
Servicing the chuck
KaVo recommends cleaning and servicing the chuck system once a week using the
collet servicing program integrated in the device.
See also:
2Instructions for use KaVo QUATTROcare PLUS
Note
Handpieces must be taken off the service couplings before the chuck service can
be started and performed.
▶ Close the front door and press the chuck service button for at least three seconds
until the spray canister control LED flashes three times consecutively.
ðThe device is in chuck service mode.
▶ Remove the service coupling of the chuck from the side hatch of the QUATTRO-
care PLUS and attach it to coupling service point four, on the far right. A MUL-
TIflex adaptor must be mounted there.
▶ Press the handpiece together with the guide bush of the chuck to be serviced
against the tip of the service coupling.
▶ Press the button marked with the chuck service symbol.
Note
Close the chuck service mode.
Option 1: Place the dental handpieces in the QUATTROcare PLUS 2124 A, close
the front door and start theservice procedure.
Option 2: After three minutes with no service procedure running, the device auto-
matically switches back to normal service mode.
See also:
2Servicing with KaVo QUATTROcare PLUS
7.6 Packaging
Note
The sterilisation bag must be large enough for the handpiece so that the bag is not
stretched.
The quality and use of the sterilisation packaging must satisfy applicable standards
and be suitable for the sterilisation procedure!
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Instructions for use SMARTmatic S80 K - 1.011.6771
7 Reprocessing steps in accordance with ISO 17664 | 7.7 Sterilisation
20 / 24
▶ Seal the medical device individually in the sterilised item packaging.
7.7 Sterilisation
Sterilisation in a steam steriliser (autoclave) in accordance with EN
13060 / ISO 17665-1
NOTICE
Improper service and care.
Premature wear and reduced product service life.
▶ Before each sterilisation cycle, service the medical device with KaVo care
products.
NOTICE
Contact corrosion due to moisture.
Damage to product.
▶ Immediately remove the product from the steam steriliser after the sterilisation
cycle.
The KaVo medical device has a maximum temperature resistance up to 138 ℃
(280.4 °F).
Select a suitable procedure (depending on the available autoclave) from the following
sterilisation processes:
▪ Autoclave with three times pre-vacuum:
- at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
▪ Steriliser using the gravity method:
- at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
▶ Use according to the manufacturer's Instructions for Use.
7.8 Storage
Prepared products must be stored, protected from germs (as far as possible) and
dust, in a dry, dark, cool room.
Note
Comply with the expiry date of the sterilised items.