KaVo SMARTtorque LUX S619 L User manual

Instructions for use
SMARTtorque LUX S619 L - 1.008.1641
SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
Always be on the safe side.

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 ........................................................................................................................................ 2
2 Safety ........................................................................................................................................................ 3
2.1 Description of safety instructions ..................................................................................................... 3
2.2 Safety instructions ........................................................................................................................... 3
3 Product description .................................................................................................................................... 5
3.1 Purpose – Proper use ..................................................................................................................... 5
3.2 Technical Specifications .................................................................................................................. 6
3.3 Transportation and storage conditions ............................................................................................ 6
4 Start up and shut down ............................................................................................................................. 7
4.1 Mount the MULTIflex (LUX) / MULTIflex LED coupling ................................................................... 7
4.2 Checking the amount of water ......................................................................................................... 7
4.3 Checking the pressures ................................................................................................................... 8
4.4 Checking the O-rings ....................................................................................................................... 8
5 Operation ................................................................................................................................................... 9
5.1 Attaching the medical device ........................................................................................................... 9
5.2 Removing the medical device ......................................................................................................... 9
5.3 Insert the milling cutter or diamond grinder ..................................................................................... 9
5.4 Removing the milling tool or diamond grinder. .............................................................................. 10
6 Troubleshooting ....................................................................................................................................... 11
6.1 Exchanging the O-rings on the coupling on the supply hose ........................................................ 11
6.2 Cleaning the spray nozzle ............................................................................................................. 11
7 Reprocessing methods according to ISO 17664 ..................................................................................... 12
7.1 Preparations at the site of use ....................................................................................................... 12
7.2 Cleaning ........................................................................................................................................ 12
7.2.1 Manual external cleaning ................................................................................................. 12
7.2.2 Automated external cleaning ............................................................................................ 12
7.2.3 Manual internal cleaning .................................................................................................. 13
7.2.4 Automated internal cleaning ............................................................................................. 13
7.3 Disinfection .................................................................................................................................... 13
7.3.1 Manual external disinfection ............................................................................................. 14
7.3.2 Manual disinfection - internal ............................................................................................ 14
7.3.3 Machine disinfection - external and internal ..................................................................... 14
7.4 Drying ............................................................................................................................................ 15
7.5 Care products and systems - Servicing ......................................................................................... 15
7.5.1 Servicing with KaVo Spray ............................................................................................... 15
7.5.2 Care with KaVo SPRAYrotor ............................................................................................ 16
7.5.3 Servicing with KaVo QUATTROcare PLUS ..................................................................... 16
7.6 Packaging ...................................................................................................................................... 17
7.7 Sterilisation .................................................................................................................................... 17
7.8 Storage .......................................................................................................................................... 18
8 Tools ........................................................................................................................................................ 19
9 Warranty terms and conditions ................................................................................................................ 20
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
Table of contents
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1 User instructions
Dear User
Congratulations on purchasing this KaVo quality product. By following the instruc‐
tions below you will be able to work smoothly, economically and safely.
© Copyright by KaVo Dental GmbH
Symbols
Refer to the chapter on Safety/Warning symbol
Important information for users and service technicians
Can be steam-sterilised at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
Thermodisinfectable
CE mark (European Community). A product bearing this mark meets the
requirements of the applicable EC directive.
Action request
Target group
This document is intended for dentists and their assistants. The section on start‐
ing up is also intended for service technicians.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
1 User instructions
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2 Safety
2.1 Description of safety instructions
Warning symbol
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.
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
moderate 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 Safety instructions
WARNING
Hazards for the care provider and the patient.
In the case of damage, irregular running noise, excessive vibration, un-typical
warming or when the cutter or grinder cannot be held.
▶Do not use further and notify Service.
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2 Safety | 2.1 Description of safety instructions
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WARNING
Hazard from contraindication.
If the soft tissue in the oral cavity is injured, the compressed air may enable sep‐
tic substances to enter the tissue.
▶Treatment must be discontinued with instruments operated by compressed
air when soft tissue is damaged in the oral cavity.
CAUTION
Burning hazard from hot instrument head and instruments cover.
If the instrument overheats, burns may arise in the oral area.
▶Never contact soft tissue with the instrument head.
CAUTION
Hazard from use as a light probe.
Do not use the device as a light probe since the rotating cutters or grinders can
cause injury.
▶Use an appropriate light probe for additional illumination of the oral cavity or
site of preparation.
CAUTION
Risk due to incorrectly stored instrument.
Injury and infection caused by chucked cutters or grinders.
Damage to clamping system from dropping the instrument.
▶After treatment, place the instrument properly in the cradle, without the cutter
or grinder.
CAUTION
Premature wear and malfunctioning from improper storage during long periods
of nonuse.
Reduced product life.
▶The medical device should be cleaned, serviced and stored in a dry location,
according to instructions, before long periods of nonuse.
Note
For safety reasons, we recommend that the tool holder system be checked an‐
nually after the warranty period expires.
To ensure proper function, the medical device must be set up according to the re‐
processing methods described in the KaVo Instructions for Use, and the care
products and care systems described therein must be used. KaVo recommends
specifying a service interval at the dental office for a licensed shop to clean, serv‐
ice and check the functioning of the medical device. This service interval depends
on the frequency of use and should be adjusted accordingly.
Service may only be carried out by KaVo-trained repair shops using original KaVo
replacement parts.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
2 Safety | 2.2 Safety instructions
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3 Product description
SMARTtorque LUX S619 L (Mat. no. 1.008.1641)
SMARTtorque Mini LUX S615 L (Mat. no. 1.008.1643)
SMARTtorque S619 C (Mat. no. 1.008.1642)
3.1 Purpose – Proper use
Purpose:
This medical device is
▪ Only intended for dental treatment. Any other type of use or alteration to the
product is impermissible and can be hazardous. The medical device is inten‐
ded for the following uses: Removal of carious material, cavities and crown
preparations, removal of fillings, processing of tooth, restoration surfaces and
surgical procedure.
▪ A medical device according to relevant national statutory regulations.
Proper use:
According to these regulations, this medical device may only be used for the de‐
scribed application by a knowledgeable user. The following must be observed:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these instructions for use
According to these regulations, it is the responsibility of the user to:
▪ only use equipment that is operating correctly,
▪ use the equipment for the proper purpose,
▪ protect him or herself, the patient and third parties from danger, and
▪ avoid contamination from the product.
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3 Product description | 3.1 Purpose – Proper use
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3.2 Technical Specifications
SURGtorque S459 L
Minimal drive pressure 2.1 bar (30 psi)
Drive pressure 2.1 to 4.2 bar (30 to 61 psi)
Air consumption 40 Nl/min
Idle Speed 350.000 to 450.000 rpm
Power > 15 W
Recommended operating
pressure
2 to 3 N
Note
The air consumption, idle speed, and power values were determined at a drive
pressure of 2.8 bar (40 psi).
Can be attached to all MULTIflex (LUX) / MULTIflex LED couplings.
3.3 Transportation and storage conditions
CAUTION
It is hazardous to start up the medical device after it has been stored strongly
refrigerated.
This can cause the medical device to malfunction.
▶Prior to start-up, very cold products must be heated 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
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3 Product description | 3.2 Technical Specifications
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4 Start up and shut down
WARNING
Hazard from non-sterile products.
Infection hazard for care provider and patient.
▶Before first use and after each use, prepare and sterilise the medical device
and accessories accordingly.
WARNING
Disposal of the product in the appropriate manner.
Prior to disposal, the product and accessories must be appropriately prepared or
sterilised if this is necessary.
CAUTION
Damage from soiled and moist cooling air.
Contaminated and moist cooling air can cause malfunctions and lead to prema‐
ture bearing wear.
▶Make sure that the supply of cooling air is dry, clean and uncontaminated ac‐
cording to ISO 7494-2.
4.1 Mount the MULTIflex (LUX) / MULTIflex LED coupling
▶ Screw the MULTIflex (LUX) / MULTIflex LED coupling onto the turbine hose
and tighten with the wrench.
▶ Rotate the spray ring on the MULTIflex (LUX) / MULTIflex LED coupling in or‐
der to regulate the fraction of water.
4.2 Checking the amount of water
CAUTION
Overheating of the tooth due to insufficient amount of cooling water.
Insufficient water can cause the medical device to overheat and damage the
pulp and tooth.
▶Adjust the water amount for the cooling to a minimum of 50 cm3/min!
▶Check the cooling water channels and clean the water nozzles with nozzle
needle 1.003.8150 according to need.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
4 Start up and shut down | 4.1 Mount the MULTIflex (LUX) / MULTIflex LED coupling
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4.3 Checking the pressures
CAUTION
Compressed air connection on devices.
Dirty and moist compressed air causes premature bearing wear.
▶Ensure that the cooling air is dry, clean and uncontaminated in accordance
with EN ISO 7494-2.
▶ Insert the test gauge (Mat. no. 0.411.8731) between the
MULTIflex (LUX) / MULTIflex LED coupling and the medical device, and check
the following pressures:
- Drive pressure: 2.8 bar (40 psi)
- Return air: < 0.5 bar (7 psi)
- Water: 0.8 to 2.5 bar (12 to 36 psi)
4.4 Checking the 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: 5
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
4 Start up and shut down | 4.3 Checking the pressures
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5 Operation
Note
At the beginning of each workday, the water-conducting systems should be
rinsed for at least 2 min. without the instrument being attached; if there is a risk
of contamination from reflux or back suction, the system must be rinsed for 20-30
seconds.
5.1 Attaching the medical device
CAUTION
Damage from inaccurate coupling.
Inaccurate coupling (especially during the afterglow period) can destroy the high-
pressure lamp or the LED of a MULTIflex (LUX) / MULTIflex LED coupling or re‐
duce its service life.
▶Check the seat of the turbine on the coupling by pulling on it.
WARNING
Release of the medical device during treatment.
A medical device that is not properly locked in place can release from the MUL‐
TIflex (LUX) / MULTIflex LED coupling during treatment.
▶Before each use, check if the medical device is securely locked onto the
MULTIflex (LUX) / MULTIflex LED coupling by pulling on it.
▶ Mount the medical device accurately on the
MULTIflex (LUX) / MULTIflex LED coupling and push it backward until the
coupling audibly locks in the medical device.
▶ Pull on it to make sure that the medical device is securely affixed to the cou‐
pling.
5.2 Removing the medical device
▶ Hold the coupling tight, and pull the medical device off while twisting slightly.
5.3 Insert the milling cutter or diamond grinder
Note
Only use carbide cutters or diamond grinders that correspond to ISO 1797-1 type
3, are made of steel or hard metal and meet the following criteria:
- Shaft diameter: 1.59 to 1.60 mm
- Overall length SURGtorque S459 L: max. 25 mm
- Shaft clamping length SURGtorque S459 L: at least 11 mm
- Blade diameter: max. 2 mm
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5 Operation | 5.1 Attaching the medical device
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WARNING
Use of unauthorised cutters or grinders.
Injury to the patient or damage to the medical device.
▶Observe the instructions for use and use the cutter or grinder properly.
▶Only use cutters or grinders that do not deviate from the specified data.
CAUTION
Injury from using worn drill bits or burs.
Drill bits or burs could fall out during treatment and injure the patient.
▶Never use drill bits or burs with worn shafts.
CAUTION
Danger of injury from cutters or grinders.
Infections or cuts.
▶Wear gloves or fingerstalls.
CAUTION
Hazard from defective chucking system.
The cutter or grinder could fall out and cause injury.
▶Pull on the cutter or grinder to check that the chucking system is okay and
the cutter or grinder is securely held. When checking, inserting and remov‐
ing, use gloves or a fingerstall to prevent an injury or infection.
▶ Forcefully press the push button with your thumb and simultaneously insert
the cutter or grinder all the way.
▶ Check that the cutter or grinder is seated by pulling on it.
5.4 Removing the milling tool or diamond grinder.
WARNING
Hazard from rotating cutter or grinder.
Lacerations and damage to the chucking system.
▶Do not touch rotating cutter or grinder.!
▶Never press the press-button while the cutter or grinder is rotating!
▶Remove the cutter or grinder from the contra-angle handpiece after treat‐
ment to avoid injury or infection while storing it.
▶ After the cutter or grinder has stopped rotating, press the press-button with
your thumb and simultaneously pull out the drill bit or bur.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
5 Operation | 5.4 Removing the milling tool or diamond grinder.
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6 Troubleshooting
6.1 Exchanging the O-rings on the coupling on the supply hose
CAUTION
Hazard from improper care of the O-rings.
Malfunctions or complete failure of the medical device.
▶Do not use Vaseline or other grease or oil.
Note
The O-ring on the coupling may only be lubricated with a cotton ball wet with KA‐
VO spray.
▶ Press the O-ring between your fingers to form a loop.
▶ Shove the O-ring to the front, and remove it.
▶ Insert new O-rings into the grooves.
6.2 Cleaning the spray nozzle
CAUTION
Hazard from insufficient cooling water.
Overheating of the medical device and damage to the tooth.
▶Check the water channels and clean the water nozzles with nozzle needle
Mat. no. 1.003.8150 according to need.
▶ Clean the water passage in the water nozzle by using the nozzle needle
Mat. no. 1.003.8150.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
6 Troubleshooting | 6.1 Exchanging the O-rings on the coupling on the supply hose
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7 Reprocessing methods according to ISO 17664
7.1 Preparations at the site of use
WARNING
Hazard from nonsterile products.
There is a risk of infection from contaminated medical devices.
▶Take suitable personal protective measures.
▶ Remove all residual cement, composite or blood without delay.
▶ Recondition the medical device as soon as possible after treatment.
▶ Remove the cutter or grinder from the medical device.
▶ The medical device must be dry when transported for reconditioning.
▶ Do not place it in a solution or similar.
7.2 Cleaning
CAUTION
Malfunctions from cleaning in the ultrasonic unit.
Defects in the product.
▶Only clean manually or in a thermodisinfector.
7.2.1 Manual external cleaning
Accessories required:
▪ Tap water 30 °C ± 5 °C (86 °F ± 10 °F)
▪ Brush, e.g. medium-hard toothbrush
▶ Brush off under flowing tap water.
7.2.2 Automated external cleaning
KaVo recommends thermodisinfectors in accordance with EN ISO 15883-1, which
are operated with alkaline cleaning agents with a pH value of max. 10 (e.g. Miele
G 7781 / G 7881 – Validation was carried out with Programme "VARIO-TD",
cleaning agent "neodisher® mediclean", neutralisation agent "neodisher® Z" and
rinsing agent "neodisher® mielclear" and only applies to the material compatibility
with KaVo products).
▶ For program settings as well as cleansers and disinfectants to be used, please
refer to the Instructions for Use of the thermodisinfector (complying with max.
pH value of 10).
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
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7 Reprocessing methods according to ISO 17664 | 7.1 Preparations at the site of use
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▶ In order to prevent negative effects on the medical device, make sure that the
interior and the exterior of the medical device are dry after completion of the
cycle, and then grease it immediately with servicing agents from the KaVo
care system.
7.2.3 Manual internal cleaning
Can only be done with KaVo CLEANspray or KaVo DRYspray.
▶ Cover the medical device with the KaVo CLEANpac bag, and place it on the
corresponding care adapter. Press the spray button three times for 2 seconds
each time. Remove the medical device from the spray attachment and let the
cleaner work for one minute.
▶ Afterwards, rinse for 3-5 seconds with KaVo DRYspray.
See also: KaVo CLEANspray / KaVo DRYspray Instructions for Use
Note
KaVo CLEANspray and KaVo DRYspray for manual interior cleaning are only
available 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 thermodisinfec‐
tors in accordance with EN ISO 15883-1.
7.2.4 Automated internal cleaning
KaVo recommends thermodisinfectors in accordance with EN ISO 15883-1, which
are operated with alkaline cleaning agents with a pH value of max. 10 (e.g. Miele
G 7781 / G 7881 – Validation was carried out with Programme "VARIO-TD",
cleaning agent "neodisher® mediclean", neutralisation agent "neodisher® Z" and
rinsing agent "neodisher® mielclear" and only applies to the material compatibility
with KaVo products).
▶ For program settings as well as cleansers and disinfectants to be used, please
refer to the Instructions for Use of the thermodisinfector (complying with max.
pH value of 10).
▶ In order to prevent negative effects on the medical device, make sure that the
interior and the exterior of the medical device are dry after completion of the
cycle, and then grease it immediately with servicing agents from the KaVo
care system.
7.3 Disinfection
CAUTION
Malfunctioning from using a disinfectant bath or disinfectant containing chlorine.
Defects in the product.
▶Only disinfect in a thermodisinfector or manually.
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7 Reprocessing methods according to ISO 17664 | 7.3 Disinfection
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7.3.1 Manual external disinfection
KaVo recommends the following products based on material compatibility.
▪ Mikrozid AF made by Schülke & Mayr (liquid or cloths)
▪ FD 322 made by Dürr
▪ CaviCide made by Metrex
Consumables required:
▪ Cloths for wiping off the medical device.
▶ Spray the disinfectant on a cloth, then thoroughly wipe down the medical de‐
vice and leave the disinfectant to soak in according to the instructions from the
disinfectant manufacturer.
▶ Follow the instructions for use of the disinfectant.
7.3.2 Manual disinfection - internal
The efficacy of manual internal disinfection must be demonstrated by the manu‐
facturer of the disinfection agent. With KaVo products, use only disinfection
agents that have been released by KaVo with respect to the compatibility of mate‐
rials (e.g. WL-cid / made by ALPRO).
▶ Immediately after internal disinfection, lubricate the KaVo medical device im‐
mediately with care agents from the KaVo care system.
▶ Follow the instructions for use of the disinfectant.
7.3.3 Machine disinfection - external and internal
KaVo recommends thermodisinfectors in accordance with EN ISO 15883-1, which
are operated with alkaline cleaning agents with a pH value of max. 10 (e.g. Miele
G 7781 / G 7881 – Validation was carried out with Programme "VARIO-TD",
cleaning agent "neodisher® mediclean", neutralisation agent "neodisher® Z" and
rinsing agent "neodisher® mielclear" and only applies to the material compatibility
with KaVo products).
▶ For program settings as well as cleansers and disinfectants to be used, please
refer to the Instructions for Use of the thermodisinfector (complying with max.
pH value of 10).
▶ In order to prevent negative effects on the medical device, make sure that the
interior and the exterior of the medical device are dry after completion of the
cycle, and then grease it immediately with servicing agents from the KaVo
care system.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
7 Reprocessing methods according to ISO 17664 | 7.3 Disinfection
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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 cutters or grinders in the medical device.
Risk of injury from sharp or pointed cutters or grinders.
▶Remove cutter or grinder.
CAUTION
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶Perform regular proper care and maintenance!
Note
KaVo only guarantees that its products will function properly when the care prod‐
ucts used are those listed as accessories, as they were tested for proper use on
our products.
7.5.1 Servicing with KaVo Spray
▶ Remove the cutter or grinder.
▶ Cover the product with the Cleanpac bag.
▶ Plug the product onto the cannula, and press the spray button for one second.
Chuck care
KaVo recommends cleaning and servicing the chuck system once a week.
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7 Reprocessing methods according to ISO 17664 | 7.4 Drying
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▶ Remove the cutter or grinder, place the INTRA spray nipple tip in the opening
and spray.
▶ Subsequently treat with the specified care agents and systems.
7.5.2 Care with KaVo SPRAYrotor
KaVo recommends servicing the product after each time it is used, i.e. after each
automatic cleaning and before each sterilisation.
▶ Place the product on the appropriate coupling of the KaVo SPRAYrotor and
cover it with a CLEANpac bag.
▶ Service the product.
See also: Instructions for use KaVo SPRAYrotor
7.5.3 Servicing with KaVo QUATTROcare PLUS
KaVo recommends servicing the product after each time it is used, i.e. after each
automatic cleaning and before each sterilisation.
▶ Remove the cutter or grinder.
▶ Servicing the product in QUATTROcare PLUS.
See also: Instructions for Use KaVo QUATTROcare PLUS 2124 A
Servicing of the clamping chuck
KaVo recommends cleaning and servicing the chuck system once a week.
See also: Instructions for Use KaVo QUATTROcare PLUS 2124 A
Note
Handpieces must be taken off the service couplings before the chuck service can
be started and performed.
▶ Remove the service coupling chuck from the side hatch of the QUATTROcare
PLUS and attach it to coupling service point four, on the far right. A MULTIflex
adapter 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 chuck.
▶ Press the button showing the chuck service symbol.
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7 Reprocessing methods according to ISO 17664 | 7.5 Care products and systems - Servicing
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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: Care 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 stand‐
ards and be suitable for the sterilisation procedure!
▶ Weld each medical device individually in a sterilised item package!
7.7 Sterilisation
Sterilisation in a steam steriliser (autoclave) in accordance with EN
13060 / ISO 17665-1
CAUTION
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶Before each sterilisation cycle, service the medical device with KaVo care
products.
CAUTION
Contact corrosion due to moisture.
Damage to product.
▶Immediately remove the product from the steam steriliser after the sterilisa‐
tion 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 fol‐
lowing 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)
▪ Autoclave using the gravity method:
– at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
7 Reprocessing methods according to ISO 17664 | 7.6 Packaging
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▶ Use according to the manufacturer's Instructions for Use.
7.8 Storage
▶ Reprocessed products should be stored protected from dust with minimum ex‐
posure to germs in a dry, dark and cool space.
▶ Comply with the expiry date of the sterilised items.
Instructions for use SMARTtorque LUX S619 L - 1.008.1641 SMARTtorque Mini LUX S615 L - 1.008.1643
SMARTtorque S619 C - 1.008.1642
7 Reprocessing methods according to ISO 17664 | 7.8 Storage
18/21