KaVo SMARTmatic S20 User manual

Instructions for use
SMARTmatic S20 - 1.011.6750
SMARTmatic S20 K - 1.011.6751
SMARTmatic S20 S - 1.011.6752

Distributed by:
KaVo Dental Corporation
11729 Fruehauf Drive
Charlotte, NC 28273 USA
Phone: [phone]
Fax: [phone]
Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
D-88400 Biberach
www.kavo.com

Table of contents
1 User instructions............................................................................................................................................. 5
2 Safety ............................................................................................................................................................. 7
2.1 Infection hazard ..................................................................................................................................... 7
2.2 Technical condition ................................................................................................................................ 7
2.3 Accessories and combination with other equipment.............................................................................. 8
2.4 Qualification of personnel ...................................................................................................................... 8
2.5 Service and repair ................................................................................................................................. 8
3 Description of the product............................................................................................................................... 9
3.1 Purpose - Intended use ......................................................................................................................... 10
3.2 Technical Specifications ........................................................................................................................ 10
3.3 Transportation and storage conditions .................................................................................................. 12
4 Startup and shut down ................................................................................................................................... 13
4.1 Checking the amount of water for the S20 S ......................................................................................... 13
5 Operation........................................................................................................................................................ 14
5.1 Attaching the medical device ................................................................................................................ 14
5.2 Removing the medical device................................................................................................................ 14
5.3 Inserting the burs ................................................................................................................................... 14
5.4 Removing the bur ................................................................................................................................. 15
6 Checking for malfunctions and troubleshooting.............................................................................................. 16
6.1 Check for malfunctions .......................................................................................................................... 16
6.2 Troubleshooting ..................................................................................................................................... 16
6.2.1 Replacing O-rings on the motor coupling.................................................................................. 16
6.2.2 Cleaning the spray tube ............................................................................................................ 16
7 Processing steps in accordance with ISO 17664 ........................................................................................... 17
7.1 Preparations at the site of use ............................................................................................................... 17
7.2 Non-fixing preliminary cleaning of the spray tube.................................................................................. 17
7.3 Cleaning................................................................................................................................................. 18
7.3.1 Manual external cleaning ......................................................................................................... 18
7.3.2 Automated external cleaning ................................................................................................... 18
7.3.3 Manual internal cleaning ........................................................................................................... 18
7.3.4 Automated internal cleaning ..................................................................................................... 18
7.4 Disinfection ............................................................................................................................................ 19
7.4.1 Manual external disinfection .................................................................................................... 19
7.4.2 Manual internal disinfection ...................................................................................................... 19
7.4.3 Automated external and internal disinfection ............................................................................ 19
7.5 Drying .................................................................................................................................................... 20
7.6 Care products and systems - Servicing ................................................................................................. 20
7.6.1 Servicing with KaVo Spray ....................................................................................................... 20
7.6.2 Servicing with KaVo QUATTROcare ....................................................................................... 21
7.6.3 Servicing with KaVo QUATTROcare PLUS ............................................................................. 21
7.7 Packaging .............................................................................................................................................. 22
7.8 Sterilization ............................................................................................................................................ 23
7.9 Storage .................................................................................................................................................. 23
Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
Table of contents
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8 Tools and consumables.................................................................................................................................. 24
9 Terms and conditions of warranty .................................................................................................................. 25
Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
Table of contents
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
1 User instructions
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
KaVo Dental Corporation
11727 Fruehauf Drive
Charlotte, NC 28273 USA
Toll-free Direct Customer Service: 1-888-ASK-KAVO (888-275-5286)
Email: [email protected]
www.kavousa.com
Please direct all questions regarding the product, service and maintenance to the
KaVo Technical Service:
Toll-free: 1-888-ASK-KAVO (888-275-5286)
Email: [email protected]
Please refer to the serial number of the product in all inquiries!
General marks and symbols
Refer to the chapter on Safety/Warning symbol
Important information for users and service technicians
Action request
Sterilization parameters
1. Sterilizer with pre-vacuum:
at least 3 minutes at
135 °C (275 °F)
Drying time: 16 min.
2. Sterilizer using the gravity method:
at least 10 minutes at
135 °C (275 °F)
Drying time: 30 min.
Suitable for disinfection in a washer disinfector
Information on the package labeling
Catalogue number
Serial number
Legal Manufacturer
5 / 28

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
1 User instructions
6 / 28
CE mark according to Medical Devices Directive EC 93/42
Consult instructions for use
Caution: Consult instructions for use
EAC conformity mark (Eurasian Conformity)
GOST R certification
Transportation and storage conditions
(Temperature limits)
Transportation and storage conditions
(Air pressure)
Transportation and storage conditions
(Humidity limitations)
Protect from moisture (Keep dry)
Fragile, handle with care
HIBC Code
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 – can lead to death or severe injury.
CAUTION
In cases which – if not prevented – can lead to moderate or mild injury.
NOTICE
In cases which – if not prevented – can lead to property damage.

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
2 Safety | 2.1 Infection hazard
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 intended use, any other type of
use is not permitted.
2.1 Infection hazard
Patients, users or third parties can be infected by contaminated medical devices.
▶ Take suitable personal protective measures.
▶ Follow the instructions for use of the components.
▶ Before initial startup and after each use, process and sterilize the medical device
and accessories appropriately.
▶ Carry out the cleaning and sterilization as described in the instructions for use.
The procedure has been validated by the manufacturer.
▶ If you deviate from this procedure, it is essential to ensure the effectiveness of the
cleaning and sterilization.
▶ Prior to disposal, the product and accessories must be appropriately processed or
sterilized.
▶ In the case of injury to soft tissue, do not continue treatment in the oral cavity with
instruments driven by compressed air.
▶ To test, use and remove the tool, use a glove or finger guard.
2.2 Technical condition
A damaged device or components can injure patients, users and third parties.
▶ Use the device and components only if there is no damage 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
To ensure optimum function and to prevent property damage, you have to comply with
the following instructions:
▶ 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 is not to be used for an extended period of time.
High torque of micromotors can lead to severe burn injuries.
▶ Service micromotors regularly.
▶ Do no use any damaged motors.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
2 Safety | 2.3 Accessories and combination with other equipment
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▶ Do not use motors for unauthorized purposes.
2.3 Accessories and combination with other equipment
Use of un-authorized accessories on the device or un-authorized modifications to the
device can 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 standardized 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 center released by
KaVo.
▶ Comply with the Instructions for Use of the treatment center.
2.4 Qualification of personnel
Application of the product by users lacking appropriate medical training can injure the
patient, the user or third parties.
▶ Make sure that the user has read and comprehends the instructions for use.
▶ Only employ the device if the user has the appropriate medical training.
▶ Comply with national and regional regulations.
Improper use of the device can lead to burns or injuries.
▶ Never touch the handpiece head or handpiece lid to soft tissue!
▶ 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 authorized to do this:
▪ Service technicians of KaVo branches after the appropriate product training
▪ Service technicians of KaVo authorized dealers after the appropriate product train-
ing
Comply with the following items during all servicing work:
▶ Have the service and testing tasks carried out in accordance with the Medical
Product Operator Ordinance.
▶ Following expiration of the warranty, have the tool holding system checked once a
year.
▶ Have the medical device evaluated by a professional shop with regard to its clean-
ing, servicing and functional needs according to an in-house service interval. De-
fine the service interval depending on the frequency of use.

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
3 Description of the product | 2.5 Service and repair
3 Description of the product
SMARTmatic S20 (Mat. No. 1.011.6750)
SMARTmatic S20 K (Mat. No. 1.011.6751)
SMARTmatic S20 S (Mat. No. 1.011.6752)
The SMARTmatic electrical-driven handpieces are dental handpieces according to 21
CFR § 872.4200 (dental handpieces and accessories) for the use by a trained profes-
sional in the field of general dentistry.
The devices are electrical-powered handpieces that are reusable and ergonomically
shaped. The devices can be sterilized by the steam autoclave method. Through the
tube and the electrical motor connected to a dental unit, the SMARTmatic handpieces
equipped with a handpiece connection according to ISO 3964 receive the energy for
the gear, the cooling water and air for cutting treatment. Dental burs and other attach-
ments according to ISO 1797-1 will be used with the SMARTmatic handpieces. Based
on the INTRAmatic connection that meets the ISO 3964 the SMARTmatic handpieces
fit with any electrical dental motor which is produced in accordance to this standard.
The electrical motors carry the energy for the gear, the cooling water and air for cut-
ting treatment from the dental treatment unit to the SMARTmatic handpieces.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
3 Description of the product | 3.1 Purpose - Intended use
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3.1 Purpose - Intended use
Indications for Use
The SMARTmatic handpieces are intended for the removal of carious material, reduc-
ing of hard tooth structure, cavity and crown preparations, root canal preparations, re-
moval of fillings, processing and finishing tooth preparations, restorations, and for pol-
ishing teeth. They are designed for use by a trained professional in the field of general
dentistry.
CAUTION
US Federal law restricts this device to sale by or on the order of a healthcare profes-
sional / dentist.
For dental use only.
Proper Use:
In accordance with these regulations, this medical device may only be used by a prop-
erly trained user and for the application described herein. You need to comply with the
following:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these Instructions for use
In accordance with these regulations, the user is required to:
▪ only use equipment that is operating properly
▪ adhere to the specified intended use
▪ protect himself or herself, the patient and third parties from danger, and
▪ avoid 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
Contra-angle handpieces S20 and S20 S can be attached to all INTRAmatic (LUX)
motors and motors with a connector in accordance with ISO 3964.
The contra-angle handpiece S20 K can be mounted on INTRA Motor 181K.
With press-button chuck.
Usable with contra-angle cutters or grinders.
Applies to S20 S only (using the spray clip and the hose):
Spray water pressure 0.8 to 2.0 bar (12 to 29 psi)
Spray air pressure 1.0 to 2.0 bar (15 to 29 psi)
Amount of air spray min. 1.5 Nl/min (at 2 bar)

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
3 Description of the product | 3.2 Technical Specifications
To use the spray:
▶ Attach the spray clip to the dental instrument as shown.
If you use the spray clip, attach the hose to the spray clip and the taper sleeve on the
dental instrument and/or the motor with external spray outlet.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
3 Description of the product | 3.3 Transportation and storage conditions
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3.3 Transportation and storage conditions
▶ Do not store in a refrigerated environment.
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 (Keep dry)

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
4 Startup and shut down | 4.1 Checking the amount of water for the S20 S
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, process the product and accessories.
WARNING
Dispose of the product in the appropriate manner.
Infection hazard.
▶ Process the product and accessories before disposal.
NOTICE
Damage from contaminated and moist cooling air.
Contaminated and moist cooling air can cause malfunctions.
▶ Make sure that the supplied cooling air is dry, clean and free of contamination in
accordance with ISO 7494-2.
4.1 Checking the amount of water for the S20 S
CAUTION
Overheating of the tooth due to insufficient amount of cooling water.
Thermal damage to the dental pulp.
▶ Adjust the water amount for the spray cooling to a minimum of 50 ml/min!
CAUTION
Hazard from insufficient amount of spray water.
Insufficient spray water can cause the medical device to overheat and damage the
tooth.
▶ Check the spray water channels and clean the spray tube with the nozzle needle
(Mat. no. 0.410.0931) according to need.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
5 Operation | 5.1 Attaching the medical device
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5 Operation
5.1 Attaching the medical device
CAUTION
Detachment of the medical device during treatment.
Injury or property damage
A medical device that is not properly locked in place can become disconnected from
the motor coupling and fall off.
▶ Carefully pull on the medical device before each treatment to make sure that it is
securely locked onto 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.
▶ Attach the medical device to 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 burs
Note
Only use carbide burs or diamond burs that conform to ISO 1797-1 type 1, are
made of steel or hard metal, and meet the following criteria:
- Shaft diameter: Ø 2.334 to Ø 2.350 mm
- Overall length: max. 22mm
WARNING
Use of unauthorized burs.
Risk of injury.
▶ Comply with the instructions for use and the intended use of the bur.
▶ Only use burs that do not deviate from the specified data.

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
5 Operation | 5.4 Removing the bur
WARNING
Hazard from rotating bur.
Lacerations.
▶ Do not touch the bur while it is rotating!
▶ Remove the bur from the medical device after treatment to avoid injury and infec-
tion when putting it away.
CAUTION
Use of burs with worn or damaged shafts.
Risk of injury, tool may fall out during treatment.
▶ Never use burs with damaged or worn shafts.
CAUTION
Hazard from defective chucking 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 finger guard when you check, insert
or remove 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.
Property 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 burs with worn or damaged shafts.
Property damage to the chuck system, tool is difficult or impossible to remove from
the chuck system.
▶ Do not use burs with damaged or worn shafts.
▶ Insert the bur into the segment of the head drive by twisting the tool slightly, and
push it to the bur stop.
▶ Check that the bur is securely attached by pulling on it.
5.4 Removing the bur
WARNING
Hazard from rotating bur.
Lacerations and damage to the chuck system.
▶ Do not touch the bur while it is rotating!
▶ Never press the push-button while the bur is rotating!
▶ Remove the bur from the contra-angle handpiece after treatment to avoid injury
and infection when putting it away.
▶ After the bur has stopped rotating, firmly press the push-button with your thumb
and simultaneously pull out the bur.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
6 Checking for malfunctions and troubleshooting | 6.1 Check for malfunctions
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6 Checking for malfunctions and troubleshooting
6.1 Check for malfunctions
CAUTION
Product heats up.
Burn injury or product damage due to over-heating.
▶ Do not continue working if the product heats up irregularly.
NOTICE
Missing or damaged O-rings.
Malfunctions and premature failure.
▶ Make sure that all O-rings are present on the coupling and are undamaged.
▶ The medical device overheats while idling:
Check the amount of cooling air.
▶ The medical device overheats while working:
Service the medical device.
▶ When the speed drops or is uneven:
Service the medical device.
▶ Missing O-ring on the motor coupling:
Replace O-ring.
6.2 Troubleshooting
6.2.1 Replacing O-rings on the motor coupling
NOTICE
Improper care of the O-rings.
Malfunction or complete failure.
▶ Do not use Vaseline or other grease or oil.
Note
The O-rings on the motor 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.
6.2.2 Cleaning the spray tube
CAUTION
Hazard from insufficient amount of spray water.
Insufficient spray water can cause the medical device to overheat and damage the
tooth.
▶ Check spray water channels and if necessary clean spray tubes with the nozzle
needle (Mat. no. 0.410.0931).

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
7 Processing steps in accordance with ISO 17664 | 7.1 Preparations at the site of use
7 Processing steps in accordance with ISO 17664
7.1 Preparations at the site of use
WARNING
Hazard from incorrectly processed products.
Contaminated products are associated with an infection risk.
▶ Take suitable personal protective measures.
▶ Remove the tool from the medical device.
▶ Remove all residual cement, composite or blood immediately.
▶ Process the medical device as soon as possible after treatment.
▶ The medical device must be dry when transported to processing.
▶ Do not immerse in solutions or the like.
7.2 Non-fixing preliminary cleaning of the spray tube
Accessories required:
▪ Demineralized water 30 °C ± 2 °C (86 °F ± 3.6 °F)
▪ Nozzle needle
▪ Brush, e.g. medium-hard toothbrush
▪ Disposable syringe
Note
Before cleaning, take the hose off the spray clip and the contra-angle handpiece.
▶ Take the spray clip with spray tube off the dental instrument to improve the clean-
ing.
▶ Check the patency of the spray tube and clean it using the nozzle needle (Mat. no.
0.410.0931).
▶ Rinse the spray tube with at least 20 ml demineralized water using a disposable
syringe.
▶ If the spray tube is not patent after the manual rinsing procedure, the medical de-
vice must be replaced.
Brush the spray tube and hose under running tap water for at least 20 seconds using
a medium-hard toothbrush.
The non-fixing preliminary cleaning is a central constituent and must be carried out
prior to the automated processing.
In the cleaning and disinfecting device, validated internal cleaning of the spray tube
necessitates preliminary non-fixing cleaning.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
7 Processing steps in accordance with ISO 17664 | 7.3 Cleaning
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7.3 Cleaning
Note
Applicable only to the S20 S (using spray clips and hose) during automated external
and internal cleaning and disinfection:
Prior to automated processing, the spray clip must be connected to the dental in-
strument using the hose.
▶ Do not plug the spray clip onto the dental instrument.
NOTICE
Never process this medical device in an ultrasonic device.
Functional damage and property damage.
▶ Clean manually or in a washer disinfector only.
7.3.1 Manual external cleaning
Accessories required:
▪ Tap water 30 oC ± 5 oC (86 oF ± 10 oF)
▪ Brush, e.g. medium-hard toothbrush
▶ Brush under flowing tap water.
7.3.2 Automated external cleaning
KaVo recommends washer disinfectors in compliance with ISO 15883-1, which are
operated using alkaline cleaning agents.
▶ 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
care products and systems supplied by KaVo.
7.3.3 Manual internal cleaning
The interior of this product is not to be cleaned manually.
7.3.4 Automated internal cleaning
KaVo recommends washer disinfectors in compliance with ISO 15883-1, which are
operated using alkaline cleaning agents.

Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
7 Processing steps in accordance with ISO 17664 | 7.4 Disinfection
▶ For program settings as well as cleansers and disinfectants to be used, please re-
fer to the Instructions for Use of the washer disinfector.
▶ 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 usually part of the cleaning program of the washer disinfector.
Note
Please comply with the instructions for use of the washer disinfector.
7.4 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.
Functional damage and property damage.
▶ Do not disinfect the device in the disinfection bath or with chlorine-containing dis-
infectants.
7.4.1 Manual external disinfection
KaVo recommends the following products based on material compatibility. The micro-
biological efficacy must be ensured by the disinfectant manufacturer and proven by
an expert opinion.
▪ 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 in accordance with the instructions of the
disinfectant manufacturer.
▶ Comply with the instructions for use of the disinfectant.
7.4.2 Manual internal disinfection
Not applicable.
This product is suitable for automated disinfection only.
7.4.3 Automated external and internal disinfection
KaVo recommends washer disinfectors in compliance with ISO 15883-1, which are
operated using alkaline cleaning agents.
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Instructions for use SMARTmatic S20 - 1.011.6750 SMARTmatic S20 K - 1.011.6751 SMARTmatic S20 S - 1.011.6752
7 Processing steps in accordance with ISO 17664 | 7.5 Drying
20 / 28
▶ For program settings as well as cleansers and disinfectants to be used, please re-
fer to the Instructions for Use of the washer disinfector.
▶ 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 usually part of the cleaning program of the washer disinfector.
Note
Please comply with the instructions for use of the washer disinfector.
7.5 Drying
Manual drying
▶ Clean the outside and inside with compressed air until no drops of water are visi-
ble.
Automated drying
The drying procedure is usually part of the cleaning program of the washer disinfector.
▶ Please comply with the instructions for use of the washer disinfector.
7.6 Care products and systems - Servicing
WARNING
Sharp bur in the medical device.
Risk of injury from sharp and/or pointed bur.
▶ Remove bur.
NOTICE
Improper service and care.
Premature wear and reduced product service life.
▶ Perform proper service regularly.
Note
KaVo only guarantees that its products will function properly when the care prod-
ucts listed as accessories are used, since these products have been tested for
proper use on our products.
7.6.1 Servicing with KaVo Spray
KaVo recommends servicing the product as part of the processing after each use, i.e.
after each cleaning, disinfection, and before each sterilization.
▶ Remove the insert.
▶ Cover the product with the Cleanpac bag.
▶ Plug the product onto the cannula, and press the spray button for one second.