KaVo SMARTmatic PROPHY S31 User manual

Instructions for use
SMARTmatic PROPHY S31 - 1.011.6760
SMARTmatic PROPHY S31 K - 1.011.6761
SMARTmatic PROPHY S33 - 1.011.6800

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.................................................................................................. 9
3.1 Intended use................................................................................................................. 10
3.2 Technical specifications for S31 and S31 K ....................................................................... 10
3.3 Technical specifications for the S 33................................................................................. 11
3.4 Transportation and storage conditions.............................................................................. 11
4 Startup and shut down.......................................................................................................12
5 Operation............................................................................................................................ 13
5.1 Attaching the medical device........................................................................................... 13
5.2 Removing the medical device.......................................................................................... 13
5.3 Inserting the prophy cups or polishing brushes ................................................................. 13
5.4 Removing prophy cups or polishing brushes ..................................................................... 14
6 Troubleshooting ................................................................................................................. 15
6.1 Troubleshooting............................................................................................................. 15
6.1.1 Replacing the O-rings.......................................................................................... 15
7 Reprocessing steps in accordance with ISO 17664 ...........................................................16
7.1 Preparations at the site of use......................................................................................... 16
7.2 Cleaning ....................................................................................................................... 16
7.2.1 Manual external cleaning ..................................................................................... 16
7.2.2 Automated external cleaning................................................................................ 16
7.2.3 Manual internal cleaning...................................................................................... 16
7.2.4 Automated internal cleaning ................................................................................ 17
7.3 Disinfection ................................................................................................................... 17
7.3.1 Manual external disinfection................................................................................. 18
7.3.2 Manual internal disinfection.................................................................................. 18
7.3.3 Automated external and internal disinfection ......................................................... 18
7.4 Drying .......................................................................................................................... 19
7.5 Care products and systems - Servicing............................................................................. 19
7.5.1 Servicing with KaVo Spray................................................................................... 19
7.5.2 Servicing with KaVo SPRAYrotor........................................................................... 19
7.5.3 Servicing with KaVo QUATTROcare ...................................................................... 20
7.5.4 Servicing with KaVo QUATTROcare PLUS .............................................................. 20
7.6 Packaging ..................................................................................................................... 20
7.7 Sterilisation................................................................................................................... 21
7.8 Storage ........................................................................................................................ 21
8 Tools and consumables ......................................................................................................22
9 Terms and conditions of warranty .....................................................................................23
Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
Table of contents
3 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
1 User instructions
4 / 26
1 User instructions
Dear User
Congratulations on purchasing this KaVo quality product. By following the in-
structions 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 dir-
ectly:
[phone]
[e-mail]
KaVo Technical Service
If you have any questions or complaints, please contact the KaVo Technical ser-
vice:
[phone]
[e-mail]
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 requirements 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
Information on the packaging
Material number
Serial number
Legal Manufacturer
CE mark according to Medical Devices Directive EC 93/42

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
1 User instructions
Please note the electronic instructions for use
Note: observe accompanying documents
EAC conformity mark (Eurasian Conformity)
GOST R certification
Transportation and storage conditions
(Temperature range)
Transportation and storage conditions
(Air pressure)
Transportation and storage conditions
(Humidity)
Protect from moisture
Protect from impact
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 in-
jury.
WARNING
In cases which – if not prevented – could lead to death or severe in-
jury.
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 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
2 Safety | 2.1 Infection hazard
6 / 26
2 Safety
The instructions for use are a component of the product and must be read care-
fully 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 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, reprocess 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 repro-
cessed 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 Ser-
vice.
▶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 prevent material damage:
▶Service the medical device with care products and systems regularly as de-
scribed in the instructions for use.
▶The device should be cleaned, serviced and stored in a dry location, accord-
ing 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.

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
2 Safety | 2.3 Accessories and combination with other equipment
▶Do no use any damaged motors.
▶Do not use motors for unauthorised purposes.
Note
The head housing is protected against the ingress of polishing paste by spe-
cial seals.
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 ap-
proved by the manufacturer of the product.
The lack of control equipment for changing the speed range and the direction of
rotation 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 injure 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
personnel. The following persons are authorised to do this:
▪ Service technicians of KaVo branches after the appropriate product training
▪ Service technicians of KaVo authorised dealers after the appropriate product
training
Observe all the following items during servicing work:
▶Have the service and testing tasks carried out according to the Medical
Product Operator Ordinance.
▶Following expiry of the warranty, have the tool holding system checked
once a year.
7 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
2 Safety | 2.5 Service and repair
8 / 26
▶KaVo recommends specifying in-house service intervals where the medical
device is brought to a professional shop for cleaning, servicing and a func-
tion check. Defined the service interval depending on the frequency of use.

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
3 Description of the product | 2.5 Service and repair
3 Description of the product
SMARTmatic PROPHY S31 (Mat. No. 1.011.6760)
SMARTmatic PROPHY S31 K (Mat. No. 1.011.6761)
SMARTmatic PROPHY S33 (Mat. No. 1.011.6800)
9 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
3 Description of the product | 3.1 Intended use
10 / 26
3.1 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
can be used in combination with a polishing tool to support the periodontal
treatment by polishing with a rotating tool.
▪ A medical device according to relevant national statutory regulations.
Proper use:
According to these provisions, this medical device may only be used for the de-
scribed application by a properly trained user. You need to comply with the fol-
lowing:
▪ 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 for S31 and S31 K
Drive speed max. 20,000 rpm
Speed transmission 8:1
Recommended drive speed max. 500 to 2,500 rpm
Cooling air flow 5.5 to 9.5 Nl/min
Note
Operate the product with clockwise rotation.
The support (spindle) for the snap-on polishing attachments can be un-
screwed.
The polishing attachments with screw-in for thread types N1-72 UNF and N1-64
UNC or supports with snap-on function in accordance with DIN EN ISO 13295,
type 5 support available in dentistry can be used.
The contra-angle handpiece S31 can be mounted on all INTRAmatic motors and
motors fitted with a connector in accordance with ISO 3964 / DIN 13940.
The contra-angle handpiece S31 K can be mounted on INTRA Motor 181K.

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
3 Description of the product | 3.3 Technical specifications for the S 33
3.3 Technical specifications for the S 33
Drive speed max. 20,000 rpm
Speed transmission 8:1
Recommended drive speed max. 500 to 2,500 rpm
The drive speed is converted into an oscillating motion of approx. 70°.
The snap-on polishing attachments available in dentistry can be attached.
The contra-angle handpiece S33 can be mounted on all INTRAmatic (LUX) mo-
tors and motors fitted with a connector in accordance with ISO 3964 / DIN
13940.
Note
The support (spindle) for the snap-on polishing attachments cannot be un-
screwed.
3.4 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
11 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
4 Startup and shut down
12 / 26
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
according 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 spray water on the supply unit before startup!

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
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 mo-
tor coupling and fall off.
▶Carefully pull on it before each treatment to ensure that the medical device
is securely 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 rotating.
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 prophy cups or polishing brushes
Note
Only use prophy cups or polishing brushes in accordance with DIN EN ISO
13295 for support (spindle) type 5.
WARNING
Use of impermissible inserts.
Injury to the patient or damage to the medical device.
▶Observe the instructions for use, and use the insert properly.
13 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
5 Operation | 5.4 Removing prophy cups or polishing brushes
14 / 26
CAUTION
Injury from using worn inserts.
The inserts can fall out during treatment and harm the patient.
▶Never use insert with worn thread.
CAUTION
Danger of injury from insert.
Infections or cuts.
▶Wear gloves or fingerstalls.
CAUTION
Risk of burn injury from hot handpiece head.
If prophylaxis cups touch the handpiece head, the head may heat up due to
friction. Burn injuries in the mouth may be caused if the handpiece overheats.
▶Do not use prophylaxis cups that touch against the handpiece head.
▶Block the catch pin of the contra-angle handpiece with the enclosed holder.
▶Screw or push the insert into/onto the head.
▶Remove the holder.
▶Check that the insert is firmly seated.
5.4 Removing prophy cups or polishing brushes
WARNING
Hazard from rotating insert.
Lacerations.
▶Do not touch rotating insert!
▶Remove the insert from the contra-angle handpiece after treatment to
avoid injury and infection during storage.
▶Block the catch pin of the contra-angle handpiece with the enclosed holder.
▶Unscrew and/or take off the insert from the head.

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
6 Troubleshooting | 6.1 Troubleshooting
6 Troubleshooting
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
6.1 Troubleshooting
6.1.1 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.
15 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
7 Reprocessing steps in accordance with ISO 17664 | 7.1 Preparations at the site of use
16 / 26
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.
▶Take screw-in and/or snap-on polishing attachments off the contra-angle
handpiece.
▶Remove all residual cement, composite or blood immediately.
▶Reprocess the medical device as soon as possible after treatment.
▶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 from Miele in accordance with EN ISO
15883-1 that are operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD programme, the cleaning
agent neodisher® MediClean and the neutralisation agent neodisher® Z.
▶The programme settings and cleansers and disinfectants that must be used
are listed in the instructions for use of the washer disinfector.
▶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 PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
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
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 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
available in the following countries:
Germany, Austria, Switzerland, Italy, Spain, Portugal, France, Luxembourg,
Belgium, Netherlands, United Kingdom, Denmark, Sweden, Finland and Nor-
way.
In other countries interior cleaning can only be carried out with washer disin-
fectors in accordance with EN ISO 15883-1.
7.2.4 Automated internal cleaning
KaVo recommends washer disinfectors from Miele in accordance with EN ISO
15883-1 that are operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD programme, the cleaning
agent neodisher® MediClean and the neutralisation agent neodisher® Z.
▶For programme settings as well as cleansers and disinfectants to be used,
please refer 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 compressed 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 thermod-
isinfector.
Note
Please comply with the instructions for use of the washer disinfector.
7.3 Disinfection
WARNING
Incomplete disinfection.
Infection hazard
▶As a matter of principle, KaVo recommends carrying out a final disinfection
of the unpackaged item in a steriliser if complete disinfection cannot be
guaranteed without this measure.
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-contain-
ing disinfectants.
17 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
7 Reprocessing steps in accordance with ISO 17664 | 7.3 Disinfection
18 / 26
7.3.1 Manual external disinfection
KaVo recommends the following products based on compatibility of the materi-
als. The microbiological efficacy must be ensured by the disinfectant manufac-
turer 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 man-
ufacturer 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 from Miele in accordance with EN ISO
15883-1 that are operated with alkaline cleaning agents.
The validations were conducted with the VARIO-TD programme, the cleaning
agent neodisher® MediClean and the neutralisation agent neodisher® Z.
▶For programme settings as well as cleansers and disinfectants to be used,
please refer 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 compressed 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 thermod-
isinfector.
Note
Please comply with the instructions for use of the washer disinfector.

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
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 thermod-
isinfector.
▶Please observe the instructions for use of the thermodisinfector.
7.5 Care products and systems - Servicing
NOTICE
Improper service and care.
Premature wear and reduced product service life.
▶Service regularly with suitable agents.
Note
Remove the insert for care.
Note
KaVo guarantees the proper function of KaVo products only if the care
products listed 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.
▶Take screw-in and/or snap-on polishing attachments off the contra-angle
handpiece.
▶Cover the product with the Cleanpac bag.
▶Plug the product onto the cannula, and press the spray button for one
second.
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.
▶Take screw-in and/or snap-on polishing attachments off the contra-angle
handpiece.
▶Place the product on the appropriate coupling on the KaVo SPRAYrotor and
cover it with the Cleanpac bag.
▶Service the product.
19 / 26

Instructions for use SMARTmatic PROPHY S31 - 1.011.6760 SMARTmatic PROPHY S31 K - 1.011.6761 SMARTmatic
PROPHY S33 - 1.011.6800
7 Reprocessing steps in accordance with ISO 17664 | 7.6 Packaging
20 / 26
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 de-
livery programme.
Follow-up product:
▶QUATTROcare PLUS 2124 A
Servicing and cleaning device with expansion pressure for the interior cleaning
of inorganic residues and optimum care.
(no validated cleaning of the interior according to German Robert Koch Institute
(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.
▶Take screw-in and/or snap-on polishing attachments off the contra-angle
handpiece.
▶Service the product.
See also:
2Instructions for use KaVo QUATTROcare 2104 / 2104A
7.5.4 Servicing with KaVo QUATTROcare PLUS
Servicing and cleaning device with expansion pressure for the interior cleaning
of inorganic residues and optimum care.
(no validated cleaning of the interior according to German Robert Koch Institute
(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.
▶Take screw-in and/or snap-on polishing attachments off the contra-angle
handpiece.
▶Service the product in the QUATTROcare PLUS.
See also:
2Instructions for use KaVo QUATTROcare PLUS
7.6 Packaging
Note
The sterilisation bag must be large enough for the instrument so that the bag
is not stretched.
The quality and use of the sterilisation packaging must comply with applic-
able standards and be suitable for the sterilisation procedure!
▶The medical device must be packed before sterilisation.