KaVo SURGmatic S201 XL Pro User manual

SURGmatic
S201 L Pro
SURGmatic
S201 XL Pro
Instructions for use
SURGmatic S201 XL Pro - 1.013.7541
SURGmatic S201 L Pro - 1.013.7540

Distributed by:
KaVo Dental Technologies, LLC
11727 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 ................................................................................................................ 4
2 Safety.................................................................................................................................. 7
2.1 Infection hazard ............................................................................................................ 7
2.2 Technical condition......................................................................................................... 7
2.3 Accessories and combination with other equipment ........................................................... 7
2.4 Qualification of personnel................................................................................................ 8
3 Product description ............................................................................................................ 9
3.1 Intended use................................................................................................................. 9
3.2 Technical Specifications .................................................................................................. 10
3.3 Transportation and storage conditions.............................................................................. 10
4 Startup and shut-down....................................................................................................... 11
4.1 Checking the water quantity ........................................................................................... 11
5 Operation............................................................................................................................ 13
5.1 Inserting the head ......................................................................................................... 13
5.2 Pulling off the head ........................................................................................................ 13
5.3 Attaching the contra-angle handpiece to the motor coupling............................................... 14
5.4 Pulling the contra-angle handpiece off the motor coupling.................................................. 14
5.5 Inserting the bur or diamond .......................................................................................... 14
5.6 Removing the bur or diamond......................................................................................... 15
6 Checking for malfunctions and troubleshooting ................................................................ 16
6.1 Check for malfunctions ................................................................................................... 16
6.2 Troubleshooting............................................................................................................. 16
6.2.1 Cleaning the spray clip and the spray tube ............................................................ 16
7 Processing steps in accordance with EN ISO 17664..........................................................17
7.1 Preparations at the site of use......................................................................................... 17
7.2 Non-fixing preliminary cleaning of the spray clip and spray tube ......................................... 17
7.3 Manual processing ......................................................................................................... 18
7.3.1 Manual internal and external cleaning and internal and external disinfection ............. 18
7.3.2 Manual drying .................................................................................................... 18
7.4 Automated processing.................................................................................................... 18
7.4.1 Automated internal and external cleaning and internal and external disinfection ........ 19
7.4.2 Automated drying............................................................................................... 19
7.5 Care products and systems - Servicing............................................................................. 20
7.5.1 Servicing with KaVo Spray................................................................................... 20
7.5.2 Servicing with KaVo QUATTROcare PLUS............................................................... 20
7.5.3 Servicing with KaVo QUATTROcare ....................................................................... 21
7.6 Packaging ..................................................................................................................... 22
7.7 Sterilization................................................................................................................... 22
7.8 Storage ........................................................................................................................ 23
8 Tools and consumables ...................................................................................................... 24
9 Terms and conditions of warranty .....................................................................................25
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
Table of contents
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
1 User instructions
4 / 28
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
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: [e-mail]
Please refer to the serial number of the product in all inquiries!
For repairs, please contact KaVo Repair Service.
For scheduling or if you have any questions, please contact:
KaVo Repair Service
KaVo Dental Technologies, LLC
11727 Fruehauf Drive
Charlotte, NC 28273 USA
Toll-free Direct Customer Service: 1-888-ASK-KAVO (888-275-5286)
Email: [e-mail]
www.kavo.com
Target group
The instructions for use are intended for medical professionals, in particular
dentists and office personnel.
The section on Commissioning 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
Sterilization parameters
▪ Sterilizer with triple pre-vacuum:
- at least 3 minutes at 135°C (275 °F)
- Drying time: 16 min.
▪ Sterilizer using the gravity method:
- at least 10 minutes at 135°C (275 °F)
- drying time 30 minutes or alternatively
- at least 30 minutes at 121°C (250 °F)
- Drying time: 15 min.
Thermodisinfectable

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
1 User instructions
Information on the packaging
Catalog number
Serial number
Legal Manufacturer
CE mark according to Medical Devices Directive EC 93/42
Please note the electronic instructions for use
Caution: Consult instructions for use
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 range)
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 property 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 – can lead to death or severe injury.
CAUTION
In cases which – if not prevented – can lead to minor or moderate in-
jury.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
1 User instructions
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NOTICE
In cases which – if not prevented – can lead to property damage.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
2 Safety | 2.1 Infection hazard
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 can be infected by contaminated medical de-
vices.
▶Take suitable personal protective measures.
▶Follow the instructions for use of the components.
▶Before initial startup and after each use, process the product and acces-
sories appropriately.
▶Carry out the processing as described in the instructions for use. The proce-
dure has been validated by the manufacturer.
▶If you deviate from this procedure, it is essential to make sure that the pro-
cessing is effective.
▶Process the product and accessories appropriately before disposal.
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 to make sure that the device is working properly and is in satisfac-
tory 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
▪ Dental bur or diamond is not firmly locked in the handpiece
To ensure optimum function and to prevent property damage, please comply
with the following instructions:
▶Service the medical device with care products and systems regularly as de-
scribed in the instructions for use.
▶The product should be processed and stored in a dry location, according to
instructions, if it is not to be used for an extended period of time.
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.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
2 Safety | 2.4 Qualification of personnel
8 / 28
▶Only use accessories that have been approved for combination with the
product by the manufacturer.
▶Do not make any modifications to the device unless these have been ap-
proved by the manufacturer of the product.
▶Use original KaVo spare parts only.
It is not permissible to combine this unit with other heads and bases as this
may lead to injury.
▶The SURGmatic S201 XL Pro / L Pro contra-angle handpiece consists of a
shank and a head and must not be combined with other heads or shanks.
▶The head, SURGmatic Head S201 L Pro Mat. no. 1.013.8648 may only be
combined with the SURGmatic S201 L Pro 1.013.7540 shank.
▶The SURGmatic Head S201 XL Pro Mat. no. 1.013.8662 may only be
combined with the SURGmatic S201 XL Pro 1.013.7541 shank.
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 / control
unit released by KaVo.
▶Comply with the Instructions for Use of the treatment center / control unit.
2.4 Qualification of personnel
Application of the product by users lacking appropriate medical training can in-
jure 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.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
3 Product description | 3.1 Intended use
3 Product description
SURGmatic
S201 XL Pro
SURGmatic S201 XL Pro Mat. no. 1.013.7541
SURGmatic
S201 L Pro
SURGmatic S201 L Pro Mat. no. 1.013.7540
The SURGmatic (S201 L/XL Pro) handpieces are electrically driven dental hand-
pieces according to 21 CFR § 872.4200 (dental handpieces and accessories) for
use by a professional trained in the field of general dentistry. The devices are
electrical-powered handpieces that are reusable and ergonomically shaped, and
provided with a fiber optic light system. The devices can be sterilized by the
steam autoclave method. Through a surgical motor connected to the surgical
control unit, the handpieces, equipped with a handpiece connection according
to ISO 3964, receives the energy, the cooling water and air for treatment and
the light for illumination the operation area. Surgical burs and cutters (with
straight handpiece shank or with contra-angle shank) according to ISO 1797
can be used. The handpieces use external spray allowing external irrigation to
the working area. Based on the speed adjusted in the surgical control unit the
handpiece bur rotates up to 40,000 rpm. The handpieces interacts with the pa-
tient through a rotating bur with the patient teeth according to the intended
use.
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 is
intended for use in the following applications: surgery e.g. placing an im-
plant, bone augmentation, sinus lift, dental extraction, implantology and
oromaxillary and facial surgery.
▪ A medical device in accordance with the relevant national statutory regula-
tions.
CAUTION
US Federal law restricts this device to sale by or on the order of a
healthcare professional / dentist.
For dental use only.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
3 Product description | 3.2 Technical Specifications
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Proper Use:
According to these regulations, this product may only be used for the described
application by a properly trained user. You need to comply with the following:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these Instructions for use
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
▪ avoid contamination from the product
3.2 Technical Specifications
Contra-angle handpiece S201 L Pro S201 XL Pro
Drive speed max. 40,000 rpm max. 40,000 rpm
Labeling 1 green ring 1 green ring
Speed transmission 20 : 1 20 : 1
Max. torque 55 Ncm 55 Ncm
Max. torque for the use of
hexagon shanks
- 80 Ncm
With push-button chuck.
Usable with surgical burs or diamonds with inner cooling or surgical tools with a
hexagon head socket at the shaft.
Internal cooling system (acc. to Kirschner and Meyer) and external cooling-
medium connection.
The contra-angle handpiece can be mounted on all INTRAmatic (LUX) motors
and motors fitted with a connector in accordance with ISO 3964.
CAUTION
The SURGmatic S201 L / XL Pro contra-angle handpiece consists of a
shank and a head.
Risk of injury.
▶It is not permissible to combine the unit with other heads / shanks.
3.3 Transportation and storage conditions
50
-29
Temperature: -29 °C to +50 °C (-20 °F to +122 °F)
Relative humidity: 5% RH to 85% RH absence of condensation
Air pressure: 700 hPa to 1060 hPa (10 psi to 15 psi)
Protect from moisture (Keep dry)

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
4 Startup and shut-down | 4.1 Checking the water quantity
4 Startup and shut-down
WARNING
Hazard from non-sterile products.
Infection hazard for dentist and patient.
▶Before first use and after each use, process and sterilize the medical device
and accessories accordingly.
WARNING
Dispose of the product in the appropriate manner.
Infection hazard.
▶Before disposal, process and sterilize the product and accessories appropri-
ately.
4.1 Checking the water quantity
CAUTION
Overheating of the tooth due to insufficient amount of cooling water.
Thermal damage to the dental pulp.
▶Set 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.
▶Switch off spray-air and spray-water supply on the treatment device.
▶Cool the dental bur or diamond via the external and/or internal feed, if
available. The supply can take place individually or via a coupling piece.
▶During surgical interventions, comply with the necessary precautions re-
garding cooling.
▶Use physiological, sterile cooling fluid.
▶Ensure that the coolant supply is free of air.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
4 Startup and shut-down | 4.1 Checking the water quantity
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▶Carefully plug the coolant hose in central position onto the media tube pro-
ceeding in axial direction.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
5 Operation | 5.1 Inserting the head
5 Operation
5.1 Inserting the head
CAUTION
The SURGmatic S201 L / XL Pro contra-angle handpiece consists of a
shank and a head.
Risk of injury.
▶It is not permissible to combine the unit with other heads / shanks.
Note
The head of the SURGmatic S201 XL Pro / L Pro contra-angle handpiece may
be taken off the shank only for the non-fixating pre-cleaning.
WARNING
Detachment of the medical device during treatment.
If the head is not properly locked in place, it can become detached during
treatment.
▶Do not mount or remove the head while it is rotating. Before each treat-
ment, check that the head is firmly seated and that the clamping ring is
tight.
▶Rotate the clamping ring in the direction of the arrow until it hits the stop
and hold it there.
▶Insert the head to the stop. Make sure that the catches engage properly.
▶Rotate the clamping ring in the direction of the arrow (-> close) and tighten
it.
▶Attach the spray clip.
▶Make sure that the spray clip is securely affixed.
5.2 Pulling off the head
▶Pull the spray clip off.
▶Rotate the clamping ring in the direction of the arrow until it hits the stop
and hold it there.
▶Removing the medical device.
▶Release the clamping ring.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
5 Operation | 5.3 Attaching the contra-angle handpiece to the motor coupling
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5.3 Attaching the contra-angle handpiece to the motor
coupling
WARNING
Detachment of the medical device during treatment.
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 straight or contra-angle handpiece while
the drive motor is rotating.
Damage to the driver.
▶Never attach or remove the straight or contra-angle handpiece while the
drive motor is rotating.
▶Lightly spray O-rings on the motor coupling with KaVo Spray.
▶Attach the medical device to the motor coupling and turn it until the guide
stud audibly snaps into place.
▶Pull on the medical device to make sure that it is securely affixed to the
coupling.
5.4 Pulling the contra-angle handpiece off the motor
coupling
▶Unlock the medical device from the motor coupling by twisting it slightly
and then pulling it along its axis.
5.5 Inserting the bur or diamond
Note
Only use carbide cutters or diamond drill bits made by Nobel Biocare that
meet EN ISO 1797 type 1 or EN ISO 17509, are made of steel or hard metal,
and meet the following criteria:
- Shaft diameter: 2.334 to 2.350 mm
- Overall length: max. 45mm
- Blade diameter: max. 10 mm
- Shaft clamping length: at least 12mm
If the torques on the rotating instrument exceed 30 Ncm, hardened drill
shafts (>500 HV) need to be used.
Using surgical handpieces with hexagon in combination with tools having a
hexagon head socket at the shaft allows deformations at the tool shaft to be
prevented.
It prevents the tool from getting lodged or being difficult to take off.
Note
If you use tools with a lower hardness (<500 HV) made by Nobel Biocare in
combination with torques in excess of 30 Ncm, the tool may only be used for
a single treatment.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
5 Operation | 5.6 Removing the bur or diamond
WARNING
Use of unauthorized burs.
Injury to the patient or damage to the medical device.
▶Comply with the instructions for use and the intended use of the bur.
▶Only use burs that do not deviate from the specified data.
CAUTION
Injury from using worn burs.
Burs could fall out during treatment and injure the patient.
▶Never use burs with worn shafts.
CAUTION
Danger of injury from bur.
Infections or cuts.
▶Wear gloves or finger guards.
CAUTION
Hazard from defective chucking system.
The bur could fall out and cause injury.
▶Pull on the bur to make sure that the chucking system works properly and
that the bur is held securely. Wear gloves or finger guards when you check,
insert or remove the insert to prevent injury and infection.
▶Insert the bur into the segment of the head drive by twisting the tool
slightly, and push it to the bur stop. Activate the button if necessary.
▶Make sure that the tool is seated securely by pulling on it.
5.6 Removing the bur or diamond
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 or diamond has stopped rotating, firmly press the button with
your thumb and simultaneously pull out the bur or diamond.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
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.
▶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.
See also:
2Instructions for use of motor
6.2 Troubleshooting
6.2.1 Cleaning the spray clip and 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).
▶Use the nozzle pin (Mat. no. 0.410.0931) to free the water passage on
the spray clip on both sides.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
7 Processing steps in accordance with EN ISO 17664 | 7.1 Preparations at the site of use
7 Processing steps in accordance with EN ISO 17664
7.1 Preparations at the site of use
WARNING
Hazard from contaminated products.
Contaminated products are associated with an infection risk.
▶Take suitable personal protective measures.
▶Remove the bur from the medical device.
▶Remove the spray clip for internal cooling.
▶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 clip and
spray tube
The non-fixing preliminary cleaning is a central constituent and must be per-
formed prior to the automated processing.
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 hand-
piece.
▶Check the patency of the spray clip and spray tube and clean them with the
nozzle pin (Mat. no. 0.410.0931).
▶Rinse the spray clip and spray tube with at least 20 ml demineralized water
using a disposable syringe.
▶If the spray clip and spray tube are not patent after the manual rinsing pro-
cedure, the medical device and/or the spray clip must be replaced.
▶Brush the spray clip and spray tube under running tap water water for at
least 20 seconds using a medium-hard toothbrush.
For validated internal cleaning of the spray clip and spray tube in the cleaning
and disinfecting device, preliminary non-fixing cleaning is required.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
7 Processing steps in accordance with EN ISO 17664 | 7.3 Manual processing
18 / 28
7.3 Manual processing
WARNING
Sharp tool in the medical device.
Injury hazard from sharp and/or pointed tool.
▶Remove the tool.
NOTICE
Never process this medical device in an ultrasonic device.
Functional damage and property damage.
▶Clean it in a washer disinfector only.
Note
The spray clip for internal cooling may be additionally cleaned in the ultra-
sonic cleaner.
7.3.1 Manual internal and external cleaning and internal
and external disinfection
Not applicable.
7.3.2 Manual drying
▶Clean the outside and inside with compressed air until no drops of water are
visible.
▶Immediately after drying, lubricate the KaVo medical device with care
agents from the KaVo care system.
See also:
27.5 Care products and systems - Servicing, Page 20
7.4 Automated processing
WARNING
Incomplete disinfection.
Infection hazard.
▶Only use disinfection procedures that are verified to be bactericidal, fungici-
dal and virucidal.
▶If the disinfectants used do not meet these requirements, the process must
be concluded by disinfection of the unit(s) without packaging using a steril-
izer.

Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
7 Processing steps in accordance with EN ISO 17664 | 7.4 Automated processing
WARNING
Sharp tool in the medical device.
Injury hazard from sharp and/or pointed tool.
▶Remove the tool.
NOTICE
Never disinfect the handpiece with chlorine-containing products.
Malfunction and material damage.
▶Only disinfect in the washer disinfector.
NOTICE
Never process this medical device in an ultrasonic device.
Functional damage and property damage.
▶Clean it in a washer disinfector only.
Note
The spray clip for internal cooling may be additionally cleaned in the ultra-
sonic cleaner.
For validated internal cleaning of the spray clip and spray tube in the cleaning
and disinfecting device, preliminary non-fixing cleaning is required.
7.4.1 Automated internal and external cleaning and
internal and external disinfection
Note
Prior to cleaning or disinfection in a washer disinfector, attach the head to an
appropriate base.
KaVo recommends washer disinfectors in accordance with ISO 15883-1, which
are operated using alkaline cleaning agents.
▶For program settings as well as cleansers and disinfectants to be used,
please refer to the Instructions for Use of the washer disinfector.
▶For the spray clip and spray tube, also use the adapter for external spray
channels.
7.4.2 Automated drying
The drying procedure is usually part of the cleaning program of the washer dis-
infector.
Note
Please comply with the instructions for use of the washer disinfector.
▶In order to prevent impairment of the KaVo medical device, make sure that
the inside and outside of the device is dry after the end of the cycle.
▶Immediately after drying, lubricate the KaVo medical device with care
agents from the KaVo care system.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540
7 Processing steps in accordance with EN ISO 17664 | 7.5 Care products and systems - Servicing
20 / 28
7.5 Care products and systems - Servicing
CAUTION
Improper service and care.
Risk of injury.
▶Perform regular proper care and servicing.
WARNING
Sharp bur in the medical device.
Risk of injury from sharp and/or pointed bur.
▶Remove bur.
Note
KaVo only guarantees that its products will function properly if the care prod-
ucts listed as accessories are used, since these products have been tested for
proper use on our products.
7.5.1 Servicing with KaVo Spray
Note
Head can be serviced alone or attached to a shank.
▶Remove the bur.
▶Cover the product with the Cleanpac bag.
▶Plug the product onto the spray head and press the spray button for one
second.
Servicing the chucking system
KaVo recommends servicing the chucking system once weekly.
▶Remove the bur, place the spray nozzle in the opening and spray.
▶Press the spray key once for 1-2 seconds.
7.5.2 Servicing with KaVo QUATTROcare PLUS
Note
Head can be serviced alone or attached to a shank.
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 bur.
▶Service the product in the QUATTROcare PLUS.