DENTSPLY Cavitron Select SPS Manual

ENGLISH • 1
Cavitron®Select™ SPS™
Ultrasonic Scaler
Cavitron®Select™ SPS™
Ultrasonic Scaler with
Cavitron®Select™
Reservoir System
Cavitron®Select™ SPS™ Ultrasonic Scaler with Cavitron®Select™ Reservoir System
Introduction
Directions For Use
Please read carefully and completely before operating unit.
DENTSPLY®Professional is an ISO9001 certified company. The
Cavitron®Select™ System is classified by Underwriters Laborato-
ries Inc. with respect to electric shock, fire, mechanical hazards
only in accordance UL 2601-1 1 and Can/CSA C22.2 NO. 601.1.
The Scaling System operates by converting ordinary AC house
current into high frequency current. The ultrasonic system consists
of two parts: an insert, and the SPS™ (Sustained Performance
System) electronic system. The system incorporates two closed
loops. One loop provides automatic tuning (operating frequency
is adjusted to be at resonance for each insert), the second
loop automatically controls the tip stroke over different working
conditions. The scaler produces 30,000 microscopically small
strokes per second at the insert’s working tip. This combined with
acoustic effects of the coolant water, produces a synergistic action
that literally “powers away” the heaviest calculus deposits while
providing exceptional operator and patient comfort.
The Pump/Reservoir accessory for the Cavitron®Select™ SPS™
is an optional lavage dispenser. Footswitch plug, handpiece plug,
water tube and power supply plug are removed from the Scaler
before mating with the Pump/Reservoir. The Scaler is snapped
together with the Pump/Reservoir. The footswitch plug, handpiece
plug and power supply plug are inserted into mating receptacles at
the rear of the Pump/Reservoir. Ultrasonic signal, footswitch and
DC power connections between the units are made via an edgecard
connector at the rear of the Scaler and the front of the Pump
module. The Reservoir has a capacity of 450 ml. Fluid from the
Reservoir is propelled from the Reservoir Bottle with 15–19 psig
compressed air generated by an internal diaphragm pump.
ON/OFF of the lavage is controlled through an internal solenoid
valve. Fluid to the Handpiece passes directly from the Pump/
Reservoir to the Handpiece. No fluid passes through the Cavitron®
Select™ SPS™ when used with this accessory. Flow through any
insert in the Handpiece will be greater than 40 cc/m water when
adjusted to maximum.
Technical Support
For technical support and repair assistance in the U.S., call
1-800-989-8826 Monday through Friday, 8:00 AM to 5:00 PM
(Eastern Time). For other areas, contact your local DENTSPLY®
representative.
Supplies & Replacement Parts
To order supplies or replacement parts in the U.S., contact
your local DENTSPLY®Distributor or call 1-800-989-8826
Monday through Friday, 8:00 AM to 5:00 PM (Eastern Time).
For other areas, contact your local DENTSPLY®representative.
Caution: U.S. Federal Law restricts this device to sale by or on the
order of a Dentist.
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Table of Contents
Section Section Title Page
Number Description of Contents Number
1 Indications for use................................................................................................................................................... 3
2 Contraindications and Warnings............................................................................................................................. 3
2.1 Contraindications
2.2 Warnings
3 Precautions ............................................................................................................................................................. 3
3.1 Precautions for All Systems
3.2 Precautions for Ultrasonic Prophylaxis Procedures
3.3 Precautions for Cavitron®Select™ Reservoir System
4 Infection Control.................................................................................................................................................... 4
4.1 General Infection Control Recommendations
4.2 Water Supply Recommendations
5 Installation Instructions for Cavitron®Select™ SPS™ Ultrasonic Scaler............................................................ 4–5
5.1 General Information
5.2 Water Line Requirements
5.3 Electrical Requirements
5.4 Unpacking the System
5.5 Power Cord/Power Connection
5.6 Foot Control Cable Assembly Connection
5.7 Water Supply Line Connection
5.8 Lavage Control Detachable Handpiece Cable Assembly Connection
6 Installation Instructions for Cavitron®Select™ SPS™ Scaler with Cavitron®Select™ Reservoir System........... 6–7
6.1 General Information
6.2 Electrical Requirements
6.3 Unpacking the System
6.4 Assembling the System
6.5 Power Cord/Power Connection
6.6 Foot Control Cable Assembly Connection
6.7 Lavage Control Detachable Handpiece Cable Assembly Connection
7 Cavitron®Select™ SPS™ Ultrasonic Scaler Description.................................................................................. 8–10
7.1 System Controls for Cavitron®SPS™ Select™ Ultrasonic Scaler
7.2 System Controls for Cavitron®Select™ SPS™ Scaler with Cavitron®Select™ Reservoir System
7.3 Handpiece
7.4 Cavitron®30KTM Ultrasonic Inserts
7.5 Foot Control Information & Operation
8 Accessories ............................................................................................................................................................ 11
8.1 Accessories List
8.2 Medicaments
9 Techniques for Use................................................................................................................................................ 11
9.1 Patient Positioning
9.2 Performing Ultrasonic Scaling Procedures
9.3 Patient Comfort Considerations
10 System Care..................................................................................................................................................12–13
10.1 Daily Maintenance — Start-Up Procedures, Between Patients, Shut-Down Procedures
10.2 Weekly Maintenance
10.3 Water Line Filter Maintenance
10.4 Pump Lavage Filter Maintenance
11 Troubleshooting.................................................................................................................................................... 14
11.1 Troubleshooting Guide
11.2 Technical Support and Repairs
12 Specifications ........................................................................................................................................................ 15
13 Classifications ....................................................................................................................................................... 15
14 Disposal of Unit.................................................................................................................................................... 15

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Section 1: Indications for Use
Section 2: Contraindications and Warnings
Section 3: Precautions
3.1 Precautions for All Systems
 •Cavitron®Inserts manufactured by DENTSPLY®
Professional should be used for optimal performance.
 • DonotplacetheSystemonornexttoaradiatoror
other heat source. Excessive heat may damage the System’s
electronics. Place the System where air is free to circulate on
all sides and beneath it.
 • TheSystemisportable,butmustbehandledwithcarewhen
moving.
 • Equipmentushinganddentalwatersupplysystem
maintenance are strongly recommended. See Water Supply
under Section 10: System Care.
 • Closethewatershut-offvalvetotheSystemeverynight
before leaving the office.
 •Neveroperatescalerwithoutuidowingthroughhandpiece.
3.2 Precautions for Ultrasonic
Prophylaxis Procedures
 • Likeatoothbrush,ultrasonicinserts“wearout”withuse.
Inserts with just 2 mm of wear lose about 50% of
their scaling efficiency. In general, it is recommended that
ultrasonic inserts be discarded and replaced after 2 mm of
wear to maintain optimal efficiency and avoid breakage.
 • Ifexcessivewearisnoted,ortheinserthasbeen
bent, reshaped or otherwise damaged, discard the
insert immediately.
2.1 Contraindications
 •UltrasonicSystemsshouldnotbeusedforrestorativedental
procedures involving the condensation of amalgam.
Ultrasonic procedures:
 •Allgeneralsupraandsubgingivalscalingapplications.
 •Periodontaldebridementforalltypesofperiodontaldiseases.
 •Endodonticprocedures.
 • Forpatientswithahistoryofsensitivitytoultrasonics.
 •Personsttedwithcardiacpacemakers,debrillatorsand
other active implanted medical devices have been cautioned
that some types of electronic equipment might interfere
with the operation of the device. Although no instance of
interference has ever been reported to DENTSPLY®, we
recommend that the handpiece and cables be kept at least 6
to 9 inches (15 to 23 cm) away from any device and their
leads during use.
 •Thereareavarietyofpacemakersandothermedically
implanted devices on the market. Clinicians should contact
the device manufacturer or the patient’s physician for
detailed information about the device.
 • Retractthelips,cheeksandtonguetopreventcontactwith
the insert tip whenever it is placed in the patient’s mouth.
 • TheDENTSPLY®power supply shipped with this unit is
approved for use with devices and must be used to operate
this system.
3.3 Precautions for Cavitron®Select™
Reservoir System
 • DonotplacetheSystemonornexttoaradiatoror
other heat source. Excessive heat may damage the System’s
electronics. Place the System where air is free to circulate on
all sides and beneath it.
 • TheSystemisportable,butmustbehandledwithcarewhen
moving.
 • Equipmentushinganddentalwatersupplysystem
maintenance are strongly recommended. See Section 10:
System Care.
 • Pourliquidintothecapopeningofthereservoirbottle.To
prevent potential leaking at the cap, do not overfill bottle
with liquid into the neck of the bottle. Ensure cap is tightly
sealed.
 • Turnunitoffbeforerellingreservoirbottletoprevent
potential leaking of fluid. Turn cap a 1/4revolution to release
air pressure and then remove the cap completely.
2.2 Warnings

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Section 5: Installation Instructions for Cavitron®Select™
SPS™ Ultrasonic Scaler
5.1 General Information
If the installation of your Cavitron®Select™ SPS™ Scaler is
performed by someone other than trained DENTSPLY®
Distributor personnel, care should be taken to observe the
following requirements and recommendations.
5.2 Water Line Requirements
• IncomingwatersupplylinepressuretotheScalermustbe
20 psi (138 kPa minimum) to 40 psi (276 kPa maximum).
If your dental water system’s supply line pressure is above 40
psi, install a water pressure regulator on the water supply line
to your Cavitron®Select™ SPS™ Scaler.
 • Amanualshut-offvalveonthedentalwatersystemsupply
line should be used so that the water can be completely shut
off when the office is unoccupied.
 • Aftertheaboveinstallationsarecompletedonthedental
water supply system, the dental office water line should be
thoroughly flushed prior to connection to the Scaler.
Section 4: Infection Control
4.1 General Infection Control Recommendations
 • Aswithalldentalprocedures,usestandardpersonal
protection equipment (i.e., wear face mask, eyewear, or face
shield, gloves and protective gown).
 • Formaximaloperatorandpatientsafety,carefullyfollow
the Infection Control Information procedures detailed in
the Cavitron Infection Control Procedures Booklet
(Form No. 81158).
 • Aswithhighspeedhandpieces,andotherdentaldevices,
the combination of water and ultrasonic vibration from your
Cavitron®Select™ SPS™ Scaler will create aerosols. With
proper technique, much of the Cavitron®Select™ SPS™
Scaler’s aerosol dispersion can be effectively controlled and
minimized. Please carefully follow the procedural guidelines
in this manual regarding the use of your System.
4.2 Water Supply Recommendations
It is highly recommended that all dental water supply systems
conform to applicable CDC (Centers for Disease Control and
Prevention) and ADA (American Dental Association) standards,
and that all recommendations be followed in terms of flushing,
chemical flushing, and general infection control procedures.
5.3 Electrical Requirements
Refer to Section 12: Specifications.
5.4 Unpacking the System
Carefully unpack your Cavitron®Select™ SPS™ Scaler and verify
that all components and accessories are included:
1. Cavitron®Select™ SPS™ Scaler.
2. Detachable AC Power Cord set.
3. Steri-Mate Detachable Sterilizable Handpiece.
4. Steri-Mate Flow Control Detachable Handpiece Cable
Assembly with Swivel.
5. Dual Position Foot Control Assembly.
6. Hose / Filter / Quick Disconnect Assembly.
7. Additional Water Line Filter.
8. Additional Pump Lavage Filters.
9. Medically Approved Power Supply.
10. Literature Packet.

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5.5 Power Cord/Power Connection
 • VerifythePowerControlknobissettotheOFFposition
before proceeding.
 • PlugthedetachableACcordintothebackoftheMedically
Approved Power Supply.
 • PlugthepowersupplyoutletintothebackoftheSystem.
 • Plugthe3pronggroundedplugintoanapprovedoutlet.
Section 5: Installation Instructions for Cavitron®Select™ SPS™ Ultrasonic Scaler, cont’d
5.6 Foot Control Cable Assembly Connection
Align the Foot Control plug with the receptacle on the back of the
System and push it in until firmly seated.
5.7 Water Supply Line Connection
 •Pushthebluehoseintotheorangewaterreceptacleuntilthe
hose cannot be pushed in any further.
 •Connectthefreeendofthesystem’swatersupplylinetothe
office water supply line.
 •Inspectallconnectionstomakecertaintherearenoleaks.
 •ToremovewaterlinefromCavitron®Select™ SPS™ Scaler,
turn off or disconnect water supply line FIRST, then push
on outer orange ring of the outlet and gently pull out
water hose.
5.8 Lavage Control Detachable
Handpiece Cable Assembly Connection
 • PlugtheHandpieceoutletintothereceptacleontheback
of the System.
 • HoldingtheHandpieceCableAssemblyseatmaleconnector
into appropriate female connector.
 • Onceseated,snapmaleconnectorintofemaleconnectorby
pushing on the end of the male connector.
 • RotateLavageControlonthehandpiecetomiddlesetting.
 • Turnontheon/offswitch(poweradjustment).

ENGLISH • 6
Section 6: Installation Instructions for Cavitron®Select™
SPS™ Scaler with Cavitron®Select™ Reservoir System
6.1 General Information
If the installation of your Cavitron®Select™ SPS™ Ultrasonic
Scaler with Cavitron®Select™ Reservoir System is performed by
someone other than trained DENTSPLY®Distributor personnel,
care should be taken to observe the following requirements and
recommendations.
6.2 Electrical Requirements
Refer to Section 12: Specifications.
6.3 Unpacking the System
Carefully unpack your Cavitron®Select™ SPS™ Scaler and verify
that all components and accessories are included:
1. Cavitron®Select™ SPS™ Scaler.
2. Cavitron®Select™ Reservoir Pump.
3. Cavitron®Select™ Reservoir Bottle.
4. Detachable AC Power Cord set.
5. Steri-Mate Detachable Sterilizable Handpiece.
6. Steri-Mate Flow Control Detachable Handpiece
Cable Assembly with Swivel.
7. Dual Position Foot Control Assembly.
8. Hose / Filter / Quick Disconnect Assembly.
9. Additional Water Line Filter.
10. Additional Pump Lavage Filters.
11. Medically Approved Power Supply.
12. Literature Packet.
6.4 Assembling the System
 • Removeprotectivestickerfromedgecardconnectoronthescaler.
 • RinseCavitron®Select™ Reservoir Bottle before using.
 • InsertCavitron®Select™ Reservoir Bottle into Cavitron®
Select™ Reservoir Pump and rotate clockwise until bottle
locks into place.
 • ConnectCavitron®Select™ SPS™ Scaler to Cavitron®
Select™ Reservoir System. Insert male edge card connector
on Cavitron®Select™ Reservoir Pump into Cavitron®
SPS™ Select™ Scaler opening on the back of the Cavitron®
Select™ SPS™ Scaler. Press down on the top of the
Cavitron®Select™ SPS™ Scaler (directly above power
setting knob) until the black striker knob located on the
Reservoir Bottle locks into place.
 • TodetachCavitron®Select™ SPS™ Scaler from Cavitron®
Select™ Reservoir Pump and Bottle, lift up on the front of
the Cavitron®Select™ SPS™ Scaler (below power setting
knob and Power/Boost light). After the striker knob is
unsnapped, pull the Cavitron®Select™ SPS™ Scaler away
from the Cavitron®Select™ Reservoir Pump.
NOTE: Always disengage striker knob before pulling the
Cavitron®Select™ SPS™ Scaler away from the Cavitron®
Select™ Reservoir Pump.

ENGLISH • 7
Section 6: Installation Instructions for Cavitron®Select Scaler with
Cavitron®Select™ SPS™ Reservoir System cont'd.
6.5 Power Cord/Power Connection
 • VerifythePowerControlknobisset to the OFF position
before proceeding.
 • Plug the detachable AC cord into the back of the Medically
Approved Power Supply.
 • PlugthepowersupplyoutletintothebackoftheCavitron®
Select™ Reservoir Pump.
 • Plugthe3pronggroundedplugintoan approved outlet.
6.6 Foot Control Cable Assembly Connection
Align the Foot Control plug with the receptacle on the back
of the Cavitron®Select™ Reservoir Pump and push it in until
firmly seated.
6.7 Lavage Control Detachable Handpiece
Cable Assembly Connection
 • PlugtheHandpieceoutletintothereceptacleonthebackof
the Cavitron®Select™ Reservoir Pump.
 • HoldingtheHandpieceCableAssemblyseatmaleconnector
into appropriate female connector.
 • Onceseated,snapmaleconnectorintofemaleconnectorby
pushing on the end of the male connector.
 • RotateLavageControlonthehandpiecetomiddlesetting.
Turn on the on/off switch (power adjustment). This
energizes the system and the ultrasonic unit is ready for
operation.

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Section 7: Cavitron®Select™ SPS™ Ultrasonic Scaler
Description
7.1 System Controls: Cavitron®Select™ SPS™ Ultrasonic Scaler
Magnetic Handpiece Holder
Holds the System's Handpiece
when system is not being used.
Power Control (ON/OFF Switch)
Turn knob to select ultrasonic power level
foroperation: clockwiseincreases system
power, counter clockwise decreases
system power.
Power & Boost Indicator Light
Greenwhen system isswitched
ON.Orangewhen“Boost”Mode
is activated.
7.2 System Controls: Cavitron®Select™ SPS™ Ultrasonic Scaler with Cavitron®Select™
Reservoir System Handpiece Holder
Holds the Handpiece when it is not being used. Amagnet is
integrated into the plastic housing.
Power Control (ON/OFF Switch)
Turn knob to select ultrasonic power
levelforoperation:clockwiseincreases
system power, counter clockwise
decreases system power.
Rellable Cavitron®Select™
Water Reservoir Cap
Reservoir Pump
Lavage dispenser.
Magnetintegrated into plastichousing.
Power & Boost Indicator Light
Greenwhen system isswitched
ON.Orangewhen“Boost”Mode
is activated.

ENGLISH • 9
Section 7: Cavitron®Select™ SPS™ Ultrasonic Scaler Description cont'd.
7.3 Handpiece
The handpiece accepts all Cavitron® 30KTM Ultrasonic Inserts.
Autoclave Symbol- Sterilizable up to the temperature specified
Lavage Control Adjustment
Holding open end of handpiece upright, lavage can be increased by holding the handpiece and gently
twisting the blue lavage adjustment knob clockwise.
HandpieceConnector-
(Handpiece & Cable
Assembly are Keyed)
Cable Assembly
Metalringis integrated
intoplastic flowcontrol
knob.
Date Codes (MMYY)
Prior to connecting, align Handpiece and Cable Assembly electrical con-
nections. If Cable Assembly does not seat into Handpiece, gently rotate
handpiece until contacts align.
DO NOT TWIST WHILE PUSHING CONNECTOR INTO HANDPIECE.
Insert Port
Steri-Mate®Handpiece
Blue Lavage Knob
30K

ENGLISH • 10
Section 7: Cavitron®Select™ SPS™ Ultrasonic Scaler Description cont'd.
O-Ring
Provides seal for handpiece
coolant.
Insert Tip
Shape and size of tip
determines access and
adaptation. Lavage
directed to tip.
Finger Grip
Connecting Body
Transfers and amplifies mechanical
motion of stack to insert tip.
Magnetostrictive Stack
Converts energy provided by the
handpiece into mechanical oscilla-
tions used to activate the insert tip.
Insert Marking
Manufacturer, Date (YYMM),
Frequency, Type, Tip Lot
Hold the handpiece in an upright position. Activate the Foot Control to bleed any air bubbles that might be trapped inside the handpiece.
Lubricate the rubber O-ring on the insert with water before placing it into the handpiece. Fully seat insert with a gentle push-twist
motion. DO NOT FORCE.
7.4 Cavitron®30KTM Ultrasonic Inserts
The many styles of Cavitron®30KTM Ultrasonic Inserts are easily interchangeable for various procedures and applications. See enclosed
booklet for specific information.
7.5 Foot Control Information & Operation
The Foot Control is a two position momentary switch, which activates both ultrasonic energy and Lavage Flow at the insert tip.
IPX1
Foot Control
released...
Both ultrasonic activation and
irrigating flow stop.
Foot Control
depressed half
way...
(1st position)
The ultrasonic insert tip is activated
and irrigating water flows.
Foot Control fully depressed...
(2nd position)
This activates the “Boost” Mode.

ENGLISH • 11
Section 8: Accessories
8.1 Accessories List
1. Cavitron®Select™ SPS™ Lavage Control Detachable
Handpiece Cable Assembly with Swivel
2. Steri-Mate Detachable Sterilizable Handpiece
3. Medically Approved Power Supply
4. AC Power Cord Set
5. Cavitron®Ultrasonic Inserts
6. Dual Position Foot Control Assembly
7. DualSelectDispensing System
8. Cavitron®Select™ Reservoir Bottle
9. Cavitron®Select™ Pump
*For detailed information, contact your local DENTSPLY®
Representative or authorized DENTSPLY®Distributor.
8.2 Medicaments
The following medicaments are compatible with the Cavitron®
Select™ SPS™ when used with the Cavitron® Select™ Reservoir
Pump:
 •ChlorhexidineGluconate0.12%
(Oris™ CHX Antimicrobial Irrigating Solution)
 •CetylpyridiniumChloride(Cepacol®)
 •EssentialOils(Listerine)
 •HydrogenPeroxide,3%USP
 •PovidoneIodine,10%Solution
 •SalineSolution
 •SanguinariaExtract(Viadent®)
 •SterileWater,USP
(For irrigating and System maintenance purposes).
Section 9: Techniques for Use
9.1 Patient Positioning
 •Foroptimalaccesstoboththeupperandlowerarches,
the backrest of the chair should be adjusted as for
other dental procedures. This assures patient comfort and
clinician visibility.
 •Havethepatientturntheirheadtotherightorleft.Also
position their chin up or down depending upon the quad-
rant and surface being treated. Evacuate irrigant using either
asalivaejectororHighVolumeEvacuator(HVE).
9.2 Performing Ultrasonic
Scaling Procedures
 •NOTE:RefertotheInfectionControlInformationcard
supplied with your System for general procedures to be fol-
lowed at the beginning of each day and between patients.
 •TheedgesofCavitron®Ultrasonic Inserts are intentionally
rounded so there is little danger of tissue laceration with
proper ultrasonic scaling technique. Whenever the insert tip
is placed in the patient’s mouth, the lips, cheek and tongue
should be retracted to prevent accidental prolonged contact
with the activated tip.
 •Turnuniton.
 •HoldtheemptyHandpieceinanuprightposition.Activate
the Foot Control until fluid exits. Once fluid exits, deactivate
foot controller.
 •LubricatetherubberO-ringontheinsertwithwaterbefore
placing it into the handpiece. Fully seat insert with a gentle
push-twist motion. DO NOT FORCE.
 •ActivatetheSystem.Holdthehandpieceoverasinkordrain.
Check spray temperature to verify fluid is reaching the work-
ing end of the insert tip. Adjust the Lavage Control knob to
ensure adequate flow for the selected Power setting. Greater
flow settings provide cooler irrigant.
 •Itmaybenecessarytoadjustlavagewiththesystemin
“Boost” mode (Foot Control fully depressed) so adequate
fluid will be available to cool tip to tooth interface.
 •Ingeneral,itissuggestedthata“feather-light-touch”beused
both supra- and subgingivally. The motion of the activated
tip and acoustic effects of the irrigating fluid, in most cases, is
adequate to remove even the most tenacious calculus.
 •PeriodicallychecktheCavitron®Ultrasonic Insert for wear
with the DENTSPLY®Insert Efficiency Indicator.
 •TheuseofasalivaejectororHighVolumeEvacuator(HVE)
is recommended during all procedures.
 •SettheSystem’sPowerAdjustmentknob to the lowest power
setting for the application and the selected insert.
9.3 Patient Comfort Considerations
Reasons for sensitivity
 • Incorrecttipplacement.Pointshouldbedirectedawayfromroot
surfaces.
 • Notkeepingtipinmotionontooth.Donotallowtheinsertto
remain in a static position on any one area of the tooth. Change
the insert’s path of motion.
 • Applyingpressure.Useextremelylightgraspandpressure,
especially on exposed cementum.
 • Ifsensitivitypersists,decreasepowersettingand/ormovefromthe
sensitive tooth to another and then return.

ENGLISH • 12
Section 10: System Care
10.1 Daily Maintenance
Start-Up Procedures at the beginning of the day (Cavitron®Select™
SPS™ Ultrasonic Scaler):
1. Open the manual shut-off valve on the dental office water
supply system.
2. Turn the System ON using the Power Control knob (see
illustrationinSection7).VerifythePowerIndicatorLight
is lighted.
3. Connect a freshly sterilized handpiece to its matching cable
connector. Set the Power Control knob to full power.
4. Set the Lavage Control on Handpiece to maximum.
5. Hold the Handpiece (without the Cavitron®Insert installed)
upright over a sink or drain. Activate the Foot Control and
flush the water line for at least 2 minutes.
6. Place a sterilized Cavitron®Insert into the Handpiece. Set
the Power and Lavage Control knobs to your preferred
operating position.
Start-Up Procedures at the beginning of the day (Cavitron®Select™
SPS™ Ultrasonic Scaler with Cavitron®Select™ Reservoir System):
1. Carefully lock Cavitron®Select™ Reservoir Bottle into
Cavitron®Select™ Reservoir Pump.
2. Fill Cavitron®Select™ Reservoir Bottle with tap, distilled
water, or medicament. Replace Cavitron®Select™ Bottle cap.
3. Connect Cavitron®Select™ Scaler to Cavitron®Select™
Reservoir Pump and Bottle (see Section 6 for complete
instructions).
4. Turn the System ON using the Power Control knob (see
illustrationinSection7).VerifythePowerIndicatorLight
is lighted.
5. Connect a freshly sterilized handpiece to its matching cable
connector. Set the Power Control knob to full power.
6. Set the Lavage Control on the Handpiece to maximum.
7. Hold the Handpiece (without the Cavitron®Insert installed)
upright over a sink or drain. Activate the Foot Control and
flush the water line for at least 2 minutes.
8. Place a sterilized Cavitron®Insert into the Handpiece. Set
the Lavage Control on the Handpiece and Power control
knobs to your preferred operating position.
Between Patients (Cavitron®Select™ SPS™ Ultrasonic Scaler):
1. Remove all ultrasonic inserts and handpiece used. Clean
and sterilize inserts and handpiece and clean and disinfect all
the surfaces of the cabinet, power cord, handpiece cable and
foot control and cable assembly as instructed in the Cavitron
Systems Infection Control Procedure booklet (#81158). To
maintain sterility of the Steri-Mate® handpiece, store it in
the steam sterilization pouch until needed.
2. Connect a freshly sterilized handpiece to its matching cable
connector. Hold the Handpiece over a sink or drain and
flush the water line of the unit as above at maximum water
flow for 30 seconds.
3. Place a freshly sterilized insert into the handpiece.
* NOTE: Water-based disinfection solutions are preferred. Some
alcohol-based disinfectant solutions may be harmful and may
discolor plastic materials.
Between Patients (Cavitron®Select™ SPS™ Ultrasonic Scaler with
Cavitron®Select™ Reservoir System):
1. Follow steps 1–2 listed in Between Patients (Cavitron®
Select™ SPS™ Ultrasonic Scaler).
2. With the power OFF, unscrew cap and fill Cavitron®Select™
Reservoir Bottle with tap, distilled water, or medicament.
3. Do not overfill Bottle with liquid into the neck of the Bottle.
Securely screw cap back on Bottle.
4. Place a freshly sterilized insert into the handpiece.
Shut-Down Procedures at the end of the day (Cavitron®Select™
SPS™ Ultrasonic Scaler):
1. Turn the System OFF.
2. Remove all ultrasonic inserts and handpiece used. Clean
and sterilize inserts and handpiece and clean and disinfect all
the surfaces of the cabinet, power cord, handpiece cable and
foot control and cable assembly as instructed in the Cavitron
Systems Infection Control Procedure booklet (#81158). To
maintain sterility of the Steri-Mate® handpiece, store it in
the steam sterilization pouch until needed.
3. Close the manual shut-off valve on the dental water supply
system.
Shut-Down Procedures at the end of the day (Cavitron®Select™
SPS™ Ultrasonic Scaler with Cavitron®Select™ Reservoir System):
1. Remove Cavitron®Insert from Handpiece.
2. Turn the System OFF.
3. Detach Cavitron®Select™ SPS™ Scaler from Reservoir
Pump and Bottle.
4. Detach Cavitron®Select™ Reservoir Bottle from Pump
(see Section 6 for complete instructions).
5. Empty entire contents of Cavitron®Select™ Reservoir Bottle.
6. Replace empty Cavitron®Select™ Reservoir Bottle to Pump.
7. Carefully lock Cavitron®Select™ Reservoir Bottle into
Cavitron®Select™ Reservoir Pump.
8. Connect Cavitron®Select™ SPS™ Scaler to Cavitron®
Select™ Reservoir System (see Section 6 for complete
instructions).
9. Turn unit ON.
10. Hold the Handpiece (without the Cavitron®Insert installed)
upright over a sink or drain.
11. To air purge the water line, activate foot control to operate
the Cavitron®Select™ SPS™ Scaler for at least 30 seconds.
(This will eliminate fluid to prevent it from settling in the
Cavitron®Select™ SPS™ System for extended periods of
time. This may also help decrease the chance of bio-film
formations in the Cavitron®Select™ SPS™ water lines.)
12. Follow steps 2–3 listed in Shut-Down Procedures at the end of
the day (Cavitron®Select™ SPS™ Ultrasonic Scaler).
It is recommended that you perform the following maintenance
procedures to help minimize bio-film formation in the lavage
path of your Cavitron Select SPS System which could affect the
lavage flow to the ultrasonic insert and scaling performance.

ENGLISH • 13
10.2 Weekly Maintenance: Cavitron®
Select™ SPS™ Ultrasonic Scaler with
Cavitron®Select™ Reservoir System
1. Remove Cavitron®Insert from Handpiece.
2. Turn the System OFF.
3. Detach Cavitron®Select™ SPS™ Scaler from
Reservoir System.
4. Detach Cavitron®Select™ Reservoir Bottle from Pump (see
Section 6 for complete instructions).
5. Empty entire contents of Cavitron®Select™ Reservoir Bottle.
6. Replace empty Cavitron®Select™ Reservoir Bottle to Pump.
7. Carefully lock Cavitron®Select™ Reservoir Bottle into
Cavitron®Select™ Reservoir Pump.
8. Connect Cavitron®Select™ SPS™ Scaler to Cavitron®
Select™ Reservoir System (see Section 6 for complete
instructions).
9. Turn the System ON.
10. Hold the Handpiece (without the Cavitron®Insert installed)
upright over a sink or drain.
11. To air purge the water line, operate the Cavitron®Select™
SPS™ Scaler for at least 30 seconds. (This will eliminate
fluid to prevent it from settling in the Cavitron®Select™
SPS™ Scaler for extended periods of time. This may also
help decrease the chance of bio-film formations in the
Cavitron®Select™ SPS™ water lines.)
12. Turn the System OFF.
13. Prepare a 1:10 hypochlorite (NaOCL) solution by mixing
1 part 5.25% sodium hypochlorite with 10 parts tap water.
14. Remove cap and pour this 1:10 solution into the Cavitron®
Select™ SPS™ Reservoir Bottle. Do not overfill with solu-
tion (see Section 3.3 for complete instructions).
15. Securely replace cap on Bottle.
16. Turn the System ON.
17. Hold the Handpiece (without the Cavitron®Insert installed)
upright over a sink or drain.
18. Operate the Cavitron®Select™ SPS™ Scaler for at least
10 seconds.
19. Turn the System OFF.
20. Leave the unit undisturbed for at least 10 minutes, BUT
FOR NO MORE THAN 30 MINUTES to allow sodium
hypochlorite solution to disinfect the system. As a suggestion,
place a sign which states that the System is being disinfected
and should not be used.
21. Unscrew cap and discard disinfectant solution.
22. Fill Cavitron®Select™ Reservoir Bottle with tap or distilled
water. Do not overfill with liquid (see Section 3.3 for
complete instructions).
23. Turn the System ON.
24. Operate the Cavitron®Select™ SPS™ Scaler for at least
60 seconds.
25. Turn off system. Detach Cavitron®Select™ SPS™ scaler
from Select™ Reservoir System.
26. Detach Cavitron®Select™ Reservoir Bottle from Pump
(see Section 6 for complete instructions).
27. Autoclave Cavitron®Select™ Reservoir Bottle.
NOTE: ALL CHEMICALS MUST BE FLUSHED FROM THE
SYSTEM BEFORE IT IS READY FOR PATIENT USE.
10.3 Water Line Filter Maintenance
When the water line filter becomes discolored, the filter should be
replaced to prevent reduced water flow to the Cavitron®Select™
SPS™ System. A 10-pack of replacement filters is available
by ordering Part Number 90158 from your local DENTSPLY®
distributor.
1. Disconnect the water supply hose from the water source. If
a quick-disconnect connector is attached to the end of the
hose, relieve the water pressure by pressing the tip of the
connector in an appropriate container and drain the water.
2. Grasp the fittings on either side of the filter disk and twist
counterclockwise. Remove the filter section from either side
of the water hose.
3. Install the replacement filter onto the water hose fittings.
The filter should be positioned to match up with the correct
hose fitting.
4. Hand tighten the two hose fittings in a clockwise direction.
Reconnect the water supply hose, operate the unit to bleed
the air and test for leaks.
10.4 Pump Lavage Filter Maintenan ce
When the pump lavage filter becomes discolored, the filter should
be replaced to prevent reduced water flow to the Cavitron®
Select™ SPS™ System. A 10-pack of replacement filters is
available by ordering Part Number 90191 from your local
DENTSPLY®distributor.
1. Empty the contents of the Cavitron®Select™ Reservoir
bottle and disconnect it from the pump.
2. Remove the old filter and discard.
3. Insert the small end of the new filter until filter is seated.
10.5 O-Ring Maintenance
Before placing Cavitron®Inserts into the handpiece, performing
the following steps will increase the O-ring life on Cavitron®
Inserts:
•Fillentirehandpiecewithwater.
•LubricateO-ring(blackorgreenrubbermaterial)withwater.
•Gentlytwisttheinsertdownintothehandpieceuntiltheinsert
is fully seated in place.
Section 10: System Care cont'd

ENGLISH • 14
Section 11: Troubleshooting
Although service and repair of the Cavitron®Select™ SPS™
should be performed by DENTSPLY®personnel, the following
are some basic trouble shooting procedures that will help avoid
unnecessary service calls. Generally, check all lines and connections
to and from the System, a loose plug or connection will often
create problems. Check the settings on the System’s knobs.
11.1 Troubleshooting Guide
System will not operate:
(Power Indicator Light is not lighted.)
1. Check that the Power Control knob is in the ON position,
and that the detachable Power Cord is fully seated in the
receptacle on back of the Cavitron® Select™ SPS™ System.
2. Check that the System’s three-prong plug is fully seated in an
appropriate AC receptacle, and that AC current is present.
3. Check that the DC power plug is properly inserted into the
DC input located on the back of the System.
(Power Indicator Light is lighted.)
1. Check that the Foot Control Connector is fully seated in the
Foot Control Receptacle on the back of the System.
2. Check that the Handpiece Cable Assembly is fully seated in
the Handpiece Receptacle.
System operates:
(No lavage flow at insert tip.)
1. Assure that Lavage control is properly adjusted.
2. Check that irrigant supply control valve/s (dental office
water supply) are open.
3. Check that the Handpiece Cable Assembly is fully seated
in the Handpiece Receptacle.
4. Check to see if Water Line or Pump Lavage Filter is
discolored—if so, replace.
5. Check to assure that liquid is available in reservoir bottle.
11.2 Technical Support and Repairs
For technical support and assistance call 1-800-989-8826 Monday
through Friday, 8:00 AM to 5:00 PM (Eastern Time). For other
areas, contact your local DENTSPLY®representative.

ENGLISH • 15
Cavitron® Select™: 100-240 VAC Systems
Electrical Voltage 30 VDC +/- 5%
Current 2 amps DC Max
Frequency 50/60 Hertz
Water Pressure 20 – 40 psig
Flow Rate Minimum setting (CCW) 0 – 15 ml/min
Maximum setting (CW) >45 ml/min
Weight 425 g / 15 oz.
Dimensions Height: 2.4 in.
Width: 3-1/8 in.
Depth: 7 1/2 in.
Handpiece Cable: 72 in.
Foot Control Cable: 72 in.
Power Cord: 2 m
Water Supply Line: 96 in.
Cavitron® Select™ Power Supply (674022001):
Electrical Voltage 100 – 240 VAC
Current 1,6 amps Max @ 100 – 240 VAC
Insulation Requirement Reinforce
Frequency 47 – 63 Hertz
Weight 550 g / 19.4 oz. Max
Dimensions Height: 14,3 cm / 5.7 in.
Width: 7,6 cm / 3.0 in.
Depth: 14,3 cm / 5.7 in.
Power Cord: 213 cm / 84 in.
Footswitch Not for operating theatres
Protection Class IPX1
Cavitron® Select™ Reservoir Pump:
Electrical Voltage 30 VDC +/- 5%
Pump Pressure 15 – 19 psig
Flow Rate 40 ml/min
Weight 513 g / 18 oz.
Dimensions Height: 10,2 cm / 4.0 in.
Width: 8,4 cm / 3.3 in.
Length: 30 cm / 11.8 in.
Operating Environment:
Temperature: 15 to 40 Deg. Celsius
Relative Humidity: 30% to 75% (non-condensing)
Transport and Storage Conditions:
Temperature: 0 to 70 Deg. Celsius
Relative Humidity: 10% to 95% (non-condensing)
Atmospheric Pressure: 500 to 1060 hPa
Section 12: Specications
Section 13: Classications
• Type of protection against electric shock: Class 1
• Degree of protection against electric shock: Type B
• Degree of protection against the harmful ingress of water: Ordinary
• Mode of operation: Continuous
• Degree of safety of application in the presence of a ammable Equipment not suitable for use in the presence
anaesthetic mixture with air or with oxygen or nitrous oxide: of flammable anesthetics or oxygen.
• According to medical device directive: IIA (rule 9)
Section 14: Disposal of Unit
• Accordance with local and state laws.
TYPE B EQUIPMENT
FOOTSWITCH
DIRECT CURRENT
REFER TO INSTRUCTION
MANUAL FOR INFORMATION
Symbology

ENGLISH • 16

DEUTSCH • 17
Cavitron®Select-™ SPS™ Ultraschall-Zahnsteinentfernungsgerät mit Cavitron®Select™ -Reservoirsystem
Einführung
Gebrauchsanweisung
Bitte vor Inbetriebnahme des Geräts sorgfältig und
vollständig durchlesen.
DENTSPLY®Professional ist ISO9001-zertifiziert. Nur in Übere-
instimmungmitVorschriftUL2601-11undCAN/CSAC22.2
Nr. 601.1 ist das Cavitron®Select-System im Hinblick auf Elektroschock,
Feuergefahr und mechanische Gefahr von Underwriters Laboratories Inc.
klassifiziert.
Die Funktionsweise des Zahnsteinentfernungssystems beruht darauf, daß
gewöhnlicher Haushaltswechselstrom in Hochfrequenzstrom umgewandelt
wird. Das Ultraschallgerät besteht aus zwei Teilen: einem Einsatzstück
und dem -Elektroniksystem SPS™ (Sustained Performance System™). Das
System enthält zwei geschlossene Regelschleifen. Eine Schleife bewirkt die
automatische Einstellung (die Betriebsfrequenz wird so eingestellt, daß
bei jedem Einsatzstück Resonanz erzeugt wird), während die zweite
Schleife automatisch die Bewegung der Spitze bei unterschiedlichen
Betriebsbedingungen steuert. Das Zahnsteinentfernungsgerät erzeugt
pro Sekunde 30.000 mikroskopisch kleine Hubbewegungen an der Arbe-
itsspitzedesEinsatzstücks.InVerbindungmitdenakustischenEffekten
des Kühlwassers wird dadurch eine synergistische Wirkung erzeugt, die
bei außergewöhnlichem Komfort für Anwender und Patient selbst stärkste
Zahnsteinablagerungen mit Leichtigkeit entfernt.
Die Reservoirsystem für das Cavitron®Select™SPS™ist ein wahlweise
verwendbares Spülflußabgabegerät. Die Stecker von Fußschalter, Hand-
stück, Wasserschlauch und Netzkabel werden vor Anschluß der Reservoir-
system vom Zahnsteinentfernungsgerät abgezogen. Das Zahnsteinentfer-
nungsgerät wird mit der Reservoirsystem verbunden. Die Stecker von
Fußschalter und Handstück sowie der Netzstecker werden in die ent-
sprechenden Buchsen auf der Rückseite der Reservoirsystem eingesteckt.
DieVerbindungenzwischendenGeräteteilenfürdasUltraschallsignal,
den Fußschalter und den Gleichstrom werden über ein Leiterkarten-
Steckverbindungsstück an der Rückseite des Zahnsteinentfernungsgeräts
undanderVorderseitedesPumpenmodulshergestellt.DasReservoirhat
eine Kapazität von 450 ml. Flüssigkeit wird aus dem Reservoir mit durch
eine interne Membranpumpe erzeugter Druckluft von 15–19 psig (103 –
131 kPa) ausgestoßen. EIN/AUS (ON/OFF) des Spülflusses wird durch
ein internes Magnetventil geregelt. Die Flüssigkeit zum Handstück fließt
direktausderReservoirsystemzumHandstück.BeiVerwendungmit
diesem Zubehörteil fließt keine Flüssigkeit durch das Cavitron® Select™
SPS™. Der Spülfluß durch die Einsatzstücke im Handstück beträgt mehr
als 40 ccm/min. Wasser, wenn maximaler Spülfluß eingestellt wurde.
Technische Unterstützung
Für technische Unterstützung und Reparaturhilfe außerhalb der U.S.A.
wenden Sie sich bitte an Ihren zuständigen DENTSPLY® Cavitron®-
Vertreter.
Zubehör und Ersatzteile
Zur Bestellung von Zubehör oder Ersatzteilen außerhalb der U.S.A.
wenden Sie sich bitte an Ihren zuständigen DENTSPLY®-Vertreter.
Achtung: Dieses Produkt darf nur von Zahnärzten bzw. auf zahnärztliche
Anordnung verkauft werden.
Cavitron®Select-™ SPS™
Ultraschall-Zahnsteinentfernungsgerät
Cavitron®Select-™ SPS™
Ultraschall-
Zahnsteinentfernungsgerät mit
Cavitron®Select™-Reservoirsystem
DEUTSCH

DEUTSCH • 18
Kapitel Titel Seiten
Nummer Inhaltsbeschreibung Zahl
1 IndikationenzurVerwendung..........................................................................................................................................19
2 Kontraindikationen und Warnhinweise ...........................................................................................................................19
2.1 Kontraindikationen
2.2 Warnhinweise
 3 Vorsichtsmaßnahmen ......................................................................................................................................................19
   3.1 VorsichtsmaßnahmenfüralleSysteme
   3.2 VorsichtsmaßnahmenfürprophylaktischeUltraschallverfahren
   3.3 VorsichtsmaßnahmenfürdieCavitron®Select-Reservoirsystem
4 Infektionskontrolle ..........................................................................................................................................................20
4.1 Allgemeine Empfehlungen zur Infektionskontrolle
4.2 Empfehlungen zur Wasserversorgung
5 Installationsanweisungen für das Cavitron®Select™ SPS™-Ultraschall-Zahnsteinentfernungsgerät .............................. 20-21
5.1 Allgemeine Informationen
5.2 Bedingungen für den Wasseranschluß
5.3 Bedingungen für die Stromversorgung
5.4 Auspacken des Systems
5.5 Stromkabel/Stromanschluß
5.6 Anschluß des Fußkontrollschalters
5.7 Anschluß der Wasserversorgungsleitung
5.8 Anschluß der Kabeleinheit des abnehmbaren Handstücks zur Spülflußregulierung
6 Installationsanweisung für das Cavitron®Select™ SPS™-Zahnsteinentfernungsgerät mit Cavitron®
Select-Reservoirsystem................................................................................................................................................ 22-23
6.1 Allgemeine Informationen
6.2 Bedingungen für die Stromversorgung
6.3 Auspacken des Systems
6.4 Aufbau des Systems
6.5 Stromkabel/Stromanschluß
6.6 Anschluß des Fußschalters
6.7 Anschluß der Kabeleinheit des abnehmbaren Handstücks zur Spülflußregulierung
7 Beschreibung des Cavitron®Select™-SPS™ Ultraschall-Zahnsteinentfernungsgeräts .................................................... 24-26
7.1 Systemregler: Cavitron®Select™SPS™-Ultraschall-Zahnsteinentfernungsgerät
7.2 Systemregler: Cavitron®Select™ SPS™-Zahnsteinentfernungsgerät mit Cavitron®Select™-Reservoirsystem
7.3 Handstück
7.4 Cavitron®30K™-Ultraschall-Einsätze
7.5 Informationen zum Fußschalter und dessen Betrieb
8 Zubehör ......................................................................................................................................................................26
8.1 Zubehörliste
8.2 Arzneimittel
 9 HinweisezurVerwendung ...............................................................................................................................................27
9.1 Lagestellung des Patienten
9.2 Durchführung von Ultraschallverfahren zur Zahnsteinentfernung
9.3 Komfort des Patienten
10 Gerätepflege............................................................................................................................................................... 28-29
10.1 Tägliche Wartung — Einschaltverfahren, Zwischen Patienten, Abschaltverfahren
10.2 Wöchentliche Wartung
10.3 Wasserleitungsfilter
10.4 Wartung des Pumpen-Irrigationsfilters
11 Informationen zur Infektionskontrolle.............................................................................................................................30
12 Fehlersuche......................................................................................................................................................................31
11.1 Hinweise zur Fehlersuche
11.2 Technische Unterstützung und Reparaturen
13 Technische Daten ............................................................................................................................................................31
14 Klassifizierung..................................................................................................................................................................31
Inhaltsverzeichnis

DEUTSCH • 19
Kapitel 1: Indikationen zur Verwendung
Kapitel 2: Kontraindikationen und Warnhinweise
Kapitel 3: Vorsichtsmaßnahmen
3.1 Vorsichtsmaßnahmen für alle Systeme
 •UmeinoptimalesErgebniszuerzielen,solltennurvon
der DENTSPLY®Professional-Abteilung hergestellte
Cavitron®-Einsatzstücke verwendet werden.
 • GerätnichtaufeinenHeizkörperodereineandereWärmequelle
stellen oder in deren Nähe aufstellen. Übermäßige Wärme kann
die elektronischen Bauteile des Geräts beschädigen. Gerät so
aufstellen, daß an allen Seiten und von unten her uneinge-
schränkte Luftzirkulation möglich ist.
 •DasGerätisttragbar,mußjedochbeimTransportmit
Vorsichtgehandhabtwerden.
 •DasDurchspülenderAusrüstungunddieWartung
des Wasserversorgungssystems der Zahnarztpraxis werden
ausdrücklich empfohlen. Siehe Wasserversorgung in
Kapitel 10: Gerätepflege.
 •AmAbendmußvordemVerlassenderPraxisdas
Absperrventil des Systems geschlossen werden
 •DenZahnsteinentfernerunterkeinenUmständeneinsetzen,
wenn keine Flüssigkeit durch das Handstück fließt.
3.2 Vorsichtsmaßnahmen für prophylaktische
Ultraschallverfahren
 •EbensowieeineZahnbürstenutzensichdieUltraschall-
EinsatzstückedurchVerwendungab.Einsätzemitnur2
mm Abnutzung verlieren etwa 50% ihrer Wirksamkeit
bei der Zahnsteinentfernung. Im allgemeinen wird emp-
fohlen, Einsätze zu verwerfen und zu ersetzen, sobald eine
Abnutzung von 2 mm eingetreten ist, um eine optimale
Wirksamkeit beizubehalten und den Bruch des Einsatzes
zu vermeiden.
 •FallsübermäßigeAbnutzungbeobachtetwirdoderder
Einsatz verbogen, verformt oder anderweitig beschädigt ist,
ist er sofort zu verwerfen.
2.1 Kontraindikationen
 •Ultraschallgerätedürfennichtbeirestaurativenzahn-
medizinischenVerfahrenverwendetwerden,bei
denen es zur Kondensation von Amalgam kommt.
2.2 Warnhinweise
 •PersonenmitHerzschrittmachern,Debrillatorenund
anderen aktiven, implantierten, medizinischen Geräten, sind
darauf hingewiesen worden, daß bestimmte Arten elek-
Ultraschallverfahren:
 • alleallgemeinenAnwendungendersupra-undsubgingivalen
Zahnsteinentfernung
 • periodontalesDébridementbeiallenArtenperiodontaler
Erkrankungen
tronischerVorrichtungendenBetriebdieserGerätestorën
konnën.ObwohlDENTSPLYnochnieeinFallvoneleck-
tronischer Interferenz mitgeteilt wurde, empfehlen wir, daß
dasHandstückunddieKabelwährendderVerwendung
wenigstens 15 bis 23 cm (6-9 Zoll) von dem Gerät und
seinen Anschlüssen ferngehalten werden.
•AufdemMarktwirdeineVielzahlvonHerzschrittmachern
und anderen medizinischen, implantierbaren Geräten ange-
boten. Daher sollte das behandelnde Personal vom Her-
steller oder vom zuständigen Arzt des Patienten genauere
Inforationen über das jeweilige Gerät einholen.
 • SpitzenvonUltraschall-Einsätzen,dieverbogen,beschädigt
oderverformtwordensind,könnenwährendderVerwendung
brechen und müssen sofort verworfen und ersetzt werden.
 •WirddasEinsatzstückindenMunddesPatientengebracht,
müssen die Lippen, die Wangen und die Zunge zurückgezo-
gen werden, um ihren Kontakt mit dem Einsatzstück zu
vermeiden.
 •DasDentsply-NetzteilimLieferumfangdieserEinheitist
für den Gebrauch mit Geräten zugelasssen und muß beim
Betrieb des Systems verwendet werden.
3.3 Vorsichtsmaßnahmen für die Cavitron®
Select-Reservoirsystem
 • GerätnichtaufeinenHeizkörperodereineandereWärmequelle
stellen oder in deren Nähe aufstellen. Übermäßige Wärme kann
die elektronischen Bauteile des Geräts beschädigen. Gerät so
aufstellen, daß an allen Seiten und von unten her uneinge-
schränkte Luftzirkulation möglich ist.
 •DasGerätisttragbar,mußjedochbeimTransportmit
Vorsichtgehandhabtwerden.
 •DasDurchspülenderAusrüstungunddieWartungdes
Wasserversorgungssystems der Zahnarztpraxis werden
ausdrücklich empfohlen. Siehe Kapitel 10: Gerätepflege.
 • FlüssigkeitindieÖffnungimDeckeldesReservoirsgießen.
Um ein evtl. Austreten von Flüssigkeit zu vermeiden, sollte
das Reservoir nicht bis in den Flaschenhals hinein überfüllt
werden. Stellen Sie sicher, daß der Deckel fest verschlossen ist.
 • GerätvordemNachfüllendesReservoirsabschalten,umein
evtl. Austreten von Flüssigkeit zu verhindern. Deckel um
90 Grad drehen, um den Luftdruck entweichen zu lassen.
Anschließend den Deckel ganz entfernen.
 • endodontischeVerfahren
• Für Patienten mit bekannter Empfindlichkeit gegen
Ultraschall.

DEUTSCH • 20
Kapitel 5: Installationsanweisungen für das Cavitron®
Select™ -SPS™ Ultraschall-Zahnsteinentfernungsgerät
5.1 Allgemeine Informationen
Wird die Installierung Ihres DENTSPLY®Cavitron®Select™ SPS™
-ZahnsteinentfernungsgerätsnichtvongeschultemVertriebspersonal
von DENTSPLY®Cavitron®durchgeführt, ist darauf zu achten, daß
die folgenden Anforderungen und Empfehlungen eingehalten werden.
5.2 Bedingungen für den Wasseranschluß
• DerDruckinderWassereingangsleitungzumZahnsteinent-
fernungsgerät muß zwischen mindestens 40 psi (276 kPa)
und höchstens 40 psi (276kPa) liegen. Ist der Druck in der
Wasserversorgungsleitung Ihrer zahnärztlichen Praxis höher
als 40 psi (276 kPa), ist die Installierung eines Wasser-
druckreglers in der Leitung zum Cavitron®Select™ SPS™ -
Zahnsteinentfernungsgerät angeraten.
• DieWasserversorgungsleitungzurZahnarztpraxissolltemit
einem manuellen Absperrventil ausgerüstet sein, damit das
Wasser vollständig abgedreht werden kann, wenn sich
niemand in der Praxis aufhält.
• NachAbschlußdervorstehendbeschriebenenInstallierun-
gen am Wasserversorgungssystem der Zahnarztpraxis ist die
Wasserleitung gründlich durchzuspülen, bevor sie an das
Zahnsteinentfernungsgerät angeschlossen wird.
Kapitel 4: Infektionskontrolle
4.1 Allgemeine Empfehlungen zur
Infektionskontrolle
 • WiebeiallenzahnmedizinischenVerfahrenist
standardmäßige Schutzausrüstung zu verwenden (d.h.
Gesichtsmaske und Augenschutz oder Gesichtsabdeckung,
Gummihandschuhe und Schutzkleidung tragen).
 • ZurGewährleistungoptimalerSicherheitfürdenAnwender
und den Patienten befolgen Sie bitte die Anweisungen
zur Infektionskontrolle im Cavitron Infektions kontrolle-
Handbuch (Bestellnr. 81158), das Sie mit Ihrem Gerät
erhalten haben.
 • WiebeihochtourigenHandstückenundanderenzahn-
medizinischenVorrichtungenerzeugtdieKombinationaus
Wasser und Ultraschallschwingungen Ihres DENTSPLY®
Cavitron®Select™ SPS™ -Zahnsteinentfernungsgeräts Aero-
sole. Bei korrekter Arbeitsweise kann der Großteil der
Aerosoldispersion des DENTSPLY®Cavitron®Select™ SPS™
-Zahnsteinentfernungsgeräts wirksam kontrolliert und auf
ein Minimum reduziert werden. Bitte halten Sie die in
diesemHandbuchangegebenenVerfahrensrichtlinienzur
Benutzung Ihres Geräts sorgfältig ein.
4.2 Empfehlungen zur Wasserversorgung
Es wird nachdrücklich empfohlen, daß alle Wasserversorgungssysteme
in der zahnärztlichen Praxis den geltenden Normen der CDC (U.S.
Centers for Disease Control and Prevention) und ADA (American
Dental Association) entsprechen und daß sämtliche Empfehlungen
bezüglichderSpülung,derchemischenSpülungundderVerfahrenzur
Infektionskontrolle eingehalten werden.
5.3 Bedingungen für die Stromversorgung
Siehe Kapitel 12: Technische Daten
5.4 Auspacken des Systems
Packen Sie Ihr DENTSPLY®Cavitron®Select™ SPS™-
Zahnsteinentfernungsgerät vorsichtig aus und überprüfen Sie,
daß alle Bauteile und sämtliches Zubehör vorhanden sind:
1. Cavitron®Select™ SPS™-Zahnsteinentfernungsgerät.
2. Abnehmbares Netzkabel-Set.
3. Sterimate abnehmbares und sterilisierbares Cavitron®
Select-Handstück.
4. Steri-Mate Flusssteuerung – Abnehmbares Handstück und
Kabel mit Drehvorrichtung
5. 2-Stufen-Fußkontrollschalter.
6. Schlauch/Filter/Schnelltrennverschluß.
7. Wasserleitungsfilter.
8. Zusätzlicher Pumpen-Irrigationsfilter.
9. Für medizinische Zwecke zugelassenes Netzteil.
10. Paket mit Referenzmaterial.