Product Overview; Technical Support; Supplies & Replacement Parts; Indications For Use - DENTSPLY Cavitron Touch Directions For Use Manual

Ultrasonic scaling system
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CAUTION: United States Federal Law restricts this
device to sale by or on the order of, a licensed dental
professional.
For dental use only.

prOduCT OvErviEw

The Cavitron Touch™ Ultrasonic Scaling System offers an
advanced experience at your fingertips. The unit features a
modern touch screen interface for ease of use with added
memory presets and customizable power settings for
improved efficiency. The system also features a lightweight,
detachable handpiece cord for improved ergonomics.

TEChNiCAL SuppOrT

For technical support and repair assistance in the U.S., call
the DENTSPLY Cavitron Care Factory Certified Service at
1-800-989-8826, Monday through Friday, 8:00 A.M. to 5:00
P.M. (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 A.M. to 5:00 P.M. (Eastern
Time). For other areas, contact your local DENTSPLY
Representative.
SECTiON 1:

indications For use

USED FOR ULTRASONIC PROCEDURES:
• All general supra and subgingival scaling applications
• Periodontal debridement for all types of periodontal
diseases
SECTiON 2:

Contraindications

• Ultrasonic Systems should not be used for restorative
dental procedures involving the condensation of
amalgam.
• Not for use on children under the age of 3.
SECTiON 3: warnings
• The use of High Volume Saliva Evacuation to reduce
the quantity of aerosols released during treatment is
highly recommended.
• Prior to beginning treatment, patients should rinse with
an antimicrobial such as Chlorhexidine Gluconate 0.12%.
Rinsing with an antimicrobial reduces the chance of
infection and reduces the number of microorganisms
released in the form of aerosols during treatment.
• It is the responsibility of the Dental Healthcare
Professional to determine the appropriate uses of this
product and to understand:
– the health of each patient,
– the dental procedures being undertaken,
– and applicable industry and governmental agency
recommendations for infection control in dental
healthcare settings,
– requirements, and regulations for safe practice of
dentistry; and
– these Directions for Use in their entirety, including
Section 4 Precautions, Section 6 Infection Control, and
Section 10 System Care.
• Where asepsis is required or deemed appropriate in
the best professional judgment of the Dental Healthcare
Professional, this product should not be used, unless
used in combination with a sterile lavage kit (P/N 81340).
Handle Cavitron
insert with care. Improper handling of
®
insert, specifically the insert tip, may result in injury and/
or cross contamination.
Failure to follow properly validated sterilization processes
and approved aseptic techniques for Cavitron inserts or
handpieces may result in cross contamination.
• Persons fitted with cardiac pacemakers, defibrillators
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 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 specific recommendations. This unit
complies with IEC 60601 Medical Device Standards.
• Insufficient water flow could result in elevated water
and tip temperature. When operated at the input water
temperature specified in the Water Line Requirements
Section 7.1 and with sufficient water flow, the water and
tip temperature should not exceed 50
to follow recommendations for environmental operating
conditions, including input water temperature, could
result in injury to patients or users. If temperature
is elevated, increase water flow. If temperature remains
elevated, discontinue use.
• During boil-water advisories, this product should not
be operated as an open water system (e.g. connected
to a public water system). A Dental Healthcare
Professional should disconnect the system from the
central water source. The Cavitron DualSelect™ system
can be attached to this unit and operated as a closed
3
o
o
C (122
F). Failure
* data on file

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