Product Overview; Technical Support; Disposal Of Unit; Indications For Use - DENTSPLY Cavitron G139 Instrucciones De Uso

Product Overview

This product is intended for installation into a dental system. The
end users are dental professionals. The devices are used to debride
light to heavy calculus deposits from the tooth and root surfaces.

Technical Support

For technical support and repair assistance in the U.S.,
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call a Cavitron Care representative at 1-800-989-8826 or
717-767-8502 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 and replacement parts in the U.S., contact your
local DENTSPLY distributor or call 1-800-989-8826 or
717-767-8502, Monday through Friday, 8:00 AM to 5:00 PM
(Eastern Time). For other areas, contact your local DENTSPLY
representative.

Disposal of Unit

Disposal of unit shall be in accordance with local regulations.
Caution: United States Federal Law restricts this device to sale by or
on the order of, a licensed dental professional.
Section 1: Indications for Use
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
procedures involving condensation of amalgam.
• Not for use on children under the age of 3.
Section 3: Warnings
• 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 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 specific
recommendations. This unit complies with IEC 60601 Medical
Device Standards.
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