Intended Use
This product is intended for installation into an existing dental
handpiece delivery system. The end users are dental professionals.
The devices are used to debride light to heavy calculus deposits from
the tooth and root surfaces. Other applications specialties include
Periodontics, Orthodontics, and Endodontics.
Technical Support
For technical support and repair assistance in the U.S.,
call a Cavitron Care
representative at 1-800-989-8826
SM
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 Professional 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
1.1 Ultrasonic procedures
The Dentsply® Cavitron® SPS Scaler System is designed for
use in general prophylaxis and periodontal treatments and other
areas of operative dentistry. It is used to debride light to heavy
calculus and plaque deposits from tooth and root surfaces.
Section 2: Contraindications
2.1 Contraindications
• Ultrasonic Systems should not be used for restorative
procedures involving condensation of amalgam.
Section 3: Warnings
3.1 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.
ENGLISH • 3