Intended Use; Technical Support; Supplies & Replacement Parts; Disposal Of Unit - DENTSPLY Cavitron SPS G90 Instrucciones Para El Uso

Intended Use

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.
Other applications specialties include Periodontics, Orthodontics,
and Endodontics.

Technical Support

For technical support and repair assistance in the U.S.,
SM
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

1.1 Ultrasonic Procedures

• All general supra and subgingival scaling applications.
• Periodontal debridement for all types of periodontal diseases.
• Endodontic procedures.
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