Publicité
Les langues disponibles
Les langues disponibles
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., call a Cavitron CareSM representative at 1-800-
989-8826 Monday through Friday, 8:00 AM to 5:00
PM (Eastern Time). For other areas, visit www.
dentsplysirona.com/eifu and search "Cavitron Repair
Centers" or contact your local Dentsply Sirona
Representative.
Supplies & Replacement Parts
To order supplies and replacement parts in the U.S.,
contact your local 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
Sirona 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.
88016 Rev (0423)_ML.indd 3
88016 Rev (0423)_ML.indd 3
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 Sirona, 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
22-06-2023 13:06:05
22-06-2023 13:06:05
Publicité
