Table Of Contents; Indications For Use; Contraindications And Warnings - DENTSPLY Cavitron Select SPS Directions For Use Manual

Ultrasonic scaler
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  • ENGLISH, page 1

Table of Contents

Section
Section Title
Number
Description of Contents
1

Indications for use ........................................................................................................................................................................................... 3

2

Contraindications and Warnings ................................................................................................................................................................ 3

2.1
Contraindications
2.2
Warnings
3
Precautions......................................................................................................................................................................................................... 3
3.1
Precautions for All Systems
3.2
Precautions for Ultrasonic Prophylaxis Procedures
3.3
Precautions for Cavitron
®
Select™ Reservoir System
4
Infection Control .............................................................................................................................................................................................. 4
4.1
4.2
5
Installation Instructions for Cavitron
®
Select™ SPS™ Ultrasonic Scaler .................................................................................... 4–5
5.1
General Information
5.2
5.3
5.4
5.5
5.6
5.7
5.8
6
Installation Instructions for Cavitron
®
Select™ SPS™ Scaler with Cavitron
6.1
General Information
6.2
6.3
6.4
6.5
6.6
6.7
7
Cavitron
®
Select™ SPS™ Ultrasonic Scaler Description .................................................................................................................8–10
7.1
System Controls for Cavitron
®
SPS™ Select™ Ultrasonic Scaler
7.2
System Controls for Cavitron
®
Select™ SPS™ Scaler with Cavitron
7.3
7.4
Cavitron
30K
Ultrasonic Inserts
®
TM
7.5
Foot Control Information & Operation
8
Accessories .......................................................................................................................................................................................................11
8.1
8.2
9
Techniques For Use ........................................................................................................................................................................................11
9.1
9.2
9.3
10
System Care.............................................................................................................................................................................................. 12–13
10.1 Daily Maintenance — Start-Up Procedures, Between Patients, Shut-Down Procedures
10.2 Weekly Maintenance
11
Troubleshooting .............................................................................................................................................................................................14
12
Speciications ..................................................................................................................................................................................................15
13
Classiications ..................................................................................................................................................................................................15
14
Disposal Of Unit ..............................................................................................................................................................................................15
ENGLISH • 2
Page
Number
®
Select™ Reservoir System ......................... 6–7
®
Select™ Reservoir System
Section 1: Indications for Use
he 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 and Warnings
2.1 Contraindications
• Ultrasonic Systems should not be used for restorative dental
procedures involving the condensation of amalgam.
2.2 Warnings
• he 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, speciically 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 may
result in cross contamination.
• Persons itted with cardiac pacemakers, deibrillators
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.
here 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 speciic recommendations. his unit
complies with IEC 60601 Medical Device Standards.
• Insuicient water low could result in elevated water
and tip temperature. When operated at the input water
temperature speciied in the Water Line Requirements
Section 7.1 and with suicient water low, the water and
tip temperature should not exceed 50o C (122o F). Failure
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 low. 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. he Cavitron DualSelect system
can be attached to this unit and operated as a closed
system until the advisory is cancelled. When the
advisory is cancelled, lush all incoming waterlines
from the public water system (e.g. faucets, waterlines
and dental equipment) in accordance with the
manufacturer's instructions for a minimum of 5 minutes.
ENGLISH • 3

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