Tabla De Contenido; Contraindications; Warnings - DENTSPLY Cavitron Select SPS Instrucciones Para El Uso

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 General Infection Control Recommendations
4.2 Water Supply Recommendations
5 Installation Instructions for Cavitron Select™ SPS™ Ultrasonic Scaler .............................................. 4-5
®
5.1 General Information
5.2 Water Line Requirements
5.3 Electrical Requirements
5.4 Unpacking the System
5.5 Power Cord/Power Connection
5.6 Foot Control Cable Assembly Connection
5.7 Water Supply Line Connection
5.8 Lavage Control Detachable Handpiece Cable Assembly Connection
6 Installation Instructions for Cavitron Select™ SPS™ Scaler with Cavitron
®
6.1 General Information
6.2 Electrical Requirements
6.3 Unpacking the System
6.4 Assembling the System
6.5 Power Cord/Power Connection
6.6 Foot Control Cable Assembly Connection
6.7 Lavage Control Detachable Handpiece Cable Assembly Connection
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 Handpiece
7.4 Cavitron 30K Ultrasonic Inserts
® TM
7.5 Foot Control Information & Operation
8 Accessories ................................................................................................................................................ 11
8.1 Accessories List
8.2 Medicaments
9 Techniques for Use..................................................................................................................................... 11
9.1 Patient Positioning
9.2 Performing Ultrasonic Scaling Procedures
9.3 Patient Comfort Considerations
10 System Care ......................................................................................................................................... 12-13
10.1 Daily Maintenance - Start-Up Procedures, Between Patients, Shut-Down Procedures
10.2 Weekly Maintenance
10.3 Water Line Filter Maintenance
10.4 Pump Lavage Filter Maintenance
11 Troubleshooting .......................................................................................................................................... 14
11.1 Troubleshooting Guide
11.2 Technical Support and Repairs
12 Specifications ............................................................................................................................................. 15
13 Classifications ............................................................................................................................................ 15
14 Disposal of Unit .......................................................................................................................................... 15
ENGLISH • 2
Page
Number
Select™ Reservoir System 6-7
®
Select™ Reservoir System
®
Section 1: Indications for Use
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 and Warnings

2.1 Contraindications

• Ultrasonic Systems should not be used for restorative dental
procedures involving the condensation of amalgam.

2.2 Warnings

• The 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, specifically 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 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 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.
• Insufficient water flow could result in elevated water
and tip temperature. When operated at the input water
temperature specified in the Water Line Requirements
Section 7.1 and with sufficient water flow, 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 flow. 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. The 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, flush 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