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•
Failure to follow the validated reprocessing
instructions provided may result in exposing
the patient to cytotoxic residuals and/or cross
contamination.
•
Air in handpiece may cause decreased stroke.
•
The frequency and decibel levels of sound emitted
by the device may impact individuals with auditory
sensitivity due to underlying conditions which may
include (but are not limited to) vestibular disorders.
7: Infection Control
7.1 General Infection Control
•
For operator and patient safety, follow the infection
control procedures detailed in the Infection Control
Information Booklet accompanying your System.
•
Dental devices that connect to air and waterlines,
such as high speed handpieces, ultrasonic scalers,
3-way air/water syringe and air polishing units
generate aerosols. Follow the procedural guidelines
in Section 10 of this manual to minimize aerosol
dispersion.
•
The objective of the following information is to
supplement published general guidelines for reducing
the potential for cross contamination when using
a Cavitron Select SPS System, Cavitron sterilizable
handpieces or reservoir bottles during routine dental
care. In the event any regulatory agency disagrees
with this information, the agency requirements take
precedence.
•
For Infection Control Procedures relating to Cavitron
ultrasonic inserts, refer to the procedures provided
with each instrument.
7.2 Water Supply Recommendations
•
It is highly recommended that all dental water
supply systems conform to applicable CDC (Centers
for Disease Control and Prevention) and ADA
(American Dental Association) standards, and that all
recommendations be followed in terms of flushing,
chemical flushing, and general infection control
procedures. See Sections 8.1 and 11.
•
As a medical device, this product must be installed
in accordance with applicable local, regional, and
national regulations, including guidelines for water
quality (e.g. drinking water). As an open water
system, such regulation may require this device to be
connected to a centralized water control device. The
Cavitron
®
Select Reservoir System may be installed to
allow this unit to operate as a closed water system.
8: Installation Instructions
Anyone installing a Cavitron Select SPS Ultrasonic Scaler should observe the following requirements and recommendations.
8.1 Waterline Requirements
8.2 Electrical Requirements
8.3 Unpacking the System
8.4 System Installation
English - 6
Cavitron Select SPS Ultrasonic Scaler with
Cavitron Select SPS Ultrasonic Scaler
Cavitron Select Reservoir System
• A water supply line with user-replaceable filter is supplied with your system. See Section 11
System Care for replacement instructions.
• Incoming water supply line pressure to the system must be 20 psi (138 kPa) to 40 psi (275
kPa). If your dental water system's supply line pressure is above 40 psi, install a water pres-
sure regulator on the water supply line to your Cavitron Select SPS Ultrasonic Scaler.
• A manual shut-off valve on the dental water system supply line should be used so that the
water can be completely shut-off when the office is unoccupied.
• In addition to the water filter supplied, it is recommended that a filter in the dental water
system supply line be installed so that any particulates in the water supply will be trapped
before reaching the Cavitron Select SPS Ultrasonic Scaler.
• After the above installations are completed on the dental water supply system, the dental
office waterline should be thoroughly flushed prior to connection to the Cavitron Select SPS
Ultrasonic Scaler.
• Incoming water temperature to the Cavitron Select SPS Ultrasonic Scaler should not exceed
25˚C (77˚F). If needed a device should be installed to maintain a temperature within this
specification, or a Cavitron Select Reservoir System attached to allow this system to be
operated as a closed water system.
• Incoming power to the system must be 100 volts AC to 240 volts AC, single phase 50/60 Hz
capable of supplying 1.0 amps.
• The system power should be supplied through the AC power cord provided with your sys-
tem.
• WARNING: To avoid risk of electric shock, this equipment must only be connected to a sup-
ply mains with protective earth.
Carefully unpack your unit and verify that all
Carefully unpack your unit and verify that all
components and accessories are included:
components and accessories are included:
1. Cavitron Select SPS Scaler.
1. Cavitron Select SPS Scaler.
2. Detachable AC Power Cord set.
2. Cavitron Select Reservoir Pump.
3. Steri-Mate Detachable Sterilizable Hand-
3. Cavitron Select Reservoir Bottle.
piece.
4. Detachable AC Power Cord set.
4. Steri-Mate Flow Control Detachable
5. Steri-Mate Detachable Sterilizable Hand-
Handpiece Cable Assembly with Swivel.
piece.
5. Dual Position Foot Control Assembly.
6. Steri-Mate Flow Control Detachable
6. Hose / Filter / Quick Disconnect Assem-
Handpiece Cable Assembly with Swivel.
bly.
7. Dual Position Foot Control Assembly.
7. Additional Waterline Filter.
8. Hose / Filter / Quick Disconnect Assem-
8. Additional Pump Lavage Filters.
bly.
9. Medically Approved Power Supply.
9. Additional Waterline Filter.
10. Literature Packet.
10. Additional Pump Lavage Filters.
11. Cavitron Ultrasonic Insert (quantity op-
11. Medically Approved Power Supply.
tional)
12. Literature Packet.
13. Cavitron Ultrasonic Insert (quantity op-
tional).
• The Cavitron Select SPS Ultrasonic Scaler is designed to rest on a level surface. Be sure unit
is stable and resting on four feet.
• The Cavitron Select SPS Ultrasonic Scaler should not be positioned such that access to the
power input and AC power cord are limited.
• Placing unit in direct sunlight may discolor plastic housing.
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