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GENERAL INFORMATION
DEFINITION OF SYMBOLS
The following symbols and terms may be used
throughout this manual:
WARNING: Failure to carefully follow the
described procedure may result in damage
to the equipment and/or injury to the patient/
operator.
Risk of electrical shock present. Make sure
power is disconnected before attempting this
procedure.
See operating instructions.
(AC) Alternating current.
Protective earth (Ground)
Manufacturing Date
Waste Electrical and Electronic Equipment.
Type B Applied part.
Conforms with the Essential Requirements of
the European Medical Device Directive 93/42/
EEC for Class I Devices.
Conforms with the Essential Requirements of
the European Medical Device Directive 93/42/
EEC for Class IIa Devices.
0473
Indicates conformity to General Requirements
for Safety is certified by Intertek Testing Ser-
vices.
General mandatory action required, important to
follow instruction. Not a caution.
Warning, strong magnetic field.
Authorized European Representative:
Medical Device and QA Services
76, Stockport Road
Timperley, Cheshire, WA15 7SN
United Kingdom
e-mail: info@mdqas.com
2
PRODUCT DISPOSAL
Contact your local authorized dealer for proper
disposal of the device to ensure compliance with your
local environmental regulations.
INTERFERENCE WITH ELECTROMEDICAL DEVICES
To guarantee the operational safety of electromedical
devices, it is recommended that the operation of mobile
radio telephones in the medical practice or hospital be
prohibited.
Strong EMI sources such as electro surgery units or
x-ray units may affect performance. If performance
problems occur, move the unit to another electrical circuit
or physical location .
INCOMPATIBLE UNITS OR ACCESSORIES
To guarantee the operational safety and function of this
device, the use of unapproved unit or accessories is not
advised. Doing so could result in potential hazard. Only
use authorized accessories and devices.
OBTAINING TECHNICAL LITERATURE
The manufacturer will make available on request circuit
diagrams, component parts lists, descriptions, calibration
instructions or other information that will assist technical
personnel to repair and replace serviceable items
STORAGE CONDITIONS:
-55°C to +50°C
10% to 90% Relative Humidity
WARNING: Only authorized service technicians
should attempt to service this equipment. Use
of other than authorized technicians will void
the warranty.
WARNING:
parts. All repairs should be performed by an
authorized dealer and/or their representatives.
WARNING:
use by trained dental/medical professionals
only.
Electrical Specifications
Volts
Cycles
115 VAC
60 HZ
230 VAC
50 HZ
All fuses are labeled at point of use. Replace
fuses only with type and rating as indicated.
IEC Medical Device Classification
Classification:
Type:
Operation Mode:
31064 R00
Use only original replacement
This product is intended for
Amps
8 A ~
4 A ~
1
B
Intermittent - 5% Duty Cycle
.
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