4
047655 r10
ELECTRICAL SPECIFICATIONS
All fuses are labeled at point of use. Replace
fuses only with type and rating as indicated.
Volts Cycles Amps
115 VAC 60 HZ 8 A ~
230 VAC 50 HZ 4 A ~
IEC Medical Device Classication
Classication: 1
Type: B
Operation Mode: Intermittent - 5% Duty Cycle
WARNING: Use only original replacement
parts. All repairs should be performed by an
authorized dealer and/or their representatives.
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 device 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.
DEFINITION OF SYMBOLS
The following symbols and terms are dened as follows:
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.
WARNING: This product is intended for use
by trained dental/medical professionals only.
Authorized European Representative:
Medical Device and QA Services
76, Stockport Road
Timperley, Cheshire, WA15 7SN
United Kingdom
e-mail: info@mdqas.com
GENERAL INFORMATION
See operating instructions.
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.
Indicates conformity to General Requirements for
Safety is certied by Intertek Testing Services.
General mandatory action required, important to fol-
low instruction. Not a caution.
Warning, strong magnetic eld.
(AC) Alternating current.
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.
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