4
062044 R02
Electrical Specifications
Volts
Cycles Amps
115 VAC
60 HZ 8 A ~
230 VAC
50 HZ 4 A ~
IEC Medical Device Classification
Classification:
I
Type:
B
Operation Mode:
Intermittent - 5% Duty Cycle
0.5 min. ON
9.5 min OFF
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 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 units or accessories is not advised. Doing so could
result in potential hazard. Using accessory equipment not complying
with the equivalent safety requirements of this equipment may lead to
a reduced level of safety of the resulting system.
Connecting electrical equipment to multiple socket outlets effectively
leads to creating an ME SYSTEM, and can result in a reduced level
of safety. All configurations shall comply with the system standard IEC
60601-1-1 or IEC 60601-1:2005
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.
WaRnInG:
This product is intended for use by
trained dental/medical professionals only.
GeneRal InfoRMaTIon
storage and Transport
Temperature -68° F to 122° F (-55°C to +50°C)
Relative humidity 10% to 90%
Working environment
Ambient temperature 68° F to 76 °F (20°C to +25°C)
Relative humidity 20% to 60% non-condensing
Atmospheric pressure: 13.1 to 15.3 PSI
fusE
IDEnTITY
VOlTaGE
(Vac)
aMps
spEED
BRakInG
capacITY
f1, f2
250
12
fasT
acTInG
750@250V
f1*, f2*
250
6
fasT
acTInG
750@250V
F1*, F2* FOR 230VAC CHAIR
Definition of Symbols
The following symbols and terms may be used throughout this
manual and your equipment:
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.
Indicates conformity to General Requirements for
Safety is certified by Intertek Testing Services.
General mandatory action required, important to
follow instruction. Not a caution.
Warning, strong magnetic field.
Off
On
Light Switch
European Authorized Representative
USB Port
ETL CLASSIFIED
EC REP
Medical Device & QA Services Ltd.
76, Stockport Road,
Timperley.
Cheshire, WA15 7SN.
United Kingdom.
Tel: +44 (0) 845 527 5078 Fax: +44 (0) 161 903 9787
Email: info@ mdqas.com www.mdqas.com
EC REP
Medical Device & QA Services Ltd.
76, Stockport Road,
Timperley.
Cheshire, WA15 7SN.
United Kingdom.
Tel: +44 (0) 845 527 5078 Fax: +44 (0) 161 903 9787
Email: info@ mdqas.com www.mdqas.com
authorized Representative:
Kaltenbach & Voigt GmbH
Bismarckring 39
88400 Biberach
Germany
0413
Manufacturing Place
DENTAL ___ __VAC__A__HZ
Summary of Contents for SP18
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