Chapter 7
TECHNICAL SPECIFICATIONS
Compliance with International Standards
The KODAK 9000 3D digital imaging Unit is compliant with the International and EEC
standards.
Manufacturer
TROPHY
A subsidiary of Carestream Health, Inc.
4, Rue F. Pelloutier, Croissy-Beaubourg
77435 Marne la Vallée Cedex 2, France
Model
KODAK 9000 3D Unit, KODAK 9000 Unit.
Compliance with International Regulations
•
Medical Device directives 93/42/ European Economic Community (EEC), Class II b
•
ElectroMagnetic Compatibility (EMC) directive 89/336/EEC
Compliance with International Standards
•
International Electrotechnical Commission (IEC) 60601-1 Class I Type B
•
IEC 60601-1-2, Group I, Class B +12db
•
IEC 60601-1-3
•
IEC 60601-2-7
•
IEC 60601-1-28
Ambient Operating Conditions
•
Temperatures: 5 ~35 °C
•
Relative humidity: 30 ~ 85%
•
Atmospheric pressure: 700 ~ 1060 hpa
Storage Conditions
•
Temperatures: -10 ~ 60 °C
•
Relative humidity: 10 ~ 95%
•
Atmospheric pressure: 700 ~ 1060 hpa
Transport Conditions
•
Temperatures: -10 ~ 60 °C
•
Relative humidity: 10 ~ 95%
•
Atmospheric pressure: 700 ~ 1060 hpa
KODAK 9000 3D Extraoral Imaging System_User Guide (SM710)_Ed 01
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