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Site~Rite Vision* Ultrasound System
Technical Specifications
ESD
EN/IEC 61000-4-2
EFT
EN/IEC 61000-4-4
Surge
EN/IEC 61000-4-5
Voltage
Dips/Dropout
EN/IEC 61000-4-11
Power Frequency
50/60 Hz
Magnetic Field
EN/IEC 61000-4-8
±6kV Contact
±8kV Air
±2kV Mains
±1kV Input/Output Lines
±1kV Differential
±2kV Common
>95% Dip for 0.5 Cycle
60% Dip for 5 Cycles
30% Dip for 25 Cycles
>95% Dip for 5 Seconds
3 A/m
±6kV Contact
±8kV Air
±2kV Mains
±1kV Input/Output Lines
±1kV Differential
±2kV Common
>95% Dip for 0.5 Cycle
60% Dip for 5 Cycles
30% Dip for 25 Cycles
>95% Dip for 5 Seconds
3 A/m
Floors should be wood, concrete or
ceramic tile. If floors are synthetic,
the relative humidity should be at
least 30%.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the Site~Rite Vision* Ultrasound
System requires continued
operation during power mains
interruptions, it is recommended
that the Site~Rite Vision* Ultrasound
System be powered from an uninter-
ruptible power supply or battery.
Power frequency magnetic fields
should be that of a typical commer-
cial or hospital environment.
Immunity Test
Compliance Level
EN/IEC 60601 Test Level
Electromagnetic Environment
Guidance
The Site~Rite Vision* Ultrasound System is intended for use in the electromagnetic environment specified below.
The customer or user of the Site~Rite Vision* Ultrasound System should ensure that it is used in such an environment.
Guidance and Manufacturer’s Declaration – Immunity