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According to the "IEC60601-1-1:2000", devices installed in the patient environment are
restricted to "electric medical devices conforming to IEC60601-1".
The Control PC, operation unit, and the magnetic card reader, etc. options that are parts of the
CXDI-C3S are classified under the data processing device standard (IEC60950), therefore these
items should not be installed in the patient environment. Otherwise the Control PC is only
classified in CXDI-C3S.
The patient environment described below is an example cited from the "IEC60601-1-1:2000" –
the measurements are only guidelines. However, the "IEC60601-1-1:2000" example must be
treated as the standard.
Therefore, the CXDI-C3S must be installed in a location further than the measurements below
(outside of the patient environment).
*Areas where the patient moves (not only during imaging but when entering and leaving
the room, etc.) are also considered as part of the patient environment, therefore the
installation location should be determined upon consultation with the user regarding
areas outside of the patient environment.
Example of patient environment
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Note: The measurements are only guidelines.
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