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BIS VISTA - Technical Documentation; Instrument Identification

BIS VISTA
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SECTION 5 PREVENTIVE MAINTENANCE, CARE AND CLEANING
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5-7
The BIS VISTA Monitor has been certified by Underwriters Laboratories to comply with
IEC60601-1, as indicated on the labeling on the rear of the monitor.
5.3 Technical Documentation
The BIS VISTA Monitoring System is designed and manufactured using state-of-the-art
components and manufacturing processes. Field repair or customer repairs are therefore
limited by design to replacement of major component assemblies such as: the Patient
Interface Cable (PIC), BISx, the BIS VISTA Monitor itself, the battery, power supply and
pole clamp. Periodic software updates are possible via the USB-A port.
This BIS VISTA Operating Manual contains the maintenance and diagnostic
troubleshooting information necessary for customer qualified technical personnel to test and
replace those parts of the equipment that are replaceable by the customer. Aspect does not
authorize nor provide information to service or repair the internal components of the BIS
VISTA monitor or the BISx.
5.4 Instrument Identification
BIS VISTA Monitor
Monitor identification information is permanently marked on the rear panel. This
information includes instrument model and serial numbers, power ratings, cautions, and the
Aspect Medical Systems’ shipping address.
BISx
The BISx identification information is permanently marked on the rear panel of the BISx.
The information includes instrument model and serial numbers, patent numbers, cautions,
and the Aspect Medical Systems’ shipping address.
Software Revision Numbers
Software revision numbers are displayed in the Configuration Information screen.

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