Operator's Manual
Table Of Contents
- 1. Introduction
- 1.1. Introduction
- 1.2. Safety Information
- 1.3. Device Description
- 1.4. Intended Purpose
- 1.5. BIS™ Advance Monitor System Indications and Contraindications
- 1.6. Patient Target Groups
- 1.7. Intended Users
- 1.8. Essential Performance
- 1.9. Adverse Events (Residual Risks)
- 1.10. The BIS™ Advance Parameters
- 1.11. Symbols
- 2. The BIS™ Advance Monitor — Equipment and Supplies
- 2.1. The BIS™ Advance System
- 2.2. Parts of the System
- 3. Installation and Preparation for Use
- 3.1. Operating Environment
- 3.2. Power Requirements and Battery Use
- 3.3. Battery Operation
- 3.4. Mounting the Docking Station
- 3.5. Preparing the Docking Station
- 3.6. Preparing the Monitor
- 3.7. Home Screen
- 3.8. Four-Channel Monitoring
- 3.9. Home Screen Trend Graphs
- 3.10. Home Screen Numeric Section
- 3.11. Home Screen Menus
- 3.12. Home Screen Options
- 3.13. Secondary Trend Selection
- 3.14. Home Screen Audio Alarm Settings
- 3.15. Settings and Maintenance
- 3.16. Info Options
- 3.17. Quick Reference Checklist
- 4. Operating the BIS™ Advance Monitoring System
- 4.1. Preparing for Operation
- 4.2. Cases
- 4.3. Alarms and Messages
- 4.4. Chart Data
- 4.5. Menu Map
- 4.6. Institutional Settings
- 5. Data Storage, Transfer, and Export
- 5.1. Cybersecurity and Data Integrity
- 5.2. Monitor Data Memory
- 5.3. BISx Data Memory
- 5.4. Types of Exported Data
- 5.5. Live Case Export
- 5.6. Saved Cases Export
- 5.7. Recording a Snapshot Event
- 5.8. BIS™ Saved Data Files
- 5.9. Logs Export
- 5.10. Viewing and Printing Saved Data in PDF Format
- 6. Service and Maintenance
- 6.1. Introduction
- 6.2. Servicing the BIS™ Advance Monitor
- 6.3. Battery Handling
- 6.4. Cleaning the BIS™ Advance Monitor
- 6.5. Instrument Identification
- 7. Diagnostics and Troubleshooting
- 7.1. Diagnostics
- 7.2. Troubleshooting
- 7.3. Administrator Mode
- 7.4. Demo Mode
- 7.5. Glossary
- 7.6. Specifications
- 7.6.1. General Specifications
- 7.6.2. Operating Environments
- 7.6.3. Power Supply
- 7.6.4. Battery Specifications
- 7.6.5. Controls and Connectors
- 7.6.6. Alarms
- 7.6.7. Display
- 7.6.8. Sound Pressure Data
- 7.6.9. BIS Specifications
- 7.6.10. EEG Specifications
- 7.6.11. BISx Module Specifications
- 7.6.12. Software/GUI Specifications
- 7.7. Electromagnetic Compatibility Specifications
- 7.8. Product Compliance
- 7.9. BIS™ Advance Components, Accessories, and Documentation
- 7.10. Warranty
- 7.11. Software License Agreement
Preparing the Monitor
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BIS™ Advance Monitor
patient’s skin may help the electrode
pass the sensor check.
The sensor check will determine if the sensor will pass the sensor check based on the
impedance of the electrodes and the ground electrode.
If the sensor passes the sensor check, monitoring will begin automatically. If the
sensor fails, monitoring will not begin. If the sensor does not pass the sensor check
process, check the functionality of the PIC cable by running a sensor check using a
Sensor Simulator. If the sensor check does not pass with the Sensor Simulator,
replace the PIC or the BISx module. If the sensor check passes with the Sensor
Simulator, replace the sensor with a new appropriate sensor. That sensor will then
undergo an automatic sensor check upon attachment. If it passes the sensor check,
monitoring will commence.
For the 2-channel system, the electrodes will be labeled as follows, starting from the
left-most electrode when viewing the sensor from the front: 1,2,4,3.
For the 4-channel system, the electrodes shall be labeled as follows, starting from the
left-most electrode when viewing the sensor from the front: LT, LE, G, C, RE, RT.
The user can determine if he wants to display the sensor check values or just a PASS,
HIGH, NOISE or POOR CONTACT indicator. By default, Display Sensor Check Values is
disabled, so PASS, HIGH, NOISE or POOR CONTACT will appear for each sensor
section. To enable sensor check values, reference 3.15.3.4 Sensor Check Values on page
134.
If the sensor is supported and impedance values are in the acceptable range, the
system shall display patient data based on the information collected by the sensor. If
there are issues that prevent the system from reading information from this sensor,
an on-screen message will display this information.