Operator's Manual
Table Of Contents
- About This Manual
- Product Description, Features and Indications for Use
- Safety Information, Warnings and Cautions
- Chapter 1: Technology Overview
- Signal Extraction Technology® (SET®)
- rainbow Pulse CO-Oximetry Technology
- Pulse CO-Oximetry vs. Drawn Whole Blood Measurements
- General Description for Total Hemoglobin (SpHb)
- General Description for Total Arterial Oxygen Content (CaO2)
- General Description for SpOC
- General Description for Carboxyhemoglobin (SpCO)
- General Description for Methemoglobin (SpMet)
- General Description for Respiration Rate (RRp)
- General Description for Oxygen Reserve Index (ORi)
- SpCO, SpMet, and SpHb Measurements During Patient Motion
- rainbow Acoustic Monitoring™ (RAM™)
- Chapter 2: Description
- Chapter 3: Setting Up
- Chapter 4: Operation
- Using the Touchscreen and Home Button
- About the Main Screen
- About the System Status Light
- Accessing Main Menu Options
- rainbow Parameter Settings
- Parameter Settings
- Temperature Settings
- Noninvasive Blood Pressure (NIBP) Settings
- NomoLine Capnography Settings
- Sounds
- Device Settings
- About
- Trends
- Call
- Rad-97 Screenshot Capture
- Patient Admit/Discharge
- EMR Push
- Chapter 5: Profiles
- Chapter 6: Temperature
- Chapter 7: Noninvasive Blood Pressure (NIBP)
- Chapter 8: NomoLine Capnography
- Chapter 9: Video Conferencing
- Chapter 10: Admit to and Discharge from Patient SafetyNet
- Chapter 11: Electronic Medical Records (EMR) Push
- Chapter 12: Third-Party Devices
- Chapter 13: Alarms and Messages
- Chapter 14: Troubleshooting
- Chapter 15: Specifications
- Pulse CO-Oximetry Specifications
- Temperature Specifications
- Noninvasive Blood Pressure (NIBP) Specifications
- NomoLine Capnography Specifications
- Electrical
- Environmental
- Physical Characteristics
- Alarms
- Display Indicators
- Compliance
- Connectors
- Wireless Specifications
- Guidance and Manufacturer's Declaration-Electromagnetic Emissions
- Guidance and Manufacturer's Declaration-Electromagnetic Immunity
- Recommended Separation Distances
- Symbols
- Citations
- Chapter 16: Service and Maintenance
- Appendix: Concepts of Alarm Response Delay
- Index
Rad-97 Chapter 16: Service and Maintenance
www.masimo.com 208 Masimo
7. Calibration is completed.
Span Point Calibration
Note: This section is provided as a reference and intended for qualified service professionals
only.
Calibration Steps
1. Enter NIBP menu and select "Calibration".
2. Enter password: 4258 and select "Span Point Calibration".
3. Connect a manometer, volume and the hand bulb to the Module using "T" adapters
and connection tubing.
4. Apply 250 mmHg to the module.
5. Touch the "Calibrate" to start the span point calibration.
6. Results are displayed for Span Point Calibration.
7. Calibration is completed.
Overpressure Test
Note: This section is provided as a reference and intended for qualified service professionals
only.
Note: This test is performed from the Main Screen.
Pass Criteria
International standards for automated NIBP devices require that the pressure must not
exceed 300 mmHg on adults and pediatric patients and 150 mmHg on neonatal patients
with a tolerance of 10% for 15 seconds or greater than 10% for 3 seconds. The overpressure
pass criteria for the Advantage module are:
Adults, Pediatrics 300 ± 10mmHg
Neonates 150 ± 5mmHg
Test Method
The steps outlined below are for manually performing an overpressure test. Some or all of
these steps may be incorporated into a service tool provided by the medical device
manufacturer.
1. Set the corresponding patient profile. See Chapter 5: Profiles on page 117.
2. Perform an NiBP measurement.
3. Connect a manometer, volume and hand bulb to Module using "T" adapters.
4. From the Main Screen, touch the Start NIBP measurement button.
5. Touch the "Test" button on the display.
6. Increase the pressure to approximately 250mmHg using the hand bulb.
7. VERY SLOWLY increase the pressure from 280 to the overpressure point. Once it is
reached, the valves will open and the pressure will rapidly reduce to 0mmHg.