Operator's Manual
Table Of Contents
- About this Manual
- Product Description
- Indications for Use
- Contraindications
- 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 Carboxyhemoglobin (SpCO)
- General Description for Methemoglobin (SpMet)
- General Description for Oxygen Reserve Index (ORI)
- SpCO, SpMet, and SpHb Measurements During Patient Motion
- rainbow Acoustic Monitoring (RAM) Technology
- Chapter 2: Radical-7 Descriptions
- Chapter 3: Setup
- Chapter 4: Operation
- Using the Touchscreen and Buttons
- Using Screen Lock
- Using the Home Button
- Standby and Power Off
- Navigating the Radical-7
- About the Display View
- Sensitivity Modes Overview
- Changing Sensitivity Modes
- Accessing the Main Menu
- Navigating the Main Menu
- Parameter Settings
- Chapter 5: Profiles
- Chapter 6: Alarms and Messages
- About Alarms
- Silencing the Alarms
- Adaptive Threshold alarm (ATA) Feature
- 3D Alarms
- Messages
- Replace Sensor Message
- Replace Cable Message
- Replace Adhesive Sensor Message
- Incompatible Sensor Message
- Incompatible Adhesive Sensor Message
- No Adhesive Sensor Connected Message
- Interference Detected Message
- SpO2 Only Mode Message
- RAM Check Sensor Message
- RAM Sensor Initializing Message
- Low Battery Message
- Low Perfusion Index Message
- Low Signal IQ Message
- Low SpCO SIQ Message
- Low SpMet SIQ Message
- Low SpHb SIQ Message
- Speaker Failure Message
- Invalid Parameter Alarm Message
- No Cable Connected Message
- No Sensor Connected Message
- Pulse Search Message
- Sensor Initializing Message
- Sensor Off Patient Message
- Incompatible Cable Message
- Near Expiration Message
- Chapter 7: Troubleshooting
- Chapter 8: Specifications
- Chapter 9: Service and Maintenance
- Appendix
- Index
Radical-7 Appendix
www.masimo.com 214 Masimo
Manufacturer's Declaration-Electromagnetic Immunity
Guidance and Manufacturer's Declaration - Electromagnetic
Immunity
The ME Equipment is intended for use in the electromagnetic
environment specified below. The customer or the user of the ME
Equipment should assure that it is used in such an environment.
Immunity Test IEC
60601
Test
Level
Compliance
Level
Electromagnetic
Environment - Guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
+6 kV
contact
+8 kV
air
+6 kV
contact
+8 kV air
Floors should be wood,
concrete or ceramic tile. If
floors are covered with
synthetic material, the
relative humidity should be
at least 30%.
Electrical fast
transient/ burst
IEC 61000-4-4
+/- 2 kV
for
power
lines
+/- 1 kV
for
input/
output
lines
Mains power quality should
be that of a typical
commercial or hospital
environment.