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 Warnings and Cautions
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as a component drop of approximately 1 meter or greater or a spillage of
blood or other liquids occurs, retest before further use. Injury to
personnel could occur.
Compliance Warnings and Cautions
Warning: Do not incinerate battery.
Caution: Dispose of used batteries according to required country or
regional instructions.
Caution: Disposal of product - Comply with local laws in the disposal of
the device and/or its accessories.
Caution: To minimize radio interference, other electrical equipment that
emits radio frequency transmissions should not be in close proximity to
Radical-7.
Note: Cleared Use Only: The device and related accessories have
obtained CE Mark for noninvasive patient monitoring and may not be
used for any processes, procedures, experiments or any other use for
which the device is not intended or cleared by the applicable regulatory
authorities, or in any manner inconsistent with the instructions for use or
labeling.
Note: This equipment has been tested and found to comply with the
Class B limits for medical devices according to the EN 60601-1-2, Medical
Device Directive 93/42/EEC. These limits are designed to provide
reasonable protection against harmful interference in a typical medical
installation.
Note: This device complies with part 15 of the FCC Rules. Operation is
subject to the following two conditions: (1) This device may not cause