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 15: Specifications
www.masimo.com 195 Masimo
Guidance and Manufacturer's Declaration - Electromagnetic Immunity
Power
frequency (50 /
60 Hz) magnetic
field.
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields
should be at levels characteristic of
typical location in a typical hospital
environment.
Portable and mobile RF communications equipment should be used no closer to any part of
the ME Equipment, including cables, than the recommended separation distance
calculated from the equation applicable to the frequency of the transmitter.
Immunity Test IEC 60601
Test Level
Compliance
Level
Recommended separation distance
Conducted RF IEC
61000-4-6
3 Vrms 3 Vrms
Radiated RF IEC
61000-4-3
20 V/m 80
MHZ to 2.5
GHz
20 V/m
80 MHz to 800 MHz
800 MHz to 2.5 GHz
where P is the maximum output
power rating of the transmitter in
watts (W) according to the
transmitter manufacturer and d is
the recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey
a
, should
be less than the compliance level in
each frequency range
b
.
Interference may occur in the
vicinity of equipment marked with
the following symbol: