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 194 Masimo
Guidance and 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
+/- 2 kV for
power lines
+/- 1 kV for
input/ output
lines
Mains power quality should be that
of a typical commercial or hospital
environment.
Surge
IEC 61000-4-5
+/-1 kV
line(s) to
line(s)
+/- 2 kV
line(s) to
earth
+/-1 kV line(s)
to line(s)
+/- 2 kV line(s)
to earth
Mains power quality should be that
of a typical commercial or hospital
environment.
Voltage dips, short
interruptions, and
voltage variations on
power supply input
lines
IEC 61000-4-11
100% dip
in mains
voltage for
0.5 cycle
60% dip in
mains
voltage for
5 cycle
30% dip in
mains
voltage for
25 cycle
100% dip in
mains voltage
for 0.5 cycle
60% dip in
mains voltage
for 5 cycle
30% dip in
mains voltage
for 25 cycle
Mains power quality should be that
of a typical commercial or hospital
environment.