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Contents
1. General Introduction
1.1 Intended Use
1.2 Restrictions for use
3.8.2 DEMO Modes
3.8.4 Data Options
3.8.5 Network Settings
3.8.6 Service settings
3.8.7 Other settings
6.11 Resetting Alarm Limit
9.4 Maintenance and replacement of the accessories
10. Accessories
10.2 NIBP
10.4 Miscellaneous
Appendix A Product Specifications
A.1 Safety Specifications
A.2 Environmental Specifications
A.3 Physical Specifications
A.4 Power Specifications
A.5 Hardware Specifications
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A.6 Measurement Specifications
Appendix B :Factory Defaults
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B.1 Date /Time
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B.2 Alarm
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B.3 Display
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B.4 Others
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B.5 SpO2
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B.6 NIBP
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B.7 Temp
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Appendix C : Guidance and Manufacturer's
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Declaration of EMC
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Appendix D Troubleshooting
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Appendix E Applicable Standards
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1. General Introduction
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1.1 Intended Use
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The RVS-100 vital signs monitor is intended to be used for monito-
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ring, displaying, reviewing, storing and sending alarms regarding
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multiple physiological patient parameters, including Pulse Oxygen
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Saturation (SpO2), Pulse Rate (PR), Non-invasive Blood Pressure
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(NIBP), and Temperature (Temp).
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The RVS-100 vital signs monitor is intended to be used in outpatient
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departments, emergency treatment rooms, and low-acuity areas
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of hospitals, community clinics, private clinics and other medical
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institutions. It is not intended for helicopter transport, hospital am-
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bulance or home use.
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Warning: The monitor is intended for use only by clinical
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professionals or under their guidance. It must only be used
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by persons who have received adequate training in its use.
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Anyone unauthorized or untrained must not perform any
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operations on it.
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1.2 Restrictions for use
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Do not use the monitor and the SpO2 sensor during ma-
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gnetic resonance imaging (MRI). Induced current could
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cause burns.
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Operating high frequency electrosurgical equipment in
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the vicinity of the monitor may produce interference and
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cause incorrect measurements.
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The following factors may influence the accuracy of
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SPO2 measurements:
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◊ Exposure to excessive illumination, such as surgical
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◊ Electromagnetic interference, such as from an MRI
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◊ Excessive patient movement;
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◊ Intravascular dyes such as indocyanine green or me-
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◊ Significant levels of dysfunctional hemoglobins
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◊ Incorrect sensor application or use;
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◊ Placement of a sensor on an extremity with a blood
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◊ Low perfusion;
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◊ Electrosurgical units.
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Do not use the SpO2 sensor on the same limb being used
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for NIBP measurement. This may result in inaccurate
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SpO2 reading due to blocked blood flow during cuff in-
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flation.
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Do not measure SpO2 on a finger painted with nail po-
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lish. This may result in unreliable measurements.
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Do not measure NIBP on patients with sickle-cell di-
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sease or any condition in which skin damage has occur-
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red or is expected.
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Use clinical judgment to decide whether to perform fre-
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quent Auto BP measurements on patients with severe
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blood clotting disorders because of the risk of hemato-
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ma in the limb fitted with the cuff.
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Use clinical judgment to decide whether to perform Auto
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BP measurement on patients with thrombasthemia.
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Do not use the NIBP cuff on a limb with an intravenous
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infusion or arterial catheter in place. This could cause
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tissue damage around the catheter when the infusion is
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slowed or blocked during cuff inflation.
lamps (especially ones with a xenon light source),
bilirubin lamps, fluorescent lights, infrared heating
lamps or direct sunlight (exposure to excessive il-
lumination can be corrected by covering the sensor
with a dark or opaque material);
device;
thylene blue;
(such as carboxyhemoglobin or methemoglobin);
pressure cuff, arterial catheter or intravascular line;
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