Riester RVS-100 Manual Del Usuario página 45

Contents
1. General Introduction
1.1 Intended Use
1.2 Restrictions for use
1.3 Configurations
1.4 Main Unit
1.4.1 Front View
1.4.2 Side View
1.4.3 Rear View
1.4.4 Bottom View
1.5 Equipment Symbols
1.6 Packaging Symbols
2. Safety
2.1 Safety Information
2.2 General Safety
2.3 Important Notes for Safety
2.4 Safe Operation Conditions
3. Operations
3.1 Unpacking and Checking Contents
3.2 Getting Started
3.3 Connect Accessories
3.4 Shutting off the Monitor
3.5 Operation Profiles
3.6 Using Menus
3.7 Clinician Management
3.8 General Setup
3.8.2 DEMO Modes
3.8.3 General Device Options
3.8.4 Data Options
3.8.5 Network Settings
3.8.6 Service settings
3.8.7 Other settings
4. Patient Management
4.1 Adding a Patient
4.2 Patient manage
5. Patient Monitoring
5.1 NIBP Measurement
5.2 SpO2 measurement
5.3 PR Measurement
5.4 Temperature Measurement
5.5 Nurse Call
6. Alarms
6.1 Alarm Categories
6.2 Alarm Levels
6.3 Alarm Indicators
6.4 Alarm Icons
6.5 Setting Alarm Volume
6.6 Alarm Parameters
6.7 Pausing Alarms
6.8 Acknowledging Alarms
6.9 Alarm Reset
6.10 Alarm Volume off and on
6.11 Resetting Alarm Limit
6.12 Alarm History
7.Reviewing
7.1 Reviewing patient measurements
7.2 Deletingpatient data
7.3 Print patient data
8. Battery
8.1 Introduction
8.2 Installing a Battery
8.3 Optimizing Battery Performance
8.4 Checking Battery Performance
8.5 Disposing of Batteries
9. Maintenance and Cleaning
9.1 Introduction
9.2 Cleaning the Monitor
9.3 Cleaning and Disinfection of Accessories
9.4 Maintenance and replacement of the accessories
10. Accessories
10.1 SpO2
10.2 NIBP
10.3 Temp
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
A.6 Measurement Specifications
Appendix B :Factory Defaults
39 B.1 Date /Time
39 B.2 Alarm
39 B.3 Display
40 B.4 Others
40 B.5 SpO2
40 B.6 NIBP
40 B.7 Temp
40 Appendix C : Guidance and Manufacturer's
41 Declaration of EMC
41 Appendix D Troubleshooting
41 Appendix E Applicable Standards
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1. General Introduction
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42
1.1 Intended Use
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43 The RVS-100 vital signs monitor is intended to be used for monito-
43 ring, displaying, reviewing, storing and sending alarms regarding
43 multiple physiological patient parameters, including Pulse Oxygen
43 Saturation (SpO2), Pulse Rate (PR), Non-invasive Blood Pressure
43 (NIBP), and Temperature (Temp).
43 The RVS-100 vital signs monitor is intended to be used in outpatient
44 departments, emergency treatment rooms, and low-acuity areas
44 of hospitals, community clinics, private clinics and other medical
45 institutions. It is not intended for helicopter transport, hospital am-
45 bulance or home use.
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Spot Check Profile: This profile is designed for taking a single set of
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45 vital signs measurements on a patient. Patient information can be
45 entered and managed, and while technical alarms are still available,
46 physiological alarms are disabled.
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46 Warning: The monitor is intended for use only by clinical
46 professionals or under their guidance. It must only be used
47 by persons who have received adequate training in its use.
47 Anyone unauthorized or untrained must not perform any
49 operations on it.
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1.2 Restrictions for use
50
• Do not use the monitor and the SpO2 sensor during ma-
51
gnetic resonance imaging (MRI). Induced current could
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cause burns.
51
• Operating high frequency electrosurgical equipment in
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51 the vicinity of the monitor may produce interference and
52 cause incorrect measurements.
52 • The following factors may influence the accuracy of
52 SPO2 measurements:
53 ◊ Exposure to excessive illumination, such as surgical
53 lamps (especially ones with a xenon light source),
53 bilirubin lamps, fluorescent lights, infrared heating
53 lamps or direct sunlight (exposure to excessive il-
lumination can be corrected by covering the sensor
53
with a dark or opaque material);
53
◊ Electromagnetic interference, such as from an MRI
54
device;
54
◊ Excessive patient movement;
54
◊ Intravascular dyes such as indocyanine green or me-
54
54 thylene blue;
54 ◊ Significant levels of dysfunctional hemoglobins
54 (such as carboxyhemoglobin or methemoglobin);
54 ◊ Incorrect sensor application or use;
54 ◊ Placement of a sensor on an extremity with a blood
54 pressure cuff, arterial catheter or intravascular line;
54 ◊ Low perfusion;
◊ Electrosurgical units.
54
• Do not use the SpO2 sensor on the same limb being used
55
for NIBP measurement. This may result in inaccurate
55
SpO2 reading due to blocked blood flow during cuff in-
55
flation.
55
• Do not measure SpO2 on a finger painted with nail po-
56
57 lish. This may result in unreliable measurements.
57 • Do not measure NIBP on patients with sickle-cell di-
57 sease or any condition in which skin damage has occur-
58 red or is expected.
58 • Use clinical judgment to decide whether to perform fre-
58 quent Auto BP measurements on patients with severe
58 blood clotting disorders because of the risk of hemato-
ma in the limb fitted with the cuff.
58
• Use clinical judgment to decide whether to perform Auto
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