Riester RVS-100 User Manual
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Riester RVS-100 User Manual

Vital signs monitor
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RVS-100
Vital Signs
Monitor User Manual
0124

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Summary of Contents for Riester RVS-100

  • Page 1 RVS-100 Vital Signs Monitor User Manual 0124...
  • Page 2 RJ11 jack for nurse call connectivity. cation. Note: For purposes of this manual, the Riester RVS-100 may be re- • The instrument is used in accordance with the user’s ma- ferred to as “the Riester RVS-100”, “the RVS-100,”...

  • Page 3: Table Of Contents

    1. General Introduction 2.3 Important Notes for Safety 2.4 Safe Operation Conditions 1.1 Intended Use The RVS-100 vital signs monitor is intended to be used for monito- 3. Operations 3.1 Unpacking and Checking Contents ring, displaying, reviewing, storing and sending alarms regarding 3.2 Getting Started...

  • Page 4: Configurations

    The monitor consists of main unit, NIBP cuff, SpO2 sensor, Tempe- to the IEC 60601-1. If you have any questions, please contact Riester. If it is not evident from the equipment rature sensor (optional) and printer (optional). It can connect to the optional RVS-200 Wall Diagnostic Station through DC output.

  • Page 5: Equipment Symbols

    2.1 Safety Information Warning: • Before putting the system into operation, verify that the RVS-100 and RVS-200 and accessories are in correct wor- king order and operating condition. • Do not use device if any electrical connections become da- maged, bent, or misaligned.

  • Page 6: General Safety

    ason make sure that all external devices operated in the 2.3 Important Notes for Safety vicinity of the monitor comply with the relevant EMC requi- • Patient Number rements. Mobile phone, X-ray equipment or MRI devices The monitor can only be applied to one patient at one time. are a possible source of interference as they may emit •...

  • Page 7: Operations

    The monitor can be used together with high-frequency electrosur- to yellow, to cyan, and then turn off, after that the device will gical units and defibrillators. produce a sound and the Riester logo will also appear on the display. • IT-NETWORK...

  • Page 8: Clinician Management

    Triage profile: This profile is designed for rapidly taking vital signs measurement information. measurements on many patients. Patient information is disabled, ALARM: Used to adjust alarm limits for each parame- in addition to physiological alarms. Here is an example of the home ter, change alarm volume settings, and review historical alarms.

  • Page 9: General Setup

    3.8 General Setup Select [SETTINGS] > [ADVANCED] > [GENERAL] > [DEMO] 3.8.1 Language settings to select demo type. There are three demo modes to choose from: Monitor profile demo, Spot check profile demo, or Triage profile demo. Select [Start]to begin the demo. 3.8.4 General Device Options Select [SETTINGS] >...

  • Page 10: Service Settings

    4. Patient Management 4.1 Adding a Patient To add a patient, Select [PATIENT] > [Add]. The patient information window will pop up. Enter or select the patient information: Patient ID: The system can automatically produce an ID for the patient. The ID can also be manually entered. First Name: Enter the patient’s first name.

  • Page 11: Patient Monitoring

    5. Patient Monitoring 5.1.2 NIBP Measurement Limitations 5.1 NIBP Measurement Accurate NIBP measurements cannot be taken when the heart rate The monitor uses the oscillometric method for measuring NIBP. It is extremely low (less than 40 bpm) or extremely high (greater than is applicable for adult, pediatric and neonatal patients.
  • Page 12 “ ” on the cuff is positioned above artery and that there are no knots in the BP cable. When wrapped around the patient’s arm, the Cuff Index Line should fall within the Range Markers printed on the cuff. If not, select another cuff size. The monitor is designed for use with standard neonatal, pediatric and adult cuffs (including arm and thigh cuffs).

  • Page 13: Spo2 Measurement

    5.1.8 Manometer Test certain arrhythmias. The pulse oximeter should not be When the NIBP value measured is inaccurate, you can select [SET- used as a replacement or substitute for ECG-based ar- TINGS] > [ADVANCED] input password > [Factory], after enter rhythmia analysis.
  • Page 14 . be inaccurate for a short time. Specifications: Peak wavelength: Red 660-666nm, IR 895-920nm 5.2.7 Riester / Biolight SpO2 Sensors and Extension cables Maximum optical output power: 2mW a) Sensors Measurement Range: SpO2 0% ~ 100% Model: 15-100-0013, 15-100-0015 Arms: 70% ~ 100% SpO2: ±2%...

  • Page 15: Pr Measurement

    F, or 33 degrees C), such as those coming out of c) Unplug the instrument before cleaning or when disinfecting. surgery. d) RVS-100 thermometer probe and probe cover are designed for • Monitor mode is suitable for continuous temperature mo- use with this thermometer.

  • Page 16: Nurse Call

    Proper Temperature Probe Positioning For any countries where no legal regulations exist for monito- ring instruments, it is recommended to examine the accuracy Oral Temperature Taking of measuring instruments in 2-year intervals • If the temperature exceeds the measurement range, the Insert the probe tip under the tongue on one side or the other.

  • Page 17: Alarm Levels

    6.2 Alarm Levels 6.3.1 Alarm Tones The monitor’s physiologic alarms are classified into three catego- The device will make the following sounds for different level alarms: ries according to the severity of the alarm issue. )538>931< 1<1B= <1B= <5F5< High level alarms: Indicate that the patient is in a life-threatening 9LL=JQ (GO $A?@ situation and an emergency treatment is necessary.

  • Page 18: Alarm Icons

    6.6.1 Alarm Switches <1B= <5F5< +9CE1< @B?=@D To turn alarm limits on or off, select [SETTINGS] > [ADVANCED]> [PARAMETERS] > [Alarm limits status] and then choose the D9JE (! >D9K@=K J=< 9L  $R AFL=JN9DK $A?@ measurement type (i.e., NIBP, PR, SpO2 or Temp). To set the alarm to be [Alarm limits on] or [Alarm limits off].

  • Page 19: Resetting Alarm Limit

    The battery can only be replaced, maintained by professi- when the storage space is insufficient. When storage is onal personnel specified by Rudolf Riester GmbH. Or the less than 10MB, a low level technical alarm occurs, and device may not be started up.

  • Page 20: Optimizing Battery Performance

    Take out the old battery. 9.2 Cleaning the Monitor Insert the new battery in the direction indicated. Common detergents and non-corrosive disinfectants com- Close the battery door. monly used in hospitals can be applied to clean the monitor. Many of these cleaners must be diluted prior to use. Please 8.3 Optimizing Battery Performance use them according to the instructions of the detergent ma- A battery needs at least two optimizing cycles when it is put into...

  • Page 21: Accessories

    10. Accessories Warnings: • Use only accessories specified in this manual. Using other accessories may cause damage to the monitor. • Disposable accessories are designed for single-patient use only. Reusing them may cause a risk of contamination and affect measurement accuracy. •...
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  • Page 37 This manual has a revision number. This revision number changes whenever the manual is updated due to software or technical specification change. Contents of this manual are subject to change without prior notice. • Document No.: 99361 • Revision number: Rev. A • Release time: July 2017 Copyright © 2017 Rudolf Riester GmbH. All rights reserved.
  • Page 38 Rudolf Riester GmbH | P.O. Box 35 | Bruckstraße 31 | 72417 Jungingen | Germany Tel.: (+49) 7477-9270-0 | Fax.: (+49) 7477-9270-70 | info@riester.de | www.riester.de...

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