User Manual
Table Of Contents
- Manufacturer
- Identification and Publication Details
- Regulatory
- Explanation of Symbols
- Conventions
- Important Information
- About
- Intended Use
- Compatibility
- Indications for Use
- Contra-indications
- Training
- Safety
- Electromagnetic Compatibility (EMC)
- Using Batteries Safely
- Examining the Shipment
- Initial Setup
- Rear Panel Connections
- Understanding Battery Operations
- Understanding Wireless Network Operations
- Advanced User Options
- Accessory List
- System Overview
- Getting Started
- Alarms
- Monitoring ECG
- ECG Monitoring Considerations for the MR Environment
- wECG Module and ECG Lead Cable
- Quadtrode Electrodes
- Work Flow for ECG Monitoring
- Selecting the ECG Lead Cable and Quadtrode Electrode Type
- Identifying the Placement Site for the Quadtrode Electrode
- Preparing the Quadtrode Electrode Site
- Attaching the ECG Lead Cable
- Checking the ECG Signal Strength
- Minimizing ECG Waveform Noise
- Positioning the ECG Lead Cable and wECG Module for Scanning
- ECG Waveforms and VS Box
- ECG Menu
- Monitoring SPO2
- Monitoring CO2 (LoFlo Option)
- Monitoring Invasive Blood Pressure
- Indications and Contraindications
- Patient Preparation for IBP Monitoring
- Transducer Component, Connection, and Feature Locations
- MR 400 Preparation for IBP Monitoring
- Adult and Pediatric Patients: Expression MR IBP DPT Kit, A/P (REF 989803194631)
- I. Connecting the Reusable Cable to the MR400
- II. Kit Set Up
- III. Purging Air from the Monitoring Line
- IV. Zeroing, Leveling and Calibration
- V. Connecting the Monitoring Kit to the Patient
- The IBP transducer must not be mounted to the patient, or patient burn may result.
- VI. Fast Flushing
- VII. Checking for Leaks
- VIII. In the MR Room
- Neonatal Patients: Expression MR IBP DPT Kit, I/N (REF 989803194641)
- Adult and Pediatric Patients: Expression MR IBP DPT Kit, A/P (REF 989803194631)
- Zeroing the Pressure Transducer
- P1 (and P2) Menu
- Monitoring Agents and Gases (AGENT Option)
- Monitoring RESP
- Monitoring Temperature
- Monitoring NIBP
- Trend Data and Printing
- Maintenance and Troubleshooting
- General Cleaning Guidelines
- Removing all Power to the MR400
- Removing Power from the Wireless Modules
- User Routine-Checks and Planned Maintenance
- Cleaning, Disinfection, and Damage Inspection
- Sterilization
- Testing Alarms
- Testing a Dropped Wireless Module
- Verification Testing
- Anesthetic Oxygen (O2) Sensor Depletion
- Updating Software
- Calibrating the Touch Screen
- Troubleshooting
- Repair
- Environmental Requirements
- Passing the Product on to another User
- Final Disposal of the Product
- Specifications
- Warranty
- Regulatory Information
- Gating Feature
- Guidelines and References
9‐4MonitoringAgentsandGases(AGENTOption) ExpressionMR400InstructionsforUse
Thebreathratelimitforaccuratelyresolvedend‐tidalgasvalues(atanI:Eratioof1:1)maybe
foundinAppendixA.TheeffectofotherI:Eratiosmaybecalculatedbydeterminingthelengthof
the
shortestinspiratory/expiratoryeventthatcanberesolvedaccurately:
t
resolved
=60/(2xBR
limit
(1:1)
BR
limit
(I:E)=60/((I+E)xt
resolved
)
Thedifferenceintheseresultswhencomparedtotherisetime'sspecificationisthatrise time's
onlytests10‐90%performance.Thisspecificationisfor(0+accuracy)to(100‐accuracy)%andis
thusmuchtougher.Theabilitytoproperlyresolveend‐tidalvaluescanbemeasuredbyusing
the
set‐updescribedinISO80601‐2‐55:2011figure201.101.Inshort,themethodconsistsof
samplinggasfromtwodifferentsourcesconnectedtoanelectricallycontrolledpneumaticvalve
topermitrapidswitchingbetweenthetwosources.Duringthetest,thevalveissettoswitchgas
sourceata
numberoffrequencies(simulatingtherangeofspecifiedbreathrates)andforeach
frequencytheend‐tidalvaluepresentedbythegasanalyzerisnoted.Fromadiagramofend‐tidal
valueoverfrequency,thefrequencyatwhich thegasanalyzerisnolongerabletoresolveend‐
tidalvalues
accordingtospecificationisidentified.Thisabilitytoproperlyresolveend‐tidalvalues
islistedinthespecification.
CO2 Low Flow and Occlusion Conditions
CO2LowFlowwillbedisplayedandanalarmwillsoundintheeventofalowflowcondition
(wheneverthegasflowfallstoanamountthatis10percentlessthanthesampleflowratefor
theselectedpatienttype),asshowninthetablebelow.
Occlusionwillbe
displayedandanalarmwillsoundintheeventofanocclusioncondition
(wheneverthegasflowratehasfallenbelow40ml/minforatleast1second. Thetypicalcauseof
Fi error
Percent
Time
Et error
- - at gas sampling site
— as presented by gas analyzer
Patient Type Sample Flow Rate Flow Rate when Low Flow is Declared
Adult 200 ml/min ≤ 180 ml/min
Pediatric 200 ml/min ≤ 180 ml/min
Neonate 150 ml/min ≤ 135 ml/min