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
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ExpressionMR400InstructionsforUse MaintenanceandTroubleshooting14‐7
WARNING
Do not use flammable or potentially explosive disinfecting sprays. Such sprays create vapors,
which can ignite, causing fatal or other serious personal injury.
CAUTION
Disinfecting a medical product room by means of sprays is not recommended, since the vapor
could penetrate the product, causing electrical short-circuits, metal corrosion or other damage to
the product.
Cleaning, Disinfecting, and Inspecting the Accessories
Anyreusablepatientaccessory(suchasECGcables,SPO2
attachmentsandprobes,temperature
sensors,etcetera)mustbecleanedanddisinfectedbeforeinitialuseandaft ereachuseto
protectpatientsandpersonnelfr omavarietyofpathogens.Usesoapandwater,andasuggested
disinfectantandmethod,tocleananddisinfect theaccessories.Thewarrantydoesnotcover
damage
causedbyunapprovedsubstancesormethods.
Duringthecleaningprocess,inspecttheaccessoryfordamage.Theaccessoriesareexposedto
potentiallydamagingsituationsduringuseandcleaning.Beforeeachuse,carefullyinspectthe
accessoriesforthefollowingsignsofdamage:
•Cracks,holes,tears,gouges,cuts,etcetera.
•Cracksorother
signsofdamagetotheconnector,includingbentordamagedpins.
• Disposableaccessoriesmustbediscardedandreplacedwithnewitems.
WARNING
Cracks, tears, cuts and gouges interfere with standard cleaning procedures and therefore
pose a potential risk to patients and personnel. If you see any sign of damage to any
accessory, immediately discontinue use.
WARNING
Single-use devices, as indicated on the device packaging, should be disposed of after use and
must never be reused.Reuse of single-use devices can result in spread of patient infection,
degradation of monitoring performance, or inaccurate measurements.
CAUTIONS
• Never immerse an accessory in any cleaning fluid.
• Do not autoclave any part of the equipment. Disinfect the accessory as determined by your
facility’s policy.