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
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.