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 MonitoringInvasiveBloodPressure8‐3
MR 400 Preparation for IBP Monitoring
FollowtheprocedurebelowtopreparetheMR400forIBPmonitoringwhenusingtheExpression
MRIBPDPTKits(Adult/Pediatric,REF989803194631;and,Infant/Neonatal,REF989803194641).
Astherearepreparationdifferences,alwaysfollowtheappropriateprocedure.
TopreparetheMR400forIBPmonitoringusingtransducerkitsotherthanthose
referenced
below,orforcomponentsaddedtothemonitoringsystem,refertoapplicablemanufacturer’s
instructionsforsetupanduse.
WARNINGS
• Invasive blood pressure transducers are sensitive to vibrations that can occur during
MRI scanning, which can lead to pressure reading inaccuracies. Always mount the invasive
blood pressure transducer away from areas where vibration is likely to occur.
• The fluid within the pressure transducer system is a conductive connection to the
patient, and must not contact other conductive parts, including earth ground.
• Do not allow fluids to enter the electrical connections of the transducer cables. Erratic
readings may result.
• Always reference the manufacturer’s instructions and follow the safe use instructions
included with the IBP transducer kit when monitoring invasive blood pressure.
• Never attach the pressure transducer(s) directly to the patient as excessive heating can
occur resulting in burn injuries to the patient.
• If air bubbles appear in the tubing system, flush the system with the infusion solution
again. Air bubbles may lead to a wrong pressure reading.
• Transducers do not protect against burns when used with high-frequency (HF)
surgical equipment.
• A transducer cable or other cable that becomes inadvertently looped during an MRI
examination may act as conductive lines for RF induced currents, resulting in
excessive heating and possible burns. When transducer cables or other cables form a
conductive loop in contact with the patient's tissue, minor to severe burning can result.
Do not allow the transducer cable or other cable to touch the patient or to become
looped. Please refer to the additional information in Appendix E to prevent excessive
heating associated with MRI procedures.
7 Press here to disconnect transducer from reusable cable
8 Reusable cable connector
9 Transducer cable connector
10 To fluid source
11 Squeeze continuous flush device