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
1‐34ImportantInformationExpressionMR400InstructionsforUse
Warning
WARNING
The MR400 has been validated with all of the accessories listed below. Only use these
specified accessories as other types or brands may compromise the safety and accuracy of
the MR400. Patient injury or loss of monitoring may result if incorrect accessories are used.
Warning
WARNING
Do not use sterile items if the packaging is damaged. Patient injury may result if non-sterile
accessories are used.
CAUTION
Modifications to the MR400 System during its service life are required to be evaluated to the
requirements of IEC 60601-1.
AGENT Original Part Number REF
CANNULA, DISP, ADULT 9012 989803152561
CANNULA, DISP, ADULT 9016 989803152601
CANNULA,DISP,INT INF,(DIVIDED) 9016B 989803152621
CANNULA,DISP,PED,(DIVIDED) 9016C 989803152631
CANNULA,DISP,INFANT,(DIVIDED) 9016A 989803152611
CANNULA, DISP, INT INFANT 9015 989803152591
CANNULA, DISP, PED 9013 989803152571
CANNULA, DISP, INFANT 9014 989803152581
ANESTHETIC OXYGEN (O2) SENSOR — 989803162051
KIT,DISPOSABLE WATER TRAP,3160 94012 989803152671
KIT,SAMPLE,AGENTS,3160 94018 989803152661
CO2 REF
LOFLO SAMPLE LINE, ADULT CANNULA, BOX 20 989803183241
LOFLO SAMPLE LINE, PED. CANNULA, BOX 20 989803183251
LOFLO SAMPLE LINE, NEO. CANNULA, BOX 20 989803183261
LOFLO LINE, ADU DVD CANNULA,BOX 20 989803183271