User's Manual

ManualsBrandsEDAN INSTRUMENTS ManualsElectronicsTelemetry Transmitter

Table Of Contents

Statement
Responsibility of the Manufacturer
Terms Used in this Manual
Chapter 1 Intended Use and Safety Guidance
- 1.1 Intended Use/Indications for Use
- 1.2 Safety Guidance
- 1.3 Explanation of Symbols on the Telemetry transmitter
Chapter 2 Overview
- 2.1 System Introduction
- 2.2 Display Screen of Telemetry Transmitter
- 2.3 Appearance of Telemetry Transmitter
- 2.4 Configuration
- 2.5 Display Screens of the MFM-CMS
Chapter 3 Installation of Telemetry Monitoring System
- 3.1 Initial Inspection
- 3.2 Installation Environment
- 3.3 Power Supply Requirement
- 3.4 Wireless Network
- 3.5 Installation Method
- 3.6 Checking the Printer
- 3.7 Checking the Telemetry Monitoring System
- 3.8 Setting Date and Time
- 3.9 Handing Over the Central Monitoring Systerm
- 3.10 FCC Statement
Chapter 4 Basic Operations
- 4.1 Basic Operations for Telemetry Transmitter
- 4.2 Basic Operations for MFM-CMS
  - 4.2.1 Mouse Operation
  - 4.2.2 Switching on/off the MFM-CMS
Chapter 5 Patient Management
- 5.1 Admitting a Patient
- 5.2 Changing Patient Information
- 5.3 Switching Patient sector
- 5.4 Discharging a Patient
- 5.5 Transferring a Patient
- 5.6 Monitoring Statistics
- 5.7 Nurse Call / Patient Call
Chapter 6 Patient Sector
- 6.1 Overview
- 6.2 Networked Monitoring Display
- 6.3 Menu in the Patient Sector
- 6.4 Parameter/ Waveform Setup
  - 6.4.1 Setting Waveforms
  - 6.4.2 Setting Parameters
- 6.5 Freeze
- 6.6 Real-Time Printing
- 6.7 Alarm Reset
Chapter 7 Viewing Single Bed
- 7.1 Display of Single Bed
- 7.2 Hiding/Showing Multi-Lead Waveform
- 7.3 Short Trend Review
- 7.4 OxyCRG
- 7.5 Freeze
Chapter 8 Setting Telemetry Transmitters via MFM-CMS
- 8.1 Changing Patient Information
- 8.2 Setting Parameters
  - 8.2.1 Parameters Alarm Setting
  - 8.2.2 Physiological Parameter Attribute and Configuration
Chapter 9 Review
- 9.1 Patient List
- 9.2 Wave Review
- 9.3 Alarm Review
- 9.4 Trend Review
Chapter 10 System Setup
- 10.1 Common Setup
- 10.2 User Maintain
Chapter 11 Alarm Management
- 11.1 Overview
- 11.2 Alarm Levels
- 11.3 Parameters Alarm Setting
- 11.4 Alarm Mute
- 11.5 Audio Pause
- 11.6 Alarm Prompt/Response
- 11.7 Testing Alarms
- 11.8 Alarms for Networking Status
Chapter 12 Alarm Information
- 12.1 Physiological Alarm Information
- 12.2 Technical Alarm Information
- 12.3 Prompts
- 12.4 Adjustable Range of Alarm Limits
Chapter 13 Printing
- 13.1 Printing Report with a Printer
- 13.2 Printing Preview/ Printing Settings
  - 13.2.1 Printing Preview
  - 13.2.2 Printing Settings
- 13.3 Exporting the PDF File
Chapter 14 Database Management
- 14.1 Database Backup
- 14.2 Reviewing Backup Database
Chapter 15 Monitoring ECG
- 15.1 Overview
- 15.2 ECG Safety Information
- 15.3 ECG Display
  - 15.3.1 ECG Display on Telemetry Transmitter Screen
  - 15.3.2 ECG Display on MFM-CMS
- 15.4 Selecting Calculation Lead
- 15.5 Changing Size of ECG Waveform
- 15.6 Changing ECG Filter Settings
- 15.7 ECG Alarm Settings
- 15.8 Monitoring Procedure
  - 15.8.1 Preparation
  - 15.8.2 Connecting ECG Cables
- 15.9 Installing Electrodes
  - 15.9.1 Electrode Placement for 3-lead
  - 15.9.2 Electrode Placement for 5-lead
- 15.10 Setting Alarm Source
- 15.11 Smart Lead Off
- 15.12 Setting Pace Status
- 15.13 ECG Calibration
- 15.14 ECG Waveform Settings
- 15.15 ST Segment Monitoring
- 15.16 Arr. Monitoring
  - 15.16.1 Arrhythmia Analysis
  - 15.16.2 ARR Analysis Menu
Chapter 16 Monitoring RESP
- 16.1 Overview
- 16.2 RESP Safety Information
- 16.3 Electrode Placement for Monitoring RESP
- 16.4 Cardiac Overlay
- 16.5 Chest Expansion
- 16.6 Abdominal Breathing
- 16.7 Selecting RESP Lead
- 16.8 Changing the Apnea Time
- 16.9 Changing the Size and Speed of the Respiration Waveform
- 16.10 RESP Alarm Settings
Chapter 17 Monitoring SpO2
- 17.1 Overview
- 17.2 SpO2 Safety Information
- 17.3 Measuring SpO2
- 17.4 Measurement Procedure
- 17.5 Assessing the Validity of a SpO2 Reading
- 17.6 SpO2 Alarm Delay
- 17.7 Setting Sensitivity
- 17.8 SpO2 Alarm Settings
Chapter 18 Monitoring PR
- 18.1 Overview
- 18.2 Selecting the Active Alarm Source
- 18.3 PR Alarm Settings
Chapter 19 Using Battery
- 19.1 Battery Status on Screen
- 19.2 Replacing the Battery
- 19.3 Recycling the Battery
Chapter 20 Safety
- 20.1 Control and Safety Index
- 20.2 Characteristics
Chapter 21 Care and Cleaning
- 21.1 General Points
- 21.2 Cleaning
  - 21.2.1 Cleaning the Telemetry Transmitter
  - 21.2.2 Cleaning the Reusable Accessories
- 21.3 Disinfection
  - 21.3.1 Disinfecting the Telemetry Transmitter
  - 21.3.2 Disinfecting the Reusable Accessories
Chapter 22 Maintenance
- 22.1 Inspecting
- 22.2 Maintenance Task and Test Schedule
Chapter 23 Warranty and Service
- 23.1 Warranty
- 23.2 Contact information
Chapter 24 Accessories
- 24.1 ECG Accessories
- 24.2 SpO2 Accessories
- 24.3 Other Accessories
A Product Specifications
- A.1 Classification of Telemetry Transmitter
- A.2 Specifications of Telemetry Transmitter
- A.3 Data Storage
- A.4 Specifications of MFM-CMS
  - A.4.1 Recommended Hardware Configuration
  - A.4.2 Software Performance
- A.5 ECG
- A.6 RESP
- A.7 SpO2
- A.8 Wi-Fi
B EMC Information
- B.1 Electromagnetic Emissions
- B.2 Electromagnetic Immunity
- B.3 Electromagnetic Immunity
- B.4 Recommended Separation Distances
C Default Settings
- C.1 Patient Information Default Settings
- C.2 Alarm Default Settings (MFM-CMS)
- C.3 ECG Default Settings
- C.4 RESP Default Settings
- C.5 SpO2 Default Settings
- C.6 PR Default Settings
D Abbreviation

Telemetry Transmitter User Manual Installation of telemetry monitoring system

WARNING

During patient monitoring, a change in date and time will influence the storage of trend

data.

NOTE:

1 The user must restart MFM-CMS to make the change effective.

2 If the system is not used for a longer period of time, its system time may be

inaccurate. In this case, reset the system time after powering on.

3 If the system time cannot be saved and resumes the default value after restart,

contact the service department of EDAN.

3.9 Handing Over the Central Monitoring Systerm

If you are handing over system to the end-users directly after installation and configuration, make

sure that it is in the monitoring mode.

The users must be adequately trained to use the system before monitoring a patient. To achieve

this, they should have access to, and read, the following documentation delivered with system:

 User Manual (this book) - for full operating instructions.

 Quick Reference Card - for quick reminders during use.

3.10 FCC Statement

This equipment has been tested and found to comply with the limits for a Class B digital device,

pursuant to part 15 of FCC Rules. These limits are designed to provide reasonable protection

against harmful interference in a residential installation. This equipment generates and can radiate

radio frequency energy and, if not installed and used in accordance with the instructions, may

cause harmful interference to radio communications. However, there is no guarantee that

interference will not occur in a particular installation. If this equipment does cause harmful

interference to radio or television reception, which can be determined by turning the equipment

off and on, the user is encouraged to try to correct the interference by one or more of the

following measures:

1. Reorient or relocate the receiving antenna.

2. Increase the separation between the equipment and receiver.

3. Connect the equipment into an outlet on a circuit different from that to which the receiver is

connected.

4. Consult the dealer or an experienced radio/TV technician for help.

This device complies with Part 15 of FCC Rules.

Operation is subject to the following two conditions:

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