User's Manual
Table Of Contents
- Statement
- Responsibility of the Manufacturer
- Terms Used in this Manual
- Chapter 1 Intended Use and Safety Guidance
- Chapter 2 Overview
- Chapter 3 Installation of Telemetry Monitoring System
- Chapter 4 Basic Operations
- Chapter 5 Patient Management
- Chapter 6 Patient Sector
- Chapter 7 Viewing Single Bed
- Chapter 8 Setting Telemetry Transmitters via MFM-CMS
- Chapter 9 Review
- Chapter 10 System Setup
- Chapter 11 Alarm Management
- Chapter 12 Alarm Information
- Chapter 13 Printing
- Chapter 14 Database Management
- Chapter 15 Monitoring ECG
- 15.1 Overview
- 15.2 ECG Safety Information
- 15.3 ECG Display
- 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
- 15.9 Installing Electrodes
- 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
- Chapter 16 Monitoring RESP
- Chapter 17 Monitoring SpO2
- Chapter 18 Monitoring PR
- Chapter 19 Using Battery
- Chapter 20 Safety
- Chapter 21 Care and Cleaning
- Chapter 22 Maintenance
- Chapter 23 Warranty and Service
- Chapter 24 Accessories
- A Product Specifications
- B EMC Information
- C Default Settings
- D Abbreviation
Telemetry Transmitter User Manual Intended Use and Safety Guidance
19 Only use patient cable and other accessories supplied by EDAN. Or else, the
performance and electric shock protection cannot be guaranteed, and the patient may
be injured. Prior to use, check if the casing of a disposable or sterilized accessory is
intact. Do not use it if its casing is damaged.
20 Wireless LAN equipment contains an intentional RF radiator that has the potential of
interfering with other medical equipment, including patient implanted devices. Be sure
to perform the electromagnetic compatibility test, as described in the Wireless LAN
System Installation, before installation and any time new medical equipment is added
to the Wireless LAN coverage area.
21 When interfacing with other equipment, a test for leakage current must be performed
by qualified biomedical engineering personnel before using with patients.
22 If multiple instruments are connected to a patient, the sum of the leakage currents
must not exceed the limits; or it may result in shock hazard.
23 During monitoring, if the power supply is off and there is no battery for standby, the
telemetry transmitter will be off. Last settings used will be recovered when the power
is restored.
24 When leakage or foul odor is detected,stop using and keep away from fire
immediately.
25 The device and accessories are to be disposed of according to local regulations after
their useful lives. Alternatively, they can be returned to the dealer or the manufacturer
for recycling or proper disposal. Batteries are hazardous waste. Do NOT dispose
them together with house-hold garbage. At the end of their life hand the batteries over
to the applicable collection points for the recycling of waste batteries. Inappropriate
disposals of waste may contaminate the environment. For more detailed information
about recycling of this product or battery, please contact your local Civic Office, or the
shop where you purchased the product.
26 The packaging is to be disposed of according to local or hospital’s regulations;
otherwise, it may cause environmental contamination. Place the packaging at the
place which is inaccessible to children.
27 After defibrillation, the ECG display recovers within 10 seconds if the correct
electrodes are used and applied based on the manufacturers’ instructions.
28 When deploying wireless network, hospital should make sure that clinicians have
acknowledged and familiarized the coverage of wireless network signal. Patients’
activity must be within that range.
29 This equipment is not intended for home usage.
30 Do not service or maintain the telemetry transmitter or any accessories during patient
monitoring.
WARNING
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