BeneVision-TM80 Operations-Manual V9.0 en
BeneVision-TM80 Operations-Manual V9.0 en
Operator’s Manual
Introduction
0123
© Copyright 2015-2019 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights
reserved.
Manufacturer’s Responsibility
Contents of this manual are subject to changes without prior notice.
All information contained in this manual is believed to be correct. Mindray shall not be
liable for errors contained herein nor for incidental or consequential damages in connec-
tion with the furnishing, performance, or use of this manual.
Mindray is responsible for the effects on safety, reliability and performance of this prod-
uct, only if:
WARNING
Warranty
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED
OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY PAR-
TICULAR PURPOSE.
Exemptions
Mindray's obligation or liability under this warranty does not include any transportation
or other charges or liability for direct, indirect or consequential damages or delay result-
ing from the improper use or application of the product or the use of parts or accessories
not approved by Mindray or repairs by people other than Mindray authorized personnel.
Company Contact
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address: Mindray Building, Keji 12th Road South, High-tech Industrial park, Nanshan, Shenzhen
518057, P.R.China
Website: www.mindray.com
E-mail Address: [email protected]
Tel: +86 755 81888998
Fax: +86 755 26582680
Preface
Manual Purpose
This manual contains the instructions necessary to operate the product safely and in
accordance with its function and intended use. Observance of this manual is a prerequi-
site for proper product performance and correct operation and ensures patient and
operator safety.
This manual is based on the maximum configuration and therefore some contents may
not apply to your product. If you have any questions, please contact Mindray.
This manual is an integral part of the product. It should always be kept close to the
equipment so that it can be obtained conveniently when needed.
Intended Audience
This manual is geared for clinical professionals who are expected to have a working
knowledge of medical procedures, practices and terminology as required for monitoring
of critically ill patients.
Illustrations
All illustrations in this manual serve as examples only. They may not necessarily reflect
the setup or data displayed on your equipment.
Conventions
■ Italic text is used in this manual to quote the referenced chapters or sections.
■ [ ] is used to enclose screen texts.
■ → is used to indicate operational procedures.
3 Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
3.1 Unpacking and Checking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
3.2 Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
3.3 Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4
3.3.1 Connecting the ECG Leadwire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4
3.3.2 Installing the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6
3.4 Powering On the TM80 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
3.5 Using the Pouch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10
3.5.1 Securing the Pouch for TM80 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11
3.5.2 Securing Pouches for TM80 and BP10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13
4 Basic Operations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
4.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
4.1.1 Display Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
4.1.2 On-Screen Keyboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
4.2 Understanding the Touch Screen Gestures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
4.3 Basic Operations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
4.3.1 Entering the Main Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
4.3.2 Understanding the Screen Display Orientation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
4.3.3 Browsing the Screen Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
4.3.4 Switching the Screen Display Orientation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
4.3.5 Displaying the Quick Keys Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 8
4.3.6 Turning the Display Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
4.3.7 Turning the Display On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
4.3.8 Configuring the Screen Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
4.3.9 Unlocking the Screen in Locked Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
4.3.10 Acknowledging the Nurse Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 10
6 Patient Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
6.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
6.2 Admitting a Patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
6.3 Changing Patient Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
6.3.1 Changing the Patient Category . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
6.3.2 Changing the Paced Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 3
6.3.3 Changing the Department Name, Room Number, and Bed Number . . . . . . . . . 6 - 4
6.4 Entering the Standby Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 5
6.5 Exiting the Standby Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 6
6.6 Discharging the Patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 6
6.6.1 Selecting the Discharge Patient Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 6
6.6.2 Restarting the TM80 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 7
7 Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
7.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
7.2 Alarm Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
7.3 Understanding the Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
7.3.1 Alarm Categories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
7.3.2 Alarm Priorities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
7.3.3 Alarm Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
7.3.4 Alarm Status Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5
7.4 Viewing Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5
7.5 Changing Alarm Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
7.5.1 Changing Alarm Properties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
7.5.2 Changing the Alarm Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
7.5.3 Initiating Auto Alarm Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
7.5.4 Restoring Default Alarm Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 7
7.6 Pausing Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8
7.7 Resetting Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
7.7.1 Resetting Physiological Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
7.7.2 Resetting Technical Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
7.8 Latching Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 10
7.9 Actions When an Alarm Occurs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 10
12 Review . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 1
12.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 2
12.2 Tabular Trends Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 2
12.2.1 Entering the Tabular Trends Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 2
12.2.2 Example Tabular Trends Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 2
12.2.3 Example Tabular Trends Data Search Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 4
12.2.4 Changing the Resolution of Trend Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 5
12.3 Events Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 5
12.3.1 Entering the Events Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 5
12.3.2 Example Events Review Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 6
12.3.3 Example Event Details Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 - 7
15 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 1
15.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 2
15.2 Battery Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 3
15.3 Installing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 5
15.4 Checking the Battery Charge Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 5
15.5 Removing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 5
15.6 Charging the Rechargeable Lithium-ion Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 6
15.7 Storing the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 7
15.7.1 Storing Rechargeable Lithium-ion Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 7
15.7.2 Storing AA Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 7
15.8 Maintaining the Rechargeable Lithium-ion Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 8
15.9 Disposing of the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 9
15.9.1 Disposing of the Rechargeable Lithium-ion Battery . . . . . . . . . . . . . . . . . . . . . . .15 - 9
15.9.2 Disposing of the AA Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15 - 9
16 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16 - 1
16.1 General Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16 - 2
16.2 Physiological Alarm Messages at the TM80 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16 - 4
16.3 Technical Alarm Messages at the TM80 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16 - 7
18 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 1
18.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 2
18.2 Maintenance Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 2
18.3 Regular Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 3
18.4 Maintenance and Testing Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 3
18.4.1 Power-on Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 4
18.4.2 ECG Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 5
18.4.3 NIBP Accuracy Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 5
18.4.4 NIBP Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 5
18.4.5 Nurse Call Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 5
18.4.6 Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 6
18.4.7 Network Print Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 6
18.4.8 Battery Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 6
18.5 Viewing System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18 - 6
19 Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 1
19.1 ECG Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 2
19.1.1 ECG Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 2
19.1.2 ECG Leadsets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 3
19.2 SpO2 Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 4
19.3 NIBP Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 5
19.4 Miscellaneous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19 - 5
A Product Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 1
A.1 Classifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 2
A.2 Environmental Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 2
A.3 Power Supply Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 3
A.4 Physical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 4
A.5 Hardware Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 5
A.6 Data Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 6
A.7 Wi-Fi Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 6
A.7.1 Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 6
A.7.2 Implemented Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 7
A.7.3 Specifications of Wireless Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 7
A.8 MPAN Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 8
A.8.1 Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 8
A.8.2 Implemented Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A - 9
E Declaration of Conformity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E - 1
Safety Information...................................................................................................1-2
Equipment Symbols................................................................................................1-7
WARNING
CAUTION
NOTE
1.1.1 Warnings
WARNING
WARNING
• Do not use patient cables or accessory cables and sensors if prior visual
inspection reveals cable damage or the presence of liquid, lint or dust
inside.
• Do not come into contact with the patient during defibrillation. Other-
wise serious injury or death could result.
• Do not touch the patient and live parts simultaneously.
• Do not rely exclusively on the audible alarm system for patient monitor-
ing. Adjustment of alarm volume to a low level may result in a hazard to
the patient. Always keep the patient under close surveillance.
• PATIENTS WITH A PACEMAKER – On ventricular paced patients, episodes
of ventricular tachycardia may not always be detected. Do not rely
entirely upon the system’s automated arrhythmia detection algorithm.
Keep pacemaker patients under close surveillance.
• The physiological data and alarm messages displayed on the TM80
Telemetry Monitor are for reference only and cannot be directly used for
diagnostic interpretation.
• Do not operate the touch screen with water on the hand.
1.1.2 Cautions
CAUTION
• Do not let the display of the TM80 Telemetry Monitor directly touch the
patient’s skin when the display is on.
• When the CMS presents the alarm “Offline”, check the network connec-
tion status.
• When disposing of the packaging material, be sure to observe the appli-
cable local waste control regulations and keep it out of children’s reach.
• The patient should be required to move in a specified area. If the patient
is at the edge of or outside the network coverage range, unstable net-
work connection may compromise the monitoring performance. The
patient’s location is of vital importance for the TM80 Telemetry Monitor.
If a life-threatening situation occurs for a patient, this patient must be
located and found by medical staff immediately.
• Mindray takes no responsibility for controlling the radio frequency envi-
ronment in a hospital. If interference for the operating frequency of
telemetry equipment exists, the telemetry equipment performance will
be affected. Exercise caution when selecting the operating frequency of
all the wireless equipment in a hospital as this is very important to avoid
mutual interference among them.
• Magnetic and electrical fields are capable of interfering with the proper
performance of the TM80 Telemetry Monitor. For this reason make sure
that all external equipment operated in the vicinity of the TM80 Teleme-
try Monitor comply with the relevant EMC requirements. Mobile phone,
X-ray equipment, micro-wave oven, interphone, or MRI equipment are a
possible source of interference as they may emit higher levels of electro-
magnetic radiation.
• Always install or carry the TM80 Telemetry Monitor properly to avoid
damage caused by drop, impact, strong vibration or other mechanical
force.
• Dry the TM80 Telemetry Monitor immediately in case of rain or water
spray.
• When the patient carrying a TM80 Telemetry Monitor moves in a hospi-
tal, signal quality can be impacted on an ambulatory patient by the con-
struction materials used within the hospital.
CAUTION
• At the end of its service life, the TM80 Telemetry Monitor and its acces-
sories must be disposed of in compliance with the guidelines regulating
the disposal of such products to prevent bringing potential negative
consequences to the environment and human health. If you have any
questions concerning disposal of the equipment, please contact Min-
dray.
1.1.3 Notes
NOTE
• Put the TM80 Telemetry Monitor in a location where you can easily see
the screen and access the operating controls.
• The software of the TM80 Telemetry Monitor was developed in compli-
ance with IEC60601-1-4. The possibility of hazards arising from software
errors is minimized.
• This manual describes all features and options. Your equipment may not
have all of them.
• If you wish to pair a TM80 Telemetry Monitor with a BeneVision N series
patient monitor, contact your service personnel. For details about pair-
ing and unpairing procedures, refer to BeneVision N Series Patient Moni-
tor Operator's Manual (PN: 046-009995-00).
• If you wish to use the 6-lead placement to derive 12-lead ECG at the
CMS, contact your service personnel. For details about this functional-
ity, refer to BeneVision Central Monitoring System Operator’s Manual (PN:
046-010282-00).
• Keep this manual in the vicinity of the equipment so that it can be
obtained conveniently when needed.
This product bears CE mark indicating its conformity with the provisions of the
0123
Council Directive 93/42/EEC concerning medical devices and fulfils the essen-
tial requirements of Annex I of this directive.
Note: The product complies with the Council Directive 2011/65/EU.
Dispose of in accordance with the local country’s requirements
NOTE
WARNING
■ ECG leadwires
■ SpO2 cables
■ SpO2 sensors
■ NIBP tubes and cuffs
2.4 Components
The TM80 Telemetry Monitor consists of the following:
5
7
4 9
6 8
10
1 2
4. Display
The touch screen display allows viewing patient information and adjusting patient
settings.
5. Alarm light indicator
Flashes in different colors and at different frequencies corresponding to the alarm
priority.
6. ECG lead connector
Connects the ECG leadset.
7. SpO2 cap
Covers SpO2 connector when SpO2 is not in use.
8. SpO2 connector
Connects the SpO2 module.
9. Speaker
10. Battery compartment
Contains the lithium-ion battery or AA battery tray.
■ Parameters and waveforms will be displayed on the screen for easy viewing.
■ If an alarm condition occurs, both audible and visual alarm indicators will be given
locally both at the TM80 and at the CMS, if networked connected.
■ If the TM80 is not connected to the CMS, the “No Central Monitoring” message will
display in the prompt message area of the TM80.
When the display of the TM80 is off:
■ No audible or visual alarm indicators are given. You can press or to turn on
the display and enter the monitoring mode. Regardless of the display status, all
measurement data is being sent to the CMS.
■ If the TM80 is disconnected from the CMS and [CMS Disconnect Alarm] is
enabled, the TM80’s display is turned on automatically. For details, refer to Config-
uring the CMS Disconnect Alarm on Page 13-2.
■ If the configured [Display Auto Off ] time is out, the display will be turned on
automatically. For how to configure the [Display Auto Off ] time, refer to
Configuring the General Menu on Page 13-2.
WARNING
• The temperature of the display rises when the TM80’s display is on and
the TM80 is connected to the CMS. If the display contacts the patient’s
skin for a long time, skin burns may occur. Do not let the display directly
touch the patient’s skin when the display is on.
WARNING
CAUTION
If the packing case is intact, open the package and remove the device and accessories
carefully. Check all materials against the packing list and check for any mechanical dam-
age. Contact Mindray in case of any problem.
WARNING
NOTE
• Save the packing case and packaging material as they can be used if the
TM80 must be reshipped.
The operating environment of the TM80 should be reasonably free from noises, vibra-
tion, dust, corrosive, flammable and explosive substances.
When the TM80 is moved from one place to another, condensation may occur as a result
of temperature or humidity difference. In this case, never start the system before the
condensation disappears.
WARNING
• Make sure that the operating environment of the TM80 meets the speci-
fications in this manual. Otherwise, unexpected consequences, e.g.
damage to the system, could result.
NOTE
3.3 Preparation
3.3.1 Connecting the ECG Leadwire
To connect the ECG leadwire, follow this procedure:
1. Align the ECG leadwire plug with the ECG connector as indicated by the arrow in
the following figure.
2. Insert the ECG leadwire plug into the ECG connector as shown in the enlarged fig-
ure below. After the ECG leadwire plug is securely plugged into the ECG connector,
the parts marked in the small red circle below become invisible.
WARNING
• Insert the ECG lead set into the ECG connector firmly. The following per-
formances may be affected by a weak connection:
◆ ECG signal quality
◆ Water resistance
• Do not use the ECG leadwire to move or lift the TM80. This may cause the
TM80 to fall, thus damaging the equipment or injure the patient.
NOTE
• Insert the SpO2 cap into the SpO2 connector when SpO2 is not in use.
NOTE
WARNING
NOTE
1. Open the battery compartment by lifting up on both bottom sides of the com-
partment door.
2. Remove the AA battery tray if present.
3. Align the raised tab in the upper part of the lithium-ion battery with the cutout in
the base of the battery compartment, as indicated by the enlarged figure below.
4. Press down the battery until it is secured, as indicated by the arrow in the follow-
ing figure.
1. Open the battery compartment by lifting up on both bottom sides of the com-
partment door.
2. Insert three AA 1.5V Alkaline batteries into the AA battery tray, matching the polar-
ity with the +indications inside the battery tray as shown below.
NOTE
• All batteries are inserted with the + polarity in the same direction.
4. Align the raised tab in the upper part of the battery tray with the cutout in the
base of the battery compartment, as indicated by the enlarged part in the follow-
ing figure.
5. Press down the battery tray until it closes firmly as indicated by the arrow in the
following figure.
When the TM80 installed with a rechargeable lithium-ion battery or AA battery tray is
■ If the TM80 is turned on for the first time, the equipment will request you to
configure first time startup. Please make your desired configurations as prompted.
■ If the TM80 is turned on next time, the equipment will prompt whether it is a new
patient. Select [Yes] or [No] as desired.
WARNING
• Check that visual and auditory alarm signals are presented correctly
when the equipment is powered on. Do not use the equipment for any
monitoring procedure on a patient if you suspect the equipment is not
working properly or if the equipment is mechanically damaged. Contact
your service personnel or Mindray.
CAUTION
• When the patient is showering, signal quality and leads off detection
may be compromised due to significant movement. Appropriate clinical
precautions must be taken.
WARNING
• While using a pouch to attach the TM80 to your patient, consider your
patient’s condition and be careful about the placement of the straps, as
the straps could present a strangulation hazard.
NOTE
• The pouch is used only for the TM80. The pouch cannot be used for car-
rying other personal devices, such as a mobile phone.
NOTE
• Do not secure the pouches for the TM80 and BP10 on the same side of
the patient’s body.
Overview.....................................................................................................................4-2
Understanding the Touch Screen Gestures....................................................4-5
Basic Operations.......................................................................................................4-5
4.1 Overview
This chapter gives you an overview of basic operations related to the TM80. The princi-
ple method of operating your TM80 is via the touch screen. Almost every element on the
display is interactive. Display elements include measurement numerics, information
prompts, waveforms, quick keys, menus, and so on.
1 234 5 6
◆ : indicates that alarms are acknowledged and the alarm system is reset.
3. MPAN indicator
◆ indicates that the TM80 is not paired with the BP10 or one TM80 is not
connected to another TM80 for configuration transfer.
◆ indicates that the TM80 is paired with the BP10 successfully or configu
ration transfer of the TM80 is in progress.
4. Wi-Fi symbol
◆ indicates that the TM80 has been connected to the Wi-Fi access point
and the signal coverage is very good. Stable data transmission via Wi-Fi net-
work can be guaranteed.
◆ indicates that the TM80 has been connected to the Wi-Fi access point
and the signal coverage is good. Stable data transmission via Wi-Fi network
can be guaranteed.
◆ indicates that the TM80 has been connected to the Wi-Fi access point
and the signal coverage can basically meet the requirements. Stable data
transmission via Wi-Fi network can be guaranteed.
◆ indicates that the TM80 has been connected to the Wi-Fi access point
and the signal coverage is weak. Wi-Fi offline may occur.
◆ indicates that the TM80 is not connected to the Wi-Fi access point.
5. Battery symbol
This symbol indicates the battery charge status. For details about the battery sta-
tus symbols, refer to Checking the Battery Charge Status on Page 15-5. Tapping
the battery symbol opens the [System Info] menu and displays the battery infor-
mation.
6. System time
7. Prompt message area
This area shows physiological alarm messages, technical alarm messages, and
informational messages. When there are multiple messages, the messages scroll.
Tapping this area displays the [Alarm List] menu where you can view all the alarm
messages. The “...” symbol indicates that there are more than one message.
8. Patient data area
This user configurable area can display parameter/waveform data. The parameter/
waveform is labeled in the upper left corner. You may also tap this area to display
the setup menu for the corresponding parameter/waveform.
6 2
5 4
7 3
6 5 4
Tap Briefly touch the surface with your fingertip to select a target.
Press and hold Touch the surface for an extended period of time.
Drag Move your fingertip over the surface without losing contact.
WARNING
• Instruct patients not to interact with the display of the device and to not
open the battery compartment while the TM80 is in use.
The main menu allows access to most of the system functions and settings.
1
4
Controls Description
4. : exits the current menu and returns to the previous menu or the main screen.
■ Portrait: both digital and waveform tiles take up the entire width of the screen.
■ Landscape: the digital tile takes up one half of the width of the screen; the
waveform tile takes up the entire width of the screen.
1. Swipe your finger down from the top of the main screen to display the following
buttons.
NOTE
• The methods given in this section only change the screen display orien-
tation temporarily. Once the TM80 is restarted, the default display ori-
entation will apply. To set the default screen display orientation, refer to
Configuring the Default Display Orientation on Page 5-2.
Discharge Patient Tap the button to enter the [Discharge Patient] menu. Refer to Dis-
charging the Patient on Page 6-6 for details.
Change Lead Tap the button to change the current first ECG lead waveform to the next
ECG lead waveform that is available in sequential order.
For example, if the current first ECG lead waveform is I lead, tap the but-
ton, the I lead waveform is changed to II lead waveform.
Alarm Pause Tap the button to pause the alarm system. Refer to Pausing Alarms on
Page 7-8 for details.
Print Tap the button to notify the CMS to start real-time print. The “Print Initi-
ated” message displays in the prompt message area.
Mark Event Tap the button to notify the CMS to save the event to the event database.
The “Event Marked” message displays in the prompt message area. The
marked event is also saved on the events review page of the TM80.
Alarm Reset Tap the button to reset the alarm system. Refer to Resetting Alarms on
Page 7-9 for details.
Alarm Limits Tap this button to enter the [Alarm Limits] menu. Refer to Changing
Alarm Settings on Page 7-6 for details.
Events Tap this button to enter the event review page. Refer to Review on Page
12-1 for details.
Monitor Mode/ When a patient moves out of the department area, you need to pay close
Telemetry Mode attention to the patient's status on the patient’s side. In this case, tap
[Monitor Mode]. Then, the TM80's display is always on and alarms are
issued locally.
If the patient returns to the department area, tap [Telemetry Mode].
You can customize the most frequently used functions to the quick keys. For details
about configuring the quick keys, refer to Changing the Quick Keys on Page 13-5.
NOTE
• While the display is off, the TM80 enters the power saving mode, and
does not provide audio or visual alarms.
• If the TM80 is not connected to the CMS, the “No Central Monitoring”
message will display in the prompt message area of the TM80. In this
case, the TM80’s display is automatically turned on and it will not time-
out. You cannot manually turn the display off.
CAUTION
• Do not let the display directly touch the patient when the display is on.
1. When the display is off, press or to turn it on and access the [Screen
Locked] menu.
2. Input the passcode to unlock the screen.
WARNING
• Do not rely exclusively on the nurse call function. The medical personnel
should also pay close attention to the patient’s condition.
For details about how to trigger a nurse call, refer to Physical View on Page 2-4.
Introduction...............................................................................................................5-2
Configuring the Display.........................................................................................5-2
Configuring the Audio Volume...........................................................................5-5
5.1 Introduction
This chapter describes the configurations that can be performed by users, such as con-
figuring the Display Setup, and Audio Volume.
1. In the [Setup] section of the [Display Setup] menu, tap [Default Orientation].
Two options display: [Portrait] and [Landscape].
2. Tap a button to set it to the default orientation.
The selected orientation displays to the right of [Default Orientation].
3. Restart the TM80 to apply the setting.
For details about the display orientation, refer to Understanding the Screen Display Ori-
entation on Page 4-7.
NOTE
• The TM80 must be restarted for the default display orientation selected
to be effective.
• Once the default display orientation takes effective, you can switch the
display orientation by following steps in Switching the Screen Display
Orientation on Page 4-7.
5. Drag the selected parameter or waveform to the desired position, and then release
it.
6. Repeat steps 4 and 5 until the desired order is configured.
1. The areas shall be displayed in the order set in the [Display Setup] menu except
that the digital area locations shall be optimized to reduce blank tiles.
2. A waveform area always takes up the entire width of the screen.
3. A digital area always takes up one half of the width of the screen. Therefore, a row
with a digital tile in it shall be split into two half tiles.
4. A digital area shall not be the only parameter in a row unless an odd number of
digital areas exist. In this case, the last digital parameter area shall have one tile on
the left side and the right half will be blank.
5. Digital areas shall be paired with the next available digital area to satisfy rule 4.
This means that a digital area may be moved ahead of a waveform area if a half of a
row needs to be filled.
For example, if the landscape display rows is set to [3] and the parameter order is as fol-
lows:
HR
SpO2
RR
NIBP
History
ECG II
ECG V
Pleth
Resp
ECG1
ECGIII
ECG aVR
ECG aVL
ECG aVF
The landscape layout displays as follows:
HR* SpO2
Resp NIBP
HISTORY
ECG II
ECG V
Pleth
Resp
ECG I
ECG III
ECG aVR
ECG aVL
ECG aVF
* Bold is displaying on screen; non-
bold data need to be scrolled to.
The icon displays to the right side of the selected parameter or waveform.
5. Drag the selected parameter or waveform to the desired position, and then release
it.
6. Repeat steps 4 and 5 until the desired order is configured.
NOTE
• The minimum sound volume cannot be lower than the minimum alarm
volume. Refer to Configuring the Alarms Menu on Page 13-4 for details.
• When [Minimum Alarm Volume] is set to [Off] and [Sounds] is turned off,
the icon is displayed on the main screen. It indicates that the alarm
sound is turned off.
• When your TM80 is connected to the CMS and [Sounds] is turned off,
[Sounds] automatically changes to [2] if the CMS is disconnected.
Introduction...............................................................................................................6-2
Admitting a Patient .................................................................................................6-2
Changing Patient Information ............................................................................6-2
Changing the Paced Status ..................................................................................6-3
Exiting the Standby Mode ....................................................................................6-6
Discharging the Patient .........................................................................................6-6
6.1 Introduction
The chapter describes how to admit a patient, change patient information, enter and
exit the Standby mode, and discharge the patient at the TM80.
After discharging the current patient, you can admit a new patient by pressing . For
how to discharge a patient, refer to Discharging the Patient on Page 6-6. After admit-
ting a patient, please check the patient category and make changes appropriately.
NOTE
NOTE
• When the TM80 is connected to the Central Station, the patient category
at the Central Station is updated if the patient category is changed at
the TM80. Refer to BeneVision Central Monitoring System Operator’s
Manual for details.
◆ When [Paced] is set to [No] or not specified at the TM80, the symbol
displays in the waveform area of the Central Monitoring System’s screen.
WARNING
• For paced patients, you must set [Paced] to [Yes]. If it is incorrectly set to
[No], the Central Station could mistake a pace pulse for a QRS and fail to
alarm when the ECG signal is too weak.
• On ventricular paced patients, episodes of ventricular tachycardia may
not always be detected.
• Do not rely entirely upon the system’s automated arrhythmia detection
algorithm. Keep paced patients under close surveillance.
WARNING
• For non-paced patients, you must set [Paced] to [No]. The pacer pulses
may be counted as QRS complexes, hence leading to wrong HR readings
or failure to diagnose certain arrhythmia symptoms. Be sure to keep a
close eye on patient’s with pacemaker devices.
• The radio frequency energy of the TM80 or other radio frequency
sources, when used in close proximity to a pacemaker, may interfere
with pacemaker performance. Internal pacemakers are less vulnerable
than external pacemakers due to the shielding effects of the body. How-
ever, caution should be exercised when monitoring any paced patient.
• In order to minimize the possibility of interference, place electrodes,
leadwires and TM80s as far away from the pacemaker as possible.
NOTE
• When [Paced] is set to [Yes] and regular pace pulses are available, the
system does not detect PVC-related arrhythmia (including PVCs) result-
ing from pacemaker but still analyzes the normal QRS complex.
You can also change the patient’s paced status from the [ECG] menu. For information
about how to set paced status in the [ECG] menu, refer to Checking the Paced Status on
Page 8-12.
For information about settings in the [Maintenance] menu, refer to Configuring Device
Location on Page 13-3.
To change department name, room number, and bed number, follow this procedure:
NOTE
• When Department and Bed No./Room No. are set to Unfixed, the depart-
ment name, room number, and bed number of the TM80 cannot be
changed at the CMS..
NOTE
2. Tap [Standby].
3. In the [Standby] confirmation menu, tap [Yes].
When a TM80 enters the Standby mode:
You can discharge the patient by selecting the [Discharge Patient] menu or restarting
the TM80.
NOTE
Introduction...............................................................................................................7-2
Alarm Safety Information......................................................................................7-2
Understanding the Alarms ...................................................................................7-3
Viewing Alarms.........................................................................................................7-5
Changing Alarm Settings......................................................................................7-6
Pausing Alarms .........................................................................................................7-8
Resetting Alarms ......................................................................................................7-9
Latching Alarms........................................................................................................7-10
Actions When an Alarm Occurs ..........................................................................7-10
Operator’s Position ..................................................................................................7-11
7.1 Introduction
This chapter describes alarm functions and alarm settings.
WARNING
• A potential hazard can exist if different alarm presets and default con-
figuration settings are used for the same or similar equipment in the
same care area.
• If the TM80 is connected to the CMS, alarms can be presented and con-
trolled at the CMS. Remote suspension or reset of alarms at the CMS may
cause a potential hazard. For more information, refer to BeneVision Cen-
tral Monitoring System Operator’s Manual.
• The TM80 telemetry monitors in the care area may each have different
alarm settings to suit different patients. Always check that the alarm set-
tings are appropriate for your patient before starting monitoring.
Always make sure that necessary alarm limits are active and set accord-
ing to the patient's clinical condition.
• Setting alarm limits to extreme values may cause the alarm system to
become ineffective. For example, setting the SpO2 high alarm limit to
100%, is equivalent to switching the alarm off.
• When the alarm sound is switched off, the TM80 gives no alarm tones
even if a new alarm occurs. Be careful when considering to switch off the
alarm sound. When the alarms are off, observe the patient frequently.
• When monitoring patients that are not continuously attended by a clini-
cal operator, properly configure the alarm system and adjust alarm set-
tings as per the patient's condition.
• Do not rely exclusively on the audible alarm system for monitoring.
Adjustment of alarm volume to a low level may result in a hazard to the
patient.
• The reception failure of alarm signals may occur in the distributed alarm
system.
Medium Low
High Priority
Alarm Indicator Priority Priority Message Comments
Alarm
Alarm Alarm
Medium Low
High Priority
Alarm Indicator Priority Priority Message Comments
Alarm
Alarm Alarm
Audible ISO Repeat pattern Repeat pat- Single beep None None
tone of triple +dou- tern of triple
ble+ triple beeps
pattern
+double beeps
Alarm message White text Black text Black text White Alarm messages
inside a red inside a yel- inside a text are displayed in
box low box cyan box the prompt mes-
sage area at the
top of the screen.
You can select
the alarm
messages to
show the alarm
list.
Parameter value White text Black text Black text None None
inside a flash- inside a flash- inside a
ing red box ing yellow flashing
box
cyan box
NOTE
NOTE
■ : indicates that alarms are acknowledged and the alarm system is reset.
1. Tap the prompt message area on the main screen. The [Alarm List] dialog is
displayed.
2. In the [Physiological Alarms] section, you can view the number of physiological
alarms and alarm messages.
3. Tap the desired physiological alarm to enter the event review page where you can
view the alarm details.
4. In the [Technical Alarms] section, you can view the number of technical alarms
and alarm messages.
◆ Press to enter the main menu →tap [Alarms] →tap [Alarm Limits].
NOTE
• Any changes to the alarm properties on the TM80 will change alarms on
the CMS and vice versa if configured.
2. Tap [Alarms].
3. Tap [Alarm Limits].
4. In the [Setup] section, tap [Auto Limits].
5. In the dialog that pops up, tap [OK].
Then the TM80 will automatically calculate alarm limits based on the latest measured
values. Before applying these automatically created alarm limits, confirm if they are
appropriate for your patient from the Limits menu. If not, you can adjust them manually.
These alarm limits will remain unchanged until you select auto limits again or adjust
them manually.
2. Tap [Alarms].
3. Tap [Alarm Limits].
1. Swipe your finger up at the bottom of the main screen to display the quick keys
area.
2. Tap [Alarm Pause].
When alarms are paused, the following indicators are given:
■ The alarm pause symbol is displayed in the upper right corner of the main
screen.
The alarm pause time is two minutes by default. You can change the alarm pause time at
the CMS. For details, refer to BeneVision Central Monitoring System Operator’s Manual.
When the pause time expires, the alarm paused status is automatically deactivated.
NOTE
• When the TM80 is connected to the CMS and the function of remotely
pausing alarms is enabled at the CMS, alarms can be paused either at the
TM80 or at the CMS. For information on pausing alarms at the CMS, refer
to BeneVision Central Monitoring System Operator’s Manual.
When an alarm occurs, follow this procedure to reset the TM80’s alarm system.
1. Swipe your finger up at the bottom of the main screen to display the quick keys
area.
2. Tap [Alarm Reset].
NOTE
• When the TM80 is connected to the CMS and the function of remotely
resetting alarms is enabled at the CMS, alarms can be reset either at the
TM80 or at the CMS. For information on resetting alarms at the CMS,
refer to BeneVision Central Monitoring System Operator’s Manual.
■ The symbol is displayed in the upper right corner of the main screen.
■ A √ mark appears before the alarm message, indicating that the alarm is
acknowledged.
■ The color of the parameter numeric background corresponds with the alarm
priority, but the parameter numeric does not flash.
■ Some technical alarms are cleared and no alarm indications are given.
■ Some technical alarms are changed to prompt messages.
■ For some technical alarms, the alarm sound will be silenced, the alarm light will
continue to indicate the alarm, a √ markwill appear before the alarm message.
■ For some technical alarms, the symbol is displayed in the upper right corner
of the main screen.
For details about the indications of technical alarms when the alarm system is reset, refer
to Technical Alarm Messages at the TM80 on Page16-7.
NOTE
NOTE
• Latching settings for physiological alarms are configured at the CMS. For
more information on how to configure latching settings, refer to BeneVi-
sion Central Monitoring System Operator’s Manual (P/N: 046-010282-00).
Introduction...............................................................................................................8-2
ECG Safety Information..........................................................................................8-2
Preparation for Monitoring ECG .........................................................................8-3
Changing ECG Settings..........................................................................................8-13
Configuring the HR Alarm Source......................................................................8-17
Understanding the ECG Display .........................................................................8-18
Arrhythmia Monitoring..........................................................................................8-20
QT/QTc Interval Monitoring .................................................................................8-33
Relearning ..................................................................................................................8-35
8.1 Introduction
The electrocardiogram (ECG) measures the electrical activity of the heart and displays it
on the TM80 as waveforms and numerics.
ECG monitoring provides 3-, 5-, and 6-lead ECG monitoring, ST-segment analysis,
arrhythmia analysis, and QT/QTc measurements.
Operations such as configuring the QRS threshold, adjusting the ST point/ISO point/J
point, configuring the ST template/QT template are performed at the CMS. For details
about these operations, refer to Monitoring with the TM80 at the CMS on Page 14-1.
WARNING
CAUTION
NOTE
1. Shave the chest hair from the electrode sites in a circular area with a diameter of 2
to 4 inches.
2. Use a dry gauze pad to remove excess skin oils, skin cells and residue from the
electrode sites. Never rub the skin until it is raw or bleeding.
NOTE
• Prepare the electrode site with alcohol only if the skin is extremely
greasy. If alcohol is used as a drying agent, always allow the skin to dry
before placing the electrode on the skin.
NOTE
NOTE
1. Peel the backing off of the electrode. Visually inspect the contact gel medium for
moistness. If the gel medium is not moist, do not use the electrode patch. Dry elec-
trode patches are not conductive.
NOTE
• To prevent evaporation of the contact gel medium, peel the backing off
of the electrode patch only when it is ready for use.
• If using the snap type lead wires, attach the electrode to the lead wire
before placing the electrode on the patient.
2. Attach the electrode patch to the skin at the prepared site. Smooth the electrode
patch down in a circular motion to ensure proper skin contact. If using soft gel
electrodes, never push down directly over the contact gel medium as this may dis-
place the gel and cause monitoring artifact. If using hard gel electrodes, it is rec-
ommended that during application, the center of the electrode should be slightly
pressed onto the skin to ensure direct contact. Consult the electrode manufac-
turer’s instructions for specific use. Ensure all the electrodes are applied to the
patient properly.
3. Secure the lead wires to the patient according to hospital practice.
CAUTION
• Route leadwires neatly. Ensure leadwires are kept away from patient’s
neck to avoid strangulation. Keep floors and walkways free of cables to
reduce risk to hospital personnel, patients and visitors.
NOTE
AHA IEC
Lead position
Label Color Label Color
RA (R) LA (L)
LL (F)
RA (R) LA (L)
V(C)
LL (F)
RL (N)
The positions of Va (Ca) and Vb (Cb) can also be placed at a proper position according to
the clinician’s needs.
RA (R) LA (L)
V6 (C6)
V1 (C1) V5 (C5)
V4 (C4)
LL (F)
RL (N)
V2 (C2)
V3(C3)
Pacemaker
RA (R) LA (L)
LL (F)
Pacemaker
RA (R) LA (L)
V(C)
LL (F)
RL (N)
Pacemaker
RA (R) LA (L)
V6 (C6)
V1 (C1) V5 (C5)
V4 (C4)
LL (F)
RL (N)
V2 (C2) V3 (C3)
Do not place an ECG electrode directly over the pacemaker generator. Place the elec-
trode patches 2 to 3 inches away from the pacemaker generator area. For example, if the
pacemaker generator is located in the right subclavian area, relocate the Right Arm elec-
trode closer in towards the center of the chest.
■ Tap the ECG lead off message in the prompt message area of the main screen.
Information bar
Lead on indicator
Lead off indicator
When any of the leads are off, the indications are as follows:
1. On the main screen, tap the HR digital area or ECG waveform area to enter the
[ECG] menu.
2. In the [Pacer] section, check if [Paced] is appropriate for the patient.
3. If it is not correct, tap [Paced] and select the correct paced status. For details about
the options, refer to Changing the Paced Status on Page 6-3.
■ On the main screen, tap the HR digital area or ECG waveform area.
■ Press to enter the main menu →tap [Parameter Setup] → select [ECG].
1. In the [Setup] section of the [ECG] menu, select the options described in the fol-
lowing table.
Lead Placement Enters the [Lead Placement] window. Refer to Checking the Lead Place-
ment on Page 8-11 for details.
Cable Type Selects the current ECG leadwire type. Auto, 3 Lead, 5 Lead, 6 Lead
Refer to ECG Leadwire Types on
Page 8-14 for details.
Smart Lead (Monitored Refer to ECG Leadwire Types on Page 8-14 for details.
Lead)
■ [Auto]: the device automatically sets the leadwire type according to the leads
connected.
■ [3 Lead]: the leadwire type is set to 3 lead.
If the leadwire type is set to 3-lead, the [Smart Lead] option becomes [Monitored
Lead]. You can select the desired lead from the [Monitored Lead] option to set
the first ECG waveform displayed on the main screen.
■ [5 Lead]: the leadwire types is set to 5 lead. The option displays [Smart Lead].
All waveform leads display on the main screen.
Drag the switch to right or left to enable or disable the Smart Lead function.
■ [6 Lead]: the leadwire types is set to 6 lead.
If the leadwire type is set to 6 lead, there will be two options [Va] and [Vb]
displayed under [Cable Type].
◆ [Va] options: Va, V1, V2, V3, V4, V5, V6. Va is the default.
◆ [Vb] options: Vb, V1, V2, V3, V4, V5, V6. Vb is the default.
All Lead Size Selects the waveform size for all the leads. 1.25 mm/mV, 2.5 mm/mV, 5 mm/
To set the waveform size for a specific mV, 10 mm/mV, 20 mm/mV, 40
lead, select that lead from the [Waveform mm/mV, Auto
Size] field.
Speed Selects the waveform sweep speed. 6.25 mm/s, 12.5 mm/s, 25 mm/s
1. In the [Pacer] section of the [ECG] menu, select the options described in the fol-
lowing table.
Pacer Reject Selects whether or not to reject the pace On, Off
pulses.
NOTE
• When [Paced] is set to [Yes], the [Markers] and [Pacer Rejection] options
can be available.
Note:
1. When you change the high limit of HR/PR, the limit of Tachy will be automatically
changed, and vice versa.
2. When you change the low limit of HR/PR, the limit of Brady will be automatically
changed, and vice versa.
3. When you change the alarm priority of HR/PR, the alarm priority of Tachy/Brady will
be automatically changed, and vice versa.
◆ [Both]: both HR and PR are used as the alarm source for HR/PR.
NOTE
• When [Alarm Source] is set to [HR], systole beep comes from heart beat.
When [Alarm Source] is set to [PR], systole beep comes from pulse rate.
1 2
5 4
1. Parameter name
2. Measurement unit
3. Heart rate value
4. PR source: PR source is displayed when ECG leads are not connected and valid PR
value is detected,
5. HR/PR alarm off symbol: when HR/PR alarm is switched on and valid HR/PR value is
detected, HR/PR alarm high and low limits in place of the alarm off symbol are dis-
played.
NOTE
• Both the HR value displayed on the TM80’s main screen and that at the
Central Station can meet relevant standards and are reliable. HR
trended, alarm checking, and arrhythmia are based on the HR calculated
at the Central Station.
• Please be noted that in case of weak wireless signals, the Central Station
faces the risk of data loss and the HR value calculated by the ECG algo-
rithm for the Central Station may have certain deviation.
1. ECG Lead
2. ECG scale bar
3. ECG waveform
4. ECG filter setting
5. ECG scale
WARNING
CAUTION
Asystole No QRS complex detected within the set time interval in the absence
of ventricular fibrillation or chaotic signal.
V-Tach The number of consecutive PVCs is greater than or equal to the V-Tach
PVCs limit, and the ventricular rate is greater than or equal to the V-
Tach rate limit.
Vent Brady The number of consecutive PVCs is greater than or equal to V-Brady
PVC limit and the ventricular rate is less than the V-Brady Rate limit.
Extreme Tachy The heart rate is greater than the extreme tachycardia limit.
Extreme Brady The heart rate is less than the extreme bradycardia limit.
R on T R on T PVC is detected.
Run PVCs More than two consecutive PVCs, but lower than the V-Brady PVCs
limit, and the ventricular rate is lower than the V-Tach rate limit.
Pacer Not Capture No QRS complex detected for 300 ms following a pace pulse (for
paced patients only).
Pacer Not Pacing No pace pulse detected for 1.75 x average R-to-R intervals following
a QRS complex (for paced patients only).
Nonsus V-Tach The number of consecutive PVCs is lower than the V-Tach PVCs limit
but greater than 2, and the ventricular rate is greater than or equal
to the V-Tach Rate limit.
Vent Rhythm The number of consecutive PVCs is greater than or equal to the V-
Brady PVCs limit, and ventricular rate is greater than or equal to the
V-Brady Rate limit but lower than V-Tach Rate limit.
Pause No QRS complex is detected within the set time threshold of pause.
Irr Rhythm End Irregular rhythm no longer detected for the irregular rhythm end
delay time.
A-Fib End Atrial fibrillation no longer detected for the A-Fib end delay time.
1. On the main screen, tap the HR digital area or ECG waveform area to enter the
[ECG] menu.
2. In the [Parameter Setup] section, tap [Arrhythmia].
3. Tap [Arrhythmia Alarm Setup]. The [Arrhythmia Alarm Setup] menu is dis-
played.
4. In the [Setup] section, select the desired option:
ǂ [All On]Ὁswitches on all arrhythmia alarms.
ǂ [All Off ]Ὁswitches off all arrhythmia alarms. This button becomes inactive
when [Lethal Arrhy Alarms Off ] is disabled in the System Setup menu of
the CMS.
ǂ [Lethals Only]: switches on all the lethal arrhythmia alarms only. Other
types of arrhythmia alarms are off.
5. In the [Alarms] section, select the options described in the following table.
R on T On, Off
WARNING
• If you switch off all arrhythmia alarms, the monitor will not alarm for any
arrhythmia event. This may result in a hazard to the patient. Always
keep the patient under close surveillance.
NOTE
• When the TM80 is connected to the CMS, any changes made either at the
TM80 or the CMS will be communicated to the other side.
• When lethal arrhythmia alarms are set to Disable at the CMS, the
symbol is displayed on the lethal arrhythmia alarms at the TM80.
NOTE
• If any of the lethal arrhythmia alarms is switched off, the ECG waveform
area displays the “Lethal Arrhys Off” message.
Asystole
V-Fib/V-Tach
V-Tach
High Priority
Vent Brady
Extreme Tachy
Extreme Brady
Beat Detection
PVC Alarm Chain Rate Alarm Chain A-Fib Alarm Chain
Alarm Chain
A-Fib/
Nonsus V-Tach Pauses/min Tachy/Brady
A-Fib End
R on T Missed Beats
Bigeminy
Trigeminy
PVCs/min
Multiform PVC
PVC
You can set the arrhythmia alarm timeout period at the CMS. For how to configure the
arrhythmia alarm timeout period, refer to Configuring the Arrhythmia Shield Time on
Page 14-11.
NOTE
• For the following alarms, alarm light and alarm tone cannot be disabled:
HR high, HR low, Tachycardia, Bradycardia, Afib End, Irr. Rhythm End.
• The timeout period is only applicable to the alarms in the medium prior-
ity chains and atrial fibrillation chain. For the alarms in the high priority
chain, alarm tone and alarm light are presented as soon as the alarm
condition is detected.
• Alarm indication rules for alarms in the atrial fibrillation chain are the
same with those for the medium priority chains.
Alarm in high priority Alarm in high priority chain Alarm light and alarm tone
chain
Alarm in medium priority During timeout period, alarm light and
chain alarm tone are disabled. When the timeout
period is reached, alarm light and alarm
tone are reactivated.
Alarm in medium priority Alarm in high priority chain Alarm light and alarm tone
chain
Alarm in the same medium Alarm light and alarm tone
priority chain, but with higher
priority
The same alarm reoccurs During timeout period, alarm light and
alarm tone are disabled. When the timeout
period is reached, alarm light and alarm
tone are reactivated.
Alarm in the same medium During timeout period, alarm light and
priority chain, but with lower alarm tone are disabled. When the timeout
priority period is reached, alarm light and alarm
tone are reactivated.
1
2 4
3 5
1. Parameter label
2. PVCs per minute label
3. PVCs per minute value
4. Pauses per minute label
5. Pauses per minute value
When the TM80 is connected to the CMS, you can adjust ST points, enter the ST graphic
window and the ST view at the CMS. For more information, refer to ST Monitoring on
Page 14-6.
WARNING
Numerics displayed in the ST digital area are different according to the lead type:
■ When the 3-lead ECG leadwires are used, the ST digital area is not displayed. A ST
value is displayed in the HR digital area.
■ When the 5-lead ECG leadwires are used, seven ST values (ST-I, ST-II, ST-III, ST-aVR,
ST-aVL, ST-aVF, ST-V) are displayed in the ST digital area.
■ When the 6-lead ECG leadwires are used, eight ST values (ST-I, ST-II, ST-III, ST-aVR,
ST-aVL, ST-aVF, ST-Va, ST-Vb) are displayed in the ST digital area.
This example shows the ST digital area when the 6-lead ECG leadwires are used. Your
screen may look slightly different:
2 3
1 4
5
)
1. Parameter label
2. ST alarm off symbol
3. Lead label
4. ST unit
5. ST numerics: a positive value indicates ST segment elevation, and a negative value
indicates ST segment depression.
The QT interval has an inverse relationship to heart rate. Faster heart rates shorten the
QT interval and slower heart rates prolong the QT interval. Therefore, several formulas
can be used to correct the QT interval for heart rate. The heart rate corrected QT interval
is abbreviated as QTc.
3
1 4
5
6
2
7
1. Parameter label
2. QT alarm off symbol
3. QTc value
4. Measurement unit
5. ΔQTc alarm off symbol
6. ΔQTc value (the difference between the current and baseline QTc values)
7. QT value
8.10 Relearning
Changes in ECG beat morphology could result in incorrect arrhythmia alarms and/or
inaccurate heart rate. ECG relearning allows the TM80 to learn the new dominant beat
morphology and thus reduce false arrhythmia alarms and inaccurate HR values. Once
learning is complete, the dominant QRS complex is stored as a reference template. The
reference template is used as the normal morphology of that patient and it is compared
with incoming beats to identify possible arrhythmias.
NOTE
1. On the main screen, tap the arrhythmia digital area to enter the [Arrhythmia]
menu.
2. Tap [Relearn].
OR
1. On the main screen, tap the ST digital area to enter the [ST] menu.
2. Tap [Relearn].
CAUTION
Introduction...............................................................................................................9-2
Resp Safety Information ........................................................................................9-2
Preparation for Monitoring Resp........................................................................9-3
Changing Resp Settings ........................................................................................9-4
Understanding the Resp Display........................................................................9-7
9.1 Introduction
Impedance respiration is measured across the thorax. When the patient is breathing or
ventilated, the volume of air changes in the lungs, resulting in impedance changes
between the electrodes. Respiration rate (RR) is calculated from these impedance
changes, and a respiration waveform appears on the screen.
WARNING
• If you do not set the detection level for the respiration correctly in man-
ual detection mode, it may not be possible for the TM80 to detect apnea.
If you set the detection level too low, the TM80 is more likely to detect
cardiac activity, and to falsely interpret cardiac activity as respiratory
activity in the case of apnea.
• If operating under conditions according to the EMC Standard IEC 60601-
1-2 (Radiated Immunity 3V/m), field strengths above 3V/m may cause
erroneous measurements at various frequencies. Therefore, it is recom-
mended to avoid the use of electrically radiating equipment in close
proximity to the respiration measurement unit.
CAUTION
• Respiration monitoring is not for use on the patients who are very
active, as this will cause false alarms.
1. Shave the chest hair from the electrode sites in a circular area with a diameter of 2
to 4 inches.
2. Use a dry gauze pad to remove excess skin oils, skin cells and residue from the
electrode sites. Never rub the skin until it is raw or bleeding.
NOTE
• Proper skin preparation is necessary for good signal quality at the elec-
trode site, as the skin is a poor conductor of electricity.
RA (R)
LL (F)
Lead II
CAUTION
NOTE
■ On the main screen, tap the Resp digital area or waveform area.
■ Press to enter the main menu →tap [Parameter Setup] → tap [Resp].
1. In the [Setup] section of the [Resp] menu, select the options described in the fol-
lowing table.
NCM Alarm Delay The TM80 will trigger the “No Chest Move- 10s, 15s, 20s, 25s, 30s, 35s, 40s
ment” alarm if the patient has stopped
breathing for longer than the set apnea
time. This alarm is displayed on the central
monitoring system only.
1. In the [Waveform] section of the[Resp] menu, select the options described in the
following table.
Gain Selects the waveform size. x0.25, x 0.5, x 1, x2, x3, x4, x5
Speed Selects the waveform sweep speed. 3mm/s, 6.25 mm/s, 12.5 mm/s, 25
mm/s
1. In the [Alarms] section of the [Resp] menu, tap [Resp Alarm Setup] .
2. Select the options described in the following table.
No Chest Movement The TM80 will trigger the “No Chest Movement” Alarm Priority: High
alarm if the patient has stopped breathing for
longer than the set apnea time. This option
defaults to be switched on.
When the TM80 is connected to the Central
Monitoring System, switching on or off this
option at the Central Monitoring System also
switches it on or off at the TM80, and vice versa.
After tapping this option, you can configure the
alarm priority.
1 2
4 3
1. Parameter name
2. Measurement unit
3. Respiration rate (RR)
4. Alarm high limit and low limit.When RR alarm is switched off, the alarm off symbol
instead of alarm limits is displayed.
Introduction...............................................................................................................10-2
SpO2 Safety Information.......................................................................................10-2
Measurement Limitations.....................................................................................10-3
Connecting and Disconnecting the SpO2 Module .....................................10-3
Changing SpO2 Settings .......................................................................................10-4
Performing SpO2 Measurement.........................................................................10-7
Understanding the SpO2 Display ......................................................................10-8
10.1 Introduction
SpO2 monitoring is a non-invasive technique used to measure the amount of oxygen-
ated hemoglobin and pulse rate by measuring the absorption of selected wavelengths
of light. The light generated in the probe passes through the tissue and is converted into
electrical signals by the photo detector in the probe. The SpO2 module processes the
electrical signal and displays a waveform and digital values for SpO2 and pulse rate.
NOTE
WARNING
• Only use SpO2 sensors specified in this manual. Follow the SpO2 sensor’s
instructions for use and adhere to all warnings and cautions.
• The operator is responsible for checking the compatibility of the pulse
oximetry monitor, sensor, and patient cable prior to use. Incompatible
components can result in degraded performance and/or device malfunc-
tion.
• When a trend toward patient deoxygenation is indicated, blood samples
should be analyzed by a laboratory co-oximeter to completely under-
stand the patient’s condition.
• Do not use SpO2 sensors during magnetic resonance imaging (MRI).
Induced current could potentially cause burns. The sensor may affect
the MRI image, and the MRI unit may affect the accuracy of the oximetry
measurements.
• Prolonged and continuous monitoring may increase the temperature of
the sensor and cause the patient discomfort. It is especially important to
check the sensor placement, and ensure proper attachment on patients
suffering from poor perfusion or skin sensitivity. Check the sensor loca-
tion every two hours and move to another location if the skin deterio-
rates. More frequent examinations may be required for different
patients.
WARNING
■ Ambient light
■ Physical movement
■ Low perfusion
■ Electromagnetic interference
■ Dysfunctional hemoglobin, such as carboxyhemoglobin (COHb) and
methemoglobin (MetHb)
■ Presence of certain dyes, such as methylene and indigo carmine
■ Inappropriate positioning of the SpO2 sensor, or use of incorrect SpO2 sensor
■ Drop of arterial blood flow to immeaurable level caused by shock, anemia, low
temperature or vasoconstrictor.
To disconnect the SpO2 module from the TM80, pinch the left and right sides near the
helix parts circled in red (as shown below) on the SpO2 module cable and pull the SpO2
module out horizontally. Do not disconnect the SpO2 module from the TM80 by pulling
out the SpO2 module cable directly.
Small red
circle
SpO2 module
SpO2 sensor
■ On the main screen, tap the SpO2 digital area or waveform area.
■ Press to enter the main menu →tap [Parameter Setup] → tap [SpO2].
1. In the [Setup] section of the [SpO2] menu, select the options described in the fol-
lowing table.
Sensitivity Selects the sensitivity mode depending upon High, Med, and Low
signal quality and patient motion.
■ High
This mode can truly reflect the patient physio-
logical state but may be slightly disturbed by
artifact.
■ Med
This mode provides the best combination of
sensitivity and anti-interference performance.
This mode is recommended for the majority of
patients.
■ Low
This mode is the least sensitive to reflect the
patient physiological state but has the best anti-
interference performance.
1. In the [Waveform] section of the [SpO2] menu, select the options described in the
following table.
Speed Selects the SpO2 pleth waveform speed. 6.25 mm/s, 12.5 mm/s, 25
mm/s
1. In the [Alarms] section of the [SpO2] menu, select the options described in the fol-
lowing table.
SpO2 Alarm Setup Configures whether to switch on SpO2 and SpO2 For SpO2:
Desat alarms. [SpO2 ] and [Desat] default to be Alarm switch: On, Off
switched on.
After tapping [SpO2] or [Desat] you can config- Alarm limit range:
ure alarm limits and alarm priority. 1% to 100%; the step is 1%.
The default alarm high limit
is [100] and the default
alarm low limit is [90].
The alarm high limit should
be at least 2% greater than
the alarm low limit.
Alarm Priority: Med, High
For Desat:
Alarm switch: On, Off
Alarm limit range:
The Desat alarm low limit
should not be higher than
the SpO2 alarm low limit.
The default alarm low limit is
[80].
Alarm Priority: High
NIBP Simul When monitoring SpO2 and NIBP on the same On, Off
limb simultaneously, you can switch on [NIBP
Simul] to lock the SpO2 alarm status until the
NIBP measurement ends. If you switch off [NIBP
Simul], low perfusion caused by NIBP measure-
ment may lead to inaccurate SpO2 readings and
therefore cause false physiological alarms.
The SpO2 measurement displays when the TM80 detects that a sensor is con-
nected to the patient.
WARNING
• When equipped with Mindray SpO2 module, use only Mindray SpO2 sen-
sors specified in this manual. Use of other SpO2 sensors may cause
improper oximeter performance.
• Do not disconnect the SpO2 sensor connector from the SpO2 module
during defibrillation.
• If the sensor is too tight because the application site is too large or
becomes too large due to edema, excessive pressure for prolonged peri-
ods may result in venous congestion distal from the application site,
leading to interstitial edema and tissue ischemia.
CAUTION
1 2 3 4 5
10
7
9 8
SpO2 digital area (for portrait display)
1. Parameter name
2. SpO2 value
3. Perfusion indicator
4. Perfusion index (PI) label
5. Perfusion index value: gives the numerical value for the pulsatile portion of the
measured signal caused by arterial pulsation. PI is an indicator of the pulsatile
strength.
◆ Above 1 is optimal.
◆ Between 0.3 and 1 is acceptable.
◆ Below 0.3 indicates low perfusion. Reposition the SpO2 sensor or find a bet-
ter site. If low perfusion persists, choose another method to measure oxygen
saturation if possible.
6. SpO2 unit of measure
7. PR measurement unit
8. PR value
9. Pulse rate (PR) label
10. Alarm high limit and low limit.When SpO2 alarm is switched off, the alarm off sym-
bol instead of alarm limits is displayed.
1. Parameter name
2. Pleth waveform
Pairing Introduction................................................................................................11-2
Pairing a TM80 with a BP10 ..................................................................................11-2
Unpairing the TM80 with the BP10 ...................................................................11-4
Screen Display after Pairing a TM80 with a BP10 .........................................11-6
Interactions after Pairing a TM80 with a BP10...............................................11-7
You can connect a TM80 to a BP10 via Mindray Patient Area Network (abbreviated as
MPAN). The process of establishing connection between the TM80 and the BP10 is called
“pairing”.
When the TM80 is paired with the BP10, measured NIBP data and NIBP-related technical
alarms will be transferred from the BP10 to the TM80. You can view NIBP data and NIBP-
related technical alarms and physiological alarms on the TM80’s screen.
For MPAN specifications, refer to MPAN Specifications on Page 11-2. For the functional-
ities and operations of the BP10, refer to BP10 NIBP Module Operator’s Manual.
1. Press the MPAN key on the right panel of the BP10. The “Pairing...” message will dis-
play in the prompt message area of the BP10.
T.
WARNING
• Before pairing a BP10 with a new TM80, unpair it with the current TM80
first.
• Do not pair a TM80 with an undesired BP10. If a TM80 is paired with an
undesired BP10, the patient category may be not applicable for the
patient and the measured NIBP data may be incorrect.
NOTE
• Make sure that you have selected the correct BP10 to pair it with the
TM80.
• If you pair a TM80 with a BP10 when NIBP measurement mode is set to
[ABPM] at BP10, the system responses after successful pairing are
slightly different from that when the NIBP measurement mode is set to
[Manual], [Auto], or [Sequence]. For the differences, see System
Responses after Successful Pairing on Page 11-3.
■ The icon will be changed to in the top-right corner of the TM80’s screen.
◆ If neither [Yes] nor [No] is selected, the wireless setup confirmation message
will disappear in three minutes. Besides, the “Pairing failure” message will be
displayed in the prompt message area of the TM80. The “MPAN
Disconnected” message is displayed in the message area of the BP10. In this
case, follow steps in Pairing a TM80 with a BP10 on Page 11-2 to pair the
TM80 with the BP10 again.
■ When NIBP measurement mode is set to [Manual], [Auto], or [Sequence] and the
BP10 is paired successfully with the TM80, the wireless setup confirmation
message “Select Yes to continue Patient in BP10. Select No to continue Patient in
Telemetry.” will not be displayed. Patient-related settings from the TM80 will be
transferred to the BP10. But NIBP-related settings displayed on the main screen of
the TM80 will come from the BP10. The patient monitored by BP10 will be dis-
charged automatically and the data history related to this patient will be cleared.
■ Patient Category can be changed at the TM80 only.
■ A patient cannot be discharged from the BP10 and NIBP-related settings are
grayed out at BP10. To discharge a patient from BP10, you need to unpair the BP10
form the TM80 by following steps in Unpairing the TM80 with the BP10 on Page
11-4.
■ The status of the BP10 unpaired will be displayed as [Disconnect] on the list of
[Devices] at the TM80.
■ The icon will be changed to in the top-right corner of the TM80’s screen
and of the BP10.
■ Measured NIBP values on the main screen of the TM80 is displayed as “---”
indicating invalid values.
■ The “MPAN Disconnected”message is displayed in the message area of the BP10.
Option 2:
■ The icon will be changed to in the top-right corner of the TM80’s screen
and of the BP10 .
■ Measured NIBP values on the main screen of the TM80 is displayed as “---”
indicating invalid values.
■ The “MPAN Disconnected”message is displayed in the message area of the BP10.
CAUTION
3 4 5 6 7
2 8
1 9
10
11
■ Press to enter the main menu →tap [Parameter Setup] → tap [NIBP].
1. In the [Setup] section of the [NIBP] menu, select the options described in the fol-
lowing table.
For pediatric:
41 mmHg to 199 mmHg; the default alarm
high limit is [120] and the default alarm low
limit is [70].
For pediatric:
11 mmHg to 149 mmHg; the default alarm
high limit is [70] and the default alarm low
limit is [40].
For pediatric:
Alarm limit range: 21 mmHg to 164 mmHg;
the default alarm high limit is [90] and the
default alarm low limit is [50].
For pediatric:
40 mmHg to 200 mmHg; the default alarm
high limit is [130] and the default alarm low
limit is [60].
For pediatric:
10 mmHg to 150 mmHg; the default alarm
high limit is [80] and the default alarm low
limit is [30].
For pediatric:
20 mmHg to 165 mmHg; the default alarm
high limit is [100] and the default alarm low
limit is [40].
NOTE
• For systolic pressure, diastolic pressure, or mean pressure, its alarm high
limit should not be greater than the high limit of SYS Extreme, DIA
Extreme, or MAP Extreme.
• For systolic pressure, diastolic pressure, or mean pressure, its alarm high
limit should beat least 5mmHg greater than its alarm low limit.
Introduction...............................................................................................................12-2
Tabular Trends Review Page.................................................................................12-2
Events Review Page ................................................................................................12-5
12.1 Introduction
You can review patients’ history data on the tabular trends review page and the events
review page.
Option 1:
2. Tap [Review].
3. Tap [Tabular Trends].
Option 2:
Tap the [Tabular Trends] button in the upper right corner of the events review page.
For how to enter the events review page, refer to Entering the Events Review Page on
Page 12-5.
3
4
1
2 6
12 11 10 9 8 7
1. Current system date and trend data time. The interval of the trend data time is
dependent on the option selected for [Interval].
2. Digital area: displays numeric values at the cursor indicated time. The background
color of numeric values indicates the alarm priority.
◆ Red: high priority alarm event
◆ Yellow: medium priority alarm event
◆ Cyan: low priority alarm event
3. Events button: tapping this button goes to the events review page.
4. Event type indicator: different color blocks indicate different types of events:
◆ Red: high priority alarm event
◆ Yellow: medium priority alarm event
◆ Cyan: low priority alarm event
◆ Green: manual event
◆ White: operation-related event such as system time change
5. Vertical bar: indicates the position of currently displayed parameters in all the
parameters.
6. Highlighted column: indicates the trend data currently selected.
7. Search button: allows searching trend data within the specific time range.
8. Next page button: tapping this button moves to the right-most column of the
review page.
9. Previous page button: tapping this button moves to the left-most column of the
review page.
10. Next event button: tapping this button locates the next event.
11. Previous event button: tapping this button locates the previous event.
12. Interval setup button: tapping this button opens the [Interval] menu. For more
information regarding this menu, refer to Changing the Resolution of Trend Data
on Page 12-5.
After you tap the button on the tabular trends review page, the tabular trends data
search page is displayed. The following figure is for reference only.
1 2
NOTE
• When the TM80 is connected to the CMS, if events of the TM80 are
deleted from the CMS, they will not be deleted from the TM80 and vice
versa.
Option 1:
2. Tap [Review].
3. Tap [Events].
Option 2:
Tap the [Events] button in the upper right corner of the tabular trends review page.
NOTE
1. The position of current page in the total pages of events: for example, 39/56 indi-
cates that there is a total of 56 pages of events and currently displayed events is on
Page 39. You can swipe your finger up and down the screen to view other events.
2. Tabular trends button: tapping this button goes to the tabular trends review page.
3. Event overview area: provides an overview of the selected event
◆ Event trigger time
■ For manual events, you can view all the monitored waveforms 16 seconds before
and after the event trigger time and all the measurement numerics at the event
trigger time.
■ For alarm events, you can view event-related waveforms 16 seconds before and
after the event trigger time and all the measurement numerics at the event trigger
time.
The following figure is for reference only.
The event trigger time is marked in a colored block along the timeline at the top of the
event details page. Different color blocks indicate different types of events:
All the measurement numerics at the event trigger time are displayed at the bottom of
the event details page. You can view these numerics by swiping your finger at the bot-
tom of the main screen. The background color of numerics indicates the alarm priority.
Introduction...............................................................................................................13-2
Entering the Maintenance Menu .......................................................................13-2
Configuring the General Menu...........................................................................13-2
Configuring the Alarms Menu.............................................................................13-4
Quick Keys Menu......................................................................................................13-5
Configuring the Network Menu .........................................................................13-7
Defaults Menu...........................................................................................................13-12
Screen Lock Menu ...................................................................................................13-14
Changing the Passwords.......................................................................................13-15
Changing the Device Name .................................................................................13-16
Configuring the CMS Disconnect Alarm .........................................................13-16
13.1 Introduction
The [Maintenance] menu provides access to the system settings such as location, device
name, alarm settings, quick keys, screen lock, and passcode updates. Entering this menu
requires a passcode.
Display Auto Off Configures the time for display auto off. 1 min, 2 min, 5 min, 15 min, 30
min, Off
Device Location Configures facility information, department information, and patient location.
Refer to Configuring Device Location on Page 13-3 for details.
Notch Filter Configures the ECG Notch filter. This 50 Hz, 60 Hz, Off
option is used to filter out AC line noise
from the ECG waveform.
ECG Lead Labeling Changes the ECG lead labeling. AHA, IEC
Date &Time Configures the time format, date format, Time Format: 12Hr, 24 Hr
specific time, and date. Date Format: DD/MM/YY, YY/MM/
DD, MM/DD/YY
NOTE
• Mindray recommends the same SpO2 tone mode be used for the TM80
within a monitoring area.
1. In the [Maintenance] menu, tap [Alarms]. The current setting displays to the right
of the option.
2. Select the options described in the following table.
Sounds
Style Allows an authorized user to set the alarm tone ISO, Mode 1, Mode 2
pattern.
Minimum value
Timeout
Reminder Interval Allows an authorized user to configure the 1 min, 2 min, 3 min, 5 min, 10 min
intervals between the alarm tones.
ECG Lead Off Allows an authorized user to configure the Low, Med, High
alarm priority.
SpO2 Sensor Off Allows an authorized user to configure the Low, Med, High
alarm priority.
WARNING
2. From the quick keys area at the bottom of the screen, tap a quick key you want to
configure.
A list of options displays.
A list of options
3. Tap the desired option from the list of options to configure the selected quick key.
4. Repeat Steps 2 to 3 to configure other quick keys, if needed.
In the [Network] menu, you can configure the network and connect the TM80 to the
BeneVision Central Monitoring System via the wireless network.
IP Address Setup Select to access the [IP Address Setup] Refer to Configuring IP Settings
menu. on Page 13-8 for details.
WLAN Setup Select to access the [WLAN Setup] menu. Refer to Configuring WLAN Set-
tings on Page 13-9 for details.
Wireless Setup Select the desired WiFi band and the Refer to Selecting WiFi Bands and
desired channel Channels on Page 13-11 for
details.
EAP Certificate Import desired certificates and delete cer- Refer to EAP Certificate Manage-
tificates from the TM80. ment on Page 13-12 for details.
NOTE
The following three options are only enabled when [DHCP] is set to Off.
IP Address Select to input the IP address. Range: 1 to 255 for the number
before the first decimal point
0 to 255 for the number after the
first decimal point
Factory default: 192.168.0.100
Subnet Mask Select to input the subnet mask. Range: 1 to 255 for the number
before the first decimal point
0 to 255 for the number after the
first decimal point
Factory default: 255.255.255.0
IP Gateway Select to input the IP gateway address. Range: 1 to 255 for the number
before the first decimal point
0 to 255 for the number after the
first decimal point
Factory default: 192.168.0.254
3. Tap [Confirm] to apply the settings and exit the [IP Address Setup] menu.
Network Name Select to input the SSID of the desired SSID of the desired WLAN
WLAN.
Security Type Configures the wireless network security Open, WPA/WPA2-PSK, WPA/
type. WPA2 EAP, WPA/WPA2 CCKM
The options are dependent on the [WiFi
Band] selected.
If [WPA/WPA2-PSK] is selected, you need
to configure [Network Password].
If [WPA/WPA2 EAP] or [WPA/WPA2
CCKM] is selected, you need to configure
[Network Password] and additional items
such as [EAP Method] and [Authentica-
tion]. You also need to import the desired
certificate into the TM80 before you can
select a certificate. For how to manage
certificates, see EAP Certificate Manage-
ment on Page 13-12.
3. Tap [Confirm] to apply the settings and exit the [WLAN Setup] menu.
NOTE
Multicast Address Select to input the multicast address. Range: 1 to 255 for the number
before the first decimal point
0 to 255 for the number after the
first decimal point
Factory default: 225.0.0.8
Port It is a public port to communicate with the 6678, grayed and unchangeable
CMS.
Multicast TTL Select to input the Multicast Time to Live Range: 1 to 255
(TTL). Factory default: 1
5. Tap [Confirm] to apply the settings and exit the [Connect CMS] menu.
5. Tap [Confirm] to apply the settings and exit the [Connect CMS] menu.
■ Select [Select CMS] from the [Connect CMS] menu. For details, refer to
Connecting the CMS in Unicast Mode on Page 13-10.
NOTE
1. Press to enter the main menu → tap [Maintenance]→ enter the required
password → tap [Network] → tap [EAP Certificate].
2. Tap [Local].
3. Select the desired certificate.
4. Tap [Delete].
Options Description
Save Departmental Defaults Allow an authorized user to save the current device settings for the selected
patient category.
Export Device Settings Copy the current settings to the external device.
Options Description
Import Device Settings Copy the settings from the external device to the TM80. Refer to Transferring
a Configuration on Page 13-13 for details.
Restore Factory Defaults Allow an authorized user to reestablish the original database power up
settings to factory default values.
To transfer the configuration from the TM80 A to TM80 B, follow this procedure::
NOTE
• The symbol displays at the top of the screen while transferring a con-
figuration.
• When TM80 is connected to the CentralStation, Import Device Settings
would not work. To use Import Device Settings, TM80 should not be con-
nected to CentralStation.
ǂ To stop the import from TM80 A, tap at TM80 B to exit the [Import
Device Settings].
ǂ To retry the import from the TM80 A, tap the external devices where the
“Failure” message is displayed and tap the [Retry] button to restart the
transfer.
You may need to repeat the retry operation several times until the transfer is suc-
cessful.
1. In the [Maintenance] menu, tap [Screen Lock] to choose a screen lock mode.
2. When [Screen Lock] is set to [Locked] or [View Only], enter a passcode.
After the passcode is entered, the TM80 exits the passcode setup menu. The
selected lock mode displays to the right of [Screen Lock].
1. In the [Maintenance] menu, tap [Screen Lock] to choose a screen lock mode.
2. Select your desired screen lock mode and then enter a passcode.
NOTE
WARNING
• When [CMS Disconnect Alarm] is disabled, the medical staff should pay
more attention to the patient’s status and check the TM80’s network
connection status at the CMS. When the offline alarm is displayed on the
CMS, medical staff should check the patient ‘s status immediately.
Introduction...............................................................................................................14-2
Network Safety Information.................................................................................14-3
Adjusting the Minimum QRS Detection Threshold .....................................14-3
QT Monitoring...........................................................................................................14-4
ST Monitoring............................................................................................................14-6
Arrhythmia Monitoring..........................................................................................14-10
Locating the TM80...................................................................................................14-12
Sending a Notification to the TM80 ..................................................................14-12
Triggering an Alarm Reminding Patients' Location.....................................14-13
14.1 Introduction
This chapter only describes the operations that you need to perform at the CMS. For
common operations such as how to set alarms and parameter settings at the CMS, refer
to BeneVision Central Monitoring System Operator’s Manual.
When the TM80 is successfully connected to the CMS (Version 07.19. or above),
■ The TM80 transmits parameter values, waveforms, alarm settings, and events to
the CMS. From the CMS, you can check the patient’s monitoring data and alarms.
■ Patient information, alarm settings, alarm status, and parameter settings can be
synchronized between the TM80 and the CMS.
■ The TM80’s screen is off.
■ The CMS will automatically send configurations to the TM80 under the following
circumstances:
◆ The TM80 is connected to the CMS for the first time.
◆ User configurations are saved at the TM80.
◆ The TM80 is connected to a different CMS.
◆ After configurations are sent, configurations are saved again at the CMS, or
◆ The department is modified at the TM80 and corresponding department
configurations are available at the CMS.
The configurations will be saved as user configurations at the TM80. They will be
automatically loaded when a patient category is changed or a patient is dis-
charged at the TM80.
When the TM80 is disconnected from the CMS and then re-establishes connection to the
CMS, it can send the following data which was not received by the CMS during the time
of connection loss.
■ Up to most recent 48 hours of tabular trends for all parameters at the trend
interval equal to or greater than 1 minute.
■ Up to 200 events
■ Up to two-hour full disclosure waveforms of ECG I, II, III, and V/Va leads.
WARNING
CAUTION
• If wireless network signal is poor, there may be a risk of CMS data loss.
• RF interference may result in wireless network disconnection.
• Disconnecting from the network may result in CMS data loss and func-
tion failure. Check the patient in case of network disconnection and
solve the network problem as soon as possible.
• Ensure that the TM80’s IP address setting is correct. Changing the net-
work settings may result in network disconnection. Contact your service
personnel if you have any problems on setting the IP address.
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. From the [ECG] tab, select the [QRS Threshold] section.
3. Select the arrow buttons to adjust the QRS threshold. Selecting [Defaults] resets
the QRS threshold to the default value (0.16 mV).
CAUTION
• The setting of QRS threshold can affect the sensitivity of arrhythmia, ST,
QT/QTc detection, and heart rate calculation.
• If QRS amplitude is low, the TM80 might not be able to calculate heart
rate and false asystole may occur.
14.4 QT Monitoring
A normal ECG waveform (as shown in the following figure) typically includes a sharp and
well defined QRS complexes with consistent spacing between R waves, and an ECG
baseline that is free of noise and artifact.
R
ISO Point
ST Point
J Point
T
P
QT Interval
The QT interval in an ECG lead is the time interval from the onset of the earliest deflec-
tion in the QRS complex to the end of the T wave. QT monitoring can assist in the detec-
tion of prolonged QT interval syndrome.
14.4.2 QT View
In the [QT View] menu, you can view a snapshot of the real-time wave and to verify that
the QT algorithm detects correct Q and T points.
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. Select the [QT] tab.
3. Select [QT View] at the bottom of the [QT] menu.
The [QT View] menu displays, as shown in the following figure:
QT View menu
Left or right arrow Select the desired lead to display on the II, I, III, aVR, aVL, aVF, V
[QT View] menu screen by selecting the Note: the leads here serve as an
left or right arrow. example only. They depend on
the [Lead Set] selected.
NOTE
14.5 ST Monitoring
R
ST deviation
ISO Point
ST Point
Depression or Elevation
J Point
P T
40 to 80 msec
S
ST Segment
The ST segment of an ECG waveform (as shown in the above figure) represents the
period from the end of ventricular de-polarization, to the beginning of ventricular re-
polarization, or the end of the QRS complex (the J point) and the beginning of the T-
wave. ST Segment analysis is used to monitor the oxygen supply and the viability of the
heart muscle.
ST deviation is the vertical distance between the isoelectric (ISO) point level and signal
level at ST point.
The ISO point is located between the end of the P-wave and the onset of the QRS com-
plex. The ISO point provides the baseline for this measurement.
The ST point is a fixed distance from the J point at the end of the QRS complex. The ST
point can be configured to 40, 60, or 80 milliseconds past the J-point, independent of
the heart rate. By default, the ST point is positioned as follows:
■ at 80 milliseconds for heart rates less than or equal to 120 beats per minute
■ at 60 milliseconds for heart rates greater than 120 beats per minute
All available ECG leads are analyzed to measure deviations in the ST segment.
Selecting leads that contain the least amount of baseline flutter will improve measure-
ment accuracy, but accurate ST deviation measurement is dependent on the correct
location of the ISO and ST points.
WARNING
• The ST algorithm has been tested for accuracy of the ST segment data.
The significance of the ST segment changes need to be determined by a
clinician.
• ST deviation is often calculated at a fixed offset from the J point.
Changes in heart rate may affect ST.
WARNING
• Always make sure that the ST measurement points are appropriate for
your patient.
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. Select the [ST] tab.
3. Select the [Adjust] section.
4. Set [ST Point].
5. Enable or disable [Auto Adjust]. This option defines the method of adjusting the
ISO point and J point.
◆ Enabled: It is enabled by default. In this case, positions of ISO point and J
point are automatically adjusted accordingly.
◆ Disabled: you need to manually adjust the position of ISO point and J point
by selecting the arrows at the right sides of ISO and J.
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. Select the [ST] tab to enter the [ST] menu.
3. From the bottom of the ST menu, select [ST Graphic].
The height of the bar indicates the ST value of corresponding ST lead. The color of the
bar indicates ST alarm status: green indicates that corresponding ST value is within alarm
limits; cyan, yellow and red indicate that the ST value exceeds the alarm limits. The color
matches ST alarm priority.
The height of gray bar indicates the baseline ST value and the green bar (cyan, yellow or
red if an alarm occurs) indicates ΔST.
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. Select the [ST] tab to enter the [ST] menu.
3. From the bottom of the menu, select [ST View].
1. On the ViewBed screen of the CMS, select the ECG digital area or waveform area to
enter the [ECG] menu.
2. Select the [Arrhythmia] tab.
3. Select the [More Threshold] section.
4. Set the desired items using the right or left arrow.
The following figure illustrates the conditions under which PVC alarms will be generated
if [V-Tach PVCs] is set to 6, [V-Tach Rate] is set to 130, [V-Brady PVCs] is set to 5, and [V-
Brady Rate] is set to 40.
If both V-Tach PVCs and V-Tach Rate are greater than or equal to the limits, a V-Tach alarm
is generated.
ƾ If consecutive PVCs is lower than the V-Tach PVCs limit (6) but greater than 2, and
the Vent rate is greater or equal to the V-Tach Rate limit (130), a Nonsus V-Tach
alarm is generated.
ƾ If consecutive PVCs is greater than or equal to the V-Brady PVCs limit (5), and the
Vent rate is lower than the V-Brady limit (40), a Vent Brady alarm is generated.
ƾ If both the V-Brady PVCs and V-Brady Rate are lower than the limits, but V-Brady
PVCs is greater than 2, a Run PVCs alarm is generated.
ƾ If the V-Brady PVCs and V-Brady Rate are greater than or equal to limits, but the
Vent rate is is lower than V-Tach Rate (130), a Vent Rhythm alarm is generated.
1. Select the system menu area in the upper left corner of the CMS screen.
2. Select [System Setup] to access the [System Setup] menu.
3. Select the [Telemetry] tab.
4. Select the [Alarm] Tab.
5. Set [Arrhy Shield Time]. When it is set to [0], it indicates that the alarm alarm
shield function is disabled.
WARNING
NOTE
• Find Device requires that the TM80 has sufficient battery power and is
within the coverage area.
1. On the ViewBed screen of the CMS, select the [Send Message] quick key from
the quick key area.
2. Enter a notification into the pop-up window.
3. Select [Send]. This message will be sent to the corresponding TM80 and displayed
on the main screen of this TM80.
4. If you wish to confirm the notification, tap [Confirm] at the TM80.
After the functionality is enabled, when a patient enter or move out of the restricted
area, the “Out of the allowed area ” alarm will be triggered at the TM80.
1. Select the system menu area in the upper left corner of the CMS screen.
2. Select [System Setup] to access the [System Setup] menu.
3. Select the [Network] tab.
4. Select the [AP Management] tab.
5. In the [Patient Movement Area Setup] section, configure [Setup Mode] and
[Department].
6. If you need to specify an AP location, enter the desired AP location in the [Please
input location information] field. If you wish to select all the locations, select
[Select All].
7. Enable or disable [Trigger an alarm when patients enter the restricted area] or
[Trigger an alarm when patients move out of the allowed area]. This option is
dependent on [Setup Mode].
8. Select [Alarm Priority].
When the “Out of the allowed area ” alarm is triggered, check patient’s location and tap
[Confirm] at the TM80.
Introduction...............................................................................................................15-2
Battery Safety Information ...................................................................................15-3
Installing the Battery ..............................................................................................15-5
Checking the Battery Charge Status .................................................................15-5
Removing the Battery ............................................................................................15-5
Charging the Rechargeable Lithium-ion Battery .........................................15-6
Storing the Batteries ...............................................................................................15-7
Maintaining the Rechargeable Lithium-ion Battery....................................15-8
Disposing of the Batteries.....................................................................................15-9
15.1 Introduction
The TM80 can be powered by a lithium-ion rechargeable battery or AA batteries. This
chapter provides instructions on how to use, maintain, and dispose of the batteries.
For how to use, maintain, and dispose of the batteries used for BP10, refer to BP10 NIBP
Module Operator’s Manual.
WARNING
• Keep the batteries in their original package until you are ready to use
them.
• Make sure to install the lithium-ion battery or the AA battery tray and
close the battery compartment during defibrillation.
• Only use recommended AA batteries or rechargeable lithium-ion bat-
tery to power the TM80. Other power supplies may cause damage to the
equipment or lead to body injury.
• While installing AA batteries, do not apply reverse polarity.
SE
WARNING
CAUTION
NOTE
NOTE
• If the “Low Battery” or “Critically Low Battery” alarm occurs, the TM80
turns off the audio, its screen displays the “Local Audio Off” message,
and the screen brightness turns dimmer.
CAUTION
NOTE
• Keep the ECG leadwire and SpO2 module connected with the TM80
while removing the battery.
1. Lift up the lithium-ion battery or AA battery tray at the bottom of the compart-
ment to pop it out.
WARNING
• Only use the specified central charger to charge to the lithium-ion bat-
teries designated by Mindray.
• Only use the approved power cord with the grounded mains plug to
firmly connect the central charger to a grounded AC mains socket. Never
refit the mains plug to fit an ungrounded AC mains socket.
• Do not use the Multiple Portable Socket Outlets (MPSO) or AC mains
extension cords. Use an IEC 60601-1 approved isolation / separation
transformer, otherwise, it may result in leakage current. Ensure that the
sum of the individual ground leakage currents does not exceed the
allowable limits.
• Do not place any shield object (such as cloth or paper) to cover the cen-
tral charger or batteries, and keep ventilated while charging the lith-
ium-ion batteries.
• Do not connect other devices to the power supply system.
• Do not use the central charger to charge the lithium-ion batteries at
high temperature above 40°C.
Use the central charger to charge the lithium-ion batteries. The central charger can
charge 10 lithium-ion batteries at one time. For details about the central charger, refer to
BeneVision Central Charger Operator’s Manual.
If you need to store the batteries for an extended period of time, place the batteries in a
cool, dry place (ideally at 15°C or 60°F) with a partial charge of about 50% capacity (two
LEDs illuminated). Storing batteries in a cool place can slow the aging process.
Stored batteries should be charged to about 50% of their capacity every six months. The
battery should be fully charged prior to first use.
NOTE
• Remove the lithium-ion battery from the equipment unit if the equip-
ment is not used for a prolonged time (for example, several weeks), and
keep the equipment in a clean place to avoid the dust or liquid entering
the battery compartment.
• Storing batteries at high temperatures for an extended period of time
will significantly shorten their life expectancy.
• Do not store the batteries in an environment above 60°C (122°F) or
lower than -20°C (-4°F).
Do not store disposable AA batteries by leaving them in the incorrect polarity position in
the TM80.
NOTE
Charge the battery Upon receipt, after use, a “Low Battery” or “Critically Low Bat-
tery” alarm occurs.
To optimize performance, a fully or almost fully discharged
battery must be charged immediately.
Clean the battery At each patient discharge, or in case that the battery is
exposed to contaminants.
Do not clean the battery contacts during cleaning.
Charge stored battery to at Once every six months if the TM80 is not in use for an
least 50% of the battery extended period of time.
capacity.
Dispose of the battery When the “Battery Maintenance Required” alarm message
displays on the TM80’s screen.
The lifetime of a lithium-ion battery depends on the frequency and duration of use. With
good maintenance, the useful life is approximately 500 complete charge-discharge
cycles. Experience indicates that the incidence of failure may increase with battery ser-
vice life due to the accumulated stresses of daily use. Therefore, Mindray strongly recom-
mends that the lithium-ion battery should be replaced after two years or 500 complete
charge-discharge cycles. Using the outdated battery may cause the device abnormity
and unacceptable performance.
The age of a lithium-ion battery begins at the date of manufacture. The date of manufac-
ture is listed on the rear of the battery.
NOTE
• The battery capacity decreases over time with the number of charge
cycles.Toward the end of its useful life, the battery capacity may be
reduced by 20% to 25%. If the reduced battery life is unacceptable for
your equipment, Mindray recommends the battery be replaced.
For methods to troubleshoot the central charger, refer to BeneVision Central Charger
Operator’s Manual. For methods to troubleshoot the BP10, refer to BP10 NIBP Module
Operator’s Manual.
ECG noise The noise interference is overlapped 1. Check that the electrodes are in good
with ECG waveforms. contact with the skin.
2. Check that the ECG leadwires are
connected securely.
3. Check that the patient does not
contact any ungrounded electric
equipment.
ECG signal saturated The TM80 detected ECG signal satu- 1. Check the ECG leadwires.
ration or overload. 2. Check that the electrodes are in good
contact with the skin.
3. Check that the electrodes are not
expired.
The TM80 or SpO2 The battery capacity for the TM80 is Replace with a known good battery.
module is started depleted.
repeatedly.
The SpO2 data is not 1. The SpO2 module is not 1. Connect the SpO2 module to the
displayed on the Cen- connected to the TM80. TM80.
tral Station. 2. There might be a problem 2. Replace the SpO2 module with a
with the SpO2 module. known good one.
The TM80 cannot be The wireless access point (AP) in the Make sure that the AP is enabled and
connected to the Cen- vicinity is not enabled. belongs to the Virtual LAN (VLAN) where the
tral Station wirelessly TM80 is covered.
and the Wi-Fi symbol
on the main screen of The TM80 is not powered on under Put the TM80 within the AP coverage area
the TM80 is displayed the AP coverage area. and restart it. Ensure that the signal strength
as . displayed on the TM80 is greater than
-65dBm.
Static IP conflict
Wireless interference
The TM80 cannot Configuration error Verify that [MPAN ] at the TM80 is set to
establish connection [Connect to BP10] and the MPAN key on the
with the BP10. BP10 is pressed.
The TM80 and BP10 When the TM80 and BP10 are Put the TM80 and BP10 closer.
are prone to offline. secured to the patient, signals may
be blocked by the patient’s body.
The TM80 and BP10 As there are many WiFi devices in Contact your service personnel.
are prone to offline in this area, communication between
certain area. the TM80 and BP10 is interfered
seriously.
Default
Measurement Alarm message Alarm Possible cause Solution
priority
ECG HR High Med* HR value has risen above Check the patient’s con-
the high alarm limit or dition and make sure
HR Low fallen below the low that the patient cate-
alarm limit. gory and alarm limit set-
tings are correct.
Default
Measurement Alarm message Alarm Possible cause Solution
priority
ECG Asystole High The patient is in arrhyth- Check the patient’s con-
mia. dition and the ECG con-
V-Fib/V-Tach nections.
V-Tach
Vent Brady
Extreme Tachy
Extreme Brady
R on T Med*
Couplet Prompt*
PVC Prompt*
Bigeminy Med*
Trigeminy
Tachy
Brady
Vent Rhythm
Pause Low*
A-Fib
PVCs/min Med*
Pauses/min
Pacer Not Cap- Prompt* The pacer appears Check the pacer.
ture abnormal.
Default
Measurement Alarm message Alarm Possible cause Solution
priority
ECG Irr Rhythm End Prompt Irregular rhythm no lon- Check the patient’s con-
ger detected for the dition and the ECG con-
irregular rhythm end nections.
delay time.
Resp RR High Med* RR value has risen above Check the patient’s con-
the high alarm limit or dition and make sure
RR Low fallen below the low that the patient cate-
alarm limit. gory and alarm limit set-
tings are correct.
No Chest Move- High The respiration signal Check the patient’s con-
ment was so weak that the dition, module and
monitor cannot perform patient connections.
respiration analysis.
SpO2 SpO2 High Med* SpO2 value has risen Check the patient’s con-
above the high alarm dition and make sure
SpO2 Low limit or fallen below the that the patient cate-
low alarm limit. gory and alarm limit set-
tings are correct.
SpO2 Desat High The SpO2 value has fallen
below the desaturation
alarm limit.
No Pulse High The pulse signal was so Check the patient’s con-
weak that the monitor dition, SpO2 sensor, and
cannot perform pulse measurement site.
analysis.
Default
Measurement Alarm message Alarm Possible cause Solution
priority
NIBP NIBP-S High Med* The NIBP systolic Check the patient’s con-
pressure has risen above dition and check if the
NIBP-S Low the high alarm limit or alarm limit settings and
fallen below the low patient category are cor-
alarm limit. rect.
NIBP NIBP-S High The NIBP systolic Check the patient’s con-
Extremely High pressure has risen above dition and check if the
the extreme alarm high alarm limit settings are
NIBP-S limit or fallen below the correct.
Extremely Low extreme alarm low limit.
The Alarm Indication column in the table below is capable of three different indication
types: A, B, C.
■ A: The alarm sound will be silenced, the alarm light will continue to indicate the
alarm, a √ will appear before the alarm message. The symbol appears on the
top of the main screen.
■ B: The technical alarm will be changed to the prompt message, it will not longer
make sound or be indicated by the alarm light.
■ C: The technical alarms are cleared, there will be no alarm indications.
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
ECG ECG Lead Low* B The electrode has Check the connec-
Off become detached from tions of the elec-
the patient or the lead trodes and
ECG XX** Low* B wire has become discon- leadwires.
Lead Off nected from the adapter
cable.
ECG Low A The ECG signal is noisy. Check for any possi-
Noisy ble sources of signal
noise around the
cable and electrode,
and check the
patient for great
motion.
Cannot Prompt / / /
Analyze
QT
Resp Elec- Prompt / The electrode has been Check the electrode
trode used for a long time or application. Reposi-
Poor the electrode contact is tion or replace the
Contact poor. electrodes if neces-
sary.
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
SpO2 SpO2 Low* B The SpO2 sensor has Check the sensor
Sensor become detached from application site and
Off the patient or the mod- the sensor type, and
ule. make sure the sen-
SpO2 Low C sor is not damaged.
Sensor There is a fault with the
Fault SpO2 sensor. Reconnect the sen-
sor or use a new sen-
SpO2 No Low B sor.
Sensor An unspecified SpO2 sen-
sor has been used.
SpO2 High A
Module
Error
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
NIBP NIBP Low Med A The battery charge is low. Replace with a new
Battery battery.
NIBP Low C The button cell does not Reset the system
Clock have sufficient charge. time for the BP10.
Needs To
Be Set
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
NIBP Cuff Low C The NIBP airway may be Check the airway
Over- occluded. and measure again.
pressure
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
NIBP NIBP Cuff Low C The NIBP airway may leak 1. Verify that the
or Air- air. cuff is prop-
way Leak erly con-
nected.
2. 2. Verify that
the airway
does not leak
air.
NIBP-D Low A
Over-
range
NIBP-M Low A
Over-
range
Default
Alarm Alarm
Measurement Alarm Possible cause Solution
message Indication
priority
Power Low Bat- Med A The battery charge is low. Replace with new
tery batteries.
Introduction...............................................................................................................17-2
Care and Cleaning Safety Information .............................................................17-2
Cleaning and Disinfecting the TM80 ................................................................17-3
Cleaning Accessories and SpO2 Module.........................................................17-8
Disinfecting Accessories and SpO2 Module...................................................17-9
Sterilization ................................................................................................................17-9
17.1 Introduction
In this chapter we describe how to clean and disinfect the TM80 and its accessories.
WARNING
CAUTION
• If liquid has accidentally entered the equipment or its parts, shut down
the equipment and have the device serviced by authorized service per-
sonnel.
• Do not pour or spray any liquid directly on the equipment or accessories
or permit fluid to seep into connections or openings.
• When cleaning, avoid the ECG leadwire connector and other connectors.
• Check the equipment after cleaning and disinfecting. If there is any sign
of damage, remove it from use.
Glutaraldehyde, 2% Liquid /
NOTE
• For equipment with the symbol , all the listed cleaning and
disinfecting agents are available for use. For equipment without the
symbol , only the cleaning and disinfecting agents marked with “*”
are available for use.
■ Install the battery pack or battery tray and firmly close to seal the battery compart-
ment.
■ Insert the SpO2 cover in the SpO2 connector when SpO2 is not in use.
■ Insert the ECG leadwire plug into the ECG connector.
To clean your TM80, follow this procedure:
CAUTION
CAUTION
• Never allow the disinfectants to spill or enter the plug, connector or bat-
tery compartment. If liquid has accidentally entered the equipment or
its parts, shut down the equipment and have the device serviced by
authorized service personnel.
■ Water
■ Mild soap
To clean the SpO2 module, follow this procedure:
CAUTION
• Never immerse cables and sensors in any fluids. Do not clean them with
harsh chemicals such as acetone or non-diluted bleach.
• Clean the cables carefully to avoid breaking internal wires by excessive
bending, strain, or flexing.
• Do not autoclave, radiation or steam sterilize the cables and sensors.
• Extended exposure to Ethylene Oxide gas may shorten life of the cables,
leading to poor signal quality.
NOTE
• Refer to the individual instruction sheets that are packaged with the
accessories for additional information.
1. Clean the SpO2 module per Disinfecting the TM80 on Page 17-7.
2. Wipe the SpO2 module using a cotton or soft cloth soaked in one of the
recommended disinfectants. Use caution to avoid the SpO2 module plug.
3. Wipe off all the disinfectant with a dry cloth if necessary.
4. Dry the SpO2 module in a ventilated, cool place.
17.6 Sterilization
Sterilization is not recommended for this equipment, related products, accessories or
supplies unless otherwise indicated in the Operating Instructions that accompany the
accessories or supplies.
Introduction...............................................................................................................18-2
Maintenance Safety Information........................................................................18-2
Regular Check ...........................................................................................................18-3
Maintenance and Testing Schedule ..................................................................18-3
Viewing System Information ...............................................................................18-6
18.1 Introduction
The chapter outlines the routine maintenance guidelines for the TM80.
The TM80 is designed for stable operation over long periods of time and under normal
circumstances should not require technical maintenance beyond that described in this
chapter. However, calibration and safety checks are recommended at least once a year or
more often as required by local statutory or hospital administration practice.
WARNING
• Do not open the TM80’s housings. All servicing and future upgrades
must be carried out by the service personnel.
• All replaced components and accessories as well as consumables are
provided or qualified by Mindray.
• If you discover a problem with any of the TM80, contact your service per-
sonnel or Mindray.
• The service personnel must be properly qualified and thoroughly famil-
iar with the TM80’s operation.
• Dispose of the TM80 and its accessories according to your local regula-
tions when they reach the end of their service life.
• When disposing of the packaging material, be sure to observe the appli-
cable local or hospital’s waste control regulations.
• The TM80 must be stored and used at the temperature and humidity
specified in this manual.
■ The housing and display screen are free from cracks or other damages.
■ All keys funtion properly.
■ Connectors are not loose, cracked, or bent and cables have no cuts, nicks, or
fraying.
■ ECG leadwires are securely connected with the equipment
■ Battery is installed and has sufficient charge.
■ Chest electrodes are free from cracks and limb electrodes can properly clamp.
After your equipment has been used for 6 to 12 months, or whenever your equipment is
repaired or upgraded, a thorough inspection should be performed by qualified service
personnel to ensure the reliability.
■ Make sure that the environment and power supply meet the requirements.
■ Inspect the devices and their accessories for mechanical damage.
■ Inspect all connectors and leadwires for damage, and make sure that their
insulation is in good condition.
■ Make sure that only specified accessories are applied.
■ Make sure that the alarm system functions correctly.
■ Make sure that the battery meet the performance requirements.
■ Make sure that the equipment is in good working condition.
In case of any damage or abnormity, do not use the TM80. Contact the hospital’s bio-
medical engineers or your service personnel immediately.
ECG verification Performance test 1. If the user suspects that the mea-
surement is incorrect.
Calibration 2. Following any repairs or replace-
ment of relevant component.
Resp test Performance test
3. At least twice a year.
SpO2 test Note: NIBP test should be performed at
least once a year.
NIBP test Pressure check
Leakage test
Nurse call test If the user suspects that the nurse call
functionality does not work properly.
■ Tap the battery symbol in the upper right corner of the main screen.
■ Press to enter the main menu →from the [System] section tap [System
Info].
ECG Accessories........................................................................................................19-2
SpO2 Accessories .....................................................................................................19-4
NIBP Accessories ......................................................................................................19-5
Miscellaneous............................................................................................................19-5
The accessories listed in this chapter comply with the requirements of IEC 60601-1-2
when in use with the TM80. The accessory material that contacts the patients has under-
taken the bio-compatibility test and is verified to be in compliance with ISO 10993-1. For
details about the accessories, refer to the instructions for use provided with the acces-
sory.
WARNING
Applicable Applicable
PN Description
property patient
Applicable Applicable
PN Description
property patient
009-004765-00 3-Lead, New Telemetry, AHA, Snap, 24" Reusable Adult, Pediatric
5-Lead
Applicable Applicable
PN Description
property patient
009-004782-00 5-Lead, New Telemetry, AHA, Snap, 24" Reusable Adult, Pediatric
6-Lead
Applicable Applicable
PN Description
property patient
009-004794-00 6-Lead, New Telemetry, AHA, Snap, 24" Reusable Adult, Pediatric
Applicable Applicable
PN Description
property patient
The information about the wavelength range and maximum photic output consump-
tion can be especially useful to clinicians (for example, when photodynamic therapy is
performed).
19.4 Miscellaneous
PN Description
Classifications............................................................................................................A-2
Environmental Specifications..............................................................................A-2
Power Supply Specifications................................................................................A-3
Physical Specifications ...........................................................................................A-4
Hardware Specifications........................................................................................A-5
Data Storage ..............................................................................................................A-6
Wi-Fi Specifications .................................................................................................A-6
MPAN Specifications ...............................................................................................A-8
Measurement Specifications ...............................................................................A-10
This chapter provides specifications of the TM80 only. For specifications of the BP10 and
the central charger, refer to BP10 NIBP Module Operator’s Manual (P/N 046-008269-
00) and BeneVision Central Charger Operator’s Manual (P/N 046-007483-00) respec-
tively.
A.1 Classifications
The TM80 Telemetry Monitor is classified, according to IEC60601-1:
Type of protection against electrical Energized from an internal electrical power source.
shock
Degree of protection against electrical Type CF defibrillation proof for ECG and SpO2.
shock for the TM80 Telemetry Monitor
WARNING
• The TM80 Telemetry Monitor may not meet the performance specifica-
tions if stored or used outside the specified temperature and humidity
ranges.
Temperature 0 °C to 40 °C -20 °C to 60 °C
AA batteries (three)
Battery type
Rechargeable lithium-ion battery (one)
Charge time for lithium-ion battery No more than 5 hours for charging a depleted battery to 90% capacity
Continuous runtime when the 5-lead ECG ≥20 hours ≥40 hours
display is off
5-lead ≥16 hours ≥32 hours
ECG+Min-
dray SpO2
Note: Prerequisites for this continuous working state: The operating temperature is at 25 °C±5°C, the
display defaults to off, no visual or audible alarm indicators are available, no alarms are issued, and the
display is lit once every two hours.
Lithium-ion battery
(P/N 022-000196-00)
Note: Prerequisites for this continuous working state: The operating temperature is at 25 °C±5°C, the
display is on, and no visual or audible alarm indicators are available by default.
Height 126 mm
Width 64 mm
Depth 23 mm
Weight
Display
LED
Audio Indicator
Speaker 1
Buttons
Nurse call 1
Power On/Off 1
Main menu 1
External Connectors
ECG connector 1
SpO2 connector 1
The TM80 Telemetry Monitor can work with APs which support POE, if the RSSI from APs
is higher than -65 dbm. One example of the APs is AIR-AP2802I-H-K9 which work with
the AC: AIR-CT2504-15- K9.
WARNING
Priority All communication data types shall have the same priority.
BP10 transmits NIBP parameters, status, and prompt messages to the TM80 Telemetry
Monitor. The TM80 Telemetry Monitor transmits control information and settings infor-
mation to the BP10.
Priority All communication data types shall have the same priority.
ECG
1 mV (peak-to-peak value)
Calibration signal
Accuracy: ± 5%
Pace Pulse
HR
Resolution 1 bpm
ST Segment Analysis
Resolution 0.01 mV
Arrhythmia Analysis
QT Analysis
A.9.2 Resp
Resp
Lead Lead II
Respiration Rate
Resolution 1 rpm
NCM alarm delay 10s, 15s, 20s, 25s, 30s, 35s, 40s
A.9.3 SpO2
NOTE
SpO2
*Measurement accuracy verification: The SpO2 accuracy has been verified in human experiments by comparing
with arterial blood sample reference measured with a CO-oximeter. Pulse oximeter measurements are statisti-
cally distributed and about two-thirds of the measurements are expected to come within the specified accuracy
range compared to CO-oximeter measurements.
Resolution 1%
*Studies were performed to validate the accuracy of Pulse Oximeter with Mindray SpO2 sensors by contrast with
a CO-Oximeter. In total, 14 healthy adults (4 male & 10 female) whose average age is 26 ±3.14 years old were vol-
untarily involved in this study. One is a black man,; one is a black woman, and the remaining are yellow people.
The average height and weight of male are 172.25±1.11cm and 67.83±6.16kg respectively. The average height
and weight of female are 160.70± 1.37cm and 55.09±2.44kg respectively. All of them conform the clinical study
requirements for age, gender, skin and health.
PR
Resolution 1 bpm
Accuracy ±3 bpm
Response Time
■ ≤ 30 s (PR 75 bpm, sensitivity set to low, no disturbance, SpO2 value rises from 70% to 100%)
■ ≤ 30 s (SpO2 value 98%, sensitivity set to low, no disturbance, PR value rises from 25 bpm to
240 bpm)
PI
Resolution 0.01
EMC ...............................................................................................................................B-2
Radio Regulatory Compliance.............................................................................B-7
Radiofrequency Radiation Exposure Information........................................B-8
B.1 EMC
The device meets the requirements of IEC 60601-1-2: 2014.
WARNING
The device is intended for use in the electromagnetic environment specified below. The customer or the user of
the device should assure that it is used in such an environment.
RF emissions Group 1 The system uses RF energy only for its internal function.
CISPR 11 Therefore, its RF emissions are very low and are not likely
to cause any interference in nearby electronic equipment.
RF emissions Class B* Only TM80 Telemetry Monitor and BP10 (subpart) compli-
CISPR 11 ance. The devices are suitable for use in all establish-
ments, including domestic establishments and those
directly connected to the public low voltage power sup-
ply network that supplies buildings used for domestic
purposes.
RF emissions Class A The system is suitable for use in all establishments other
CISPR 11 than domestic and those directly connected to the public
low-voltage power supply network that supplies build-
Harmonic Emissions Class A ings used for domestic purposes.
IEC61000-3-2
Note: The TM80 Telemetry Monitor and BP10 (subpart) are classified by is their using environment or intended
function.
NOTE
If the system is operated within the electromagnetic environment listed in Table Guid-
ance and declaration - electromagnetic immunity, the system will remain safe and pro-
vide the following essential performance:
■ Operating mode
■ Accuracy
■ Function
■ Accessories identification
■ Data stored
■ Alarm
■ Detect for connection
The device is intended for use in the electromagnetic environment specified below. The customer or the user of
the device should assure that it is used in such an environment.
Electrical fast ±2 kV for power ±2 kV for power Mains power quality should be that of a typi-
transient/burst supply lines supply lines cal commercial or hospital environment.
IEC 61000-4-4 ±1 kV for input/out- ±1 kV for input/
put lines output lines
(length greater (length greater
than 3 m) than 3 m)
Voltage dips 0% UT for 0,5 cycle 0% UT for 0,5 Mains power quality should be that of a typi-
and Voltage cycle cal commercial or hospital environment. If
interruptions 0% UT for 1 cycle the user of our product requires continued
0% UT for 1 cycle operation during power mains interruptions,
IEC 61000-4-11 and 70% UT for
and 70% UT for 25/ it is recommended that our product be pow-
30 cycles 25/30 cycles ered from an uninterruptible power supply
or a battery.
0% UT for 250/300 0% UT for 250/
cycle 300 cycle
Note: UT is the A.C. mains voltage prior to application of the test level.
The device is intended for use in the specified electromagnetic environment. The customer or the user of the
device should assure that it is used in such an environment as described below.
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
a
: The ISM (industrial, scientific, and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz;
13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz. The amateur radio bands
between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3
MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to
24,99 MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
b
: Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site
survey should be considered. If the measured field strength in the location in which the device is used exceeds
the applicable RF compliance level above, the device should be observed to verify normal operation. If abnor-
mal performance is observed, additional measures may be necessary, such as re-orienting or relocating the
device.
c
: Over the frequency ranges 150 kHz to 80 MHz, field strengths should be less than 3V/m.
Recommended Separation Distances between Portable and Mobile RF, Communications Equipment and
This Equipment
The equipment is intended for use in an electromagnetic environment in which radiated RF disturbance are con-
trolled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the device
as recommended below, according to the maximum output power of the communication equipment.
100 12 12 23
For transmitters at a maximum output power not listed above, the recommended separation distanced in
meters (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
0123
The radio device used in this product is in compliance with the essential requirements
and other relevant provisions of Directive 2014/53/EU.
This device complies with part 15 of the FCC Rules and with RSS-210 of Industry Canada.
Operation is subject to the condition that this device does not cause harmful interfer-
ence.
This device must accept any interference received, including interference that may cause
undesired operation.
The following electrical safety tests are recommended as part of a comprehensive pre-
ventive maintenance program. They are a proven means of detecting abnormalities that,
if undetected, could prove dangerous to either the patient or the operator. Additional
tests may be required according to local regulations.
All tests can be performed using commercially available safety analyzer test equipment.
These procedures assume the use of a 601PROXL International Safety Analyzer or equiv-
alent safety analyzer. Other popular testers complying with IEC 60601-1 used in Europe
such as Fluke, Metron, or Gerb may require modifications to the procedure. Follow the
instructions of the analyzer manufacturer.
The consistent use of a safety analyzer as a routine step in closing a repair or upgrade is
emphasized as a mandatory step if an approved agency status is to be maintained. The
safety analyzer also proves to be an excellent troubleshooting tool to detect abnormali-
ties of line voltage and grounding, as well as total current loads.
The power plug The power plug pins No broken or bent pin. No discolored pins.
The following outlet conditions apply when performing the Earth Leakage test:
For UL60601-1,
LIMITS
The following outlet conditions apply when performing the Mains on Applied Part test.
■ Normal Polarity;
■ Reversed Polarity
LIMITS
LIMITS
NOTE
Units..............................................................................................................................D-2
Symbols .......................................................................................................................D-3
Abbreviations ............................................................................................................D-3
D.1 Units
A ampere
Ah ampere hour
bpm beats per minute
°C centigrade
cc cubic centimeter
cm centimeter
dB decibel
DS dyne. second
°F fahrenheit
g gram
hr hour
hPa hundred pascal
Hz hertz
in inch
k kilo
kg kilogram
kPa kilopascal
l litre
lb pound
m meter
mg milligrams
min minute
ml milliliter
mm millimeters
ms millisecond
mV millivolt
mW milliwatt
nm nanometer
ppm part per million
s second
V volt
VA volt ampere
Ω ohm
μA microampere
μm micron
μV microvolt
W watt
D.2 Symbols
- minus
% percent
/ per; divide; or
^ power
+ plus
= equal to
< less than
> greater than
≤ less than or equal to
≥ greater than or equal to
± plus or minus
× multiply
© copyright
D.3 Abbreviations
P power
PD photodetector
PR pulse rate
QRS interval of ventricular depolarization
(QRS complex)
RA(R) right arm
RL(N) right leg
ROM read-only memory
SpO2 arterial oxygen saturation from pulse oximetry