T1 Patient Monitor and Docking Station Operators Manual Nov 2014

Copyright 2014 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved. For this Operator’s Manual, the issue date is November 2014.

WARNING 

Federal Law (USA) restricts this device to sale by or on the order of a physician.

T1 Patient Monitor Operator’s Manual

I

Intellectual Property Statement SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray) owns the intellectual property rights to this Mindray product and this manual. This manual may refer to information protected by copyrights or patents and does not convey any license under the patent rights of Mindray, nor the rights of others.

Mindray intends to maintain the contents of this manual as confidential information. Disclosure of the information in this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden.

Release, amendment, reproduction, distribution, rental, adaption and translation of this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden.

,

,

and

are the registered trademarks or trademarks owned

by Mindray in China and other countries. All other trademarks that appear in this manual are used only for editorial purposes without the intention of improperly using them. They are the property of their respective owners.

Responsibility on the Manufacturer Party Contents of this manual are subject to changes without prior notice.

All information contained in this manual is believed to be correct. Mindray is not be liable for errors contained herein nor for incidental or consequential damages in connection with the furnishing, performance, or use of this manual.

Mindray is responsible for the effects on safety, reliability and performance of this product, only if: 

all installation operations, expansions, changes, modifications and repairs of this product are conducted by Mindray authorized personnel;



the electrical installation of the relevant room complies with the applicable national and local requirements;



the product is used in accordance with the instructions for use.

WARNING 

This equipment must be operated by skilled/trained clinical professionals.



It is important for the hospital or organization that employs this equipment to carry out a reasonable service/maintenance plan. Neglect of this may result in machine breakdown or personal injury.

II

T1 Patient Monitor Operator’s Manual

Warranty THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR 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 resulting 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.

This warranty does not extend to 

Malfunction or damage caused by improper use or man-made failure.



Malfunction or damage caused by unstable or out-of-range power input.



Malfunction or damage caused by force majeure such as fire and earthquake.



Malfunction or damage caused by improper operation or repair by unqualified or unauthorized service people.



Malfunction of the instrument or part whose serial number is not legible enough.



Others not caused by instrument or part itself.

Company Contact Manufacturer:

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Address:

Mindray Building, Keji 12th Road South,Hi-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

Distributor:

Mindray DS USA, Inc.

Address:

800 MacArthur Boulevard Mahwah, New Jersey 07430, USA

Tel:

1.800.288.2121, 1.201.995.8000

Website:

www.mindray.com

T1 Patient Monitor Operator’s Manual

III

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 prerequisite 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 question, please contact us.

This manual is an integral part of the product. It should always be kept close to the equipment so that it can be conveniently referenced 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 patient monitor.

Conventions

IV



Italic text is to quote the referenced chapters or sections.



[ ] is used to enclose screen text.



→ is used to indicate operational procedures.

T1 Patient Monitor Operator’s Manual

Contents 1 Safety ... 1-1 1.1 Safety Information ... 1-1 1.1.1 Warnings ... 1-2 1.1.2 Cautions ... 1-3 1.1.3 Notes ... 1-3 1.2 Equipment Symbols... 1-4

2 The Basics ... 2-1 2.1 Intended Use ... 2-1 2.2 Main Unit ... 2-2 2.2.1 Front View ... 2-2 2.2.2 Left View ... 2-3 2.2.3 Right View ... 2-4 2.2.4 Bottom View ... 2-5 2.3 T1 handle ... 2-5 2.3.1 Left View ... 2-5 2.3.2 Right View ... 2-6 2.4 T1 Docking Station ... 2-6 2.4.1 Left View ... 2-6 2.4.2 Right View ... 2-7 2.4.3 Rear View... 2-7 2.5 External Parameter Modules ... 2-8 2.6 Installation ... 2-8 2.7 Display Screen ...2-11

3 Basic Operations... 3-1 3.1 Installation ... 3-1 3.1.1 Unpacking and Checking ... 3-1 3.1.2 Environmental Requirements ... 3-2 3.2 Getting Started ... 3-2 3.2.1 Turning Power On ... 3-2 3.2.2 Starting Monitoring ... 3-2 3.3 Turning Off the Monitor ... 3-3 3.4 Using the Touchscreen... 3-3 3.5 Using the On-screen Keyboard ... 3-3 3.6 Using the Main Menu ... 3-4 3.7 Changing General Settings ... 3-4 3.7.1 Setting up a Monitor... 3-4 3.7.2 Changing Language ... 3-4 3.7.3 Setting the Date and Time ... 3-5 3.8 Setting Parameters ... 3-5 3.8.1 Switching the Parameters On/Off ... 3-5 3.8.2 Accessing the Parameters Menu ... 3-5 T1 Patient Monitor Operator’s Manual

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3.9 Operating Mode ... 3-5 3.9.1 Monitoring Mode ... 3-5 3.9.2 Privacy Mode... 3-6 3.9.3 Night Mode ... 3-6 3.9.4 Outdoor Mode ... 3-7 3.9.5 Configuration Mode ... 3-7 3.9.6 Demo Mode ... 3-7 3.9.7 Standby Mode ... 3-8

4 User Screens... 4-1 4.1 Adjusting the Screen Brightness... 4-1 4.2 Adjusting Volume ... 4-1 4.3 Configuring Your Screens ... 4-2 4.3.1 Changing the Wave Line Size ... 4-2 4.3.2 Changing Measurement Colors ... 4-2 4.3.3 Choosing a Screen... 4-2 4.3.4 Changing Screen Layout ... 4-3 4.4 Understanding the Big Numerics Screen ... 4-4

5 Managing Patients ... 5-1 5.1 Admitting a Patient ... 5-1 5.2 Quick Admitting a Patient ... 5-2 5.3 Querying and Obtaining Patient Information ... 5-2 5.4 Associating Patient Information ... 5-3 5.5 Editing Patient Information ... 5-3 5.6 Discharging a Patient ... 5-3 5.7 Transferring Patient Data ... 5-4 5.7.1 Transferring Patient Data via a USB Drive ... 5-4 5.8 Auto Deleting History Data from SD Card ... 5-5 5.9 Connecting to a Central Monitoring System ... 5-5

6 Managing Configurations ... 6-1 6.1 Introduction ... 6-1 6.2 Entering the Manage Configuration Menu ... 6-2 6.3 Changing Department ... 6-2 6.4 Setting Default Configuration ... 6-3 6.5 Saving Current Settings ... 6-3 6.6 Editing Configurations... 6-4 6.7 Deleting a Configuration ... 6-4 6.8 Transferring a Configuration ... 6-5 6.9 Loading a Configuration ... 6-5 6.10 Restoring the Latest Configuration Automatically ... 6-6 6.11 Modifying Password... 6-6

7 Alarms ... 7-1 7.1 Alarm Categories ... 7-1 2

T1 Patient Monitor Operator’s Manual

7.2 Alarm Levels... 7-2 7.3 Alarm Indicators ... 7-2 7.3.1 Alarm Lamp... 7-2 7.3.2 Audible Alarm Tones ... 7-2 7.3.3 Alarm Message ... 7-3 7.3.4 Flashing Numeric ... 7-3 7.3.5 Alarm Status Symbols ... 7-4 7.4 Alarm Tone Configuration ... 7-4 7.4.1 Changing the Alarm Volume ... 7-4 7.4.2 Setting the Minimum Alarm Volume ... 7-4 7.4.3 Changing the Alarm Tone Pattern ... 7-4 7.4.4 Setting the Interval between Alarm Sounds ... 7-5 7.4.5 Setting the Reminder Tones... 7-6 7.5 Understanding the Alarm Setup Menu ... 7-6 7.5.1 Setting Alarm Properties for All Parameters ... 7-7 7.5.2 Adjusting Alarm Limits Automatically ... 7-7 7.5.3 Setting Alarm Delay Time ... 7-9 7.5.4 Setting SpO2 Technical Alarm Delay ... 7-9 7.5.5 Setting Recording Length... 7-9 7.5.6 Entering CPB Mode ...7-10 7.6 Pausing Alarms ...7-10 7.7 Switching Off All Alarms...7-10 7.8 Resetting Alarms ...7-11 7.9 Latching Alarms...7-12 7.10 Testing Alarms ...7-12 7.11 When an Alarm Occurs ...7-12

8 Monitoring ECG ... 8-1 8.1 Introduction ... 8-1 8.2 Safety ... 8-1 8.3 Preparing to Monitor ECG ... 8-2 8.3.1 Preparing the Patient and Placing the Electrodes ... 8-2 8.3.2 Choosing AHA or IEC Lead Placement ... 8-2 8.3.3 ECG Lead Placements ... 8-2 8.3.4 Checking Paced Status... 8-4 8.4 Understanding the ECG Display ... 8-5 8.5 Changing ECG Settings... 8-5 8.5.1 Accessing ECG Menus ... 8-5 8.5.2 Choosing the Alarm Source ... 8-5 8.5.3 Changing ECG Wave Settings ... 8-6 8.5.4 Changing the ECG Filter Settings ... 8-6 8.5.5 Setting Pacemaker Rate (For Mortara only) ... 8-6 8.5.6 Choosing an ECG Display Screen ... 8-7 8.5.7 Setting the Notch Filter ... 8-7 8.5.8 Changing the Pacer Reject Settings ... 8-7 8.5.9 Enabling Smart Lead Off ... 8-8 T1 Patient Monitor Operator’s Manual

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8.5.10 Setting the Alarm Level for ECG Lead Off Alarms... 8-8 8.5.11 Adjusting QRS Volume ... 8-8 8.5.12 About the Defibrillator Synchronization ... 8-8 8.6 About ST Monitoring... 8-9 8.6.1 Switching ST On and Off ... 8-9 8.6.2 Changing ST Filter Settings ... 8-9 8.6.3 Understanding the ST Display ... 8-10 8.6.4 Saving the Current ST Segment as Reference ... 8-10 8.6.5 Changing the Reference Segment ... 8-11 8.6.6 Deleting a Reference Segment ... 8-11 8.6.7 Changing the ST Alarm Limits ... 8-11 8.6.8 Setting the ST Alarm Delay Time ... 8-11 8.6.9 Adjusting ST Measurement Points ... 8-11 8.7 About Arrhythmia Monitoring ... 8-12 8.7.1 Understanding the Arrhythmia Events... 8-12 8.7.2 Changing Arrhythmia Alarm Settings... 8-14 8.7.3 Changing Arrhythmia Threshold Settings ... 8-14 8.7.4 Setting the Extended Arrh. (For Mindray ECG Algorithm Only) ... 8-15 8.7.5 Reviewing Arrhythmia Events... 8-15 8.8 ECG Relearning ... 8-16 8.8.1 Initiating an ECG Relearning Manually ... 8-16 8.8.2 Automatic ECG Relearning ... 8-16 8.9 12-Lead ECG Monitoring... 8-17

9 Monitoring Respiration (Resp) ... 9-1 9.1 Introduction ... 9-1 9.2 Safety Information ... 9-1 9.3 Understanding the Resp Display ... 9-2 9.4 Placing Resp Electrodes ... 9-2 9.4.1 Optimizing Lead Placement for Resp ... 9-3 9.4.2 Cardiac Overlay ... 9-3 9.4.3 Abdominal Breathing... 9-3 9.4.4 Lateral Chest Expansion ... 9-3 9.5 Choosing the Respiration Lead ... 9-3 9.6 Changing the Apnea Alarm Delay... 9-4 9.7 Changing Resp Detection Mode... 9-4 9.8 Changing Resp Wave Settings ... 9-5 9.9 Setting Respiration Rate (RR) Source... 9-5 9.10 Setting Alarm Properties ... 9-5

10 Monitoring PR... 10-1 10.1 Introduction ... 10-1 10.2 Setting the PR Source ... 10-1 10.3 Selecting the Active Alarm Source ... 10-1 10.4 QRS Tone ... 10-2

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T1 Patient Monitor Operator’s Manual

11 Monitoring SpO2... 11-1 11.1 Introduction ...11-1 11.2 Safety ...11-2 11.3 Identifying SpO2 Modules ...11-2 11.4 Applying the Sensor ...11-2 11.5 Changing SpO2 Settings ...11-3 11.5.1 Accessing SpO2 Menus ...11-3 11.5.2 Setting SpO2 Sensitivity ...11-3 11.5.3 Changing Averaging Time ...11-3 11.5.4 Monitoring SpO2 and NIBP Simultaneously ...11-3 11.5.5 Sat-Seconds Alarm Management ...11-3 11.5.6 Changing the Speed of the Pleth Wave ...11-5 11.5.7 Setting the Alarm Level for SpO2 Sensor Off Alarm ...11-5 11.5.8 Setting the SpO2 Tone Mode ...11-5 11.5.9 Adjusting the Desat Alarm ...11-5 11.6 Measurement Limitations ...11-5 11.7 Masimo Information ...11-6 11.8 Nellcor Information ...11-6

12 Monitoring NIBP ... 12-1 12.1 Introduction ...12-1 12.2 Safety ...12-2 12.3 Measurement Limitations ...12-2 12.4 Measurement Methods ...12-2 12.5 Setting Up the NIBP Measurement ...12-3 12.5.1 Preparing to Measure NIBP ...12-3 12.5.2 Starting and Stopping Measurements ...12-3 12.5.3 Correcting the Measurement if Limb is not at Heart Level ...12-3 12.5.4 Enabling NIBP Auto Cycling and Setting the Interval ...12-3 12.5.5 Starting a STAT Measurement ...12-4 12.6 Understanding the NIBP Numerics ...12-4 12.7 Changing NIBP Settings ...12-4 12.7.1 Setting the Initial Cuff Inflation Pressure ...12-4 12.7.2 Setting NIBP Alarm Properties ...12-4 12.7.3 Displaying NIBP List ...12-5 12.7.4 Setting the Pressure Unit ...12-5 12.7.5 Switching On NIBP End Tone...12-5 12.8 Assisting Venous Puncture...12-5

13 Monitoring Temp ... 13-1 13.1 Making a Temp Measurement ...13-1 13.2 Understanding the Temp Display ...13-1 13.3 Setting the Temperature Unit ...13-1

14 Monitoring IBP ... 14-1 14.1 Introduction ...14-1 T1 Patient Monitor Operator’s Manual

5

14.2 Safety ... 14-1 14.3 Zeroing the Transducer ... 14-2 14.4 Setting Up the Pressure Measurement ... 14-3 14.5 Understanding the IBP Display ... 14-4 14.6 Changing IBP Settings ... 14-4 14.6.1 Changing a Pressure for Monitoring ... 14-4 14.6.2 Setting Alarm Properties ... 14-5 14.6.3 Setting the IBP Wave ... 14-5 14.6.4 Changing Averaging Time ... 14-5 14.6.5 Setting the Pressure Unit ... 14-6

15 Monitoring Carbon Dioxide... 15-1 15.1 Introduction ... 15-1 15.2 CO2 Module ... 15-2 15.3 Preparing to Measure CO2... 15-2 15.4 Changing CO2 Settings ... 15-4 15.4.1 Setting the CO2 Unit ... 15-4 15.4.2 Accessing CO2 Menus ... 15-4 15.4.3 Setting up Gas Compensations ... 15-4 15.4.4 Setting up Humidity Compensation ... 15-4 15.4.5 Setting the Apnea Alarm Delay ... 15- 15.4.6 Setting the Flow Rate ... 15-5 15.4.7 Setting up the CO2 Wave ... 15-5 15.4.8 Setting RR Source... 15-5 15.4.9 Entering the Standby Mode ... 15-6 15.5 Measurement Limitations ... 15-6 15.6 Leakage test ... 15-6 15.7 Troubleshooting the CO2 Sampling System ... 15- 15.8 Removing Exhaust Gases from the System ... 15-7 15.9 Zeroing the Sensor ... 15-7

16 Review ... 16-1 16.1 Accessing Respective Review Windows ... 16-1 16.2 Reviewing Graphic Trends ... 16-1 16.3 Reviewing Tabular Trends ... 16-2 16.4 Reviewing Events ... 16-3 16.4.1 Marking Events ... 16-3 16.4.2 Reviewing Events ... 16-3 16.5 Reviewing Waveforms ... 16-4

17 Printing ... 17-1 17.1 Printer ... 17-1 17.2 Connecting a printer... 17-1 17.3 Setting the Printer ... 17-2 17.4 Starting Report Printouts ... 17-2 6

T1 Patient Monitor Operator’s Manual

17.5 Stopping Report Printouts ...17-3 17.6 Setting Up Reports ...17-3 17.6.1 Setting Up ECG Reports ...17-3 17.6.2 Setting Up Tabular Trends Reports ...17-3 17.6.3 Setting Up Graphic Trends Reports ...17-3 17.6.4 Setting Up Realtime Reports ...17-4 17.7 End Case Reports...17-4 17.8 Printer Statuses ...17-4 17.8.1 Printer Out of Paper ...17-4 17.8.2 Printer Unavailable ...17-4

18 Other Functions... 18-1 18.1 Analog Output...18-1 18.2 Transferring Data ...18-1 18.2.1 Data Export System ...18-1 18.2.2 Transferring Data by Different Means ...18-1 18.3 Network Connection ...18-2 18.3.1 Setting the Network Type...18-2 18.3.2 Setting the IP Address, Subnet Mask and eGateway ...18-2

19 Battery ... 19-1 19.1 Overview ...19-1 19.2 Safety ...19-2 19.3 Installing the Battery ...19-2 19.4 Charging the Battery ...19-3 19.5 Conditioning the Battery ...19-3 19.6 Checking Battery Performance ...19-4 19.7 Storing the Battery...19-4 19.8 Recycling the Batteries ...19-5

20 Care and Cleaning ... 20-1 20.1 General Points ...20-1 20.2 Cleaning ...20-2 20.3 Disinfecting ...20-2

21 Maintenance ... 21-1 21.1 Regular Inspection ...21-1 21.2 Maintenance and Testing Schedule...21-2 21.3 Checking Monitor and Module Information ...21-3 21.4 ECG Verification ...21-3 21.5 NIBP Leakage Test ...21-4 21.CO2 Leakage Test .........21-6 21. Calibrating the Touchscreen ... 21-9

T1 Patient Monitor Operator’s Manual

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22 Accessories... 22-1 22.1 ECG Accessories ... 22-1 22.2 SpO2 Accessories ... 22-3 22.3 NIBP Accessories... 22-5 22.4 Temp Accessories ... 22-6 22.5 IBP/ICP Accessories... 22-6 22.6 CO2 Accessories... 22-7 22.7 Others... 22-7

A Product Specifications ... A-1 A.1 Classifications ... A-1 A.2 Environmental Specifications ... A-1 A.3 Power Supply Specifications ... A-2 A.4 Physical Specifications ... A-3 A.5 Hardware Specifications ... A-3 A.6 Data Storage ... A-5 A.7 Measurement Specifications ... A-6 A.8 CO2 ... A-14

B EMC... B-1 B.1 EMC... B-1

C Default Configurations ... C-1 C.1 Parameters Configuration ... C-1 C.2 Routine Configuration ... C-9 C.3 User Maintenance Items ...C-13

D Alarm Messages ... D-1 D.1 Physiological Alarm Messages ...D-1 D.2 Technical Alarm Messages ...D-3

E Electrical Safety Inspection ... E-1 E.1 Power Cord Plug ... E-1 E.2 Device Enclosure and Accessories... E-2 E.3 Device Labelling... E-2 E.4 Protective Earth Resistance... E-2 E.5 Earth Leakage Test... E-3 E.6 Patient Leakage Current... E-3 E.7 Mains on Applied Part Leakage... E-4 E.8 Patient Auxiliary Current ... E-4

F Symbols and Abbreviations... F-1 F.1 Symbols... F-1 F.2 Abbreviations... F-2

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T1 Patient Monitor Operator’s Manual

1 Safety 1.1 Safety Information

WARNING 

Indicates a potential hazard or unsafe practice that, if not avoided, could result in death or serious injury.

CAUTION 

Indicates a potential hazard or unsafe practice that, if not avoided, could result in minor personal injury or product/property damage.

NOTE 

Provides application tips or other useful information to ensure that you get the most from your product.

T1 Patient Monitor Operator’s Manual

1-1

1.1.1 Warnings

WARNINGS 

This equipment is used for single patient at a time.



The equipment is not intended to be used within the Magnetic Resonance (MR) environment.



Before putting the system into operation, the operator must verify that the equipment, connecting cables and accessories are in correct working order and operating condition.



The equipment must be connected to a properly installed power outlet with protective earth contacts only. If the installation does not provide for a protective earth conductor, disconnect it from the power line and operate it on battery power, if possible.



To avoid explosion hazard, do not use the equipment in the presence of oxygen-rich atmospheres, flammable anesthetics, or other flammable agents (such as gasoline).



Do not open the equipment housings. All servicing and future upgrades must be carried out by the personnel trained and authorized by our company only.



Do not come into contact with patients during defibrillation. Otherwise serious injury or death could result.



Do not touch the equipment’s metal parts or connectors when in contact with the patient; otherwise patient injury may result.



Do not rely exclusively on the audible alarm system for patient monitoring. Adjustment of alarm volume to a low level or off may result in a hazard to the patient. Remember that alarm settings should be customized according to different patient situations and always keeping the patient under close surveillance is the most reliable way for safe patient monitoring.



The physiological data and alarm messages displayed on the equipment are for reference only and cannot be directly used for diagnostic interpretation.



To avoid inadvertent disconnection, route all cables in a way to prevent a stumbling hazard. Wrap and secure excess cabling to reduce risk of entanglement or strangulation by patients or personnel.



Dispose of the package material, observing the applicable waste control regulations and keeping it out of children’s reach.



Remove the DC adapter from use in case of a damaged cable.



Never mix patient electrode types or brands. Dissimilar metals or other incompatibilities may cause considerable baseline drift and may increase trace recovery time after defibrillation.

1-2

T1 Patient Monitor Operator’s Manual

1.1.2 Cautions

CAUTIONS 

Use only parts and accessories specified in this manual.



At the end of its service life, the equipment, as well as its accessories, must be disposed of in compliance with the guidelines regulating the disposal of such products. If you have any questions concerning disposal of the equipment, please contact us.



Magnetic and electrical fields are capable of interfering with the proper performance of the equipment. For this reason make sure that all external devices operated in the vicinity of the equipment comply with the relevant EMC requirements. Mobile phone, X-ray equipment or MRI devices are a possible source of interference as they may emit higher levels of electromagnetic radiation.



Before connecting the equipment to the power line, check that the voltage and frequency ratings of the power line are the same as those indicated on the equipment’s label or in this manual.



Always install or carry the equipment properly to avoid damage caused by drop, impact, strong vibration or other mechanical force.



Dry the equipment immediately in case of rain or water spray.

1.1.3 Notes NOTES 

Put the equipment in a location where you can easily see the screen and access the operating controls.



Keep this manual in the vicinity of the equipment so that it can be conveniently referenced when needed.



The software was developed in compliance 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.

T1 Patient Monitor Operator’s Manual

1-3

1.2 Equipment Symbols

ON/OFF for a part of equipment

Direct current

Battery indicator

Network connector

Multifunctional connector

Serial number

Unlocking

Equipotentiality

Lock; tighten

Alternating current

Date of Manufacture

Symbol for “MANUFACTURER”

Input/output

Defibrillation-proof Type CF applied part

Protected against vertically falling water drops per IEC 60529

Direction and angle of rotation

USB connector

Caution, consult accompanying documents

Dispose of in accordance to your country’s requirements

Conforms to UL Std.60601-1, IEC Std.60601-2-25, IEC Std.60601-2-27, IEC Std.60601-2-30, IEC Std.60601-2-34, IEC Std.60601-2-49 Certified to CSA Std.C22.2 No 601.1, IEC Std.60601-2-25, CSA Std. C22.2 No 60601-2-27, CSA Std.C22.2 No 60601-2-30, CSA Std.22.2 No 60601-2-34, CSA Std.C22.2 No 60601-2-49

NOTE 

1-4

Some symbols may not appear on your equipment.

T1 Patient Monitor Operator’s Manual

2 The Basics 2.1 Intended Use T1 patient monitor, hereafter referred to as “the monitor” or “the equipment”, is intended for monitoring, displaying, reviewing, storing and transferring of multiple physiological parameters including ECG, respiration (Resp), temperature (Temp), SpO2, pulse rate (PR), non-invasive blood pressure (NIBP), invasive blood pressure (IBP), and carbon dioxide (C O2).

All the parameters can be applied to a single adult, pediatric or neonatal patient with the exception of the following: arrhythmia detection and ST Segment analysis of Mortara ECG algorithm are intended for adult and pediatric patients; arrhythmia detection of Mindray ECG algorithm is intended for adult and pediatric patients; ST Segment analysis of Mindray ECG algorithm is intended for adult patients only.

The monitor is intended to be used in a hospital environment including, but not limited to, ICU, CCU, PICU, NICU, RICU, emergency room, operating room, postoperative observation ward, etc. It can also be used during patient transport both inside the hospital and with an ambulance. For patient transport monitoring with an ambulance, only ECG, HR, Resp, Temp, SpO2, PR, NIBP, and IBP can be monitored. The monitor is not intended for helicopter transport or home use.

This patient monitor is intended for use only by clinical professionals or under their guidance. It must only be used by those who have received adequate training in its use. Anyone unauthorized or untrained must not perform any operation on it.

The monitor can be used as a stand-alone patient monitor.

T1 Patient Monitor Operator’s Manual

2-1

2.2 Main Unit 2.2.1 Front View

1

2

3 4 5

7

6 1.

Alarm lamp The Alarm lamp flashes in different color and frequency to match the alarm level.

2.

Display Screen

3.

Ambient light sensor When [Brightness] is set to [Auto], the system automatically adjusts screen according to the strength of ambient light.

4.

5.

External power supply indicator 

On:

when external DC power supply is connected.



Off:

when external DC power supply is not connected.

Battery indicator 

On:

when the battery is installed and the external DC power supply is connected.



Off:

when no battery is installed, or the installed battery is malfunctioning, or no external DC power supply

is connected when the patient monitor is power off. 

6.

Flashing: when the patient monitor operates on battery power.

Power On/Off Switch 

Pressing this switch turns the patient monitor on.



When the monitor is on, pressing and holding this switch turns the monitor off.

An indicator is built into this switch. It turns on when the patient monitor is on and turns off when the patient monitor is off. 7.

Lock/unlock switch: Sliding this switch to the right locks/unlocks the touch screen.

2-2

T1 Patient Monitor Operator’s Manual

2.2.2 Left View

1

2

3

4

4

1.

External DC power supply connector

2.

Main unit multi-pin connector: connects T1 to the T1 handle or T1 docking station.

3.

Infrared filter:

4.

Contact: is for future use.

is for future use.

NOTE 

To ensure good contact, clean the contacts regularly, as dust and dirt may collect on them. When cleaning the contacts, wipe them with cotton, dampened with alcohol. Using forceps is recommended.

T1 Patient Monitor Operator’s Manual

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