Accutorr 7 Vital Signs Monitor Operating Instructions Rev 17.00 Nov 2021

© Copyright 2013-2021 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved. Release date: November 2021 Revision: 17.0

WARNING

• Federal Law (USA) restricts this device to sale by or on the order of a physician or other practitioner licensed by U.S. state law to use or order the use of this device.

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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. This posting serves as notice under 35 U.S.C.§287(a) for Mindray patents: http:// www.mindrayna.com/patents.

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 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:

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

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

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

Accutorr 7 Operator’s Manual

WARNING

• Only skilled/trained clinical professionals shall operate this equipment. • 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.

Service Mindray maintains a network of service representatives and factory-trained distributors. Prior to requesting service, perform a complete operational check of the instrument to verify proper control settings. If operational problems continue to exist, contact Mindray service. In North America contact the Service Department at (800) 288-2121, ext: 8116 for Technical Support or (201) 995-8000 for assistance in determining the nearest field service location. Please include the instrument model number, the serial number, and a description of the problem with all requests for service. Any questions regarding the warranty should be directed to your local sales or service representative.

NOTE

• Upon request, Mindray provides circuit diagrams, component part lists, descriptions, calibration instructions, or other information which assist the user’s appropriately qualified technical personnel to repair those parts of the equipment which are designated by Mindray DS USA, Inc. as repairable.

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Company Contact

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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

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

Accutorr 7 Operator’s Manual

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 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 patient monitor.

Conventions ■

Italic text is used in this manual to quote the referenced chapters or sections.

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[ ] is used to enclose screen texts.

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→ is used to indicate operational procedures.

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Contents 1 Safety ...1 - 1 1.1 Safety Information ...1 - 1 1.1.1 Warnings ...1 - 1 1.1.2 Cautions ...1 - 2 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 Applied Parts ...2 - 1 2.3 Main Unit ...2 - 2 2.3.1 Front View ...2 - 2 2.3.2 Side View ...2 - 4 2.3.3 Rear View ...2 - 5 2.3.4 Bottom View ...2 - 6 2.4 Main Screen ...2 - 7 2.5 Menu ... 2 - 11 2.6 Operating Modes ... 2 - 12 2.6.1 Monitor Mode ... 2 - 12 2.6.2 Spot Check Mode ... 2 - 12 2.6.3 Standby Mode ... 2 - 13 3 Basic Operation ...3 - 1 3.1 Installation ...3 - 1 3.1.1 Unpacking and Checking ...3 - 2 3.1.2 Environmental Requirements ...3 - 2 3.2 General Operation ...3 - 3 3.2.1 Connection to AC Power ...3 - 3 3.2.2 Using a Battery ...3 - 3 3.2.3 Connecting Accessories ...3 - 3 3.3 Turning On/Off Power ...3 - 4 3.3.1 Turning Power On ...3 - 4 3.3.2 Turning off the Monitor ...3 - 4 3.4 Using Key, Knob, Touchscreen ...3 - 5 3.4.1 Using Keys ...3 - 5 3.4.2 Using the Knob ...3 - 6 3.4.3 Using the Touchscreen ...3 - 6 3.5 Using the Timer ...3 - 6 3.5.1 Displaying the Timer ...3 - 6 3.5.2 Controlling the Timer ...3 - 6 3.6 Changing General Settings ...3 - 7

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3.6.1 Setting up a Monitor ...3 - 7 3.6.2 Changing Language ...3 - 7 3.6.3 Configuring the Timeout of Clinician ID ...3 - 7 3.6.4 Showing/Hiding Patient Name ...3 - 7 3.6.5 Adjusting Alarm Volume ...3 - 8 3.6.6 Adjusting Key Volume ...3 - 8 3.6.7 Adjusting the Screen Brightness ...3 - 8 3.6.8 Setting Screen ...3 - 8 3.6.9 Configuring the Timeout of Measured Value ...3 - 9 3.6.10 Configuring Measurement Colors ...3 - 9 3.6.11 Setting the Date and Time ...3 - 9 3.6.12 Changing the Time Zone ...3 - 9 3.6.13 Enabling Auto Daylight Savings Time ... 3 - 10 3.6.14 Configuring Unit ... 3 - 10 3.6.15 Configuring Printout ... 3 - 10 4 Patient Data Management ...4 - 1 4.1 Admitting a Patient ...4 - 1 4.1.1 Admitting a Patient by the Admit Patient Hardkey ...4 - 1 4.1.2 Admitting a Patient by Barcode Scanner ...4 - 2 4.1.3 Admitting a Patient from [Patient List] ...4 - 4 4.2 Manually Input Patient Data ...4 - 5 4.2.1 Setting the Manual Input Area ...4 - 5 4.2.2 Adding Custom Manual Input Parameters ...4 - 7 4.3 Setting the Monitor Location ...4 - 7 4.4 Setting the Location Protection ...4 - 8 4.5 Manually Save Patient Data ...4 - 8 4.6 Reviewing Patient Data ...4 - 9 4.6.1 Spot Check Trends ...4 - 9 4.6.2 Continuous Trends ... 4 - 11 4.6.3 Graphic Trends ... 4 - 12 4.6.4 Scoring Review ... 4 - 13 4.7 VitalsLink Instructions ... 4 - 14 4.8 Transferring Data from the Monitor to USB Drive ... 4 - 15 4.9 Managing Patient Data ... 4 - 15 5 Managing Configurations ...5 - 1 5.1 Overview ...5 - 1 5.2 Accessing [Manage Configuration] Menu ...5 - 1 5.2.1 Setting Default Configuration ...5 - 2 5.3 Saving Current Settings ...5 - 2 5.4 Deleting a Configuration ...5 - 2 5.5 Transferring a Configuration ...5 - 3 5.6 Loading a Configuration ...5 - 3 5.7 Restoring the Latest Configuration Automatically ...5 - 3

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6 Alarms ...6 - 1 6.1 Alarm Categories ...6 - 1 6.2 Alarm Levels ...6 - 2 6.3 Alarm Indicators ...6 - 2 6.3.1 Alarm Lamp ...6 - 2 6.3.2 Audible Alarm Tones ...6 - 3 6.3.3 Alarm Messages ...6 - 3 6.3.4 Flashing Numerics ...6 - 4 6.3.5 Alarm Status Symbols ...6 - 4 6.4 Setting Alarms ...6 - 4 6.5 Selecting Alarm Properties ...6 - 5 6.5.1 Changing the Alarm Volume ...6 - 5 6.5.2 Setting the Minimum Alarm Volume ...6 - 5 6.5.3 Setting the Interval between Alarm Sounds ...6 - 5 6.5.4 Adjusting Alarm Limits Automatically ...6 - 6 6.6 Pausing Alarms ...6 - 9 6.7 Switching Off Alarm Sound ...6 - 9 6.8 Switching Off [No CO2 Change Detected] Alarm ...6 - 9 6.9 Resetting Alarms ... 6 - 10 6.10 Setting the Reminder Tone ... 6 - 11 6.11 Latching Alarms ... 6 - 11 6.12 Actions for Alarm Occurrence ... 6 - 12 6.13 Nurse Call ... 6 - 12 7 Monitoring SpO2 ...7 - 1 7.1 Overview ...7 - 1 7.2 Safety ...7 - 2 7.3 Identifying SpO2 Module ...7 - 3 7.4 Applying the Sensor ...7 - 3 7.5 Changing SpO2 Settings ...7 - 4 7.5.1 Accessing SpO2 Menu ...7 - 4 7.5.2 Adjusting the Desat Alarm ...7 - 4 7.5.3 Setting SpO2 Sensitivity ...7 - 4 7.5.4 Changing Averaging Time ...7 - 4 7.5.5 Monitoring SpO2 and NIBP Simultaneously ...7 - 4 7.5.6 Sat-Seconds Alarm Management ...7 - 5 7.5.7 Changing the Speed of Pleth Wave ...7 - 6 7.5.8 Setting the Alarm Level for SpO2 Sensor Off Alarm ...7 - 6 7.6 Measurement Limitations ...7 - 6 7.7 Masimo Information ...7 - 6 7.8 Nellcor Information ...7 - 7 8 Monitoring PR ...8 - 1 8.1 Overview ...8 - 1

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8.2 PR Source ...8 - 1 8.3 Pulse Tone ...8 - 1 9 Monitoring NIBP ...9 - 1 9.1 Overview ...9 - 1 9.2 Safety ...9 - 2 9.3 Measurement Limitations ...9 - 3 9.4 NIBP Measurement Mode ...9 - 3 9.5 Measuring NIBP ...9 - 3 9.5.1 Preparing the Patient ...9 - 3 9.5.2 Preparing to Measure NIBP ...9 - 4 9.5.3 Starting NIBP measurement ...9 - 5 9.5.4 Stopping NIBP Measurement ...9 - 5 9.5.5 Initiating An NIBP Averaging Program ...9 - 5 9.5.6 Correcting the Measurement when Cuff is not at Heart Level ...9 - 5 9.6 Understanding the NIBP Numerics ...9 - 6 9.6.1 NIBP Numerics for a Single Measurement ...9 - 6 9.6.2 NIBP Numerics for an Averaging Program ...9 - 6 9.7 Setting NIBP ...9 - 7 9.7.1 Setting NIBP Measurement Mode ...9 - 7 9.7.2 Configuring an NIBP Averaging Program ...9 - 8 9.7.3 Setting Interval ...9 - 8 9.7.4 Setting the Initial Cuff Inflation Pressure ...9 - 8 9.7.5 Setting NIBP End Tone ...9 - 9 9.7.6 Switching On/Off Measurement on Clock ...9 - 9 9.7.7 Configuring a Custom Program ...9 - 9 9.7.8 Setting NIBP Alarm Properties ... 9 - 10 9.7.9 Setting the Pressure Unit ... 9 - 10 9.8 Assisting Venous Puncture ... 9 - 10 9.9 Care and Cleaning of Reusable Cuffs ... 9 - 11 9.9.1 Reusable Cuffs with Bladders ... 9 - 11 9.9.2 Cleaning ... 9 - 11 9.9.3 Disinfection ... 9 - 11 9.9.4 Reusable Bladderless Cuffs ... 9 - 12 10 Monitoring Temp ...10 - 1 10.1 Overview ... 10 - 1 10.2 Monitoring Temp with SmarTemp™ Module ... 10 - 1 10.2.1 Setting Temp ... 10 - 2 10.2.2 Preparation ... 10 - 2 10.2.3 Disinfecting Temperature Probe ... 10 - 5 10.3 Monitoring Temp with Exergen TemporalScanner™ Thermometer ... 10 - 5 10.3.1 Safety Information ... 10 - 5 10.3.2 Taking a Temperature with the TemporalScanner™ ... 10 - 6 10.3.3 Understanding the Numerics ... 10 - 8 10.3.4 Understanding the TemporalScanner™ Thermometer LED Display ... 10 - 8

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10.3.5 Fahrenheit or Celsius Conversion ... 10 - 9 10.3.6 Replacing the Battery ... 10 - 9 10.3.7 Troubleshooting ... 10 - 9 10.3.8 Cleaning the TemporalScanner™ Thermometer ...10 - 10 11 Monitoring CO2 ... 11 - 1 11.1 Overview ... 11 - 1 11.2 Safety ... 11 - 1 11.3 Measurement Limitations ... 11 - 2 11.4 CO2 Display ... 11 - 2 11.5 Automatic CO2 Module Zeroing ... 11 - 2 11.6 Measuring CO2 ... 11 - 3 11.7 Changing CO2 Settings ... 11 - 4 11.7.1 Changing CO2 Alarm Settings ... 11 - 4 11.7.2 Setting the “No CO2 Changes Detected” Alarm Delay ... 11 - 4 11.7.3 Setting the CO2 Waveform ... 11 - 5 11.7.4 Entering the Standby Mode ... 11 - 5 11.7.5 Setting the Auto Standby ... 11 - 5 11.7.6 Setting Humidity Compensation ... 11 - 6 11.7.7 Setting Gas Compensation ... 11 - 6 11.7.8 Automatic Barometric Pressure ... 11 - 6 11.7.9 Calibrating the CO2 Module ... 11 - 6 12 Clinical Scoring ...12 - 1 12.1 Overview ... 12 - 1 12.1.1 MEWS (Modified Early Warning Score) ... 12 - 2 12.1.2 NEWS (National Early Warning Score) ... 12 - 2 12.1.3 Customizable Scoring ... 12 - 2 12.2 Entering the Calculation Screen ... 12 - 3 12.2.1 Scoring Screen ... 12 - 3 12.2.2 Score Tile ... 12 - 3 12.3 Calculating a Score ... 12 - 3 12.4 Clinical Scoring Screen ... 12 - 4 12.4.1 Score Tile in the Main Screen ... 12 - 4 12.4.2 Scoring Screen ... 12 - 4 12.5 Obtaining the Total Score ... 12 - 5 12.6 Unfreezing the Scoring Screen ... 12 - 7 12.7 Managing Scorings ... 12 - 7 12.7.1 Allowing Measured Values to be Edited ... 12 - 7 12.7.2 Importing Scoring ... 12 - 7 12.7.3 Selecting a Default Scoring ... 12 - 8 12.7.4 Deleting a Scoring ... 12 - 8 12.7.5 Loading a Scoring ... 12 - 8 13 Recording ...13 - 1

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13.1 Using a Recorder ... 13 - 1 13.2 Loading Paper ... 13 - 2 13.3 Setting the Recorder ... 13 - 2 13.4 Starting and Stopping Recordings ... 13 - 2 13.5 Reports ... 13 - 3 13.5.1 Real-time Recording ... 13 - 3 13.5.2 Graphic Trend Recording ... 13 - 3 13.5.3 Continuous Trends Recording ... 13 - 3 13.5.4 Spot Check Trends Recording ... 13 - 4 13.6 Removing a Paper Jam ... 13 - 4 13.7 Cleaning the Recorder Printhead ... 13 - 4 14 Network ...14 - 1 14.1 Network Connection ... 14 - 1 14.1.1 Selecting a Network Type ... 14 - 2 14.1.2 Setting the Wired Network ... 14 - 2 14.1.3 Setting the Wireless Network (Optional) ... 14 - 2 14.1.4 WLAN Test ... 14 - 3 14.1.5 Selecting WLAN Band and Channels ... 14 - 4 14.1.6 Setting up the Wireless Network (Optional) ... 14 - 4 14.2 Setting Data Send Method ... 14 - 5 14.2.1 DNS Setup ... 14 - 5 14.2.2 ADT Communication Setup ... 14 - 5 14.2.3 EMR Communication Setup ... 14 - 6 14.2.4 NTP Server Setup ... 14 - 6 14.2.5 Realtime Data Send Interval (for HL7 only) ... 14 - 7 14.2.6 Alarm Server Settings (for HL7 only) ... 14 - 7 14.2.7 Setting the Data Encryption Switch ... 14 - 7 14.3 Connecting the monitor to the CMS ... 14 - 7 14.3.1 Setting the CMS ... 14 - 8 14.3.2 Selecting a CMS ... 14 - 8 14.3.3 Clearing the Selected CMS at Startup ... 14 - 8 14.4 Managing Certificates ... 14 - 8 14.5 Setting the Multicast Parameters ... 14 - 9 14.5.1 DIAP Communication Setup ... 14 - 9 14.6 MLDAP ... 14 - 9 14.6.1 Setting MLDAP ... 14 - 9 14.6.2 Selecting Password for User Authentication ...14 - 10 14.7 Setting the VitalsLink ...14 - 11 14.7.1 Setting the VitalsLink Switch ...14 - 11 14.7.2 Setting the General Connectivity ...14 - 11 14.7.3 Setting the Security ...14 - 11 14.7.4 Setting the Clinician and Patient ...14 - 11 14.7.5 Setting the Barcode Format ...14 - 12 14.7.6 Importing Aliases/Bearer/Certificate ...14 - 12

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15 Battery ...15 - 1 15.1 Overview ... 15 - 1 15.2 Charging a Battery ... 15 - 2 15.3 Replacing a Battery ... 15 - 2 15.4 Battery Guidelines ... 15 - 2 15.5 Battery Maintenance ... 15 - 3 15.5.1 Conditioning a Battery ... 15 - 3 15.5.2 Checking a Battery ... 15 - 4 15.6 Recycling a Battery ... 15 - 4 16 Care and Cleaning ...16 - 1 16.1 General Points ... 16 - 1 16.2 Cleaning and Disinfecting the Main Unit ... 16 - 2 16.2.1 Approved Cleaning and Disinfecting Agents ... 16 - 2 16.2.2 Cleaning the Main Unit ... 16 - 4 16.2.3 Disinfecting the Main Unit ... 16 - 4 16.3 Cleaning and Disinfecting the Accessories ... 16 - 5 16.3.1 Approved Accessories Cleaning and Disinfecting Agents ... 16 - 5 16.3.2 Cleaning the Accessories ... 16 - 8 16.3.3 Disinfecting the Accessories ... 16 - 8 16.4 Sterilization ... 16 - 8 17 User Maintenance ...17 - 1 17.1 General Inspection ... 17 - 1 17.2 Maintenance and Testing Schedule ... 17 - 2 17.3 Checking Monitor Information ... 17 - 3 17.4 Visual Inspection ... 17 - 4 17.5 Power-on Test ... 17 - 4 17.6 Calibrating CO2 ... 17 - 4 17.7 Battery Check ... 17 - 5 17.8 Calibrating the Touchscreen ... 17 - 6 17.9 Formatting the Storage Card ... 17 - 6 18 Accessories ...18 - 1 18.1 SpO2 Accessories ... 18 - 1 18.2 NIBP Accessories ... 18 - 3 18.3 Temp Accessories ... 18 - 4 18.3.1 SmarTemp™ Accessories ... 18 - 4 18.3.2 Exergen TemporalScanner™ Thermometer Accessories ... 18 - 5 18.4 CO2 Accessories ... 18 - 5 18.5 Others ... 18 - 5 A Product Specifications ... A - 1 A.1 Classifications ... A - 1 Accutorr 7 Operator’s Manual

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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.5.1 LEDs ... A - 4 A.5.2 Audio Indicator ... A - 4 A.5.3 Monitor Interface Specifications ... A - 4 A.5.4 Outputs ... A - 4 A.5.5 Data Storage ... A - 5 A.6 Wireless Network (Optional) ... A - 5 A.7 Measurement Specifications ... A - 6 A.7.1 SpO2 ... A - 6 A.7.2 PR ... A - 8 A.7.3 NIBP ... A - 9 A.7.4 Temp ...A - 11 A.7.5 CO2 ...A - 12 B EMC and Radio Regulatory Compliance ...B - 1 B.1 EMC ...B - 1 B.2 Radio Regulatory Compliance ...B - 6 C Default Configurations ...C - 1 C.1 Parameter Configuration ... C - 1 C.1.1 NIBP ... C - 1 C.1.2 SpO2 ...C - 2 C.1.3 PR ... C - 3 C.1.4 Temp ... C - 3 C.1.5 CO2 ...C - 4 C.2 General Configuration ... C - 5 C.2.1 Alarm ... C - 5 C.2.2 Review ... C - 6 C.2.3 Record ... C - 6 C.2.4 Others ... C - 6 C.3 User Maintenance Items ... C - 8 D Alarm Messages ... D - 1 D.1 Physiological Alarm Messages ... D - 1 D.2 Technical Alarm Messages ... D - 2 D.2.1 NIBP Alarm Messages ... D - 2 D.2.2 SpO2 Alarm Messages ... D - 5 D.2.3 Temperature Alarm Messages ... D - 7 D.2.4 CO2 Alarm Messages ... D - 8 D.2.5 Recorder Alarm Messages ...D - 10 D.2.6 Power Alarm Messages ...D - 11 D.2.7 System Alarm Messages ...D - 12

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E Symbols and Abbreviations ...E - 1 E.1 Symbols ...E - 1 E.2 Abbreviations ...E - 3 F Anomalies ... F - 1 F.1 NIBP Smart Inflation Anomaly ...F - 1

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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.

1.1.1

Warnings WARNING

• This equipment is restricted to one patient at a time. • 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.

• To avoid risk of electric shock, this equipment must only be connected to a properly grounded power outlet. If a properly grounded power outlet is not available, operate the monitor on battery power.

• Ensure that the equipment is supplied with continuous electric power during operation. Sudden power failure may lead to the loss of patient data. • The equipment is magnetic resonance (MR) unsafe. To avoid an explosion hazard, do not use the equipment in the presence of oxygen–rich

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atmospheres, flammable anesthetics, or other flammable agents (such as gasoline).

• Before connecting the equipment to a 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.

• Do not open the equipment housings. All servicing or future upgrades must be carried out by Mindray trained and authorized personnel. • 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 should be reviewed by a clinician before being used for diagnostic interpretation and treatment.

• 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 by patients or personnel.

• The equipment uses a mains plug as isolation means to the mains power supply. Please do not position the equipment in a place difficult to operate the mains plug.

• 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 phones and X-ray equipment are a possible source of interference as they may emit higher levels of electromagnetic radiation.

1.1.2

Cautions CAUTION

• Only use parts and accessories specified in this manual. • Remove the battery before shipping the monitor or if it will not be used for an extended period of time. • Carefully route patient cabling to reduce the possibility of patient entanglement.

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Accutorr 7 Operator’s Manual

• Disposable accessories are not designed to be reused. Reuse may cause a risk of contamination and affect the measurement accuracy. • Always install or carry the equipment properly to avoid damage caused by a drop, impact, strong vibration or other mechanical force. • Dry the equipment immediately in case of rain or water spray. • When no battery is installed, make sure that the power supply is continuous. A power interruption will result in patient data loss. • Store and use the equipment in specified environmental condition. The monitor and accessories may not meet the performance specification due to aging, stored or used outside the specified temperature and humidity range.

• Contact the Mindray service personnel for replacements if you find the housing is broken. • Data communication must be performed within a closed network or within a virtually isolated network provided by a hospital for all network functions. The hospital is responsible for ensuring the security of the virtually isolated network.

1.1.3

Notes NOTE

• Keep this manual in the vicinity of the equipment so that it can be easily located 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 the equipment features and options. Your equipment may not have all of them. • During normal use, the operator is expected to face the front of the equipment. • Put the equipment in a location where you can easily view and operate the equipment. • The equipment uses a mains plug as a means of isolation to the mains power supply. Do not position the equipment in a place difficult to access the mains plug.

• When disposing of the packaging material, be sure to observe the applicable waste control regulations and keep it out of children’s reach. • At the end of its service life, the equipment, and 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 Mindray.

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