Mindray MEC-1000 User manual

MEC-1000
Portable Multi-parameter
Patient Monitor
Operation Manual

I
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called
Mindray) owns the intellectual property rights to this 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 does not assume any
liability arising out of any infringements of patents or other rights of third parties.
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,
rent, 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.
Contents of this manual are subject to changes without prior notice.
For this Operation Manual, the issued Date is July 2005 (Version: 1.3).
© 2002-2005 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.

II
Manufacturer’s Responsibility
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 safety, reliability and performance of this product only in the
condition that:
 all installation operations, expansions, changes, modifications and repairs of this
product are conducted by Mindray authorized personnel; and,
 the electrical installation of the relevant room complies with the applicable national
and local requirements; and,
 this product is operated under strict observance of this manual.
Warranty
This warranty is exclusive and is in lieu of all other warrantyies, 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 shall not extend to
 any Mindray product which has been subjected to misuse, negligence or accident;
or
 any Mindray product from which Mindray's original serial number tag or product
identification markings have been altered or removed; or
 any product of any other manufacturer.

III
Return Policy
In the event that it becomes necessary to return a unit to Mindray, follow the instructions
below.
1. Obtain a return authorization.
Contact the Mindray Service Department and obtain a Mindray Customer Service
Authorization Number. The Mindray Customer Service Authorization Number must appear on
the outside of the shipping container. Return shipments will not be accepted if the Mindray
Customer Service Authorization Number is not clearly visible. Please provide the model
number, serial number, and a brief description of the reason for return.
2. Freight policy
The customer is responsible for freight charges when this product is shipped to Mindray for
service (including any relevant customs fees or other freight related charges).
3. Return address
Please send the part(s) or equipment to the address offered by Customer Service
Department.

IV
Contact Information
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
Tel: [phone] [phone]
Fax: [phone] [phone]
Website: www.mindray.com.cn
EC Representative: Shanghai International Holding Corp. GmbH (Europe)
Address: Eiffestraße 80, 20537 Hamburg Germany
Tel: [phone]
Fax: [phone]

V
Equipment Symbols
This symbol means 'BE CAREFUL '. Refer to the manual.
This symbol indicates that the instrument is IEC 60601-1 Type CF
equipment. The unit displaying this symbol contains an F-Type isolated
(floating) patient applied part providing a high degree of protection
against shock, and is suitable for use during defibrillation.
Equipotential grounding system.
Protective earth ground.
Power On/Off
This mark means that this device is fully in conformance with the
Council Directive Concerning Medical Devices 93/42/EEC. The
number adjacent to the CE marking (0123) is the number of the
EU-notified body that certified meeting the requirements of Annex II of
the Directive.
The following definition of the WEEE label applies to EU member
states only.
This symbol indicates that this product should not be treated as
household waste. By ensuring that this product is disposed of correctly,
you will help prevent bringing potential negative consequences to the
environment and human health. For more detailed information with
regard to returning and recycling this product, please consult the
distributor from whom you purchased it.
* For system products, this label may be attached to the main unit only.
NOTE: Points to be noted.
CAUTION: Points to be noted to avoid damage to the equipment.
WARNING: Points to be noted to avoid injury to the patient and the
operator.

VI
FOR YOUR NOTES

1
Contents
Chapter 1 Introduction........................................................................................................1-1
1.1 General Information .................................................................................................. 1-2
1.2 Screen Display.......................................................................................................... 1-4
1.3 Button Functions ....................................................................................................... 1-7
1.4 Interfaces ................................................................................................................ 1-10
1.5 Built-in battery ......................................................................................................... 1-12
Chapter 2 Getting Started ................................................................................................. 2-1
2.1 Unpacking and Checking .......................................................................................... 2-1
2.2 Connect the Power Cables ....................................................................................... 2-1
2.3 Power On the Monitor ............................................................................................... 2-2
2.4 Connect Sensors/Probes .......................................................................................... 2-2
2.5 Check the Recorder .................................................................................................. 2-2
Chapter 3 System Menu ................................................................................................... 3-1
3.1 Patient Setup............................................................................................................. 3-2
3.2 Default Setup............................................................................................................. 3-4
3.3 System Setup ............................................................................................................ 3-5
3.4 Selection Setup ....................................................................................................... 3-10
3.5 Monitor Version ....................................................................................................... 3-11
3.6 Drug Calculation...................................................................................................... 3-12
3.7 Maitenance .............................................................................................................. 3-12
3.8 DEMO Function....................................................................................................... 3-15
Chapter 4 Face Select ...................................................................................................... 4-1
4.1 Standard Screen ....................................................................................................... 4-1
4.1 Viewbed Screen ........................................................................................................ 4-2
Chapter 5 Alarm................................................................................................................ 5-1
5.1 Alarm Modes ............................................................................................................. 5-1
5.2 Alarm Self-test........................................................................................................... 5-4
5.3 Alarm Cause.............................................................................................................. 5-4
5.4 SILENCE/CLOSE/PAUSE ........................................................................................ 5-5
5.5 Parameter Alarm ....................................................................................................... 5-6
5.6 When an Alarm Occurs ............................................................................................. 5-6
Chapter 6 Freeze ............................................................................................................... 6-1
6.1 General Description .................................................................................................. 6-1
6.2 Entering and Exiting Frozen Mode............................................................................ 6-1
6.3 Frozen Menu ............................................................................................................. 6-2
6.4 Recording Frozen Waveform .................................................................................... 6-2
Chapter 7 Recording .......................................................................................................... 7-1
7.1 General Description .................................................................................................. 7-1
7.2 Recording Type ......................................................................................................... 7-1
7.3 Start Recording ......................................................................................................... 7-4

Contents
2
7.4 Recorder Operations and Status Information ........................................................... 7-5
Chapter 8 Trend and Event .............................................................................................. 8-1
8.1 Trend Graph .............................................................................................................. 8-1
8.2 Trend Table................................................................................................................ 8-3
8.3 NIBP Recall ............................................................................................................... 8-5
8.4 Alarm Event Recall .................................................................................................... 8-5
Chapter 9 Drug Calculation and Titration Table................................................................ 9-1
9.1 Drug Calculation........................................................................................................ 9-1
9.2 Titration Table ............................................................................................................ 8-4
Chapter 10 Patient Safety................................................................................................. 10-1
Chapter 11 Maintenance / Cleaning ................................................................................. 11-1
11.1 System Check ....................................................................................................... 11-1
11.2 General Cleaning .................................................................................................. 11-1
11.3 Cleaning Agents .................................................................................................... 11-2
11.4 Sterilization ............................................................................................................ 11-3
11.5 Disinfection............................................................................................................ 11-3
Chapter 12 ECG/RESP Monitoring ................................................................................ 12-1
12.1 What Is ECG Monitoring ....................................................................................... 12-1
12.2 Precautions ........................................................................................................... 12-1
12.3 Monitoring Procedure............................................................................................ 12-2
12.4 ECG Screen Hot Keys .......................................................................................... 12-5
12.5 ECG Menu ............................................................................................................ 12-6
12.6 ECG Alarm Information and Prompt ................................................................... 12-10
12.7 ST Segment Monitoring (optional) ...................................................................... 12-11
12.8 Arr. Monitoring (optional)..................................................................................... 12-15
12.9 Measuring RESP................................................................................................. 12-20
12.10 Maintenance and Cleaning ............................................................................... 12-24
Chapter 13 SpO2 Monitoring ............................................................................................ 13-1
13.1 What is SpO2Monitoring....................................................................................... 13-1
13.2 Precautions ........................................................................................................... 13-2
13.3 Monitoring Procedure............................................................................................ 13-3
13.4 Limitations for Measurement................................................................................. 13-5
13.5 SpO2Menu............................................................................................................ 13-6
13.6 Alarm Description and Prompt .............................................................................. 13-8
13.7 Maintenance and Cleaning ................................................................................... 13-9
Chapter 14 NIBP Monitoring............................................................................................. 14-1
14.1 Introduction ........................................................................................................... 14-1
14.2 NIBP Monitoring .................................................................................................... 14-1
14.3 NIBP SETUP menu............................................................................................... 14-6
14.4 NIBP Alarm Message.......................................................................................... 14-11
14.5 Maintenance and Cleaning ................................................................................. 14-13
Chapter 15 TEMP Monitoring ........................................................................................... 15-1
15.1 TEMP Monitoring .................................................................................................. 15-1
15.2 TEMP SETUP Menu ............................................................................................. 15-2