Mindray Hypervisor VI User manual

HYPERVISOR VI

Central Monitoring System

Service Manual

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, adaptation 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 manual, the issued Date is January 2006 (Version: 1.0).

© 2005 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved

I

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 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 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.

II

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.

III

Contact Information

Manufacturer:

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Address:

Tel:
Fax:
Website:

EC-Representative:
Address:
Tel:
Fax:

Mindray Building, Keji 12th Road South, Hi-tech Industrial
Park, Nanshan, Shenzhen 518057 P.R. China

[phone] [phone]

[phone] [phone]

www.mindray.com.cn

Shanghai International Holding Corp. GmbH (Europe)

Eiffestraße 80, 20537 Hamburg Germany

0049-40-2513175

0049-40-255726

IV

Safety Precautions

1. Meaning of Signal Words

In this service manual, the signal words

CAUTION and NOTE are used regarding safety and other important instructions.

The signal words and their meanings are defined as follows. Please understand their

meanings clearly before reading this manual.

DANGER, WARNING,

DANGER

 Indicates an imminent hazard situation that, if not avoided, will result in

death or serious injury.

WARNING

 Indicates a potential hazard situation 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.

V

2. Meaning of Safety Symbols

Symbol Description

Type-BF applied part

"Attention" (Refer to the operation manual.)

3. Safety Precautions

Please observe the following precautions to ensure patient and operator safety when

using this system.

CAUTION

 Malfunctions due to radio waves

 Use of radio-wave-emitting devices in the proximity of this kind of

medical electronic system may interfere with its operation. Do not
bring or use devices which generate radio waves, such as cellular
telephones, transceivers, and radio controlled toys, in the room where
the system is installed.

 If a user brings a device which generates radio waves near the system,

they must be instructed to immediately turn OFF the device. This is
necessary to ensure the proper operation of the system.

 Do not allow fluids such as water to contact the system or peripheral

devices. Electric shock may result.

DANGER

 Do not use flammable gasses such as anesthetics, or flammable liquids

such as ethanol, near this product, because there is danger of
explosion.

WARNING

 Do not connect this system to outlets with the same circuit breakers

and fuses that control current to devices such as life-support systems.
If this system malfunctions and generates an overcurrent, or when there
is an instantaneous current at power ON, the circuit breakers and fuses
of the building’s supply circuit may be tripped.

VI

Contents

Intellectual Property Statement·············································································I

Manufacturer’s Responsibility··············································································II

Warranty................................................................................................................... II

Exemptions............................................................................................................... II

Return Policy········································································································III

Contact Information ···························································································· IV

Safety Precautions··································································································V

Contents ···················································································································1

1 Introduction········································································································· 1-1

1.1 Overview............................................................................................................... 1-1

1.2 System Components.............................................................................................. 1-3

2 Installation···········································································································2-1

2.1 About the installation of the Central Monitoring System ..................................... 2-1

2.2 Requirements on Environment.............................................................................. 2-2

2.3 Installation of Windows XP Professional.............................................................. 2-3

2.4 Installation of the Drivers...................................................................................... 2-4

2.4.1 Driver of the display card.............................................................................. 2-4

2.4.2 Driver of network card .................................................................................. 2-5

2.4.3 Driver of sound card...................................................................................... 2-8

2.4.4 Installation of printer..................................................................................... 2-8

2.4.5 Installation of recorder .................................................................................. 2-8

2.4.6 Installation of USB watchdog driver............................................................. 2-9

2.4.7 Shutoff of Windows XP Fire Wall................................................................. 2-9

2.5 Adjusting the System .......................................................................................... 2-10

2.5.1 Setting the time delay of the system startup and recovery .......................... 2-10

2.5.2 Overrwriting Mode of Log Files ................................................................. 2-10

1

Contents

2.5.3 Disabling sound............................................................................................2-11

2.5.4 Setting Power Management Property.......................................................... 2-12

2.6 Installation of MSDE .......................................................................................... 2-14

2.7 Installation of the Central Monitoring System.................................................... 2-15

3 Quick Recovery ··································································································· 3-1

3.1 Overview............................................................................................................... 3-1

3.1.1 Application Scope ......................................................................................... 3-1

3.1.2 Precautions .................................................................................................... 3-1

3.2 Installation Procedure............................................................................................ 3-2

3.2.1 Making the Recovery Start Floppy Disk....................................................... 3-2

3.2.2 Quick Recovery Procedure............................................................................ 3-3

4 Maintenance and Cleaning················································································· 4-1

4.1 Maintenance .......................................................................................................... 4-1

4.1.1 General Inspection ........................................................................................ 4-1

4.1.2 System Performance Test .............................................................................. 4-1

4.2 Cleaning ................................................................................................................ 4-3

5 Troubleshooting··································································································· 5-1

5.1 Recorder/printer-related technical alarm messages............................................... 5-1

5.2 The CMS fails to display information of a monitor.............................................. 5-1

5.3 No waveform displayed in waveform review ....................................................... 5-1

5.4 “Display Mode Error” appears on the dual-screen CMS ...................................... 5-1

5.5 Dual-screen changes to Single-screen during the CMS installation...................... 5-1

5.6 Slow wave speed or database error message occurs during waveform reviewing 5-4

2

1 Introduction

1.1 Overview

HYPERVISOR VI Central Monitoring System (CMS) is intended for professional

physicians or paramedics to conduct centralized monitoring over multiple patients

monitored by individual monitors in hospitals or medical institutions.

The central monitoring system comprises powerful system software and

high-performance computer. It constructs a monitoring network by connecting

monitors. By collecting, processing, analyzing and outputting the information coming

from monitors, the central monitoring system can achieve centralized monitoring over

multiple patients so as to greatly promote the efficiency and quality of the monitoring

work.

The central monitoring system:

 Is capable of connecting up to 64 monitors that supports the CMS or CMS+

network protocol.

 Is capable of connecting up to 16 telemetry transmitters and supporting 1-16

transmitter frequency configurations.

 Supports multi-screen display mode, including two primary displays and

multiple secondary displays.

 Is capable of displaying information from 16 monitors in the single-screen mode

and 32 monitors in the dual-screen mode.

 Allows you to view a single patient emphatically.

 Allows you to review up to 240 hours of trend data for each online patient.

 Allows you to review up to 720 alarm events for each online patient.

 Allows you to save and review a 4-hour dynamic short trend for each online

patient.

 Allows you to review up to 720 CO measurements for each online patient.

 Allows you to review up to 72 hours of 64 waveforms.

 Allows you to review up to 720 NIBP measurements for each online patient.

 Allows you to search for, review and maintain the data of up to 20,000 history

patients.

 Provides the patient information management function.

1-1

Introduction

 Provides four alarm indications: audible alarm, visual alarm, alarm icon and

alarm message.

 Provides the functions of drug calculation, titration table calculation and

hemodynamics calculation.

 Provides the functions to record, print and save data.

 Provides comprehensive help information, prompts and operational guide.

 Supports 1280×1024 high display resolution.

 Facilitates the setup of language, waveform and parameter color.

 Supports such peripherals as the keyboard, mouse, thermal recorder, laser printer,

speaker, etc.

 Supports wire and wireless network.

The central monitoring system has a USB watchdog to protect the copyright. You

must plug the watchdog into the system’s USB interface before starting the system.

Otherwise, the system cannot start.

1-2

Introduction

1.2 System Components

Hardware components of the central monitoring system should be highly reliable and

stable. The hardware components of your system should meet the following

requirements at least.

Components Requirements

System

Host

Display 1280×1024 17"TFT, with CE marking.

Mouse PS/2 or other standard interface, with CE marking

Keyboard PS/2 or other standard interface, with CE marking.

Recorder Thermal array, serial port

Printer HP LaserJet series, supporting A4 paper

Speaker Internal speakers (of the computer or the display).

Meet the IEC60950 requirements defined for ITE equipment, and

Comply with CE low voltage directives (LVD) and EMC directives.

PC compatible, with CE marking

CPU: PIV 2.0GHz

256M RAM

40G Fixed Diskette

Network card: 10M/100M Base-T, Ethernet 802.3, RJ45 interface

3 USB interfaces

1 serial port

1 parallel port;

NOTE

 The configuration above is for reference only.

1-3