EasyManua.ls Logo

Biolight Meditech M850 User Manual

Default Icon
103 pages
To Next Page IconTo Next Page
To Next Page IconTo Next Page
Page #1 background imageLoading...
Page #1 background image
Product Information
z Product Model: M850
z Product Name: Patient monitor
z Manufacturer: Guangdong Biolight Meditech Co., Ltd.
z After Service Contact Information:
Address: No.2 Innovation First Road, Technical
Innovation Coast, Hi-tech Zone, Zhuhai ,
P.R.China
Fax: +86-756-3399919
Postcode: 519085
Toll-free consultation hot line: +86-400-8818-233
Revision History
This manual has a revision number. This revision
number changes whenever the manual is updated due to
software or technical specification change. Contents of this
manual are subject to change without prior notice.
z Document No.: J/M850-I-002
z Revision number: V1.0
z Release time: Oct.2016
Copyright © 2016 Guangdong Biolight Meditech Co., Ltd.
All rights reserved.

Table of Contents

Question and Answer IconNeed help?

Do you have a question about the Biolight Meditech M850 and is the answer not in the manual?

Biolight Meditech M850 Specifications

General IconGeneral
ECGYes
SpO2Yes
NIBPYes
Respiration RateYes
TemperatureYes
EtCO2Optional
IBPOptional
Display TypeTFT LCD
Touch ScreenYes
Battery LifeUp to 4 hours
Alarm SystemAudible and visual alarms
Resolution1024 x 768
ParametersECG, SpO2, NIBP, Respiration Rate, Temperature
ConnectivityUSB, Wi-Fi

Summary

Chapter 1 General Introduction

1.1 Intended Use

M850 Patient monitor is intended for continuously monitoring or spot checking of SpO2, PR, ECG, HR and RR signals of single adult, pediatric and neonatal patient.

1.3 Display Views

This device has a function of automatic display rotation (Gravity Activated) which provides for vertical and horizontal positioning to maximizing space utilization and visibility.

Chapter 2 Safety

2.1 Safety Information

Explosion hazard: Do not use the monitor in the presence of flammable anesthetics mixture with air, oxygen, or hydrogen.

2.2 Explanation of Symbols

Defines symbols used in the manual, such as Type CF applied part, defibrillation protected.

Chapter 3 Basic Operations

3.1 Unpacking and Checking

Open the package. Parts are as follows in the package .Take out the monitor and its accessories.

3.2 Getting Started

Before you start to make measurements, carry out the following checks on the monitor including all connected modules.

3.3 Starting the Monitor

Press the button about two seconds to turn on the monitor. The alarm indicating lamp flashes, and then goes out.

3.4 Screen Brightness Setting

You can set the screen brightness to a value between 1 to 5.

3.5 Auto-Rotate Setting

If you select 【On】, the screen can react to the gravity. When the monitor rotates, the screen will rotate the display direction automatically.

3.6 Date & Time Setting

After starting up, you need to set date and time of this monitor.

3.7 Patient Information Setting

Please select patient information correctly before measuring.

3.8 Demo Mode Setting

To enter the demo mode: Select 【Menu】→【System】→【Maintenance】→enter the required password.

3.9 Language Setting

Enter the required password. On 【Factory Mainten.】interface, you can select 【Language】and then choose a desired language.

3.10 Checking the Version

Select【Menu】→【System】to check the version of the monitor software.

3.11 Restoring the Factory Configuration

If you have changed the system’s configuration and want to restore the factory configuration, follow this procedure.

3.12 Shutting off the Monitor

Pressing power button about 2s can turn off the monitor.

Chapter 4 Alarm

4.1 Alarm Categories

By nature, the monitor’s alarms can be classified into three categories: Physiological alarms, Technical alarms, Prompt messages.

4.2 Alarm Levels

By severity, the monitor’s physiological alarms can be classified into three categories: high level alarms, medium level alarms and low level alarms.

4.3 Alarm Indicators

When an alarm occurs, the monitor will raise user’s attention by the following indications: Alarm tone, Alarm lamp, Alarm message, Flashing numeric.

4.4 Alarm Status Symbol

Symbols to identify controls for alarm pause, alarm sound status, and alarm reset.

4.5 Alarm Tone Configuration

Set the minimum alarm volume and alarm volume levels.

4.6 Pausing Alarms

Press the button on the front panel of monitor to suspend all alarm indicators.

4.7 Shutting off the Alarm Volume

Set the minimum alarm volume and alarm volume to 【off】 to shut off the alarm volume.

4.8 Alarm Reset

Turn on alarm reset. Alarm reset will be displayed on the interface of system.

4.9 When an Alarm Occurs

Check the alarm message appeared on screen. It is needed to identify the alarm and action appropriately, according to the cause of the alarm.

Chapter 5 Measuring ECG

5.1 Introduction

Explains the principle of ECG measurement and how the monitor works.

5.2 Safety Information

Imperative to only use ECG electrodes and cables provided by manufacturer or specified in this manual.

5.3 Monitoring Procedure

Describes the steps for monitoring ECG, including skin preparation and electrode placement.

5.4 Checking Paced Status

It is important to set the paced status correctly when you start monitoring ECG.

5.5 ECG Display

Shows the ECG waveform, HR parameter, and associated labels and limits.

5.6 Setting ECG

Allows configuration of HR alarm, limits, scan speed, gain, lead type, and QRS volume.

Chapter 6 Measuring RESP

6.1 Principle of Measuring

Monitor measures RESP with the method of impedance. Respiration rate is calculated based on impedance changes.

6.2 Preparatory Steps of Measurement

Steps include plugging the ECG cable, placing electrodes, and setting relevant parameters.

6.3 Resp Display

Shows the respiration waveform, rate, and associated limits and units.

6.4 Resp Setup

Allows configuration of Resp alarm, limits, scan speed, gain, lead, and apnea alarm.

Chapter 7 Measuring SpO2

7.1 Introduction

Explains the measurement of oxygen saturation using light spectra and volume tracing principles.

7.2 Safety Information

Use only SpO2 sensors specified, avoid use during MRI, and monitor skin for prolonged use.

7.3 Monitoring Procedure

Steps for selecting, connecting, and applying the SpO2 sensor to the patient.

7.4 SpO2 Display

Displays SpO2 percentage, high/low alarm limits, SpO2 value, and unit.

7.5 PR Display

Shows Pulse Rate (PR) value, high/low alarm limits, and unit.

7.6 SpO2 Setup

Configure SpO2 alarm level, limits, scan speed, average time, and QRS volume.

7.7 Desat limit Setup

Sets the SpO2 desaturation limit, triggering a high physiological alarm when crossed.

Chapter 8 Trend Review

8.1 Introduction

Enter trend reviewing window to review ECG, Reap, SpO2 and PR data stored before.

8.2 Review Interface

Displays stored data in a tabular format, allowing navigation between pages.

8.3 Review Setup

Allows selection of patient ID to review patient's trend data.

Chapter 9 Battery

9.1 Introduction

Describes the rechargeable battery and indicates battery status through icons.

9.2 Charging the Battery

Connect the Micro USB to the power adapter and then to the monitor to charge the battery.

9.3 Optimizing Battery Performance

Recommends initial optimizing cycles and regular conditioning for battery maintenance.

9.4 Checking the Lithium Battery

Procedure to check battery performance by charging and discharging cycles.

9.5 Disposing of the Batteries

Batteries should be replaced and discarded properly according to local regulations.

Chapter 10 Maintenance and Cleaning

10.1 Introduction

Keep equipment and accessories free of dust and dirt. Follow rules to avoid damage.

10.2 Seasonal Safety Checking

Ensures performance and safety of equipment by checks after one year and annually.

10.3 Cleaning the Monitor

Use common detergent and non-corrosive disinfectant. Avoid alcohols and abrasive materials.

10.4 Cleaning ECG Cable

Recommended disinfectants include glutaric dialdehyde and 10% decolourant solution.

10.5 Cleaning SpO2 Sensor

Clean sensor casing with medical alcohol; sensor cable with Hydrogen Peroxide or isopropyl alcohol.

10.6 Disposal

Dispose of the monitor, SpO2 sensor, and ECG cable in accordance with local regulations.

Chapter 11 Accessories

Appendix A Product Specifications

A.1 Safety Specifications

Details CFDA classification, CE classification, and protection degrees against electric shock and liquid ingress.

A.2 Physical Specifications

Provides mainframe weight and dimensions.

A.3 Environmental Specifications

Specifies operating and storage conditions for temperature, atmospheric pressure, and humidity.

A.4 Charging Specifications

Details power adapter input/output and Micro USB function.

A.5 Hardware Specifications

Covers display size, resolution, touch, autorotation, and indicating lamps.

A.7 Measurement Specifications

Lists ECG, RESP, and SpO2 measurement ranges, resolution, accuracy, and other parameters.

Appendix B Factory Defaults

B.1 Alarm Setup

Lists factory default settings for alarm volume, SpO2, HR, and RESP alarm levels.

B.2 System Setup

Includes factory default settings for QRS volume, brightness, and scan speed.

B.3 ECG Setup

Shows factory default HR and RESP high/low limits for Adult, Pediatric, and Neonate.

B.4 SpO2 Setup

Details factory default SpO2 and PR high/low limits for different patient types.

B.5 Trend Setup

Specifies the factory default interval for trend data storage.

Appendix C Alarm Message

C.1 Physiological Alarm

Lists physiological alarm messages, their causes, and adjustable alarm levels.

C.2 Technical Alarm

Details technical alarm messages, their causes, and associated alarm levels.

C.3 Prompt Message

Describes prompt messages, their causes, and display level.

Appendix D EMC

Appendix E Warranty Registration Card

Related product manuals