Medipost-Nutristoma MD300K2 User Manual

Copyright
Our company owns all rights of this unpublished work and intends to maintain it as a
condential work. We may also seek to maintain this work as an unpublished copyright. This
publication is to be used solely for the purpose of reference or operation of our software
system. No part of this work can be disseminated for other purposes.
In the event of inadvertent or deliberate publication, we intend to enforce its right to this work
under copyright laws as a published work. Those having access to this work may not copy,
use, or disclose the information in this work unless expressly authorized by our company.
All information contained in this publication is believed to be correct. We shall not be liable for
errors contained herein nor for incidental or consequential damages in connection with the
furnishing, performance, or use of this material. The information this publication refers to is
protected by copyrights or patents and does not convey any license under the patent rights
of our company, nor the rights of others. We do not assume any liability arising out of any
infringements of patents or other rights of third parties.
Content of the manual is subject to change without prior notice.
Model: MD300K2
Version: Ver 1.0K2
Revised Date: March 10, 2017

Medipost-Nutristoma MD300K2 Specifications

General

Brand	Medipost-Nutristoma
Model	MD300K2
Category	Medical Equipment
Language	English

Summary

Copyright

1 INTRODUCTION

1.1 Brief Introduction

Provides a general overview of the MD300K2 pulse oximeter functions and capabilities.

1.2 Intended Use

Specifies the target patients and clinical applications for the MD300K2 Pulse Oximeter.

1.3 Measurement Principle

Explains the underlying photoelectric technology and mathematical formula used for measurements.

1.4 Safety Information

Covers crucial warnings, cautions, notes, and potential hazards for safe operation.

1.5 Electromagnetism Interference

1.6 Explanation of Symbols

1.7 Product Features

1.8 Contraindication

2 GENERAL DESCRIPTION

2.1 Appearance

Describes the physical layout, components, and ports of the pulse oximeter.

2.2 Power Supply

3 TIME AND DATE SETTINGS

4 TAKE A MEASUREMENT

4.1 Install the Probe

Guides on correctly connecting the SpO2 sensor probe to the pulse oximeter unit.

4.2 Measurement Screens

Describes the different display modes and the data presented during SpO2 and PR measurements.

5 SETTING

5.1 System Setting

Allows configuration of alarm volume, pause, beep tone, backlight, language, and screen sleep mode.

5.2 Alarm Setting

Enables configuration of alarm parameters, limits, and password management for settings.

6 DATA MANAGEMENT

6.1 Data Review

Allows users to view stored measurement data, including time, SpO2, PR, and alarm markers.

6.2 SpO2 Trend

Displays historical SpO2 readings over time in a graphical trend format.

6.3 PR Trend

Displays historical Pulse Rate readings over time in a graphical trend format.

6.4 Delete All Data

Provides a function to erase all stored measurement data from the device.

7 ALARM

8 MAINTENANCE AND REPAIR

8.1 Maintenance

Provides guidelines for cleaning, disinfecting, and general upkeep of the pulse oximeter.

8.2 Safety Checks

Outlines periodic inspection procedures to ensure the device's reliability and proper function.

8.3 Troubleshooting

Lists common malfunctions, their probable causes, and recommended solutions for user assistance.

8.4 Warranty and Repair

8.4.1 Maintenance Method

Specifies the response and repair times for technical support and service.

8.4.2 Exempt and limitation

Lists conditions and situations for which the manufacturer is not responsible for damage or loss.

8.4.3 User Guarantees

Outlines user responsibilities regarding operation, maintenance, and environmental conditions.

8.4.4 No-guarantee principle

Lists specific conditions or damage types that will void the product's warranty.

8.4.5 User's Special Request for Guarantee Time

Discusses procedures and considerations for extending the warranty period beyond the standard term.

8.4.6 Repackage

Provides instructions for properly repackaging the product, accessories, and original packaging.

APPENDIX A SPECIFICATIONS

APPENDIX B CLINICAL STUDY SUMMARY

APPENDIX C DECLARATION