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IV

CONTENTS

1 Safety ...................................................................1

1.1 Instructions for safe operations................ 1
1.2 Warning ..................................................... 1
1.3 Attention.................................................... 2

2 Overview.............................................................4

2.1 Features...................................................... 5
2.2 Major applications and scope of
application........................................................... 5
2.3 Environment requirements....................... 5

3 Principle..............................................................6

4 Technical specifications ....................................7

4.1 Main performance..................................... 7
4.2 Main Parameters ....................................... 7

5 Installation..........................................................8

5.1 View of the front panel............................. 8
5.2 Battery installation.................................... 8
5.3 Accessories................................................ 9

6 Operating Guide................................................9

6.1 Application method................................... 9
6.2

Attention for operation ......................... 14

6.3 Clinical restrictions................................. 15

7 Maintain

transportation and storage........16

7.1 Cleaning and Disinfecting...................... 16
7.2 Maintain................................................... 16
7.3 Transportation and storage ..................... 17

8 Troubleshooting ...............................................17
9 Key of Symbols ................................................19

10 Function Specification .....................................21

1

1 Safety

1.1 Instructions for safe operations

Check the main unit and all accessories

periodically to make sure that there is no visible
damage that may affect patient

s safety and

monitoring

performance

about

cables

and

transducers. It is recommended that the device
should be inspected once a week at least. When there
is obvious damage, stop using the device.

Necessary maintenance must be performed by

qualified service engineers ONLY. Users are not
permitted to maintain it by themselves.

The oximeter cannot be used together with

devices not specified in User

s Manual.Only the

accessory that appointed or recommendatory by
manufacture can be used with this device.

This product is calibrated before leaving factory.

1.2 Warning

Explosive hazard

DO NOT use the oximeter in

environment with inflammable gas such as some
ignitable anesthetic agents.

DO NOT use the oximeter while the testee

measured by MRI and CT.

The person who is allergic to rubber can not use

this device.

Summary of Contents for CMS-50D Plus

Page 1: ......

Page 2: ...the Pulse Oximeter s features and requirements main structure functions specifications correct methods for transportation installation usage operation repair maintenance and storage etc as well as th...

Page 3: ...evice ceaselessly especially for the microcirculation barrier patients It is recommended that the sensor should not be applied to the same finger for over 2 hours For the special patients there should...

Page 4: ...s Check the main unit and all accessories periodically to make sure that there is no visible damage that may affect patient s safety and monitoring performance about cables and transducers It is recom...

Page 5: ...r is not permitted Refer to User Manual in the relative chapter 7 1 for 3 instructions of cleaning and disinfection Do not have the oximeter immerged in liquid When it needs cleaning please wipe its s...

Page 6: ...able It is only necessary for patients to put one of his fingers into a probe for diagnosis and a display screen will directly show the measured value of pulse oxygen saturation with the high veracity...

Page 7: ...sitive element information acquired through which will be shown on screen through treatment in electronic circuits and microprocessor Figure 1 7 4 Technical specifications 4 1 Main performance A SpO2...

Page 8: ...nm 6 75mW 5 Installation 5 1 View of the front panel Figure 2 front view 5 2 Battery installation A Refer to Figure 3 and insert the two AAA size batteries properly in the right direction 9 B Replace...

Page 9: ...tion The icon of SpO2 is a program for receiving real time data which is shown as figure 5 the icon of SpO2 Review is a program for receiving stored data which is shown as figure 6 11 a Please connect...

Page 10: ...nds and then the screen will be automatically shut down only a flashing yellow dot appear on screen If short press the button at this moment the sign Recording would appear on the screen and then the...

Page 11: ...sensor should not be used at a location 15 or limb tied with arterial canal or blood pressure cuff or receiving intravenous injection E Do not fix the SpO2 sensor with adhesive or else it may result i...

Page 12: ...n shows C Take out the battery if leave the equipment unused for long time D The device needs to be calibrated once a year or according to the calibrating program of hospital It also can be performed...

Page 13: ...vice 1 Please change batteries 2 Please Install the battery again 3 Please contact the local service center The display is off suddenl y 1 The device s malfunction 2 The battery is drained away or alm...

Page 14: ...ion Specification Information Display Mode The Pulse Oxygen Saturation SpO2 2 digit digital OLED display Pulse Rate PR 3 digit digital OLED display Pulse Intensity bar graph bar graph OLED display SpO...

Page 15: ...Moving calculate the Average pulse rate every 4 cardio beat s cycle The deviation between average value and true value does not exceed 1 Safety Type Interior Battery Type 23 Pulse Intensity Range Con...

Page 16: ...24 Dimensions 58 5 L 31 W 32 H mm Weight About 50g with the batteries...

Page 17: ...File Ver 0 9 Release Date March 2009...

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