Contec CMS50QB Instructions To User

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Dear users, thank you very much for purchasing the Pulse Oximeter.

This Manual is written and compiled in accordance with the council directive MDD93/42/EEC for

medical devices and harmonized standards. In case of modifications and software upgrades, the

information contained in this document is subject to change without notice.

The Manual describes, in accordance with 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 the safety procedures to protect both the user and

equipment. Refer to the respective chapters for details.

Please read the User Manual carefully before using this product.The User Manual which describes

the operating procedures should be followed strictly. Failure to follow the User Manual may cause

measuring abnormality, equipment damage and human injury. The manufacturer is NOT responsible

for the safety, reliability and performance issues and any monitoring abnormality, human injury and

equipment damage due to users' negligence of the operation instructions. The manufacturer's

warranty service does not cover such faults.

Owing to the forthcoming renovation, the specific products you received may not be totally in

accordance with the description of this User Manual. We would sincerely regret for that.

This product is medical device, which can be used repeatedly.

WARNING:

�

� Discomfort

Discomfort

Discomfort or or or or pain

microcirculation

microcirculation barrier

used

on on

the

same

used

used on

on the

the

the same

same finger

same

�

� For

�

For

For the

the

the special

special

special patients,

special

patients,

patients, there

The

device

can

not

not be be be be clipped

not

The

The device

device can

can not

�

� The

The

The light

light

light (the

(the infrared

(the

infrared

infrared is is is is invisible)

infrared

user

and

the

maintenance

user

user and

and the

the maintenance

maintenance man

�

� Testee

Testee

can

not

use

Testee

Testee can

can

can not

not

not use

use

use enamel

�

� Testee

Testee

Testee' ' ' ' s s s s fingernail

fingernail

fingernail can

�

� Please

Please

refer

refer to to to to the

the

Please refer

the correlative

� This

This

This device

device is is is is not

device

not

not intended

Instructions

Instructions to to to to User

Instructions

pain

may

appear

appear if if if if using

pain may

may appear

barrier

barrier patients.

patients.

patients. It It It It is is is is recommended

finger

for

than

than 2 2 2 2 hours.

finger for

finger

for more

for

more than

than

there

there should

should be be be be a a a a more

should

clipped

on on

the

edema

clipped on

on the

the edema

edema and

invisible)

invisible) emitted

emitted

emitted from

man

should

man should

should not

enamel or or or or other

enamel

other

makeup.

enamel

other

other makeup.

makeup.

can

can not

not

not be be be be too

too

too long.

long.

correlative

literature

correlative literature

literature about

intended

intended for

intended

for

for treatment.

treatment.

User

using

the

device

ceaselessly,

using the

the device

device ceaselessly,

ceaselessly, especially

recommended

recommended tha

recommended

tha

that t t t the

tha

the

the pulse

hours.

more prudent

prudent

prudent inspecting

prudent

inspecting

inspecting in in in in the

and

tender

tissue.

and tender

tender tissue.

tissue.

from

from the

from

the

the device

device

device is is is is harmful

not

look

look at at at at the

the

light

source

source. . . .

not look

the light

light source

about

the

clinical

restrictions

about the

the clinical

clinical restrictions

restrictions and

especially

for

especially for

pulse

pulse oximeter

pulse

oximeter

oximeter should

oximeter

should

should not

the

the placing

placing

placing process.

process.

harmful

harmful to to to to the

the

the eyes,

the

eyes,

eyes, so so so so the

and

caution.

and caution.

caution.

for

the

for the

the

not

not be be be be

the

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Summary of Contents for Contec CMS50QB

Page 1 Instructions Instructions Instructions to to to to User User User Instructions User Dear users, thank you very much for purchasing the Pulse Oximeter. This Manual is written and compiled in accordance with the council directive MDD93/42/EEC for medical devices and harmonized standards. In case of modifications and software upgrades, the information contained in this document is subject to change without notice.
Page 2: Table Of Contents
Contents Contents Contents Contents 1 1 1 1 Safety Safety Safety ......................................................................................1 1 1 1 Safety.............................. 1.1 Instructions for safe operations..................... 1 1.2 Warning............................ 1 1.3 Attention...........................1 2 2 2 2 Overview Overview Overview ..................................................................................2 2 2 2 Overview............................
Page 3 Appendix Appendix Appendix Appendix A A A A ..................................................................................................................................10 10 10 10...
Page 4: Safety Safety
1 1 1 1 Safety Safety Safety Safety Instructions Instructions safe safe operations operations 1.1 Instructions Instructions for for safe safe operations 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.It is recommended that the device should be inspected weekly at least.
Page 5: Features
␇ DO NOT operate button on front panel with sharp things. ␇ High temperature or high pressure steam disinfection for the oximeter is not permitted. Refer to User Manual in the relative chapter (7.1) for cleaning and disinfection. ␇ Do not have the oximeter immerged in liquid. When it needs cleaning, please wipe its surface with medical alcohol by soft material.
Page 6: Major Applications And Scope Of Application
2.2 Major Major Major Major applications applications applications applications and and scope scope scope scope of of of of application application application application The Pulse Oximeter can be used in measuring the pulse oxygen saturation and pulse rate through finger.The product is fit for family, hospital, oxygen bar, community healthcare, physical care in sports (It can be used before or after doing sports and it is not recommended to use the device during the process of having sport) and etc.
Page 7: Main Parameters
� Pulse sound indication � Low-power indication: when the battery is low in power,the symbol will blink. � With alarm function � With screen overturn function Main Main Main p p p p arameters arameters arameters 4.2 Main arameters A A A A Measurement Measurement Measurement Measurement of of of of SpO...
Page 8: Battery Installation
5. 5. 5. 5.2 2 2 2 Battery Battery Battery Battery installation installation installation installation Figure 3.Battery installation A. Refer to the polarity and put the edge of the battery on the mouth of the battery box ,along the bottom of the battery box, gently push the battery into the box until the whole battery has been in-place.(Refer to Figure 3) B B B B .
Page 9: Attention For Operation
Fingernails and the luminescent tube should be in the same side. 6.1.2 6.1.2 Pulse Pulse sound sound setting setting 6.1.2 6.1.2 Pulse Pulse sound sound setting setting After turning the device on,the pulse sound is open.Long press the button can close the pulse sound and the pulse sound indication icon disappears.Long press button again, the pulse sound is turned on and pulse sound indication icon appears.
Page 10: Clinical Restrictions
measure of SpO and pulse rate. F. F. F. F. Excessive ambient light may affect measurement accuracy. It includes fluorescent lamp, dual ruby light, infrared heater, direct sunlight and etc. G. G. G. G.Intense activity of the subject or extreme electrosurgical interference may also affect the accuracy. H.
Page 11: 8 8 8 Troubleshooting Troubleshooting Troubleshooting
8 8 8 8 Troubleshooting Troubleshooting Troubleshooting Troubleshooting Trouble Trouble Trouble Trouble Possible Possible Possible Possible Reason Reason Reason Reason Solution Solution Solution Solution The SpO and Pulse Pulse Pulse Pulse The finger is not properly positioned. Place the finger properly and try 2 2 2 2 Rate Rate...
Page 12: 10 10 10 Function
The pulse sound indication Type BF IPX1 Ingress of liquids rank UROPEAN EPRESENTATIVE WEEE (2002/96/EC) This item is compliant with Medical Device Directive 93/42/EEC of June 14, 1993, a directive of the European Economic Community. battery positive electrode battery cathode electrode 10 10 10 10 Function Function Function s s s s pecification...
Page 13 Battery Battery Requirement Requirement Battery Battery Requirement Requirement Voltage 3.6 rechargeable buttony battery × 1 Battery Battery Battery Battery working working working working life life life life Charge and discharge not less than 300 times. Dimension Dimensions s s s and Weight Dimension Dimension...
Page 14 The CMS50QB Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the user of CMS50QB Pulse Oximeter should assure that it is used in such an environment. Electromagnetic Electromagnetic...
Page 15 If abnormal performance is observed, additional Pulse Oximeter measures may be necessary, such as reorienting or relocating the CMS50QB Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Page 16 RF disturbances Pulse Oximeter are controlled. The customer or the user of the CMS50QB can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the...

Contec CMS50QB Instructions To User

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