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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. 

 

The  disposal  of  scrap  instrument  and  its  accessories  and  packings  (including  battery,  plastic 

bags, foams and paper boxes) should follow the local laws and regulations. 

 

Please  check  the  packing  before  use  to  make  sure  the  device  and  accessories  are  totally  in 

accordance with the packing list, or else the device may have the possibility of working abnormally.   

 

Please  choose  the  accessories  and  probe  which  are  approved  or  manufactured  by  the 

manufacturer, or else it may damage the device. 

 

The device can only be matched with the compatible probe. 

 

Please don't measure this device with functional tester for the device's related information. 

1.3.    Attention 

 

Keep the oximeter away from dust, vibration, corrosive substances, explosive materials, high 

temperature and moisture. 

 

If the oximeter gets wet, please stop operating it. 

 

When it is carried from cold environment to warm or humid environment, please do not use it 

immediately.   

 

DO NOT operate keys on front panel with sharp materials. 

 

High temperature or high pressure steam disinfection of the oximeter is not permitted. Refer to 

User Manual in the relative chapter (7.1) for instructions of 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. Do not spray any liquid on the device directly. 

 

When cleaning the device with water, the temperature should be lower than 60 °C . 

 

As to the fingers which are too thin or too cold, it would probably affect the normal measure 

of  the  patients'  SpO

2

  and  pulse  rate,  please  clip  the  thick  finger  such  as  thumb  and  middle  finger 

deeply enough into the probe. 

 

The pulse oximeter can be used to adult or infant. Whether the device is used to adult or infant, 

it depends on the probe selected.   

Summary of Contents for OXY-50

Page 1: ...I Cod 35100 OXY 50 Pulse Oximeter User manual ...

Page 2: ...onitoring 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 use...

Page 3: ...Installation 4 5 1 View of the front panel 4 5 2 Under side View and Left View 5 5 3 Battery and probe installation 5 5 3 Accessories 6 6 Operating Guide 6 6 1 Application method 6 6 2 Attention for operation 10 6 3 Clinical restrictions 11 7 Maintain transportation and storage 11 7 1 Cleaning and Disinfecting 11 7 2 Maintain 11 7 3 Transportation and storage 12 8 Troubleshooting 12 9 Key of Symbo...

Page 4: ...r else the device may have the possibility of working abnormally Please choose the accessories and probe which are approved or manufactured by the manufacturer or else it may damage the device The device can only be matched with the compatible probe Please don t measure this device with functional tester for the device s related information 1 3 Attention Keep the oximeter away from dust vibration ...

Page 5: ...se the decrease of SpO2 in the blood furthermore some other causes such as the malfunction of human body s self adjustment damages during surgery and the injuries caused by some medical checkup would also lead to the difficulty of oxygen supply in human body and the corresponding symptoms would appear as a consequence such as vertigo impotence vomit etc Serious symptoms might bring danger to human...

Page 6: ... two beams of different wavelength of lights can be focused onto human nail tip through perspective clamp finger type sensor Then measured signal can be obtained by a photosensitive element information acquired through which will be shown on screen through treatment in electronic circuits and microprocessor Figure 1 4 Technical specifications 4 1 Main performance A SpO2 value display B Pulse rate ...

Page 7: ...2 and pulse rate can be shown correctly when pulse filling ratio is 0 4 SpO2 error is 4 pulse rate error is 2 bpm or 2 select larger E Resistance to surrounding light The deviation between the value measured in the condition of man made light or indoor natural light and that of darkroom is less than 1 F Power supply requirement 2 6 V DC 3 6V DC G Optical Sensor Red light wavelength is 660nm 6 65mW...

Page 8: ...Refer to Figure 4 and insert the two AA size batteries properly in the right direction Figure 4 Batteries installation B Replace the cover C Inserting the SpO2 probe of the pulse oximeter in the upper jack The probe is limited to be produced by our company never replace it with the similar ones by other manufacturers Please take care when you insert the batteries for the improper insertion may dam...

Page 9: ... e The data can be read directly from the screen on the measuring interface Fingernails and the luminescent tube should be on the same side If the alarm function is on the device will provide medium priority alarm signal when probe or finger is out Intermittent alarm will occur and the user interface presents FINGER OUT Medium priority indicating that prompt operator response is required B Pause a...

Page 10: ...ine shows the PR trend waveform the time underside shows the starting time of dispalying the date in the screen the middle and underside the screen means the operation direction of the Down button Press right button it will show in the position then press Down button to enter next hour Press left button it will show in the position then press Down button to enter last hour d The Review Interface 2...

Page 11: ...se the parameter to be adjusted then press the left button or right button to change data Each press of the left button or right button the data will raise or descend for one time accordingly If the alarm function is on the device will provide medium priority alarm signal when the data of SpO2 or pulse rate is beyond the limit Intermittent alarm will occur and the measurement shows in yellow Mediu...

Page 12: ...gure 10 if it is in recording state will come into figure 11 Figure 10 b In the status shown in Figure 10 press left button or right button can change the setting of the item then press menu button to exit the status in Figure 10 and perform setting YES for starting recording NO for do not recording c In the status shown in Figure 11 press left button or right button can change the setting press m...

Page 13: ...anges of time due to improper operation You can change the state by press the left button or right button choose yes to reset the time choose no to forbid time resetting b Press the up button or down button to select the parameter that you want to change then adjust the data by press the left button or right button c Exit the clock setting menu directly by press the menu button If you have reset t...

Page 14: ...a subject with weak pulse due to shock low ambient body temperature major bleeding or use of vascular contracting drug the SpO2 waveform PLETH will decrease In this case the measurement will be more sensitive to interference B For those with a substantial amount of staining dilution drug such as methylene blue indigo green and acid indigo blue or carbon monoxide hemoglobin COHb or methionine Me Hb...

Page 15: ... a diagnosis if you are sure the device works all right The SpO2 and Pulse Rate are not displayed stably 1 The finger is not placed inside deep enough 2 The finger is shaking or the patient is moving 1 Place the finger properly and try again 2 Let the patient keep calm The device can not be turned on 1 The battery is drained away or almost drained away 2 The battery is installed incorrectly 3 The ...

Page 16: ...on Fully charged battery Low battery Power on off button Left button Alarm pause button Menu button Right button Down button Up button USB Type BF SN Serial number 1 The finger clip falls off no finger inserted 2 Probe error 3 Signal inadequacy indicator IPX1 Ingress of liquids rank WEEE 2002 96 EC ...

Page 17: ...viation between average value and true value does not exceed 1 Pulse Parameter Specification Measuring range 30bpm 250bpm the resolution is 1bpm Accuracy 2bpm or 2 select larger Average pulse rate 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 BFType Pulse Intensity Range Continuo...

Page 18: ...ght About 180g with Dry battery 2AA Appendix 1 State Alarm condition delay Alarm signal generation delay Low voltage alarm 1s 20ms Spo2 alarm 330ms 20ms Pulse rate alarm 330ms 20ms Probe error alarm 16ms 20ms ...

Page 19: ...ts due to production reasons Labor costs and personnel traveling expenses and packaging not included All components subject to wear are not included in the warranty The repair or replacement performed during the warranty period shall not extend the warranty The warranty is void in the following cases repairs performed by unauthorized personnel or with non original spare parts defects caused by neg...

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