Omron P300 Intelli IT Pulse Handleiding

Omron Niet gecategoriseerd P300 Intelli IT Pulse

Lees hieronder de ๐Ÿ“– handleiding in het Nederlandse voor Omron P300 Intelli IT Pulse (2 pagina's) in de categorie Niet gecategoriseerd. Deze handleiding was nuttig voor 30 personen en werd door 2 gebruikers gemiddeld met 4.5 sterren beoordeeld

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3. Read the data.
Note
โ€ข If the measurement falls below the threshold (SpO
2<90%), the color
of the measurement becomes orange.
If it continues to become orange, we recommend to consult with
the physician.
โ€ข If the display shows the โ€œ?โ€ symbol, it means the signal is unstable.
Please keep hands still and retry.
โ€ข If the battery power reduces to half, the โ€œ โ€ appears. If it
becomes low, the โ€œ ๎˜ƒยด๎˜ƒร€๎˜ƒDVKHV๎˜ƒLQ๎˜ƒUHG๎˜‘๎˜ƒ:H๎˜ƒUHFRPPHQG๎˜ƒWR๎˜ƒUHSODFH๎˜ƒ
2 AAA alkaline batteries with new ones.
โ€ข The โ€œ ๎˜ƒยด๎˜ƒV\PERO๎˜ƒVWRSV๎˜ƒร€๎˜ƒDVKLQJ๎˜ƒZKHQ๎˜ƒWKH๎˜ƒGHYLFH๎˜ƒLV๎˜ƒFRQQHFWHG๎˜ƒZLWK๎˜ƒ
the app successfully.
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connected with the app.
4. Press the power button once to switch the display mode.
Maintenance and Storage
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โ€ข Dispose of batteries properly; follow any applicable local battery disposal laws.
Cleaning and Disinfecting the Device
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recommended alcohol of 70% isopropyl or 70% ethanol before and after each use.
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thoroughly before reuse.
The Fingertip Pulse Oximeter requires no routine calibration or maintenance other than replacement of batteries.
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patient, or cause damage to the equipment or other property.
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6SHFLยฟ๎˜ƒFDWLRQV
1. Product category
Pulse oximeter
2. Product description
Fingertip pulse oximeter
3. Model(code)
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4. Display Type
OLED display
5. SpO2
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Accuracy (A
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Low Perfusion Accuracy (A
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Note
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2. Clinical testing is used to establish the SpO
2 accuracy. The measured arterial hemoglobin
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2) of the sensors is compared to arterial hemoglobin oxygen (SaO
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2
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Medical Electrical Equipmentโ€“Particular requirements for the basic safety and essential performance of pulse oximeter equipment
for medical use.
โ€ข A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor or sensor. A functional tester is used to
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6. Pulse Rate
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Accuracy (A
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Low Perfusion Accuracy (A
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Note
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8. Power Requirements
Two AAA alkaline batteries (LR03)
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It is used for 2000 measurements and 30 seconds per one measurement.
9. Environment Requirements
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10. Equipment data update period
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11. &ODVVLยฟ๎˜ƒFDWLRQ
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12. Wireless Communication
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13. Transmission method
Bluetoothยฎ Low Energy
14. Weight
$SSUR[LPDWHO\๎˜ƒ๎˜™๎˜“๎˜ƒJ๎˜ƒ๎˜‹LQFOXGLQJ๎˜ƒEDWWHULHV๎˜Œ
15. Dimensions
$SSUR[LPDWHO\๎˜ƒ๎˜–๎˜•๎˜ƒPP๎˜ƒ๎˜‹Z๎˜Œ๎˜ƒรฎ๎˜ƒ๎˜™๎˜”๎˜‘๎˜˜๎˜ƒPP๎˜ƒ๎˜‹K๎˜Œ๎˜ƒรฎ๎˜ƒ๎˜–๎˜”๎˜‘๎˜˜๎˜ƒPP๎˜ƒ๎˜‹O๎˜Œ
16. Internally stored data
Up to 30
Clinical Study Summary
7KH๎˜ƒIROORZLQJ๎˜ƒGHWDLOV๎˜ƒDUH๎˜ƒSURYLGHG๎˜ƒWR๎˜ƒGLVFORVH๎˜ƒDFWXDO๎˜ƒSHUIRUPDQFH๎˜ƒREVHUYHG๎˜ƒLQ๎˜ƒWKH๎˜ƒFOLQLFDO๎˜ƒYDOLGDWLRQ๎˜ƒVWXG\๎˜ƒRI๎˜ƒ๎˜”๎˜•๎˜ƒKHDOWK\๎˜ƒDGXOW๎˜ƒYROXQWHHUV๎˜ƒ
๎˜‹DJHV๎˜ƒ๎˜”๎˜›๎˜๎˜—๎˜˜\U๎˜๎˜ƒPL[HG๎˜JHQGHU๎˜๎˜ƒOLJKW๎˜ƒWR๎˜ƒGDUN๎˜ƒVNLQ๎˜ƒSLJPHQWDWLRQ๎˜Œ๎˜‘๎˜ƒ7KH๎˜ƒ$
rms๎˜ƒYDOXH๎˜ƒDQDO\VLV๎˜ƒVWDWHPHQW๎˜ƒDQG๎˜ƒ%ODQG๎˜$OWPDQ๎˜ƒSORW๎˜ƒRI๎˜ƒGDWD๎˜ƒLV๎˜ƒVKRZQ๎˜ƒDV๎˜ƒ
IROORZLQJ๎˜
Arms๎˜ƒ9DOXH๎˜ƒ$QDO\VLV๎˜ƒ6WDWHPHQW๎˜ƒ %ODQG๎˜$OWPDQ๎˜ƒ3ORW๎˜ƒ*UDSKLF
Item ๎˜œ๎˜“๎˜๎˜๎˜”๎˜“๎˜“ ๎˜›๎˜“๎˜๎˜๎˜Ÿ๎˜œ๎˜“ ๎˜š๎˜“๎˜๎˜๎˜Ÿ๎˜›๎˜“
#pts ๎˜›๎˜“ ๎˜›๎˜˜ ๎˜›๎˜•
Bias ๎˜”๎˜‘๎˜•๎˜˜ ๎˜”๎˜‘๎˜”๎˜“ ๎˜”๎˜‘๎˜“๎˜•
Arms ๎˜”๎˜‘๎˜™๎˜— ๎˜”๎˜‘๎˜™๎˜™ ๎˜”๎˜‘๎˜š๎˜“
Time
Pulse rate
(bpm: beats per
minute)
Pulse waveform
Communication indication
Signal indication
Battery indication
Oxygen saturation
:DYHOHQJWK Radiant Power
RED 3.2mw๎˜™๎˜™๎˜“๎š“๎˜–QP
IR ๎˜œ๎˜“๎˜˜๎š“๎˜”๎˜“QP 2.4mw
Diff.SpO2๎˜6D22
SaO2
๎˜™
๎˜˜
4
3
2
๎˜”
0
๎˜๎˜”
๎˜๎˜•
๎˜๎˜–
๎˜๎˜—
๎˜™๎˜˜ ๎˜š๎˜˜ ๎˜›๎˜“ ๎˜›๎˜˜ ๎˜œ๎˜˜ ๎˜”๎˜“๎˜“70 90
๎˜”# subject
2# subject
3# subject
4# subject
๎˜˜๎˜†๎˜ƒVXEMHFW
๎˜™๎˜†๎˜ƒVXEMHFW
7# subject
๎˜›๎˜†๎˜ƒVXEMHFW
9# subject
๎˜”๎˜“๎˜†๎˜ƒVXEMHFW
๎˜”๎˜”๎˜†๎˜ƒVXEMHFW
๎˜”๎˜™๎˜†๎˜ƒVXEMHFW
General Description
2[\JHQ๎˜ƒELQGV๎˜ƒWR๎˜ƒKHPRJORELQ๎˜ƒLQ๎˜ƒUHG๎˜ƒEORRG๎˜ƒFHOOV๎˜ƒZKHQ๎˜ƒPRYLQJ๎˜ƒWKURX ๎˜ƒEORRG๎˜‘๎˜ƒ$๎˜ƒJK๎˜ƒWKH๎˜ƒOXQJV๎˜‘๎˜ƒ,W๎˜ƒLV๎˜ƒWUDQVSRUWHG๎˜ƒWKURXJKRXW๎˜ƒWKH๎˜ƒERG\๎˜ƒDV๎˜ƒDUWHULDO
pulse oximeter uses two frequencies of light (red and infrared) to determine the percentage (%) of hemoglobin in the blood that is saturated
with oxygen. The percentage is called blood oxygen saturation, or SpO
2. A pulse oximeter also measures and displays the pulse rate at the
same time it measures the SpO
2๎˜ƒOHYHO๎˜‘
Measurement Principle
3ULQFLSOH๎˜ƒRI๎˜ƒWKH๎˜ƒSXOVH๎˜ƒR[LPHWHU๎˜ƒLV๎˜ƒDV๎˜ƒIROORZV๎˜๎˜ƒ7KH๎˜ƒSXOVH๎˜ƒR[LPHWHU๎˜ƒZRUNV๎˜ƒE\๎˜ƒDSSO\LQJ๎˜ƒD๎˜ƒVHQVRU๎˜ƒWR๎˜ƒD๎˜ƒยฟ๎˜ƒQJHUWLS๎˜‘๎˜ƒ7KH๎˜ƒVHQVRU๎˜ƒFRQWDLQV๎˜ƒD๎˜ƒGXDO๎˜ƒOLJKW๎˜ƒ
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VHQVRU๎˜ƒFROOHFWV๎˜ƒDQG๎˜ƒFRQYHUWV๎˜ƒWKH๎˜ƒOLJKW๎˜ƒLQWR๎˜ƒDQ๎˜ƒHOHFWURQLF๎˜ƒVLJQDO๎˜ƒZKLFK๎˜ƒLV๎˜ƒSURSRUWLRQDO๎˜ƒWR๎˜ƒWKH๎˜ƒOLJKW๎˜ƒLQWHQVLW\๎˜‘๎˜ƒ7KH๎˜ƒDUWHULROH๎˜ƒQRUPDOO\๎˜ƒSXOVDWHV๎˜ƒ
DQG๎˜ƒDEVRUEV๎˜ƒYDULDEOH๎˜ƒDPRXQWV๎˜ƒRI๎˜ƒOLJKW๎˜ƒGXULQJ๎˜ƒV\VWROH๎˜ƒDQG๎˜ƒGLDVWROH๎˜๎˜ƒDV๎˜ƒEORRG๎˜ƒYROXPH๎˜ƒLQFUHDVHV๎˜ƒDQG๎˜ƒGHFUHDVHV๎˜‘๎˜ƒ7KH๎˜ƒUDWLR๎˜ƒRI๎˜ƒOLJKW๎˜ƒDEVRUEHG๎˜ƒDW๎˜ƒ
systole and diastole is translated into an oxygen saturation measurement. This measurement is referred to as SpO
2.
Diagram of Operation Principle
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2. 5HG๎˜ƒDQG๎˜ƒ,QIUDUHG๎˜UD\๎˜ƒ/LJKW๎˜ƒ6RXUFH
Intended Use
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(SpO2๎˜Œ๎˜ƒDQG๎˜ƒSXOVH๎˜ƒUDWH๎˜ƒRI๎˜ƒDGXOW๎˜๎˜ƒDGROHVFHQW๎˜ƒDQG๎˜ƒFKLOG๎˜ƒSDWLHQWV๎˜ƒLQ๎˜ƒKRVSLWDOV๎˜๎˜ƒKRVSLWDO๎˜W\SH๎˜ƒIDFLOLWLHV๎˜ƒDQG๎˜ƒKRPH๎˜FDUH๎˜ƒHQYLURQPHQWV๎˜‘๎˜ƒ
Precautions For Use
โ€ข Before use, carefully read the manual.
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โ€ข 7KH๎˜ƒGHYLFH๎˜ƒPXVW๎˜ƒEH๎˜ƒDEOH๎˜ƒWR๎˜ƒPHDVXUH๎˜ƒWKH๎˜ƒSXOVH๎˜ƒSURSHUO\๎˜ƒWR๎˜ƒREWDLQ๎˜ƒDQ๎˜ƒDFFXUDWH๎˜ƒ6S2
2 measurement. Verify that nothing is hindering the
pulse measurement before relying on the SpO
2 measurement.
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signs and symptoms.
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less than half an hour.
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sterilization.
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โ€ข :KHQ๎˜ƒWKH๎˜ƒVLJQDO๎˜ƒLV๎˜ƒQRW๎˜ƒVWDEOH๎˜๎˜ƒWKH๎˜ƒUHDGLQJ๎˜ƒPD\๎˜ƒEH๎˜ƒLQDFFXUDWH๎˜‘๎˜ƒ3OHDVH๎˜ƒGR๎˜ƒQRW๎˜ƒUHIHU๎˜ƒWR๎˜ƒWKH๎˜ƒUHVXOW๎˜๎˜ƒDQG๎˜ƒWU\๎˜ƒWKH๎˜ƒPHDVXUHPHQW๎˜ƒDJDLQ๎˜‘
โ€ข The patient is an intended operator.
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Contraindication
Not found yet.
Inaccurate Measurements may be Caused by
โ€ข 6LJQLยฟ๎˜ƒFDQW๎˜ƒOHYHOV๎˜ƒRI๎˜ƒG\VIXQFWLRQDO๎˜ƒKHPRJORELQ๎˜ƒ๎˜‹VXFK๎˜ƒDV๎˜ƒFDUERQ\O๎˜ƒ๎˜๎˜ƒKHPRJORELQ๎˜ƒRU๎˜ƒPHWKHPRJORELQ๎˜Œ๎˜‘
โ€ข ,QWUDYDVFXODU๎˜ƒG\HV๎˜ƒVXFK๎˜ƒDV๎˜ƒLQGRF\DQLQH๎˜ƒJUHHQ๎˜ƒRU๎˜ƒPHWK\OHQH๎˜ƒEOXH๎˜‘
โ€ข +LJK๎˜ƒDPELHQW๎˜ƒOLJKW๎˜‘๎˜ƒ6KLHOG๎˜ƒWKH๎˜ƒVHQVRU๎˜ƒDUHD๎˜ƒLI๎˜ƒQHFHVVDU\๎˜‘
โ€ข ([FHVVLYH๎˜ƒSDWLHQW๎˜ƒPRYHPHQW๎˜‘
โ€ข +LJK๎˜IUHTXHQF\๎˜ƒHOHFWURVXUJLFDO๎˜ƒLQWHUIHUHQFH๎˜ƒDQG๎˜ƒGHยฟ๎˜ƒEULOODWRUV๎˜‘
โ€ข Venous pulsations.
โ€ข :KHQ๎˜ƒWKH๎˜ƒGHYLFH๎˜ƒLV๎˜ƒXVHG๎˜ƒRQ๎˜ƒWKH๎˜ƒVDPH๎˜ƒDUP๎˜ƒDV๎˜ƒD๎˜ƒEORRG๎˜ƒSUHVVXUH๎˜ƒFXII๎˜๎˜ƒDUWHULDO๎˜ƒFDWKHWHU๎˜๎˜ƒRU๎˜ƒLQWUDYDVFXODU๎˜ƒOLQH๎˜‘
โ€ข 7KH๎˜ƒSDWLHQW๎˜ƒKDV๎˜ƒK\SRWHQVLRQ๎˜๎˜ƒVHYHUH๎˜ƒYDVRFRQVWULFWLRQ๎˜๎˜ƒVHYHUH๎˜ƒDQHPLD๎˜๎˜ƒRU๎˜ƒK\SRWKHUPLD๎˜‘
โ€ข The patient is in cardiac arrest or is in shock.
โ€ข )LQJHUQDLO๎˜ƒSROLVK๎˜ƒRU๎˜ƒIDOVH๎˜ƒยฟ๎˜ƒQJHUQDLOV๎˜‘
โ€ข :HDN๎˜ƒSXOVH๎˜ƒTXDOLW\๎˜ƒ๎˜‹ORZ๎˜ƒSHUIXVLRQ๎˜Œ๎˜‘
โ€ข Low hemoglobin.
Product Features
โ€ข 6LPSOH๎˜ƒWR๎˜ƒRSHUDWH๎˜ƒDQG๎˜ƒFRQYHQLHQW๎˜ƒWR๎˜ƒFDUU\๎˜‘
โ€ข 6PDOO๎˜ƒYROXPH๎˜๎˜ƒOLJKW๎˜ƒZHLJKW๎˜ƒDQG๎˜ƒORZ๎˜ƒSRZHU๎˜ƒFRQVXPSWLRQ๎˜‘
โ€ข Colorful color OLED displays SpO
2๎˜๎˜ƒ35๎˜ƒDQG๎˜ƒSXOVH๎˜ƒZDYHIRUP๎˜‘
โ€ข 2 display modes.
โ€ข ๎˜•SFV๎˜ƒ$$$๎˜VL]H๎˜ƒDONDOLQH๎˜ƒEDWWHULHV๎˜ƒ๎˜‹/5๎˜“๎˜–๎˜Œ๎˜ž๎˜ƒEDWWHU\๎˜ƒLQGLFDWRU๎˜‘
โ€ข Bluetoothยฎ for data transmission.
โ€ข Automatically power on/off.
โ€ข :HDN๎˜ƒRU๎˜ƒXQVWDEOH๎˜ƒVLJQDO๎˜ƒSURPSW๎˜ƒSURYLGHV๎˜ƒPRUH๎˜ƒDFFXUDWH๎˜ƒPHDVXUHPHQWV๎˜‘
โ€ข :KHQ๎˜ƒQR๎˜ƒVLJQDO๎˜ƒRU๎˜ƒORZ๎˜ƒVLJQDO๎˜ƒLV๎˜ƒGHWHFWHG๎˜๎˜ƒLW๎˜ƒZLOO๎˜ƒGLVSOD\๎˜ƒยณ)LQJHU๎˜ƒ2XWยด๎˜ƒDQG๎˜ƒZLOO๎˜ƒSRZHU๎˜ƒRII๎˜ƒ
DXWRPDWLFDOO\๎˜ƒLQ๎˜ƒ๎˜›๎˜ƒVHFRQGV๎˜‘
Battery Installation
๎˜”๎˜‘๎˜ƒ Install two AAA alkaline batteries.
๎˜”๎˜‘๎˜”๎˜‘๎˜ƒ Push up the battery case along the arrow to open the battery case.
๎˜”๎˜‘๎˜•๎˜‘๎˜ƒ ,QVWDOO๎˜ƒWZR๎˜ƒ$$$๎˜ƒDONDOLQH๎˜ƒEDWWHULHV๎˜ƒLQWR๎˜ƒWKH๎˜ƒEDWWHU\๎˜ƒFDVH๎˜‘๎˜ƒ0DWFK๎˜ƒWKH๎˜ƒSOXV๎˜ƒ๎˜‹๎˜Ž๎˜Œ๎˜ƒDQG๎˜ƒPLQXV๎˜ƒ๎˜‹๎˜๎˜Œ๎˜ƒVLJQV๎˜ƒLQ๎˜ƒWKH๎˜ƒFDVH๎˜‘๎˜ƒ,I๎˜ƒWKH๎˜ƒSRODULWLHV๎˜ƒDUH๎˜ƒQRW๎˜ƒ
PDWFKHG๎˜๎˜ƒGDPDJH๎˜ƒPD\๎˜ƒEH๎˜ƒFDXVHG๎˜ƒWR๎˜ƒWKH๎˜ƒGHYLFH๎˜‘
๎˜”๎˜‘๎˜–๎˜‘๎˜ƒ Push down the battery case to close.
Note
โ€ข 3OHDVH๎˜ƒUHPRYH๎˜ƒWKH๎˜ƒEDWWHULHV๎˜ƒLI๎˜ƒWKH๎˜ƒGHYLFH๎˜ƒZLOO๎˜ƒQRW๎˜ƒEH๎˜ƒXVHG๎˜ƒIRU๎˜ƒORQJ๎˜ƒSHULRGV๎˜ƒRI๎˜ƒWLPH๎˜‘
โ€ข 3OHDVH๎˜ƒUHSODFH๎˜ƒWKH๎˜ƒEDWWHULHV๎˜ƒZKHQ๎˜ƒWKH๎˜ƒEDWWHU\๎˜ƒLQGLFDWLRQ๎˜ƒVWDUWV๎˜ƒร€๎˜ƒDVKLQJ๎˜‘
โ€ข 2QO\๎˜ƒXVH๎˜ƒWZR๎˜ƒ$$$๎˜ƒDONDOLQH๎˜ƒEDWWHULHV๎˜ƒZLWK๎˜ƒWKLV๎˜ƒGHYLFH๎˜‘๎˜ƒ'R๎˜ƒQRW๎˜ƒXVH๎˜ƒRWKHU๎˜ƒW\SHV๎˜ƒRI๎˜ƒEDWWHULHV๎˜‘๎˜ƒ'R๎˜ƒQRW๎˜ƒXVH๎˜ƒQHZ๎˜ƒDQG๎˜ƒXVHG๎˜ƒEDWWHULHV๎˜ƒ
together. Do not use different brands of batteries together.
Warning: ,QGLFDWHV๎˜ƒD๎˜ƒSRWHQWLDOO\๎˜ƒKD]DUGRXV๎˜ƒVLWXDWLRQ๎˜ƒZKLFK๎˜๎˜ƒLI๎˜ƒQRW๎˜ƒDYRLGHG๎˜๎˜ƒFRXOG๎˜ƒUHVXOW๎˜ƒLQ๎˜ƒGHDWK๎˜ƒRU๎˜ƒVHULRXV๎˜ƒLQMXU\๎˜‘
โ€ข .HHS๎˜ƒWKH๎˜ƒGHYLFH๎˜ƒDZD\๎˜ƒIURP๎˜ƒ\RXQJ๎˜ƒFKLOGUHQ๎˜‘๎˜ƒ6PDOO๎˜ƒLWHPV๎˜ƒVXFK๎˜ƒDV๎˜ƒWKH๎˜ƒEDWWHU\๎˜ƒFDVH๎˜ƒDQG๎˜ƒEDWWHULHV๎˜ƒDUH๎˜ƒFKRNLQJ๎˜ƒKD]DUGV๎˜‘
Download the โ€œOMRON connectโ€ app on the Smart Device
๎˜”๎˜‘๎˜ƒ Enable Bluetoothยฎ๎˜ƒRQ๎˜ƒWKH๎˜ƒVPDUW๎˜ƒGHYLFH๎˜‘
2. 'RZQORDG๎˜ƒDQG๎˜ƒLQVWDOO๎˜ƒWKH๎˜ƒยณ20521๎˜ƒFRQQHFWยด๎˜ƒDSS๎˜ƒRQWR๎˜ƒWKH๎˜ƒVPDUW๎˜ƒGHYLFH๎˜‘
3. Press the power button to access the measurement interface. Press and hold
the power button for more than 2 seconds to enter the pairing setting interface.
4. 2SHQ๎˜ƒWKH๎˜ƒDSS๎˜ƒRQ๎˜ƒ\RXU๎˜ƒVPDUW๎˜ƒGHYLFH๎˜๎˜ƒDQG๎˜ƒIROORZ๎˜ƒWKH๎˜ƒSDLULQJ๎˜ƒLQVWUXFWLRQV๎˜‘๎˜ƒ
Uploading the Data via Bluetooth
:KHQ๎˜ƒWDNLQJ๎˜ƒD๎˜ƒPHDVXUHPHQW๎˜๎˜ƒRSHQ๎˜ƒWKH๎˜ƒDSS๎˜ƒIRU๎˜ƒXSORDGLQJ๎˜ƒWKH๎˜ƒGDWD๎˜‘
:KHQ๎˜ƒWKH๎˜ƒยณ๎˜ƒ ๎˜ƒยด๎˜ƒV\PERO๎˜ƒVWRSV๎˜ƒร€๎˜ƒDVKLQJ๎˜ƒGXULQJ๎˜ƒD๎˜ƒPHDVXUHPHQW๎˜๎˜ƒWKH๎˜ƒGHYLFH๎˜ƒLV๎˜ƒFRQQHFWHG๎˜ƒZLWK๎˜ƒWKH๎˜ƒDSS๎˜ƒVXFFHVVIXOO\๎˜‘
Note
โ€ข :KHQ๎˜ƒWKH๎˜ƒUHDGLQJ๎˜ƒLV๎˜ƒVWDEOH๎˜๎˜ƒWKH๎˜ƒGDWD๎˜ƒLV๎˜ƒXSORDGHG๎˜ƒWR๎˜ƒWKH๎˜ƒDSS๎˜‘๎˜ƒ7KH๎˜ƒGHYLFH๎˜ƒZLOO๎˜ƒSRZHU๎˜ƒRII๎˜ƒDXWRPDWLFDOO\๎˜ƒDIWHU๎˜ƒWKH๎˜ƒGDWD๎˜ƒVKRZV๎˜ƒRQ๎˜ƒWKH๎˜ƒGLVSOD\๎˜ƒ
DERXW๎˜ƒ๎˜”๎˜˜๎˜ƒVHFRQGV๎˜‘
โ€ข 7KH๎˜ƒGHYLFH๎˜ƒVWRUHV๎˜ƒGDWD๎˜ƒXS๎˜ƒWR๎˜ƒ๎˜–๎˜“๎˜ƒZLWKRXW๎˜ƒXVLQJ๎˜ƒWKH๎˜ƒDSS๎˜ƒGXULQJ๎˜ƒWKH๎˜ƒPHDVXUHPHQW๎˜‘๎˜ƒ:KHQ๎˜ƒWDNLQJ๎˜ƒD๎˜ƒPHDVXUHPHQW๎˜ƒZLWK๎˜ƒWKH๎˜ƒDSS๎˜๎˜ƒDOO๎˜ƒVWRUHG๎˜ƒGDWD๎˜ƒ
ZLOO๎˜ƒEH๎˜ƒXSORDGHG๎˜ƒRQ๎˜ƒWKH๎˜ƒDSS๎˜‘๎˜ƒ7KH๎˜ƒGHYLFH๎˜ƒGHOHWHV๎˜ƒIURP๎˜ƒWKH๎˜ƒROGHVW LQJ๎˜ƒWKH๎˜ƒDSS๎˜‘๎˜ƒGDWD๎˜ƒLI๎˜ƒWKH๎˜ƒPHDVXUHPHQW๎˜ƒLV๎˜ƒWDNHQ๎˜ƒPRUH๎˜ƒWKDQ๎˜ƒ๎˜–๎˜“๎˜ƒWLPHV๎˜ƒZLWKRXW๎˜ƒXV
Operation Instructions
Open the app when taking a measurement.
๎˜”๎˜‘๎˜ƒ 3ODFH๎˜ƒRQH๎˜ƒRI๎˜ƒยฟ๎˜ƒQJHUV๎˜ƒRWKHU๎˜ƒWKDQ๎˜ƒD๎˜ƒWKXPE๎˜ƒRU๎˜ƒD๎˜ƒOLWWOH๎˜ƒยฟ๎˜ƒQJHU๎˜๎˜ƒLQWR๎˜ƒWKH๎˜ƒUXEEHU๎˜ƒRSHQLQJ๎˜ƒRI๎˜ƒWKH๎˜ƒGHYLFH๎˜‘๎˜ƒ
7KH๎˜ƒGHYLFH๎˜ƒZLOO๎˜ƒWXUQ๎˜ƒRQ๎˜ƒDXWRPDWLFDOO\๎˜‘๎˜ƒ,W๎˜ƒJRHV๎˜ƒIURP๎˜ƒWKH๎˜ƒVWDUWXS๎˜ƒVFUHHQ๎˜ƒWR๎˜ƒWKH๎˜ƒPHDVXUHPHQW๎˜ƒ
interface.
2. .HHS๎˜ƒKDQGV๎˜ƒVWLOO๎˜ƒIRU๎˜ƒWKH๎˜ƒPHDVXUHPHQW๎˜‘๎˜ƒ'R๎˜ƒQRW๎˜ƒVKDNH๎˜ƒWKH๎˜ƒยฟ๎˜ƒQJHU๎˜ƒGXULQJ๎˜ƒD๎˜ƒPHDVXUHPHQW๎˜‘๎˜ƒ,W๎˜ƒLV๎˜ƒ
UHFRPPHQGHG๎˜ƒQRW๎˜ƒWR๎˜ƒPRYH๎˜ƒWKH๎˜ƒERG\๎˜ƒZKLOH๎˜ƒWDNLQJ๎˜ƒD๎˜ƒPHDVXUHPHQW๎˜‘
1
2
Power button
Display
Battery case
Back side of the device
7R๎˜ƒJHW๎˜ƒVWDUWHG๎˜ƒJR๎˜ƒWR๎˜
omronconnect.com/setup
Possible Problems and Solutions
Problems Possible reason Solution
SpO2 or PR can not be
shown normally.
๎˜”๎˜‘๎˜ƒ Finger is not inserted correctly
2. Patientโ€™s SpO2๎˜ƒYDOXH๎˜ƒKDV๎˜ƒYDULDWLRQV๎˜ƒRU๎˜ƒLV๎˜ƒLQDFFXUDWH๎˜‘
๎˜”๎˜‘๎˜ƒ 5HWU\๎˜ƒE\๎˜ƒXVLQJ๎˜ƒWKH๎˜ƒVDPH๎˜ƒRU๎˜ƒD๎˜ƒGLIIHUHQW๎˜ƒยฟ๎˜ƒQJHU๎˜ƒ๎˜‹RWKHU๎˜ƒ
WKDQ๎˜ƒD๎˜ƒWKXPE๎˜ƒRU๎˜ƒD๎˜ƒOLWWOH๎˜ƒยฟ๎˜ƒQJHU๎˜Œ๎˜‘
2. 7KHUH๎˜ƒLV๎˜ƒH[FHVVLYH๎˜ƒLOOXPLQDWLRQ๎˜‘
3. Try some more times. If you can make sure
no problem exist in the product, please go to a
hospital timely for exact diagnosis.
The display continues
WR๎˜ƒVKRZ๎˜ƒยณ๎˜๎˜๎˜ยด๎˜ƒDQG๎˜ƒยณ)LQJHU๎˜ƒ
Outโ€.
SpO2 or PR is shown
unstably.
๎˜”๎˜‘๎˜ƒ Finger might not be inserted deep enough.
2. ([FHVVLYH๎˜ƒSDWLHQW๎˜ƒPRYHPHQW
๎˜”๎˜‘๎˜ƒ 5HWU\๎˜ƒE\๎˜ƒLQVHUWLQJ๎˜ƒWKH๎˜ƒยฟ๎˜ƒQJHU๎˜‘
2. Be calm.
The display continues to
show โ€œ?โ€.
7KH๎˜ƒGHYLFH๎˜ƒFDQQRW๎˜ƒEH๎˜ƒ
powered on.
๎˜”๎˜‘๎˜ƒ No battery or low power of battery
2. Batteries might be installed incorrectly.
3. 7KH๎˜ƒGHYLFH๎˜ƒPLJKW๎˜ƒEH๎˜ƒGDPDJHG
๎˜”๎˜‘๎˜ƒ Please replace batteries.
2. Please reinstall the batteries.
3. 3OHDVH๎˜ƒFRQWDFW๎˜ƒZLWK๎˜ƒORFDO๎˜ƒFXVWRPHU๎˜ƒVHUYLFH๎˜ƒFHQWHU๎˜‘
The display is suddenly
off.
๎˜”๎˜‘๎˜ƒ 7KH๎˜ƒGHYLFH๎˜ƒLV๎˜ƒDXWRPDWLFDOO\๎˜ƒSRZHUHG๎˜ƒRII๎˜ƒZKHQ๎˜ƒQR๎˜ƒ
VLJQDO๎˜ƒLV๎˜ƒGHWHFWHG๎˜ƒORQJHU๎˜ƒWKDQ๎˜ƒ๎˜›๎˜ƒVHFRQGV๎˜‘
2. The battery power is too low to work.
๎˜”๎˜‘๎˜ƒ Normal
2. Replace the batteries.
Any communication issue
occurs.
)ROORZ๎˜ƒWKH๎˜ƒLQVWUXFWLRQV๎˜ƒVKRZQ๎˜ƒLQ๎˜ƒWKH๎˜ƒVPDUW๎˜ƒGHYLFH๎˜๎˜ƒRU๎˜ƒYLVLW๎˜ƒWKH๎˜ƒยณ+HOSยด๎˜ƒVHFWLRQ๎˜ƒLQ๎˜ƒWKH๎˜ƒยณ20521๎˜ƒFRQQHFWยด๎˜ƒDSS๎˜ƒIRU๎˜ƒ
further help. If the problem still persists, contact your OMRON retail outlet or distributor.
6\PERO๎˜ƒ'Hยฟ๎˜ƒQLWLRQV
Symbol 'Hยฟ๎˜ƒQLWLRQ Symbol 'Hยฟ๎˜ƒQLWLRQ Symbol 'Hยฟ๎˜ƒQLWLRQ
Type BF applied part Atmospheric pressure
limitation IP32
The degree of
protection against
ingress of dust and
water
Follow instruction for
use Date of Manufacture Manufacturerโ€™s
information
No SpO2 Alarm European union
DSSURYDO
Authorized
UHSUHVHQWDWLYH๎˜ƒ
in the European
community
Temperature limitation &RQIRUPLW\๎˜ƒWR๎˜ƒ:(((๎˜ƒ
'LUHFWLYH For medical use
+XPLGLW\๎˜ƒOLPLWDWLRQ Serial No.
Box Contents
๎˜”๎˜‘๎˜ƒ Fingertip Pulse Oximeter
2. Two AAA alkaline batteries (LR03)
3. Instruction manual
4. Storage case
Note
โ€ข The illustrations used in this manual may differ slightly from the appearance of the actual product.
โ€ข 7KH๎˜ƒVSHFLยฟ๎˜ƒFDWLRQV๎˜ƒDUH๎˜ƒVXEMHFW๎˜ƒWR๎˜ƒFKDQJH๎˜ƒZLWKRXW๎˜ƒSULRU๎˜ƒQRWLFH๎˜‘
Limited Warranty
Thank you for buying an OMRON product. This product is constructed of high quality materials and great care has been taken in its
PDQXIDFWXULQJ๎˜‘๎˜ƒ,W๎˜ƒLV๎˜ƒGHVLJQHG๎˜ƒWR๎˜ƒJLYH๎˜ƒ\RX๎˜ƒD๎˜ƒKLJK๎˜ƒOHYHO๎˜ƒRI๎˜ƒFRPIR FULEHG๎˜ƒLQ๎˜ƒWKH๎˜ƒUW๎˜๎˜ƒSURYLGHG๎˜ƒWKDW๎˜ƒLW๎˜ƒLV๎˜ƒSURSHUO\๎˜ƒRSHUDWHG๎˜ƒDQG๎˜ƒPDLQWDLQHG๎˜ƒDV๎˜ƒGHV
instruction manual.
This product is warranted by OMRON for a period of 2 years after the date of purchase.
The proper construction, workmanship and materials of this product is warranted by OMRON. During this period of warranty OMRON will,
ZLWKRXW๎˜ƒFKDUJH๎˜ƒIRU๎˜ƒODERXU๎˜ƒRU๎˜ƒSDUWV๎˜๎˜ƒUHSDLU๎˜ƒRU๎˜ƒUHSODFH๎˜ƒWKH๎˜ƒGHIHFW๎˜ƒSURGXFW๎˜ƒRU๎˜ƒDQ\๎˜ƒGHIHFWLYH๎˜ƒSDUWV๎˜‘
7KH๎˜ƒZDUUDQW\๎˜ƒGRHV๎˜ƒQRW๎˜ƒFRYHU๎˜ƒDQ\๎˜ƒRI๎˜ƒWKH๎˜ƒIROORZLQJ๎˜
A. Transport costs and risks of transport.
B. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.
&๎˜‘๎˜ƒ 3HULRGLF๎˜ƒFKHFN๎˜XSV๎˜ƒDQG๎˜ƒPDLQWHQDQFH๎˜‘
'๎˜‘๎˜ƒ ๎˜ƒ)DLOXUH๎˜ƒRU๎˜ƒZHDU๎˜ƒRI๎˜ƒRSWLRQDO๎˜ƒSDUWV๎˜ƒRU๎˜ƒRWKHU๎˜ƒDWWDFKPHQWV๎˜ƒRWKHU๎˜ƒWKDQ๎˜ƒWKH๎˜ƒPDLQ๎˜ƒGHYLFH๎˜ƒLWVHOI๎˜๎˜ƒXQOHVV๎˜ƒH[SOLFLWO\๎˜ƒZDUUDQWHG๎˜ƒDERYH๎˜‘
(๎˜‘๎˜ƒ &RVWV๎˜ƒDULVLQJ๎˜ƒGXH๎˜ƒWR๎˜ƒQRQ๎˜DFFHSWDQFH๎˜ƒRI๎˜ƒD๎˜ƒFODLP๎˜ƒ๎˜‹WKRVH๎˜ƒZLOO๎˜ƒEH๎˜ƒFKDUJHG๎˜ƒIRU๎˜Œ๎˜‘
F. Damages of any kind including personal caused accidentally or from misuse.
6KRXOG๎˜ƒZDUUDQW\๎˜ƒVHUYLFH๎˜ƒEH๎˜ƒUHTXLUHG๎˜ƒSOHDVH๎˜ƒDSSO\๎˜ƒWR๎˜ƒWKH๎˜ƒGHDOHU๎˜ƒZKRP๎˜ƒWKH๎˜ƒSURGXFW๎˜ƒZDV๎˜ƒSXUFKDVHG๎˜ƒIURP๎˜ƒRU๎˜ƒDQ๎˜ƒDXWKRULVHG๎˜ƒ20521๎˜ƒ
distributor. For the address refer to the product packaging / literature or to your specialised retailer.
,I๎˜ƒ\RX๎˜ƒKDYH๎˜ƒGLIยฟ๎˜ƒFXOWLHV๎˜ƒLQ๎˜ƒยฟ๎˜ƒQGLQJ๎˜ƒ20521๎˜ƒFXVWRPHU๎˜ƒVHUYLFHV๎˜๎˜ƒYLVLW๎˜ƒRXU๎˜ƒZHEVLWH๎˜ƒ๎˜‹ZZZ๎˜‘RPURQ๎˜KHDOWKFDUH๎˜‘FRP๎˜Œ๎˜ƒIRU๎˜ƒFRQWDFW๎˜ƒLQIRUPDWLRQ๎˜‘
5HSDLU๎˜ƒRU๎˜ƒUHSODFHPHQW๎˜ƒXQGHU๎˜ƒWKH๎˜ƒZDUUDQW\๎˜ƒGRHV๎˜ƒQRW๎˜ƒJLYH๎˜ƒULVH๎˜ƒWR๎˜ƒDQ\๎˜ƒH[WHQVLRQ๎˜ƒRU๎˜ƒUHQHZDO๎˜ƒRI๎˜ƒWKH๎˜ƒZDUUDQW\๎˜ƒSHULRG๎˜‘
7KH๎˜ƒZDUUDQW\๎˜ƒZLOO๎˜ƒEH๎˜ƒJUDQWHG๎˜ƒRQO\๎˜ƒLI๎˜ƒWKH๎˜ƒFRPSOHWH๎˜ƒSURGXFW๎˜ƒLV๎˜ƒUHWXUQHG๎˜ƒWRJHWKHU๎˜ƒZLWK๎˜ƒWKH๎˜ƒRULJLQDO๎˜ƒLQYRLFH๎˜ƒ๎˜’๎˜ƒFDVK๎˜ƒWLFNHW๎˜ƒLVVXHG๎˜ƒWR๎˜ƒWKH๎˜ƒFRQVXPHU๎˜ƒ
by the retailer.
Electromagnetic Compatibility
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Emissions Test Compliance
RF Emissions
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Instruction Manual
Fingertip Pulse Oximeter
P300 Intelli IT (HPO-300T)
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Beijing Choice Electronic Technology Co., Ltd.
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No. 2 Building, No. 9 Shuangyuan Road, Shijingshan
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OMRON HEALTHCARE EUROPE B.V.
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OMRON SANTร‰ FRANCE SAS
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Shanghai International Holding Corp. GmbH
(Europe)
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Made in China

Product specificaties

Merk: Omron
Categorie: Niet gecategoriseerd
Model: P300 Intelli IT Pulse

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