Instrukcja obsล‚ugi Omron P300 Intelli IT Pulse

Omron Niesklasyfikowane P300 Intelli IT Pulse

Przeczytaj poniลผej ๐Ÿ“– instrukcjฤ™ obsล‚ugi w jฤ™zyku polskim dla Omron P300 Intelli IT Pulse (2 stron) w kategorii Niesklasyfikowane. Ta instrukcja byล‚a pomocna dla 15 osรณb i zostaล‚a oceniona przez 8 uลผytkownikรณw na ล›rednio 4.9 gwiazdek

Strona 1/2
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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7. 3UREH๎˜ƒ/('๎˜ƒ6SHFLยฟ๎˜ƒFDWLRQV
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
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Table 2: Electromagnetic Immunity
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OMRON SANTร‰ FRANCE SAS
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Made in China


Specyfikacje produktu

Marka: Omron
Kategoria: Niesklasyfikowane
Model: P300 Intelli IT Pulse

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