Instrukcja obsługi Omron P300 Intelli IT Pulse

Omron Niesklasyfikowane P300 Intelli IT Pulse

Przeczytaj poniżej 📖 instrukcję obsługi w języku polskim dla Omron P300 Intelli IT Pulse (2 stron) w kategorii Niesklasyfikowane. Ta instrukcja była pomocna dla 6 osób i została oceniona przez 2 użytkowników na średnio 4.5 gwiazdek

Strona 1/2
3. Read the data.
Note
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.
• If the display shows the “?” symbol, it means the signal is unstable.
Please keep hands still and retry.
• If the battery power reduces to half, the “ ” appears. If it
becomes low, the “ ´ÀDVKHVLQUHG:HUHFRPPHQGWRUHSODFH
2 AAA alkaline batteries with new ones.
The “ ´V\PEROVWRSVÀDVKLQJZKHQWKHGHYLFHLVFRQQHFWHGZLWK
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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• 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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1. Product category
Pulse oximeter
2. Product description
Fingertip pulse oximeter
3. Model(code)
3,QWHOOL,7+327
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 Equipment–Particular requirements for the basic safety and essential performance of pulse oximeter equipment
for medical use.
• 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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12. Wireless Communication
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13. Transmission method
Bluetooth® Low Energy
14. Weight
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15. Dimensions
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16. Internally stored data
Up to 30
Clinical Study Summary
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Item   
#pts   
Bias   
Arms   
Time
Pulse rate
(bpm: beats per
minute)
Pulse waveform
Communication indication
Signal indication
Battery indication
Oxygen saturation
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IR QP 2.4mw
Diff.SpO26D22
SaO2
4
3
2
0
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# subject
2# subject
3# subject
4# subject
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9# subject
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General Description
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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
2OHYHO
Measurement Principle
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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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Intended Use
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Precautions For Use
• Before use, carefully read the manual.
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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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:KHQWKHVLJQDOLVQRWVWDEOHWKHUHDGLQJPD\EHLQDFFXUDWH3OHDVHGRQRWUHIHUWRWKHUHVXOWDQGWU\WKHPHDVXUHPHQWDJDLQ
• The patient is an intended operator.
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Contraindication
Not found yet.
Inaccurate Measurements may be Caused by
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,QWUDYDVFXODUG\HVVXFKDVLQGRF\DQLQHJUHHQRUPHWK\OHQHEOXH
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([FHVVLYHSDWLHQWPRYHPHQW
+LJKIUHTXHQF\HOHFWURVXUJLFDOLQWHUIHUHQFHDQGGH¿EULOODWRUV
Venous pulsations.
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• The patient is in cardiac arrest or is in shock.
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Low hemoglobin.
Product Features
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• Colorful color OLED displays SpO
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• 2 display modes.
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Bluetooth® for data transmission.
• Automatically power on/off.
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Battery Installation
 Install two AAA alkaline batteries.
 Push up the battery case along the arrow to open the battery case.
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PDWFKHGGDPDJHPD\EHFDXVHGWRWKHGHYLFH
 Push down the battery case to close.
Note
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together. Do not use different brands of batteries together.
Warning: ,QGLFDWHVDSRWHQWLDOO\KD]DUGRXVVLWXDWLRQZKLFKLIQRWDYRLGHGFRXOGUHVXOWLQGHDWKRUVHULRXVLQMXU\
.HHSWKHGHYLFHDZD\IURP\RXQJFKLOGUHQ6PDOOLWHPVVXFKDVWKHEDWWHU\FDVHDQGEDWWHULHVDUHFKRNLQJKD]DUGV
Download the “OMRON connect” app on the Smart Device
 Enable Bluetooth®RQWKHVPDUWGHYLFH
2. 'RZQORDGDQGLQVWDOOWKH³20521FRQQHFW´DSSRQWRWKHVPDUWGHYLFH
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. 2SHQWKHDSSRQ\RXUVPDUWGHYLFHDQGIROORZWKHSDLULQJLQVWUXFWLRQV
Uploading the Data via Bluetooth
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Note
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Operation Instructions
Open the app when taking a measurement.
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interface.
2. .HHSKDQGVVWLOOIRUWKHPHDVXUHPHQW'RQRWVKDNHWKH¿QJHUGXULQJDPHDVXUHPHQW,WLV
UHFRPPHQGHGQRWWRPRYHWKHERG\ZKLOHWDNLQJDPHDVXUHPHQW
1
2
Power button
Display
Battery case
Back side of the device
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omronconnect.com/setup
Possible Problems and Solutions
Problems Possible reason Solution
SpO2 or PR can not be
shown normally.
 Finger is not inserted correctly
2. Patient’s SpO2YDOXHKDVYDULDWLRQVRULVLQDFFXUDWH
 5HWU\E\XVLQJWKHVDPHRUDGLIIHUHQW¿QJHURWKHU
WKDQDWKXPERUDOLWWOH¿QJHU
2. 7KHUHLVH[FHVVLYHLOOXPLQDWLRQ
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
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Out”.
SpO2 or PR is shown
unstably.
 Finger might not be inserted deep enough.
2. ([FHVVLYHSDWLHQWPRYHPHQW
 5HWU\E\LQVHUWLQJWKH¿QJHU
2. Be calm.
The display continues to
show “?”.
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powered on.
 No battery or low power of battery
2. Batteries might be installed incorrectly.
3. 7KHGHYLFHPLJKWEHGDPDJHG
 Please replace batteries.
2. Please reinstall the batteries.
3. 3OHDVHFRQWDFWZLWKORFDOFXVWRPHUVHUYLFHFHQWHU
The display is suddenly
off.
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VLJQDOLVGHWHFWHGORQJHUWKDQVHFRQGV
2. The battery power is too low to work.
 Normal
2. Replace the batteries.
Any communication issue
occurs.
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further help. If the problem still persists, contact your OMRON retail outlet or distributor.
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Symbol 'H¿QLWLRQ Symbol 'H¿QLWLRQ Symbol 'H¿QLWLRQ
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 Manufacturer’s
information
No SpO2 Alarm European union
DSSURYDO
Authorized
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in the European
community
Temperature limitation &RQIRUPLW\WR:(((
'LUHFWLYH For medical use
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Box Contents
 Fingertip Pulse Oximeter
2. Two AAA alkaline batteries (LR03)
3. Instruction manual
4. Storage case
Note
• The illustrations used in this manual may differ slightly from the appearance of the actual product.
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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
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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,
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A. Transport costs and risks of transport.
B. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.
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' )DLOXUHRUZHDURIRSWLRQDOSDUWVRURWKHUDWWDFKPHQWVRWKHUWKDQWKHPDLQGHYLFHLWVHOIXQOHVVH[SOLFLWO\ZDUUDQWHGDERYH
( &RVWVDULVLQJGXHWRQRQDFFHSWDQFHRIDFODLPWKRVHZLOOEHFKDUJHGIRU
F. Damages of any kind including personal caused accidentally or from misuse.
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distributor. For the address refer to the product packaging / literature or to your specialised retailer.
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by the retailer.
Electromagnetic Compatibility
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2 accuracy and pulse rate accuracy or an indication of abnormal operation. Accuracies may be
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Table 1: Electromagnetic Emissions Limits and Compliance
Emissions Test Compliance
RF Emissions
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Table 2: Electromagnetic Immunity
Immunity Test Compliance
Electrostatic Discharge (ESD)
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Rated Power Frequency Magnetic Fields
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30 A/m
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Radiated RF
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of Apple Inc.
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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 SANTÉ FRANCE SAS
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Made in China


Specyfikacje produktu

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

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