iHealth PO3M Manuale utente

Wireless Pulse Oximeter

Oxymètre de pouls sans l

Ossimetro wireless per il rilevamento del battito

Pulsioxímetro inalámbrico

Funkgesteuertes Pulsoximeter

Oxímetro de Pulso Wireless

Draadloze Pulse-Oxymeter

Ασύρματο Οξύμετρο Παλμού

OPERATION MANUAL

Manuel de presentation

Manuale dell’utente

Manual de Introducción

Bedienungsanleitung

Manual de Funcionamento

Gebruikshandleiding

Εγχειρίδιο Λειτουργίας

MODEL PO3M

Wireless Pulse Oximeter

OPERATION MANUAL

TABLE OF CONTENT

EN

SYMBOLS

INTENDED USE

PARTS AND DISPLAY INDICATORS

PARTS AND DISPLAYS

DEVICE DESCRIPTION

CONTRAINDICATIONS

WARNINGS

Notice

USING YOUR PULSE OXIMETER

CARE AND MAINTENANCE

SPECIFICATIONS

TROUBLESHOOTING

IMPORTANT INFORMATION REQUIRED BY THE FCC

IMPORTANT INFORMATION REQUIRED BY THE INDUSTRY CANADA

Manufacturer Information

ELECTROMAGNETIC COMPATIBILITY INFORMATION

1

2

3

4

6

9

10

12

13

14

15

SYMBOLS

The symbols below associate with your PO3M

1

Symbols

Symbol for” THE OPERATION MANUAL MUST BE READ”

Symbol for “WARNING”

Symbol for “Type BF Applied Part”

Symbol for ”ENVIRONMENT PROTECTION-Waste electrical products

should not be disposed of with household waste. Please recycle

where facilities exist. Check with your local Authority of retailer for

recycling advice”.

Symbol for “no alarm for SpO2”

Symbol for “Use by date”

Symbol for “Manufacturer”

Symbol for “SERIAL NUMBER”

Symbol for “EUROPEAN REPRESENTATIVE”

Symbol for “KEEP DRY”

Symbol for “COMPILIES WITH MDD93/42/EEC REQUIREMENTS”

Denition of Symbol

SN

EC REP

INTENDED USE

The PO3M Wireless Pulse Oximeter is a non-invasive device intended for spot-checking

of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate.

The wireless pulse oximeter is intended to measure blood oxygen saturation and pulse

rate of adults above 16 years old in home and hospital environments (including clinical

use in internist/surgery, anesthesia, intensive care, etc.).

The Wireless Pulse oximeter is not intended for continuous monitoring.

Compatibility

The Wireless Pulse Oximeter PO3M is designed for use with the following devices:

iPhone 4S or later

iPad Air or later

iPad mini or later

iPad (3rd generation) or later

iPod touch (5th generation) or later

The iOS version of these devices should be V5.0 or higher.

The Wireless Pulse Oximeter PO3M is also compatible with a number of Android

devices,the Android version should be V4.3 or higher. For a complete list of compatible

devices, please visit the support page on www.ihealthlabs.com

PARTS AND DISPLAY INDICATORS

One (1) Wireless Pulse Oximeter PO3M

One (1) Lanyard

One (1) Operation Manual

One (1) Quick Start Guide

One (1) USB cable

2

DEVICE DESCRIPTION

PARTS AND DISPLAYS

3

Display screen

Bluetooth indicator

Start button

PO3M pulse oximeter measures the amount of oxygen in

your blood and the pulse rate. The oximeter works by

shining two light beams into the small blood vessels or

capillaries of the nger; the measured signal is then

obtained by a photosensitive element and processed by

the microprocessor. The oxygen saturation (SpO2) is

measured as a percentage of full capacity.

Typically, a SpO2 reading between 94%-99% is considered normal. High altitudes and

other factors may aect what is considered normal for a given individual. Concerns

about your readings should be shared with your physician or healthcare professional.

4

IEC 60601-1: 2005 + CORR. 1 (2006) + CORR. 2 (2007)/EN 60601-1:2006 /AC:2010

Medical electrical equipment-Part1: General requirements for basic safety and essential

performance

IEC60601-1-2:2007/EN 60601-1-2:2007 /AC:2010 (Medical electrical equipment -- Part

1-2: General requirements for basic safety and essential performance - Collateral

standard: Electromagnetic compatibility - Requirements and tests)

IEC 60601-1-11 (First Edition): 2010 Medical electrical equipment-Part 1-11: General

requirements for basic safety and essential performance – Collateral Standard:

Requirements for medical electrical equipment and medical electrical systems used in

the home healthcare environment

ISO 80601-2-61:2011 (Medical electrical equipment-Particular requirements for the

basic safety and essential performance of pulse oximeter equipment for medical use).

Hereby, [Andon Health CO.,LTD], declares that this [PO3M] is in compliance with the

essential requirements and other relevant provisions of Directive 1999/5/EC. Directive

1999/5/EC declaration of conformity can be downloaded on the following link :

https://www.ihealthlabs.eu/support/certications

CONTRAINDICATIONS

The PO3M Wireless Pulse Oximeter cannot be used on infant babies.

WARNINGS

1.This device is for use on adults only.

2.Certain activities may pose a risk of injury, including strangulation, if the lanyard

should become wrapped around your neck. Use the lanyard with caution.

3.Do not use the device in a magnetic resonance (MR) environment.

Notice

5

1.Do not use the device as the only basis for making medical decisions. It is intended

only to be used as additional information that you can give to your licensed health

care professional.

2.The device might misinterpret excessive movement as good pulse strength. Limit

nger movement as much as possible when using the device.

3.Do not use the device on the same hand/arm when using a blood pressure cu or

monitor.

4.The device has no alarms of blood oxygen saturation and pulse rate, and it will not

sound if the amount of oxygen in your blood is too low or your pulse rate is abnormal.

If the measurement of SpO2 and pulse rate is not in the normal range, please contact

your health care professional.

5.Do not place the device in liquid or clean it with agents containing ammonium

chloride or products that are not listed in this Operation Manual.

6.Any of the following conditions may reduce the performance of the device:

a)Flickering or very bright light;

b)Excessive Movement;

c)Weak pulse quality (low perfusion);

d)Low hemoglobin;

e)Nail polish, and/or articial nails;

f)Any tests recently performed on you that required an injection of intravascular dyes

7. The device may not work if you have poor circulation. Rub your nger to increase

circulation, or place the device on another nger.

8.The device measures oxygen saturation of functional hemoglobin. High levels of

dysfunctional hemoglobin (caused by sickle cell anemia, carbon monoxide, etc.)

could aect the accuracy of the measurements.

9.Do not use the device in a combustible environment (oxygen enriched environ

ment).

6

10.Do not use the device outside the specied operating temperature range, and do

not store the device outside the specied storage temperature ranges

11.The materials used in the device conform to the biocompatibility and nontoxic

regulations and present no hazard to the body.

12.Use in emergency vehicles with communication systems may aect accuracy of the

measurements.

13.The packaging of the device is recyclable, and it must be collected and disposed

according to the related regulation in the country or region where the package of

the device or its accessories is opened.

14.Any material of the device that may cause pollution must be collected and disposed

according to local rules and requirements.

15.Any single functional tester cannot be used to assess the accuracy of a pulse

oximeter.

16.Do not stare at the lighting LED, as it may irritate your eyes.

17.The device is calibrated to display FUNCTIONAL OXYGEN SATURATION

18.Do not use the device for more than 30 minutes.

19.The wavelength range of pulse oximeter can be especially useful to clinicians

20.Because the pulse oximeter measurements are statistically distributed, only about

two-thirds of pulse oximeter measurements can be expected to fall within ±Arms of

the value measured by a oximeter.

21.The SpO2 accuracy was tested by comparing it to a Co-oximeter and the pulse rate

accuracy was tested by comparing it to a function tester.

22.The device shall not be installed close to or stacked with other devices. When it is

necessary to be close to or stacked with other devices, please observe if the device

can operate normally under such setting rst. For recommended measures of

avoiding or reducing such interference, please refer to the section of "ELECTROMAG-

NETIC COMPATIBILITY INFORMATION".

Charge the battery before rst use

Link the wireless Pulse Oximeter to a USB port of a electrical power source (may be a

PC), and press the “start” button. Then the battery indicator " " will blink, which

means the battery charging is started. When the battery indicator " " stops blinking,

it means the battery has

been fully charged.

DOWNLOAD THE APP ON IOS :

Download the iHealth MyVitals app from Apple app store and install it. (Your

compatible IOS device should be version 5.0 or later)

7

USING YOUR PULSE OXIMETER

Before Using Pulse Oximeter

The wireless pulse oximeter may be used when the user is seated, standing or lying

down. The user should not walk or run during measurements and should take care of

not excessively moving the nger where the device is attached and the corresponding

hand and arm.

It is recommended that the user should wash hands before use. Nail polish, especially

dark shades, may aect the accuracy of the measurement and it is suggested that any

polish be removed prior to monitoring.

The device is suitable for using on any nger excluding the thumb. It is preferred to use

the index or middle nger.

8

DOWNLOAD THE APP ON ANDROID :

Download the iHealth MyVitals app from Google play store and install it. .(Your

compatible Android device should be version 4.3 or later and 4.0 bluetooth).

Create User and Cloud Account

After downloading the app, register and set up your user account following the

on-screen instructions.

When setting up your user account, you will also have access to a free, secure iHealth

Cloud account. Go to www.ihealthlabs.com, then click “Sign In” to access your cloud

account fromPC or Mac.

9

USING WITHOUT SMART DEVICE

1. Clean the device once per week or more frequently if handled by multiple users.

2. Wipe the device with a soft cloth dampened with rubbing alcohol to avoid cross

infection. Do not pour the alcohol directly on or into the device. Dry with a soft

cloth, or allow to air dry.

3. Avoid dropping this device on a hard surface.

4. Do not immerse the device in water or other liquid, as this will result in damage to

the device.

5. If this device is stored below 0 , please acclimate the device to room temperature

before use.

6. Do not try to disassemble this device.

7. The PO3M is a precision electronic instrument and must be repaired/serviced by an

accredited iHealth service center.

8. Incorrect replacement of battery by inadequately trained personnel could result in

an unacceptable risk (e.g., excessive temperatures, re or explosion).

9. The patient simulator « Index 2 », made by the Fluke company, can be used to verify

operation of the oximeter.

10.The expected service life of the PO3M is about 5 years.

CARE AND MAINTENANCE

After it has been used for the rst time, the date and time of the Pulse Oximeter PO3M

will be synchronized with your device. It can also be used without being connected to

an smart device. In this case, the measurement data is stored in the memory and can be

uploaded to the app when the connection is re-established. The Pulse Oximeter PO3M

can store up to 100 measurements. When the memory is full, any new measurement

overwrites the oldest ones.

1.Model: PO3M

2.Classication: Internally powered, type BF

3.Enclosure degree of ingress protection: IPX1

4.Display System: LED

5.Power Source: battery 3.7V Lithium-ion 330mAh

6.Peak wavelength: 660nm/880nm;

7.Maximum optical output power: 1mW;

8.SpO2 Measuring Range: 70-99%

9.Average Root Mean Square (ARMS) of SpO2 Accuracy: 80% 99% ±2%, 70% 79%

±3% ,<70%: no denition.

10.

SPECIFICATIONS

The gure below shows the graphical plot of all SaO2 versus SpO2 with linear regression

t for all the sample data in the clinical protocol.

Range

90%~100%

80%~89%

70%~79%

Arms

1.2215

1.3282

1.7277

10

Scatter plot of SaO2 versus SpO2 with linear

regression t

The gure below shows the graphical plot of

SaO2 versus error (SpO2 – SaO2) with upper

95% and lower 95% limits of agreement:

Scatter plot of dierence between methods

against the SaO2

11.Pulse Rate Measuring Range: 30/min-250/min

12.Pulse Rate Accuracy: 30/min ~ 99/min: ±2, 100/min ~ 250/min: ±2%.

13.Data update period: 15s

14.Automatic Shut-o: After 8 seconds of no indication on the sensors

15.Operation Environment: 5 -40 ; Humidity <80%; Atmospheric pressure:

700hPa-1060hPa

16.Storage Environment: -20 -55 ; Humidity <95%; Atmospheric pressure:

700hPa-1060hPa

11

TROUBLESHOOTING

12

Problem Possible Cause

Solution

SpO2 or pulse rate shows

no value, or the number

uctuates.

1.Finger may not be

inserted correctly.

2.Finger or hand may be

moving.

3.The device may be

damaged

1.Remove nger and

reinsert, as directed.

2.Try to keep perfectly still

and test again.

3.Please contact the iHealth

Customer Service

The device does

not turn on.

1.The battery may be low.

2.The device might be

damaged.

1.Charge the battery and

try again.

2.Please contact the iHealth

Customer Service

“E1” is displayed on the

screen

The sensor is damaged

Please contact the iHealth

Customer Service

Low Battery indicator is

blinking.

The battery is low.

Charge the battery and

try again.

The app cannot nd the

Wireless Pulse Oximeter

PO3M.

The Bluetooth does not

work

Reestablish the Bluetooth

connection. If still not

successful, restart your

wireless device (iPod,

iPhone or iPad).

try again.

13

IMPORTANT INFORMATION REQUIRED BY THE FCC

This device complies with Part 15 of the FCC Rules. Its operation is subject to the

following two conditions:

(1) This device may not cause harmful interference.

(2) This device must accept any interference received, including interference that may

cause undesired operation.

Note: This product has been tested and found to comply with the limits for a Class B

digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide

reasonable protection against harmful interference in a residential installation. This

product generates, uses, and can radiate radio frequency energy and, if not installed

and used in accordance with the instructions, may cause harmful interference to radio

communications. However, there is no guarantee that interference will not occur in a

particular installation. If this product does cause harmful interference to radio or

television reception, which can be determined by turning the equipment of and on, the

user is encouraged to try to correct the interference by one or more of the following

measures:

—Reorient or relocate the receiving antenna.

—Increase the separation between the equipment and receiver.

—Connect the equipment into an outlet on a circuit dierent from that to which the

receiver is connected.

—Consult the dealer or an experienced radio/TV technician for help.

IMPORTANT INFORMATION REQUIRED BY THE INDUSTRY CANADA

Under Industry Canada regulations, this radio transmitter may only operate using an

antenna of a type and maximum (or lesser) gain approved for the transmitter by

Industry Canada. To reduce potential radio interference to other users, the antenna

type and its gain should be so chosen that the equivalent isotropically radiated power

(e.i.r.p.) is not more than that necessary for successful communication.

This device complies with Industry Canada license-exempt RSS standard(s). Operation

is subject to the following two conditions: (1) this device may not cause interference,

and (2) this device must accept any interference, including interference that may cause

undesired operation of the device.

14

Manufacturer Information

ANDON HEALTH CO., LTD.

No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.

Tel: 86-22-60526081

IHealthLabs Europe SARL

3 rue Tronchet, 75008, Paris, France

Tel: +33 1 44 94 04 81

Email: [email protected]

Health is a trademark of iHealth Lab Inc. Bluetooth® associated logos are registered

trademarks owned by Bluetooth SIG, Inc. and any use of such marks by iHealth Lab Inc. is

permitted under license. Other trademarks and trade names are those of their respective

owners.

EC REP

ELECTROMAGNETIC COMPATIBILITY INFORMATION

15

Table 1

For all ME EQUIPMENT and ME SYSTEMS

Guidance and manufacture’s declaration - electromagnetic emissions

The PO3M is intended for use in the electromagnetic environment specied below.

The customer or the user of the PO3M should assure that it is used in such an environment.

Emissions test

Compliance Electromagnetic environment - guidance

RF emissions

CISPR 11

Group 1

The PO3M uses RF energy only for its internal

function. Therefore, its RF emissions are very

low and are not likely to cause any interference

in nearby electronic equipment.

RF emissions

CISPR 11

Class B

The PO3M is suitable for use in all establish-

ments other than domestic and those directly

connected to the public low-voltage power

supply network that supplies buildings used

for domestic purposes.

Harmonic emissions

IEC/EN 61000-3-2

Not applicable

Voltage uctuations/

icker emissions

IEC/EN 61000-3-3

Not applicable

Table 2

For all ME EQUIPMENT and ME SYSTEMS

16

Guidance and manufacturer’s declaration - electromagnetic immunity

The PO3M is intended for use in the electromagnetic environment specied below. The

customer or the user of the PO3M should assure that it is used in such an environment.

IMMUNITY

test

IEC 60601test

level

Compliance

level

Electromagnetic environment

- guidance

Electrostatic

discharge (ESD)

IEC/EN 61000-4-2

± 6 kV contact

± 8 kV air

± 6 kV contact

± 8 kV air

Floors should be wood, concrete

or ceramic tile. If oors are covered

with synthetic material, the

relative humidity should be at

least 30 %.

Power frequency

(50/60 Hz)

magnetic eld

IEC/EN 61000-4-8

3 A/m 3 A/m

Power frequency magnetic elds

should be at levels characteristic of

a typical location in a typical

commercial or hospital

environment.

NOTE: UT is the A.C. mains voltage prior to application of the test level.

17

Table 3

For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING

Guidance and manufacturer’s declaration - electromagnetic immunity

The PO3M is intended for use in the electromagnetic environment specied below.

The customer or the user of the PO3M should assure that it is used in such an environment.

IMMUNITY

test

IEC/EN 60601

test level

Compliance

level

Electromagnetic environment

- guidance

Radiated RF

IEC/EN 61000-4-3

3 V/m 80 MHz to

2.5 GHz

3 V/m

Portable and mobile RF

communications equipment

should be used no closer to any

part of the [PO3M], including

cables, than the recommended

separation distance calculated from

the equation applicable to the

frequency of the transmitter.

Recommended separation

distance

d=1.2 p

80 MHz to 800 MHz

d=2.3 p

800 MHz to 2,5 GHz

Where P is the maximum output

power rating of the transmitter in

watts (W) according to the

transmitter manufacturer and d is

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is

aected by absorption and reection from structures, objects and people.

A) Field strengths from xed transmitters, such as base stations for radio (cellular/cordless)

telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV

broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic

environment due to xed RF transmitters, an electromagnetic site survey should be

considered. If the measured eld strength in the location in which the PO3M is used exceeds

the applicable RF compliance level above, the PO3M should be observed to verify normal

operation. If abnormal performance is observed, additional measures may be necessary,

such as re-orienting or relocating the [PO3M].

B) Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than [V1] V/m.

18

the recommended separation

distance in meters (m).

Field strengths from xed RF

transmitters, as determined by an

electromagnetic site survey,a should

be less than the compliance level in

each frequency range.b

Interference may occur in the vicinity

of equipment marked with the

following symbol:

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