iHealth PO3M Wireless Pulse Oximeter, PO3M Operation manual

Wireless Pulse Oximeter
Oxymètre de pouls sans fil
Ossimetro wireless per il rilevamento del battito
Pulsioxímetro inalámbrico
Funkgesteuertes Pulsoximeter
Oxímetro de Pulso Wireless
EN
MODEL PO3M
Wireless Pulse Oximeter
OPERATION MANUAL
TABLE OF CONTENT
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
2
3
3
4
4
4
6
9
10
12
13
13
14
14
The symbols below associate with your PO3M
Symbols
Definition of Symbol
Symbol for” THE OPERATION MANUAL MUST BE READ”
Symbol for “WARNING”
Symbol for “Type BF Applied Part”
Symbol for “no alarm for SpO2”
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 “Use by date”
Symbol for “Manufacturer”
EC
REP
SN
Symbol for “EUROPEAN REPRESENTATIVE”
Symbol for “SERIAL NUMBER”
Symbol for “KEEP DRY”
Symbol for “COMPILIES WITH MDD93/42/EEC REQUIREMENTS”
1
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:
iPod touch 5th generation
iPhone 4S
iPhone 5
New iPad
iPad 4
with an iOS version of V5.0 or higher.
iPhone and iPod touch are trademarks of Apple Inc., registered in the U.S. and other
countries. iPad is a trademark of Apple Inc.
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
PARTS AND DISPLAYS
Bluetooth indicator
Display screen
Start button
DEVICE DESCRIPTION
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 finger; 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 affect what is considered normal for a given individual. Concerns
about your readings should be shared with your physician or healthcare professional.
3
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).
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
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.
4
2.The device might misinterpret excessive movement as good pulse strength. Limit
finger 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 cuff 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 artificial 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 finger to increase
circulation, or place the device on another finger.
8.The device measures oxygen saturation of functional hemoglobin. High levels of
dysfunctional hemoglobin (caused by sickle cell anemia, carbon monoxide, etc.)
could affect the accuracy of the measurements.
9.Do not use the device in a combustible environment (oxygen enriched environ
ment).
10.Do not use the device outside the specified operating temperature range, and do
not store the device outside the specified storage temperature ranges
5
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 affect 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.
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 finger where the device is attached and the corresponding
hand and arm.
6
It is recommended that the user should wash hands before use. Nail polish, especially
dark shades, may affect 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 finger excluding the thumb. It is preferred to use
the index or middle finger.
Charge the battery before first 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 App
Download the app from the App Store and install it. Search for “iHealth MyVitals”. (Your
compatible iOS device should be version 5.0 or later.)
Create User and Cloud
Account
After downloading the
app, register and set up
your user account
following the on-screen
instructions.
7
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 from PC or Mac.
Turn Bluetooth “On”
Turn Bluetooth “On” under the “Settings” menu of your iOS device (The date and time of
the Pulse Oximeter will be synced with your iOS device upon first successful
connection). Once your Bluetooth is on, the Pulse Oximeter will connect automatically
when the app is launched and the Bluetooth indicator on the screen of oximeter will
turn on.
TESTING INSTRUCTIONS
1.Open the clamp of the Pulse Oximeter PO3M, then place the
middle, ring or index finger of your left hand into the rubber
opening of the oximeter with nail side down, as pictured.
2. On the front panel, press the “Start” button once to turn the
oximeter on.
3. Keep your hand still for the reading.
Note: If the pulse signal is too weak to measure, dashes (- - -) will appear on the
display.
4. After a few seconds, your SpO2 reading will appear on the oximeter display screen
and the app if the app is turned on.
5. If the signal strength is too low, switch to another finger and perform the test again.
6. Remove the oximeter from the finger. The oximeter will automatically turn off after 8
seconds.
8
USING WITHOUT iOS DEVICE
After it has been used for the first time, the date and time of the Pulse Oximeter PO3M
will be synchronized with your iOS device. It can also be used without being connected
to an iOS 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.
CARE AND MAINTENANCE
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, fire 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.
9
SPECIFICATIONS
1.Model: PO3M
2.Classification: 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 definition.
10.
Arms
Range
90%~100%
1.2215
80%~89%
1.3282
70%~79%
1.7277
The figure below shows the graphical plot of all SaO2 versus SpO2 with linear
regression fit for all the sample data in the clinical protocol.
10
Scatter plot of SaO2 versus SpO2 with
linear regression fit
The figure below shows the graphical
plot of SaO2 versus error (SpO2 – SaO2)
with upper 95% and lower 95% limits of
agreement:
Scatter plot of difference 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-off: 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
1.Finger may not be
inserted correctly.
2.Finger or hand may be
moving.
3.The device may be
damaged
1.Remove finger and
reinsert, as directed.
2.Try to keep perfectly still
and test again.
3.Please contact the iHealth
Customer Service
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 find 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).
Problem
SpO2 or pulse rate shows
no value, or the number
fluctuates.
The device does
not turn on.
12
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 different 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
13
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.
Manufacturer Information
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.
Tel: 86-22-60526081
EC
REP
IHealthLabs Europe SARL
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
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.
ELECTROMAGNETIC COMPATIBILITY INFORMATION
14
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 specified below.
The customer or the user of the PO3M should assure that it is used in such an environment.
Compliance
Group 1
Class B
Harmonic emissions
IEC/EN 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions
IEC/EN 61000-3-3
Not applicable
Electromagnetic environment - guidance
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.
The PO3M is suitable for use in all establishments other than domestic and those directly
connected to the public low-voltage power
supply network that supplies buildings used
for domestic purposes.
15
Table 2
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacturer’s declaration - electromagnetic immunity
The PO3M is intended for use in the electromagnetic environment specified below. The
customer or the user of the PO3M should assure that it is used in such an environment.
IMMUNITY
test
Compliance
level
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 floors are covered
with synthetic material, the
relative humidity should be at
least 30 %.
Power frequency
(50/60 Hz)
magnetic field
IEC/EN 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields
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.
16
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 specified below.
The customer or the user of the PO3M should assure that it is used in such an environment.
IMMUNITY
test
Radiated RF
3 V/m 80 MHz to
IEC/EN 61000-4-3 2.5 GHz
Electromagnetic environment
- guidance
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
17
the recommended separation
distance in meters (m).
Field strengths from fixed 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:
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
affected by absorption and reflection from structures, objects and people.
A) Field strengths from fixed 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 fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field 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, field strengths should be less than [V1] V/m.
18
Table 4
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between
portable and mobile RF communications equipment and the [PO3M]
The PO3M is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the PO3M can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the PO3M as recommended
below, according to the maximum output power of the communications equipment.
Rated maximum
output
power of
transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
d=1.2 p
d=1.2 p
d=2.3 p
0,01
0.12
0.12
0.23
0,1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
19
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be determined using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
20
1
2
2
3
3
4
4
PRÉCAUTIONS
UTILISATION DE VOTRE OXYMÈTRE DE POULS
SOINS ET ENTRETIEN
SPÉCIFICATIONS
DÉPANNAGE
Informations sur le fabricant
INFORMATIONS SUR LA COMPATIBILITE ÉLECTROMAGNÉTIQUE
4
6
9
10
11
12
12
EC
REP
Symbole de « REPRÉSENTATION EUROPÉENNE »
IPX1
SN
PARTIES COMPOSANTES ET AFFICHAGES
Indicateur Bluetooth
Écran d’affichage
Bouton Marche/Arrêt
PRÉCAUTIONS
4
7
10
Solution
Bluetooth ne fonctionne
pas
11
Informations sur le fabricant
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, Chine.
Tél. : +86-22-60526081
EC
REP
IHealthLabs Europe SARL
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
12
Non applicable
13
Contact ± 6 kV
± 8 kV air
Contact
± 6 kV
± 8 kV air
3 A/m
3 A/m
14
3 V/m 80 MHz à
2,5 GHz
15
16
m
150 kHz à 80 MHz
d=1.2 p
d=1.2 p
d=2.3 p
0,01
0.12
0.12
0.23
0,1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
17
18
1
2
2
3
3
4
4
4
6
9
10
11
12
12
EC
REP
IPX1
SN
COMPONENTI E DISPLAY
Indicatore Bluetooth
Schermo display
ATTENZIONE
4
7
10
11
Informazioni di produzione
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, Cina.
Tel: 86-22-60526081
EC
REP
IHealthLabs Europe Co., Ltd.
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
12
Test sulle emissioni
Emissioni RF
CISPR 11
Emissioni RF
CISPR 11
13
Test IMMUNITÀ
3 A/m
3 A/m
14
Test IMMUNITÀ
RF irradiate
IEC 61000-4-3
15
d=1.2 p
d=2.3 p
16
d=1.2 p
d=1.2 p
d=2.3 p
0,01
0.12
0.12
0.23
0,1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
da 150 kHz a
80 MHz
17
18
ES
MODELO PO3M
Pulsioxímetro para la yema de los dedos
MANUAL DE INTRODUCCIÓN
ÍNDICE
SÍMBOLOS
USO PREVISTO
PIEZAS E INDICADORES DE LA PANTALLA
PIEZAS Y PANTALLAS
DESCRIPCIÓN DEL DISPOSITIVO
CONTRAINDICACIONES
ADVERTENCIAS
1
2
2
3
3
4
4
4
6
9
10
11
12
12
EC
REP
IPX1
SN
PIEZAS Y PANTALLAS
Indicador de
Bluetooth
PRECAUCIONES
4
7
10
RESOLUCIÓN DE PROBLEMAS
Problema
11
REP
IHealthLabs Europe SARL
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
12
Emisiones de RF
CISPR 11
Grupo 1
Emisiones de RF
CISPR 11
13
3 A/m
3 A/m
14
Prueba de
INMUNIDAD
RF irradiada
IEC 61000-4-3
3 V/m
15
d=1.2 p
d=2.3 p
16
De 800 MHz a
2,5 GHz
d=1.2 p
d=1.2 p
d=2.3 p
0,01
0,12
0,12
0,23
0,1
0,38
0,38
0,73
1
1,2
1.2
2,3
10
3,8
3,8
7,3
100
12
12
23
De 150 kHz a
80 MHz
17
18
1
2
2
3
3
4
4
4
6
9
10
11
12
12
SYMBOLE
Die folgenden Symbole betreffen Ihr PO3M:
Symbole
EC
REP
IPX1
SN
Display
7
10
FEHLERBEHEBUNG
Problem
11
Herstellerangaben
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.
Tel: 86-22-60526081
EC
REP
IHealthLabs Europe SARL
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
12
Gruppe 1
HF-Emissionen
CISPR 11
13
Konformitä
tsniveau
± 6 kV
Kontakt
± 8 kV Luft
± 6 kV
Kontakt
± 8 kV Luft
3 A/m
3 A/m
14
Konformitä
tsniveau
3 V/m
Empfohlene Trenndistanz:
d=1.2 p
d=1.2 p
d=2.3 p
15
16
d=1.2 p
d=1.2 p
d=2.3 p
0,01
0,12
0,12
0,23
0,1
0,38
0,38
0,73
1
1,2
1.2
2,3
10
3,8
3,8
7,3
100
12
12
23
150 kHz bis
80 MHz
17
18
1
2
3
3
3
4
4
5
7
10
11
13
14
14
15
16
REP
SN
Display
AVISOS
4
5
6
7
Aviso
Ligue o Bluetooth
8
INSTRUÇÕES DE TESTE
CUIDADOS E MANUTENÇÃO
9
10
RESOLUÇÃO DE PROBLEMAS
1,2215
80%~89%
1,3282
70%~79%
1,7277
11
12
13
INFORMAÇÕES IMPORTANTES EXIGIDAS PELA INDUSTRY CANADA
(INDÚSTRIA DO CANADÁ)
14
Emissions test
Emissões de FR
CISPR 11
Informações do fabricante
ANDON HEALTH CO., LTD.
No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.
Tel: 86-22-60526081
EC
REP
IHealthLabs Europe SARL
3 rue Tronchet, 75008, Paris, France
Tel: +33 1 44 94 04 81
3 A/m
d=1.2 p
80 MHz a 800 MHz
d=2.3 p
800 MHz a 2,5 GHz
16
17
18
19
80 MHz a 800 MHz 800 MHz a 2,5 GHz
d=1.2 p
0,01
0.12
0,1
0.38
1
1.2
10
3.8
100
12
20
d=1.2 p
d=2.3 p
0.12
0.23
0.38
0.73
1.2
2.3
3.8
7.3
12
23
21
PO3M-SMSP01 V1.0