Qardio QardioArm A100 User manual

QARDIO
QardioArm A100
A Smarter Read on Blood Pressure
User Guide
Draft 0.9 –drawings to be replaced.
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QardioArm: Welcome to a smarter read on blood pressure!
Your new QardioArm blood pressure monitor is a reliable medical device for taking measurements on
the upper arm. This device was developed in collaboration with physicians and clinical tests were carried
out prove its measurement accuracy.
Every day, we at Qardio put our passion and effort into bringing you products of superior quality, design
and technology that can change your life for the better.
With its ease of use and accuracy, QardioArm is ideal for monitoring your blood pressure in your home,
office or wherever is convenient for you.
Please read through these instructions carefully so you understand all functions and safety information.
We want you to be happy with your QardioArm. If you have any questions, problems or suggestions,
please contact Qardio’s Customer Service on www.getqardio.com/support, or visit our website
www.getqardio.com, for more information.
Track your revolution with Qardio.
Intended Use
QardioArm is a fully automatic, non-invasive wireless blood pressure monitor. QardioArm is a blood
pressure measurement system intended to measure the diastolic and systolic blood pressures and pulse
rate of an adult individual. QardioArm utilizes an inflatable cuff that is wrapped around the upper arm.
This device is not intended to be a diagnostic device. Contact your physician if hypertensive values are
indicated. The cuff circumference is limited to 22cm-37cm (8.7in -14.6in).
Important safety information
Please read the User Guide carefully before using the QardioArm blood pressure monitor. In the case of
pregnancy, arrhythmia and arteriosclerosis, consult your doctor before use.
Package contents
QardioArm blood pressure monitor
Four AAA alkaline batteries, already pre-installed in the QardioArm.
User Guide.
Quick start leaflet.
Requirements
The QardioArm blood pressure monitor requires iOS 7.0 or later, and an iOS device with Bluetooth 4.0.
These include: iPhone 4S, iPhone 5 or later, iPad 4th generation or later, iPad mini, iPod Touch 5th
generation or later.
In order to use your QardioArm blood pressure monitor, you have to install the Qardio app available for
free on the Apple App Store, or on www.getqardio.com.
Using QardioArm for the first time
1. Download the Qardio app: On your mobile phone or tablet go to
www.getqardio.com and when prompted, download the app. Alternatively,go on
the Apple App Store. The Qardio app is available for free.
2. Open the Qardio app on your phone or tablet. If requested, you should
enable Bluetooth on your device, You can enable Bluetooth under the Settings
menu on your smartphone or tablet
3. Create a new user login, or login with your existing user name and
password. Follow the on-screen instructions to register and set up your personal account.

4. Fit the Qardio Arm on the upper arm
5. With the Qardio app open, touch your device on the QardioArm to perform the pairing of your
QardioArm with your phone or tablet. You should accept the pairing request.
6. On the Qardio app, press the green START button to initiate the blood pressure measurment.
Blood pressure can be affected by the position of the cuff and your physiologic condition. It is
very important that the cuff is correctly placed, please read the Detailed instructions on correct
cuff placement and the Checklist for measuring your blood pressure correctly and reliably
sections of this User Guide with particular care.
Detailed instructions on correct cuff placement
1. Ideally, remove close-fitting garments from the upper arm, or ensure that rolling the sleeve up
does not cause constriction. If you are unable to remove or roll-up your shirtsleeve, then ensure
it remains flat under the cuff.
2. Always ensure that the cuff fits correctly, verifying the markings on the cuff. You should fit the
cuff closely, but not too tight.
3. Make sure that the cuff is positioned 2cm (0.8in) above the elbow. The QardioArm must be
positioned over the artery that runs down the inner side of the arm. The Qardio logo should be
on the bottom, towards your hand. Support your arm so it is relaxed, and ensure that the
QardioArm is at the same height as your heart. Your arm should lightly bend while taking the
measurement.
Body Posture
Sitting Comfortably During Measurement
1. Be seated with your feet flat on the floor without crossing your legs.
2. Place your hand, palm-side up, in front of you on a flat surface such as a desk or a table.
3. The middle of the cuff should be at the level of the right atrium of your heart.
Lying Down During Measurement
1. Lie on your back.
2. Place your arm straight along your side with your hand palm-side up.
3. The cuff should be placed at the same level as your heart.
Note: Blood pressure can be affected by the position of the cuff and your physiologic condition.

Detailed instructions on taking a blood pressure measurement
Taking a blood pressure measurement with the QardioArm is easy and is done
in a few simple steps:
1. Open the Qardio App on your iOS device.
2. Unwrap the cuff from around the QardioArm to switch on the device.
3. Fit the QardioArm cuff around your upper arm. You can review the
instructions to do so at any point.
4. Press the green START button on the Qardio App Blood Pressure
measurement screen to start measuring.
5. The cuff will now inflate automatically. Relax, do not move and do not
tense your arm muscles until the measurement result is displayed. Breathe
normally and do not talk.
6. When the correct pressure is reached, the inflation stops and the
pressure gradually decrease. If the required pressure was not reached, the device will
automatically inflate additional air into the cuff.
7. The result, comprising the systolic and the diastolic blood pressure and the pulse rate, is
displayed on the Qardio App.
8. When the device has finished measuring, remove the cuff and wrap it around the QardioArm to
switch it off automatically.
Checklist for measuring your blood pressure correctly and reliably
Avoid activity, eating or smoking immediately before the measurement.
Sit down and relax for a few minutes before the measurement.
Always measure on the same arm (normally left, or as instructed by your doctor).
Ideally, remove close-fitting garments from the upper arm, or ensure that rolling the sleeve up
does not cause constriction. If you are unable to remove or roll-up your shirtsleeve, then ensure
it remains flat under the cuff.
Always ensure that the cuff fits correctly, verifying the markings on the cuff. You should fit the
cuff closely, but not too tight.
Make sure that the cuff is positioned 2cm (0.8in) above the elbow. The QardioArm must be
positioned over the artery that runs down the inner side of the arm. The Qardio logo should be
on bottom, towards your hand.
Support your arm so it is relaxed, and ensure that the QardioArm is at the same height as your
heart. Your arm should lightly bend while taking the measurement.
The traffic light indicator
The blood pressure measurement screen shows you the range within which the indicated blood
pressure value lies. Depending on the values detected, the bar is colored in green (optimum values),
yellow (high values), orange (very high values), or red (dangerously high values). The classification
corresponds to the 4 ranges in the table as defined by the international guidelines (ESH, AHA, JSH), as
described in “How to evaluate your blood pressure”.
Selecting multiple measurements averaging
Because blood pressure constantly fluctuates, a result determined with multiple measurements is more
reliable than one produced by a single measurement.

There is a break of 30 seconds between the measurements. A count
down indicates the remaining time.The individual results are not
displayed. Your blood pressure will only be displayed after all
measurements are taken. Do not remove the cuff between
measurements.
Visualizing your historical blood pressure data
Press the History button on the Blood Pressure page to visualize your
historical blood pressure and heart rate data in a table or chart format.
Important Facts about Blood Pressure and Self-Measurement
QardioArm measures your blood pressure. Blood pressure is the
pressure of the blood flowing in the arteries generated by the pumping
of the heart. Two values, the systolic (upper) value and the diastolic
(lower) value, are always measured.
QardioArm also measures your pulse rate. Pulse rate is the number of
times the heart beats in a minute.
High blood pressure, especially when permanent or recurrent, can
negatively affect your health and must be treated by your doctor.
Always discuss your measurement readings with your doctor and tell him/her if you have noticed
anything unusual or feel unsure. Never rely on a single blood pressure reading.
There are several potential causes of high blood pressure. Your doctor will explain them in more detail
and offer treatment where appropriate. Besides medication, weight loss and exercise can also help
lowering your blood pressure.
You should never alter the dosages of any medications prescribed by your doctor.
Blood pressure is subject to wide fluctuations throughout the day, depending on various potential
factors, including physical exertion and condition. You should routinely take your measurements in quiet
conditions when you feel relaxed. Ideally, you should take two readings every time (in the morning and
in the evening) or as prescribed by your doctor.
Deviations between measurements taken by your doctor or in the pharmacy and those taken at home
are quite normal, as these situations are completely different.
It is recommended to have at least 30 seconds in between measurements.
If you are pregnant, consult your healthcare provider before use. Monitor your blood pressure regularly
throughout pregnancy as it can change drastically during this time. When you detect unusual high
readings during pregnancy, you should measure again after at least four hours. If the reading is still too
high, consult your doctor or obstetrician.
Physical activity including eating, drinking, and smoking as well as excitement, stress, and many other
factors influence blood pressure results.
How to evaluate your blood pressure?
The World Health Organization (WHO) has created the following guide for assessing high blood pressure
(without regard to age or gender). It is important to note that various factors (e.g. diabetes, obesity,
smoking, etc.) also need to be considered. Consult with your physician for an accurate assessment and
diagnosis of your health condition.
This chart is not intended to provide a basis for any type of diagnosis or emergency assessment; this
chart only depicts different classifications of blood pressure. Consult your physician for an interpretation
and diagnosis based on your blood pressure results.

Replacing the AAA alkaline batteries
When the batteries are approximately 75% empty the battery symbol will appear on the Qardio app
blood pressure measurement screen. Although the QardioArm will continue to measure reliably, you
should obtain replacement batteries.
If the empty battery symbol appears on the Qardio app, your QardioArm batteries are depleted and it’s
time to replace them. You cannot take any further measurements and must replace the batteries. You
should replace all four AAA alkaline batteries at the same time. Use 4 new, long-life 1.5V, size AAA
batteries. Do not use batteries beyond their expiration date.
To replace batteries:
1. Release the batteries compartment hatch by pressing the button under the
cuff as shown in the drawing.
2. Replace all four AAA alkaline cells with new ones, ensuring that the polarities
are correctly aligned: the + (positive) and –(negative) polarities should match the
polarities indicated on the AAA alkaline batteries compartment.
3. Put the batteries compartment hatch back in place, pushing until it clicks in
place.
4. You will see a green light shining through the batteries compartment hatch.
Resetting the pairing
In order to reset the pairing, unwrap the cuff from around the QardioArm to switch
on the device and use a paper clip to press the button on the pinhole on the battery
compartment hatch. You should see a green light shining through.
If necessary, go in the Settings of your phone or tablet, select the QardioArm and
select forget device.
Accuracy testing and maintenance
QardioArm comprises sensitive components and must be treated with caution. Observe the storage and
operating conditions described in the “ Technical Specifications” section.
If you can’t fix the problems using the troubleshooting instructions, please contact Qardio customer
service on www.getqardio.com
We recommend the QardioArm is tested for accuracy every 2 years or after mechanical impact (e.g.
being dropped). Please contact Qardio customer service on www.getqardio.com to arrange the test.
Contraindication
It is not recommended for people with serious arrhythmia to use this blood pressure monitor.

Caution
Self-diagnosis of measurement results and self-treatment are potentially dangerous. You should always
consult your doctor.
People with severe blood flow problems, or blood disorders, should consult a doctor before using the
blood pressure monitor as cuff inflation might cause internal bleeding.
Complicating factors such as common arrhythmias, ventricular premature beats, atrial fibrillation,
arterial sclerosis, poor perfusion, diabetes, age, pregnancy, preeclampsia or renal disease can affect the
performance of the automated sphygmomanometer and/or its blood pressure reading.
If you suffer from an irregular heartbeat, measurements taken with this device should be evaluated with
your doctor.
This device may only be used for the purposes described in this User Guide. The manufacturer cannot be
held liable for damage or injury caused by incorrect use. Always follow the operating procedures
described in this User Guide to measure your blood pressure accurately and safely.
QardioArm is not suitable for checking the frequency of heart pacemakers.
General usage, safety and precautions, cleaning
Do not use the QardioArm blood pressure monitor for any purpose other than measuring blood
pressure.
Do not take measurement immediately after bathing, drinking alcohol, smoking, exercising or eating.
Do not use the QardioArm blood pressure monitor while operating a mechanical vehicle or in a
moving vehicle (e.g. during air travel)
Do not leave the QardioArm blood pressure monitor unattended around children or persons who
cannot express their consent to use.
Do not inflate the arm cuff when it is not wrapped around your arm.
Do not wrap the cuff inside-out.
Do not apply strong shocks and vibrations to the QardioArm blood pressure monitor, as this may
result in damage to the device.
Do not drop the QardioArm blood pressure monitor.
Do not expose the cuff and/or the QardioArm blood pressure monitor to temperatures outside the
storage or operating range.
Do not expose the cuff and/or the QardioArm blood pressure monitor to direct sunlight for extensive
periods of time.
Do not expose the arm cuff and/or the QardioArm blood pressure monitor to water, liquids or
moisture.
Do not expose the arm cuff and/or the QardioArm blood pressure monitor to dust or particulate.
Improper continuous pressure of cuff or too frequent measurements may interfere with blood flow ,
and result harmful injury to the users. Especially, cuff’s inflating pressure on the patients who have
intravascular access or therapy, or an arterio-venous (A-V) shunt, or same side of mastectomy will
have danger on injury.

Improper continuous pressurization from cuff’s inflation on the same limb will cause loss of function
of device.
Do not apply the cuff over the users’ arm bearing a wound or medical treatment and so on, as this
can cause further influence on the therapy.
When cuff inflation, always check the device will not result in prolonged impairment of the
circulation of the blood on users.
Do not disassemble the QardioArm blood pressure monitor.
Do not use an alcoholic-based or solvent agent to clean the device. Clean the device only with a soft,
dry cloth. Clean the cuff carefully with a humid cloth and soap. Do not submerse any part of the
QardioArm in water at any time.
AAA alkaline cells usage, storage
If AAA alkaline batteries fluid should get on your skin or clothing, immediately and thoroughly rinse with
plenty of clean water.
Use only four AAA alkaline batteries with the QardioArm blood pressure monitor. Do not use any other
types of AAA batteries.
When replacing batteries, insert the four AAA alkaline batteries with their polarities aligned as indicated
on the QardioArm blood pressure monitor.
Immediately replace the AAA alkaline batteries when they are depleted.
Always replace all four AAA alkaline batteries at the same time: do not use new and old AAA alkaline
batteries together.
If the QardioArm blood pressure monitor will not be used for a long period of time, the batteries should
be removed.
Store the device and the components in a clean, dry and safe location
Error messages and troubleshooting
Problem
Cause
Remedy
START button is gray,
not green
QardioArm is not connected to
your smartphone or tablet.
1) Close the QardioArm cuff and reopen it again.
2) Ensure that Bluetooth is enabled on your phone or
tablet and the QardioArm is nearby your phone or
tablet.
3) Replace the batteries of the QardioArm. Reset the
pairing.
Measurement could
not be performed
During the measurement, error
signals were auto-detected by
the device, or the pulse signals
on the cuff are too weak..
Re-position the cuff and repeat the measurement
keeping your arm still and without talking. Check the
marks on the cuff and the instructional videos on the
Qardio App to verify you are positioning the
QardioArm correctly. If the problem occurs again,
please contact customer service.
No pressure in the
cuff
An adequate pressure cannot
be generated in the cuff. A leak
may have occurred.
1) Check that the cuff is correctly positioned and fit to
the arm.
2) Replace the batteries if necessary.
Repeat the measurement. If the problem occurs
again, please contact customer service.
Abnormal result
The measuring signals are
inaccurate and no result can
therefore be displayed. This
could be due to cuff not fully
1) Read through instructions for performing reliable
measurements. Re-position the cuff and repeat the
measurement keeping your arm still and without
talking. If the problem occurs again, please contact

deflated before measurement,
noise interference, user talking,
user movements, cuff not
correctly fastened, cuff broken,
pump or valve failure, pressure
overflow, or user special
characteristics.
customer service.
2) If user has special characteristics, please contact
your physician.
Batteries depleted
Battery level is too low.
Replace batteries according to instructions. If the
problem occurs again, please contact customer
service..
Irregular heart beat
Pulse irregularity was detected
during measurement, and the
blood pressure measurement
might not be fully reliable.
Repeat the measurement after one hour. If irregular
heart beat is detected several times in a day or week,
we recommend you to discuss this with your doctor.
If irregular heartbeat is detected during the
measurement procedure, the IHB symbol will be
displayed. Under this condition, the wireless blood
pressure monitor can keep functioning, but the
results may be inaccurate. Please consult your
physician for accurate assessment.
Though the batteries
are installed, the
START button on the
Qardio app is still
gray.
Batteries are not inserted
correctly. Batteries level is too
low.
1) Close the device and wait five seconds. Unwrap
the cuff from around the QardioArm and try again.
2) Check the AAA alkaline cells polarities, and correct,
if required.
3) Replace the AAA alkaline cells.
Each measurement
has significantly
different results.
Under normal measuring
circumstance, the reading at
home is different from that of
the clinics. The variation is due
to the different environments.
The blood pressure is changing
according to the physiological
or psychological status of your
body.
1) Relax for a few minutes before each measurement.
Try to measure your blood pressure at consistent
times and locations.
Discuss your blood pressure values with your
physician.
2) If the problem occurs again, please contact
customer service.
The cuff does not fit
The cuff circumference is
limited to 22cm-37cm
(measured by close fitting in
the centre of the upper arm).
Contact Qardio customer service.
Customer service contact
Qardio customer service is available on www.getqardio.com.
Guarantee
This device is covered by a three-year guarantee from the date of purchase. The guarantee is valid only
on presentation of the purchase receipt confirming date of purchase.
Batteries and wearing parts are not included.
Opening or altering the device invalidates the guarantee.
The guarantee does not cover damage caused by improper handling, discharged batteries, accidents or
non-compliance with the operating instructions.
The cuff has a functional guarantee (bladder tightness) for two years.
QardioArm Technical Specifications
1) Weight: 350g (0.77 lb) including batteries
2) Dimensions: 140 x 68 x 38 mm (5.5 x 2.7 x 1.5 in) when closed

3) Measurement: Oscillometric method with automatic inflation and controlled pressure release valve.
4) Measurement range: 40~250 mmHg for blood pressure, 40~200 beats/minute for pulse.
5) Technical measuring precision:
Cuff pressure Accuracy: ±3mmHg or ±2% of readout value for blood pressure. ±5% of readout for pulse.
6) Measurement resolution: 1mmHg for blood pressure. 1 beat/min for pulse.
7) Power source: 4 x 1.5V Batteries; size AAA, supplied.
8) Operating conditions: 10~40C (50~104F) temperature, 15~90% relative maximum humidity, atmospheric
pressure 86Kpa~106kpa, maximum altitude: 2000m.
9) Storage and transport conditions: -25~70C (-13~158F) temperature, 10~95% relative maximum humidity,
atmospheric pressure 86Kpa~106kpa, maximum altitude: 2000m.
10) Compatibility: iPhone 4S or later, iPad 4th generation or later, iPad mini, iPod Touch 5th generation or
later. Free companion app with iOS 7.0 or later.
11) Product life : 5 years
12) Clinical Test : In accordance with EN1060-4 :2004 & ANSI/AAMI/ISO 81060‐2:2009
Specifications are subject to change without prior notice or any obligation on the parts of the
manufacturer.
Disposal
Actuation of European directives 2002/95/EC, 2002/96/EC and 2003/108/EC, for reduction in
use of dangerous substances in the electric and electronic device and for garbage disposal.
The symbol applied on the device or its packaging means that at the end of its useful life the
product must not be disposed of with domestic waste.
At the end of devices useful life, the user must deliver it to the able collecting centers for
electric and electronic garbage, or give back to the retailer when purchasing a new device. Disposing of
the product separately prevents possible negative consequences for the environment and for health,
deriving from inadequate disposal. It also allows the recovery of materials of which it’s made up in order
to obtain an important saving of energy and resources and to avoid negative effects to the environment
and health. In case of abusive disposal of device by the user, will be applied administrative
endorsements in compliance with current standard. The device and its parts is mared with regard to
disposal, as appropriate, in accordance with national or regional regulations.
Certifications
This device complies with the following normative documents:
COUNCIL DIRECTIVE 93/42/EEC of 14 June 1993 concerning medical devices as amended by Directive 2007/47/EC
EN ISO 13485:2003/AC: 2009:Medical devices - Quality management systems –Requirements for regulatory
purposes (ISO 13485:2003) Reference to standards contd.
EN ISO14971:2012: Medical devices - Application of risk management to medical devices (ISO 14971:2007,
Corrected version 2007-10-01)
IEC60601-1: 2005 + CORR. 1 (2006) + CORR. 2 (2007); EN 60601-1:2006+AC (2010) : Medical electrical equipment -
Part 1:General requirements for basic safety and essential Performance
EN1060-3:1997+A1:2005+A2:2009: Non-invasive sphygmomanometers, Part 3: Supplementary requirements for
electromechanical blood pressure measuring systems
EN1060-4: 2004 Non-invasive sphygmomanometers. Test procedures to determine the overall system accuracy of
automated non-invasive sphygmomanometers.

IEC/EN 60601-1-11 : 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
IEC 80601-2-30: 2009 (First Edition) for use in conjunction with IEC 60601-1:2005
EN 80601-2-30: 2010/ ANSI/AAMI 80601-2-30: 2009 : Particular requirements for the basic safety and essential
performance of automated non-invasive sphygmomanometers
EN300328 V1.7.1 :2006 Electromagnetic compatibility and Radio spectrum Matters (ERM); Wideband
transmission systems; Data transmission equipment operating in the 2,4 GHz ISM band and using wide band
modulation techniques; Harmonized EN covering the essential requirements of article 3.2 of the R&TTE Directive
EN301489-1-3 V1.9.2 :2011 Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic
Compatibility (EMC) standard for radio equipment and services; Part 1: Common technical requirements
EN301489-1-17 V2.2.1 :2012 Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic
Compatibility (EMC) standard for radio equipment and services; Part 1: Common technical requirements
EN60601-1-2: 2007 /AC 2010: Medical electrical equipment: Part 1‐2: General requirements for basic safety and
essential performance-collateral standard electromagnetic compatibility
EN 55011Group 1 Class B: 2009+A1:2010 : Industrial, scientific and medical equipment - Radio-frequency
disturbance characteristics - Limits and methods of measurement
FCC part B 15B: 2013 Electromagnetic Compatibility
FCC Rule Part: 15.247 Cat: DSS (Bluetooth) FCC Rule Part: 15.247 Cat: DTS (BT4.0)
EN ISO 10993-1:2009 Biological evaluation of medical devices-Part 1: Evaluation and testing within a risk
management process (ISO 10993-1:2009)
ANSI/AAMI SP10: 2002/A1 2003(R) 2008: Manual, electronic or automated sphygmomanometers
ANSI/AAMI/ISO 81060‐2:2009 Non‐invasive sphygmomanometers Part 2: Clinical validation of automated
measurement type
FCC statement
Federal Communications Commission (FCC) Statement 15.21
You are cautioned that changes or modifications not expressly approved by the part responsible for
compliance could void the user’s authority to operate the equipment.
15.105(b)
This equipment 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 equipment 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 equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off 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.

FCC/IC Caution:
1. This device complies with Part 15 of the FCC rules/ Industry Canada licence‐exempt RSS standard(s).
Operation is subject to the following two conditions :
1) this device may not cause harmful interference and
2) this device must accept any interference received, including interference that may cause undesired
operation.
2. This Transmitter must not be colocated or operating in conjunction with any other antenna or transmitter.
3. Any changes or modifications not expressly approved by the party responsible for compliance could
void the user's authority to operate this equipment.
IMPORTANT NOTE : (For Portable Device Configuration)
Federal Communication Commission (FCC) Radiation Exposure Statement This EUT is compliance with S
AR for general population/uncontrolled exposure limits in ANSI/IEEE C95.1‐1999 and had been tested
in accordance with the measurement methods and procedures specified in OET Bulletin 65
Supplement C.
ICES-003
This Class B digital apparatus complies with Canadian ICES‐003.
Cet appareil numérique de la classe [B] est conforme à la norme NMB‐003 du Canada.
FCC RF Radiation Exposure Statement:
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment.
End users must follow the specific operating instructions for satisfying RF exposure compliance. This
transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.
Industry Canada Caution:
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.
Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts
de licence. L'exploitation est autorisée aux deux conditions suivantes:
(1) il ne doit pas produire de brouillage et
(2) l’ utilisateur du dispositif doit étre prêt à accepter tout brouillage radioélectrique reçu, même si ce
brouillage est susceptible de compromettre le fomctionnement du dispositif.
IC IMPORTANT NOTE : (For Portable Device Configuration)
IC Radiation Exposure Statement
This device has been evaluated and complied with IC RSS-102 RF exposure requirement.
Ce dispositif a ete evalue et respecte IC RSS-102 condition d'exposition aux RF.
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
potentialradio 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.
En vertu de la réglementation de l'industrie du Canada, cet émetteur de radio ne peuvent fonctionner
en utilisant une antenne d'un type et maximum (ou moins) Gain approuvé pour l'émetteur par Industrie
Canada. pour réduire risque d'interférence aux autres utilisateurs, le type d'antenne et son gaindoivent
être choisis de sorte que lapuissance isotrope rayonnée équivalente (PIRE) ne dépasse pas ce qui est
nécessaire pour la réussite de communication.
RF Statement
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and
put into service according to the EMC information provided in the following.
•Interference may occur in the vicinity of equipment marked with
•Portable and mobile RF communication equipment (e.g. cell phones) can affect Medical Electrical
Equipment.
•The use of accessories and cables other than those specified may result in increased emissions or
decreased immunity.
•The device 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 device is suitable for use in all establishments, including domestic establishments and those
directly connected to the public low voltage power supply network that supplies buildings used for
domestic purposes.
•Portable and mobile RF communications equipment should be used no closer to any part of the
device, including cables, than the recommended separation distance calculated from the equation
applicable to the frequency of the transmitter.
•The device is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. Any other accessories, transducers and cables may result in increased emissions or
decreased immunity and EMC performance.
•The device should not be used adjacent to or stacked with other equipment and that if adjacent or
stacked use is necessary, which should be observed to verify normal operation in the configuration
in which it will be used.
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and
put into service according to the EMC information provided in the following. Portable and mobile RF
communication equipment (e.g. cell phones) can affect Medical Electrical Equipment. The use of
accessories and cables other than those specified may result in increased emissions or decreased
immunity of the unit.
Guidance and manufacturer’s declaration-electromagnetic emissions
The Wireless Blood Pressure Monitor is intended for use in the electromagnetic environment specified
below. The customer or the user of the Wireless Blood Pressure Monitor should assure that it is used
in such an environment.
Emissions test
Compliance
Electromagnetic environment - guidance
CE emissions CISPR11
Group 1
The BP-801 Wireless Blood Pressure Monitor 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.
RE emissions CISPR11
Class B

Harmonic emissions
IEC 61000-3-2
Not applicable
The BP-801 Wireless Blood Pressure Monitor is
suitable for use in all establishments, including
domestic establishments and those directly
connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.
Voltage fluctuations/
Flicker emissions
IEC 61000-3-3
Not applicable
Declaration –electromagnetic emissions and immunity for equipment and systems that are not life-
supporting and are specified for use only in a shielded location
The Wireless Blood Pressure Monitor declaration-
electromagnetic immunity
Declaration –electromagnetic immunity
The Wireless Blood Pressure Monitor system is
intended for use in the electromagnetic environment
specified below. The customer or the user of the
Wireless Blood Pressure Monitor system should
assure that it is used in such an environment.
The Wireless Blood Pressure Monitor system is
intended for use in the electromagnetic environment
specified below.
The customer or the user of the Wireless Blood
Pressure Monitor system should assure that it is used
in such an environment.
Immunity
test
IEC
60601
test level
Compliance
level
Electromagnetic
environment -
guidance
Immunity
test
IEC
60601
test level
Compliance
level
Electromagnetic
environment -
guidance
Electrostatic
discharge
(ESD)
IEC 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 %.
Conducted
RF IEC
61000-4-6
3 Vrms
150 kHz
to 80
MHz
N/A
Portable and
mobile RF
communications
equipment should
be used no closer
to any part of the
EQUIPMENT or
SYSTEM including
cables, than the
recommended
separation
distance
calculated from
the equation
applicable to the
frequency of the
transmitter.
Interference may
occur in the
vicinity of
equipment
marked with the
following symbol.
Electrical
fast
transient/
Burst IEC
61000-4-4
2 kV for
power
supply
lines 1 kV
for input
/output
lines
N/A
Mains power
quality should be
that of a typical
commercial or
hospital
environment.
Surge IEC
61000-4-5
1 kV
differenti
al mode
2 kV
common
mode
N/A
Mains power
quality should be
that of a typical
commercial or
hospital
environment.
Radiated
RF IEC
61000-4-3
3 V/m
80 MHz
to 2.5
GHz
N/A
Voltage dips,
short
interruption
s and
voltage
variations on
power
supply input
lines IEC
61000-4-11
-5 % UT
(95 %
dip in
UT) for
0.5 cycle
, -40 %
UT (60 %
dip in
UT) for 5
cycles
-70 % UT
(30 %
dip in
N/A
Mains power
quality should be
that of a typical
commercial or
hospital
environment. If
the user of the
EQUIPMENT or
SYSTEM requires
continued
operation during
power mains
interruptions, it is

UT) for
25 cycles
-5 % UT
(95 %
dip in
UT) for
5 sec
recommended
that the
EQUIPMENT or
SYSTEM be
powered from an
uninterruptible
power supply or a
battery.
Power
frequency
(50/60 Hz)
magnetic
field
IEC 61000-4-
8
3 A/m
N/A
Power frequency
magnetic fields
should be at
levels
characteristic of a
typical location in
a typical
commercial or
hospital
environment.
Manufactured for Qardio, Inc. 340 S Lemon Ave #1104F, Walnut, California 91789, USA.
www.getqardio.com
iPhone, iPad, iPod and iOS are trademarks of Apple Inc., registered in the U.S. and other countries.
The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any
use of such marks by Qardio, Inc. is under license. Other trademarks and trade names are those of their
respective owners.
Qardio, QardioArm, QardioCore and the Qardio logo are trademarks of Qardio, Inc.
Copyright Qardio, Inc. All rights reserved.
User Guide v. 2.0.
FACTORY:ATTEN ELECTRONIC(DONGGUAN) CO.,LTD.
2013
US Importer
Qardio, Inc
340 S Lemon Ave #1104F, Walnut, California 91789,
USA.
Kahl Handelsvertretung
Add.: Isarstr.33 40699 Erkrath, Germany
Tel: [phone]
Type BF Applied Part (cuf
WEEE
IP22 Ingress of water or particulate matter
FCC ID : 2ABF2-888ARM-1
IC : 11885A-888ARM01