actiiv ACMMD001 User manual

Please read the user manual carefully and thoroughly so as to ensure the
safe usage of this product, and keep the manual for further reference in
case you have problems.
Thank you very much for selecting the Actiiv Wrist Blood Pressure
Monitor ACMMD001.
MODEL: ACMMD001
WRIST BLOOD PRESSURE MONITOR
User Manual

1
INTRODUCTION............................................................................................................... 2
Indications for Use
LCD Display Signal
Monitor Components
BEFORE YOU START...................................................................................................... 6
MEASUREMENT .............................................................................................................. 9
INFORM ATION FOR USER............................................................................................... 15
Tips for Measurement
Maintenance
ABOUT BLOOD PRESSURE............................................................................................. 17
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure vary, even in one day?
Why is the blood pressure I get from the hospital different from home?
Will I get the same result if I measure on the right wrist?
TROUBLESHOOTING...................................................................................................... 19
SPECIFIC ATIONS............................................................................................................ 20
THE MATCHED COMPONENTS...................................................................................... 21
CONTACT INFORMATION............................................................................................... 21
Safety Information
Charging your Device
Setting Date and Time
Positioning the Cuff
Start Measurement
DATA MANAGEMENT....................................................................................................... 13
Recall the Records
Delete the Records
COMPLIED EUROPEAN STANDARDS LIST.................................................................... 22
Pair up the Blood Pressure Monitor with your Device
Table of Contents
Measurement Principle
General Description
EMC GUIDANCE.............................................................................................................. 23
APPENDIX........................................................................................................................ 24
Table of Contents

INTRODUCTION INTRODUCTION
Thank you for selecting the Actiiv blood pressure Monitor (ACMMD001 .
)
The
monitor features blood pressure measurement, pulse rate measurement and
storage of results.
Readings taken by the device are equivalent to those obtained by a trained
observer using the cuff and stethoscope auscultation method.
step instructions for using the product.
This manual contains important safety and care information, and provides step by
Please read this user manual carefully and thoroughly before use.
FEATURES:
Systolic Blood Pressure
Diastolic Blood Pressure
Pulse Rate
Memory: Up to 60 readings can be
recorded
This product uses the Oscillometric Measuring Method to detect blood pressure.
Before every measurement, the unit establishes a “zero point” equivalent to the
atmospheric pressure. Then it starts inflating the cuff. Meanwhile, the unit detects
pressure oscillation generated by beat-to-beat pulsatile, which is used to deter-
mine the systolic pressure and diastolic pressure as well as pulse rate.
The device also compares the longest and the shortest intervals of detected
pulse wave with the average value, and then calculates the standard deviation.
The monitor will light up a warning symbol when the calculated standard deviation
is larger than or equal to 15.
Measurement Principle
General Description
The below signs might appear in the user manual, labeling or other components.
Safety information
23
Indications for use
The Actiiv Blood Pressure Monitor is a digital monitor intended for use in
measuring blood pressure and heartbeat rate with a wrist circumference ranging
from 13.5 cm to 21.5 cm ( about 5-8.5 inches ).
It is intended for adult indoor use only.
CAUTION
* It is intended for adult indoor use only. Pregnant women, pre-eclamptic patients
and patients with severe obesity should not use this device. If required, please consult a
professional doctor.
* This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is
not intended for use on extremities other than the wrist or for functions other than obtaining a
blood pressure measurement.
* Please use the device under the specified environment as instructed in this user manual,
otherwise the accuracy of the device will be influenced.
* Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood
pressure. Please only start or end any medical treatments based solely on a physician's treatment
advice.
* If you are taking medication, consult your physician to determine the most appropriate time for
your measurement. Never change a prescribed medication without your physician’s consent.
* This unit is not suitable for continuous monitoring during medical emergencies or operations.
After the cuff has been inflated for a long time, the patient’s wrist and fingers blood supply will
become insufficient and could result in distending pain and ecchymosis.
* If the pressure of the cuff exceeds 40 kPa (300 mmHg), the unit will automatically deflate. If the
cuff doesn’t deflate when its pressure exceeds 40 kPa (300 mmHg), detach the cuff from the wrist
and press the START/STOP button to stop inflation.
* Do not use the monitor under strong electromagnetic field conditions (e.g. medical RF equipment)
that radiate an interference signal or electrial fast transient/ burst signal.
* The maximum temperature that the applied part can achieve is 42.5℃ while the
environmental temperature is 40℃.
* The device is not AP/APG equipment. It is not suitable for use in the presence of a flammable
anesthetic mixture with air (or oxygen, nitrous oxide).
* Please keep the unit out of reach of infants, children or pets, since inhalation or swallowing of
small parts is dangerous or even fatal.
* Please use the accessories and detachable parts as specified and authorised by the manufacturer.
Otherwise, it may cause damage to the unit or danger to the user / patient.
* The patient is an intended operator. The patient can measure, transmit data and charge the battery
under normal circumstances and maintain the device and its accessories according to the user
manual.
* The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient
environment. If you are allergic to dacron or plastic, please don’t use this device.
*This device cannot be used with HF surgical equipment at the same time.
* There is a PTC current limiter in the monitor, with a specification of 8V and 0.5A. When the voltage
and current exceed the limiting value, the monitor will stop working.
* The device is not suitable for public use.
T1A/250V Φ3.6*10CCC
F1
For indoor use only
Symbol for “TYPE BF
APPLIED PARTS”
Symbol for “DIRECT
CURRENT”
The Bluetooth Combination
Mark
Symbol for “THE OPERATION
GUIDE MUST BE READ”

INTRODUCTION INTRODUCTION
4
LCD Display Signal
Systolic
Blood Pressure High blood pressure
Diastolic
Blood Pressure Low blood pressure
Pulse beat/minute
Unit Measurement unit of blood pressure
Time Hour:Minute (Month/Day/Year)
Low Battery
Please use the USB cable provided to recharge the battery.
Error
Memory Recalling the history records
Bluetooth Successful Bluetooth Connection
IHB Detector Irregular Heartbeat Detector
Error
5
SYSTOLIC
DIASTOLIC
MEM/UP
BUTTON
SET/DOWN
BUTTON
START/STOP BUTTON
CUFF
(Type BF applied part)
PULSE RATE
TIME
USB Interface
Monitor Components
List
1.Blood Pressure Monitor
(ACMMD001)
2.USB Cable
3.User Manual
MEM
SET

BEFORE YOU START BEFORE YOU START
6
1. The battery for ACMMD001 is a built-in rechargeable
lithium-ion battery, with a current of 420 mAh.
2. Please use the USB cable provided to charge the battery
just like the picture below:
Power Supply and Charge Power
Your device will require charging under the following circumstances:
displays on the LCD
The LCD display dims
When powering on the monitor, the LCD doesn’t light up.
CAUTION
1. The battery used is a built-in rechargeable lithium-ion battery,
please do not disassemble it by an unauthorized maintenance personel.
2. Under normal use, it can be charged about 300 times.
If measured three times per day, and the battery
is fully charged, it can be used for about 20 days.
3. Store and use the blood pressure monitor in a cool, dry and
ventilated environment. Avoid close proximity to fire and heat sources or it
may cause the battery explode.
4. You cannot use the blood pressure monitor during the charging process.
5. During the process of charging, the blood pressure monitor will
display this symbol:
When charging is complete, please remove plug before use.
6. When charging, do not touch the charging connector and the patient
simultaneously.
7
Setting Date and Time
2.As pictured in the right, the
blinking number “12” representing
[HOUR]. Press “MEM” button to
change the number. Each press
will increase the number by one
in a cycling manner.
1.When the monitor is OFF, press
and hold the “SET” button for 3
seconds to enter Time Setting
Mode.
3.Press “SET” button again to
confirm [HOUR]. Then the
number representing [MINUTE]
blinks.
Please proceed to set the time before your initial use to
ensure each record is labelled with a time stamp. (Year
Range: 2012-2052; Time Format: 12 Hours)

BEFORE YOU START MEASUREMENT
8
4.Repeat step 2 and 3 to confirm
[MINUTE].
5.Repeat step 2 and 3
to confirm [MONTH],
[DAY] and [YEAR].
7.After confirming the [YEAR], the LCD
will display “dONE” and the
monitor will shut off.
9
Positioning the Cuff
1.Remove all accessories (watch, bracelet, etc) from your left wrist. If your
physician has diagnosedyou with poor circulationin your left wrist, use your
right wrist.
2.Roll or push up your sleeve to expose the skin.
3.Apply the cuff to your left wrist with your palm facing up.
4. Position the edge of the cuff about 1-2 cm from bottom of hand.
5. Fasten the wristcuff around your wrist,leaving no extra roombetweenthe cuff
and your skin. If the cuff is too loose, the measurement will not be accurate.
Rest for 5 minutes before measuring.
Wait at least 3 minutes between measure ments. This allows your blood
circulation to recover.
For a meaningful comparison, try to measure under similar conditions. For
example, take daily measurementsat approximatelythe same time, on the same
wrist
6.Patients with Hypertension:
The middle of the cuff should be at the same level as the right atrium of the heart.
Before starting the measurement, please sit comfortably with legs uncrossed,
feet flat on the floor, back and arm supported.

MEASUREMENT MEASUREMENT
10
Bluetooth Module No.: AW2540MV1
RF Frequency Range: 2.4 GHz
Output Power Range: -1 dBm
Supply Voltage: 2 V to 3.6 V
Transmitting Distance: 10 meters
11
START
STOP
1.After correctly positioning the cuff,
press the START button to turn on the
monitor, and it will complete the
measurement process.
Adjust to zero.
Inflating and measuring. Display and save the
measuring result.
Start Measurement
Install App and Pair-Up
(Supports Bluetooth 4.0 only)
With the advanced Bluetooth 4.0 technology applied to this blood pressure
monitor, mobile phones which are equipped with Bluetooth functionality are
able to receive your personal health data. Just simply install the specially-
designed app and pair up your blood pressure monitor with your mobile
phone by following the instructions below
1.The App is now available in the App Store and Google Play.
App name is "LIFESENSE INTERNATIONAL"
You may search for the app, then download and install the app on
your iPhone or Android Phone. Simple and convenient!
1. Turn on Bluetooth and the app.
Make sure both are ON when
pair-up is proceeding.
3. The monitor wil shut off after
pair-up process is complete
IF SUCCESSFULL, symbol
will be shown on the LCD.
IF FAILED, symbol
will be shown on the LCD.
2. When the monitor is OFF, press
and hold the START button to start
pair-up. The symbol and the
symbol will be shown on the
LCD alternatively, indicating pair-up
is proceeding.

MEASUREMENT DATA MANAGEMENT
12
START
STOP
4. Press STOP button to turn off
the monitor.
2.The device will proceed to transmit
data after taking the measurement.
The Bluetooth symbol
blinks on the LCD
to indicate data is transmitting to your phone.
3. If the data is successfully
transmitted, the LCD will then
display “dONE”.
If the data transmission fails, the
LCD will display “ ” instead.
CAUTION
1. When using this device, please pay attention to the following situations which may
interrupt blood flow and influence blood circulation of the patient, thus causing harm or
injury to the patient: too frequent and consecutive multiple measurements;
the application of the CUFF and it’s pressurization on any wrist where intravascular
access or therapy, or an arterio-venous (A-V) shunt, is present;
Inflating the cuff on the wrist on the side of a mastectomy.
2. Do not apply the cuff over a wound, otherwise it can cause further injury.
3. Do not inflate the cuff on the same limb which other monitoring ME EQUIPMENT
is applied simultaneously, because this could cause temporary loss of function
of those simultaneously-used monitoring ME EQUIPMENT.
4. Do not use the device in such a way as to cause prolonged impairment of blood
circulation in the patient.
13
Recall the Records
1.Press the “MEM” button to access the
memory. The monitor will display the
calculated average of the last three
readings first.
2. Press “MEM/UP” button or
“SET/DOWN” button to rotate the
history records.
“MEM/UP” to go forward;
“SET/DOWN” to go backward.
The most recent record (1) is shown first. Each new measurement
is assigned to the first (1) record. All other records are pushed back
one digit (e.g., 2 becomes 3, and so on), and the last record (60) is
dropped from the list.
CAUTION
CAUTION
5. The cuff pressure may continuously increase which can prevent blood
flow and result in harmful injury to the PATIENT. Sensitive people,
including pregnant women, pre-eclamptic patients, patients with
implanted medical electronic instruments and have atrial fibrillation (AF),
premature ventricular beats and peripheral arterial disease (PAD), should
avoid using the unit whenever possible.

DATA MANAGEMENT INFORMATION FOR USER
14
When you have not obtained an accurate measurement, you can clear all the
measuring results by following the below steps:
Delete the Records
1.Under Memory Recalling Mode, press
and hold both the “MEM” button and the
“SET” button for 3 seconds.
2.The LCD will display “dEL dONE”,
indicating that memory clearing is
complete. It will then shutdown.
Under Memory Recalling Mode, if you
wish to give up clearing, press
“START/STOP” to turn off the monitor.
3.When there is no memory in the monitor,
if you press the “MEM” button to look up the
history, the LCD will display as pictured
to the right.
CAUTION
15
Tips for Measurement
Within 1 hour
after eating or drinking
Within 20 minutes
after taking a bath
In a very cold enviroment
Immediate measurement
after tea, coffee, smoking
When talking or moving your fingers
When you want to discharge urine
Measurements could be inaccurate if taken in the following circumstances:

INFORMATION FOR USER ABOUT BLOOD PRESSURE
MEM
SET
MEM
SET
MEM
SET
16
Maintenance
To obtain the best performance, please follow the below instructions.
Keep your device in a cool
dry place, avoid direct sunlight
and high temperatures
Avoid dropping or direct impact Avoid dusty environments and
unstable surrounding temperatures
Use a slightly damp cloth to
remove any dirt Avoid washing the cuff
MEM
SET
MEM
SET
MEM
SET
CAUTION
1. Please make sure the unit functions safely and that it is in proper working condition before use.
Don’t service or maintain while the device is in use.
2. If you have any problems with this device, such as setting up, maintaining or using, please
go to www.actiivfitness.com. Don’t open or repair the device by yourself.
3. Please report to Actiiv if any unexpected operation or events occur.
4. Cleaning: Dusty environments may affect the performance of the unit.
Please use a soft cloth to remove any dirt from the device and cuff before and after use.
17
What are systolic pressure and diastolic pressure?
press
artery vein
blood discharging
Systolic
relax
blood entering
Diastolic
What is the standard blood pressure classification?
When ventricles contract and pump blood out
of the heart, the blood pressure reaches its
maximum value in the cycle, which is called
systolic pressure. When the ventricles relax,
the blood pressure reaches its minimum
value in the cycle, which is called diastolic
pressure.
Irregular Heartbeat Detector
This Blood Pressure Monitor is equipped with an intelligent Irregular
Heartbeat (IHB) Detector function. During each measurement, this equipment records
the heartbeat intervals and works out the standard deviation. If the calculated value is
larger than or equal to 15, this equipment will light up the IHB symbol on the screen
when displaying the measuring result.
CAUTION
The appearance of the IHB icon indicates that a pulse irregularity consistent with
an irregular heartbeat was detected during measurement. Usually this is NOT a
cause for concern. However, if the symbol appears often, we recommend you
seek medical advice. Please note that the device does not replace a cardiac
examination, but serves to detect pulse irregularities at an early stage.
Only a doctor can tell your normal BP range. Please
contact your doctor if your measuring result falls out of the
range. Kindly note that only a doctor can tell whether
your blood pressure value has reached a dangerous point.
The blood pressure classification published by the
World Health Organization (WHO) and the
International Society of Hypertension (ISH) in
1999 is as follows:
SYS
DIA
<120
<80
120-129
80-84
130-139
85-89
140-159
90-99
160-179
100-109
≥180
≥110
Level
Blood
Pressure (mm Hg)
Optimal Normal High-normal Mild Moderate Severe
CAUTION
Avoid immersing your device
in liquid

ABOUT BLOOD PRESSURE TROUBLESHOOTING
1918
Why does my blood pressure vary,
even in one day?
PROBLEM SYMPTOM CHECK THIS REMEDY
No power
Low
batteries
Error
message
Display is dim or
will not light up.
Show on
the display
shows Data communication
has failed
Make sure that phone’s
Bluetooth is on or within
the distance range
E 2 shows The cuff is very tight Refasten the cuff and
then measure again.
E 3 shows The pressure of the
cuff is in excess.
Relax for a moment
and then measure again.
E 9 shows Product has not been
activated. Reactivated
E 10 or
E 11 shows
The monitor detected
motion while measuring.
Movement can affect the
measurement. Relax for a
moment and then
measure again.
E 20 shows
E 21 shows Relax for a moment and
then measure again.
EExx,shows on
the display.
A calibration error
occurred.
Retake the measurement.
If the problem persists,
contact the retailer or our
customer service
department for further
assistance.
The measurement
process does not detect
the pulse signal.
Loosen the clothing on
the arm and then
measure again.
Measured incorrectly.
Power is exhausted. Charge the power
Power is low. Charge the power
1. Individual blood pressure varies every
day. It is also affected by the way you tie
your cuff and your measurement
position, so please take the measure-
ment in the same conditions.
2. Blood pressure variation is greater if
the person takes medication.
3. Make sure you wait at least 3 minutes
before taking another measurement.
Will I get the same result if I
measure on the right wrist?
It is ok to use the device on both wrists, but
the results may differ depending on the
person. It is recommended that you measure
on the same wrist every time to maintain an
accurate record of measurements.
Why is the blood pressure
I get from the hospital different from home?
Blood pressure can vary even during a 24 hour period due to influences like
the weather, emotions, exercise etc. You may experience different
environmental and emotional conditions at a hospital compared to at home
which can affect your blood pressure measurements.
This section includes a list of error messages and frequently
asked questions for problems you may encounter with your
blood pressure monitor. If the product is not operating as
you think it should, check here before contacting support.

SPECIFICATIONS CONTACT INFORMATION
20
Power supply 3.7V 420mAH Built-in rechargeable lithium-ion
battery, 5V / 1A USB
Display Digital LCD V.A.46.5x36.5mm
Measurement mode Oscillographic testing mode
Measurement range
Accuracy
Normal working condition
Storage & transportation
condition
Measurement perimeter
of the wrist About 13.5cm-21.5cm
Net Weight Approx.110g
External dimensions
Attachment
Approx.79.8×72.5×13.2mm
USB cable, User manual
Mode of operation Continuous operation
Degree of protection Type BF applied part
Protection against
ingress of water
IP22, It means the device could be protected
against solid foreign objects of 12.5 mm and
greater, and against vertically falling water
drops when ENCLOSURE is tilted up to 15°
Software version
Device classification
V01
Battery Powered Mode:
Internally Powered ME Equipment
WARNING: No modification of this equipment is allowed.
Rated cuff pressure:
0kpa-40kpa (0mmHg-300mmHg)
pulse value:(40-199)beat/minute
Pressure:
5℃-40℃within±0.4kpa(3mmHg)
0℃-45℃(out of 5℃-40℃)
within±0.7kpa(5mmHg)
pulse value:±5%
Temperature:-20℃to 60℃ RH: 10% to 93%
Atmospheric pressure: 50kPa to 106kPa
Temperature:5℃to 40℃ Relative humidity ≤85%
Atmospheric pressure: 86kPa to 106kPa
21
For customer support, please visit www.actiivfitness.com
Contact Information
Measurement pressure: 4kPa-34kPa
(30mmHg-255mmHg)

22 23
EMC Guidance
1. The Blood Pressure Monitor needs special precautions
regarding EMC and needs to be installed and put into service
according to the EMC information provided in the
ACCOMPANYING DOCUMENTS
2. Wireless communications equipment such as wireless home
network devices, mobile phones, cordless telephones and their
base stations, walkie-talkies can affect this equipment and should
be kept at least a distance d = 3,3 m away from the equipment.
(Note. As indicated in Table 6 of IEC 60601-1-2:2007 for ME
EQUIPMENT, a typical cell phone with a maximum output power
of 2 W yields d = 3,3 m at an IMMUNITY LEVEL of 3 V/m)
Complied European Standards List
Risk management
Labeling
User manual
General Requirements
for Safety
Electromagnetic
compatibility
Performance
requirements
Clinical investigtion
Usability
Software life-cycle
processes
ISO/EN 14971:2012 Medical devices — Application of risk
management to medical devices
ISO/EN 15223-1:2012 Medical devices. Symbols to be used
with medical device labels, labelling and information to be
supplied. General requirements
EN 1041: 2008 Medical equipment manufacturers to provide
information
IEC/EN 60601-1: 2006+A1：2012 Medical electrical
equipment - Part 1: General requirements for basic safety and
essential performance
IEC/EN 60601-1-11: 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
IEC/EN 80601-2-30:2009 Medical electrical equipment - Part
2-30: Particular requirements for the basic safety and
essential performance of automated noninvasive
sphygmomanometers
IIEC/EN 60601-1-2:2007 Medical electrical equipment - Part
1-2: General requirements for basic safety and essential
performance - Collateral standard:Electromagnetic
compatibility - Requirements and tests
EN 1060-1:1995+A2:2009 Non-invasive blood pressure Part
1: General requirements
EN 1060-3:1997+A2:2009 Non-invasive blood pressure Part
3: Supplementary requirements for electromechanical blood
pressure measuring system
EN 1060-4: 2004 Automatic Blood Pressure Monitor overall
system Interventional accuracy of the testing process
IEC/EN 60601-1-6: 2010 Medical electrical equipment --
Part 1-6: General requirements for basic safety and essential
performance - Collateral Standard: Usability
IEC/EN 62366: 2007 Medical devices - Application of
usability engineering to medical devices
IEC/EN 62304:2006+AC: 2008 Medical device software -
Software life cycle processes
COMPLIED EUROPEAN
STANDARDS LIST
EMC GUIDANCE

2524
APPENDIX
Installing App and Pairing
The following steps are for use with iPhone.
The App is also available for Android
through Google Play.
1. Search for the App in the App Store.
The App name is “Lifesense
International”. Download and install the
App onto your phone.
2. Ensure Bluetooth is turned “ON”
on your phone
3. Run the App,
the following screen
should appear
4. Create a new account
or sign in
5. The following screen will
appear after you
have signed in.
6. Press “Edit” at the bottom right corner,
untick “Weight”, press the back button
and “Yes” to save Data. (this will
remove the weight measurement) and
return to the Start menu.
7. Press the “Settings” button
in the top right corner ( )
8. Press the “Add” button to
add a device ( )
9. Press the Bluetooth logo
10. Please ensure you pressand hold the
“Start” button on the blood pressure
monitor to initiate Pairing Mode.
11. Once connected, the device will show
[ ]. It is now ready to use.
12. Your readings will be
recorded on the App, you
can find the readings by
selecting Blood Pressure
in the App as per the image
shown here
13. The following screen
will appear
14. To see records, press the “list” button
at the top of the screen ( )
15. The following screen
will appear
16. To delete any unwanted
readings, slide to the left
on the reading and the
delete button will appear