Kinetik Wellbeing WBP2 User manual

Blood Pressure Monitor
Instruction Manual
WBP2

TABLE OF CONTENTS
INTRODUCTION.......................................................................2 - 8
Support
General Description
Indications for Use
Contraindications
Measurement Principle
Safety Information
LCD Display Signal
Monitor Components
List
TROUBLESHOOTING..................................................................22
SPECIFICATIONS......................................................................23
COMPLIED STANDARDS LIST........................................................25
EMC GUIDANCE.........................................................................26 - 28
AUTHORISED COMPONENTS.........................................................24
Authorised Components
Manufacturer Information
Return Policy
ABOUT BLOOD PRESSURE...........................................................20 - 21
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Irregular heartbeat detector
Why does my blood pressure fluctuate throughout the day?
Why do I get a different blood pressure at home compared to the hospital?
Is the result the same if measuring on the right arm?
TAKING A MEASUREMENT...........................................................14 - 15
Tie the Cuff
Start the Measurement
DATA MANAGEMENT.................................................................16 -18
Recall the Records
Delete the Records
INFORMATION FOR USER............................................................19
Tips for measurement
Maintenance
1
The Choice of Power Supply
Installing and Replacing the Batteries
Setting Date, Time
Select the user ID
BEFORE YOU START..................................................................9 - 13

INTRODUCTIONINTRODUCTION
2 3
Features:
Maximum 90 records per each user
3rd Generation Technology: Measuring during inflation
80mm×58.5mm Digital LCD display
The Kinetik Blood Pressure Monitor is digital monitors intended for use in
measuring blood pressure and heartbeat rate with arm circumference ranging
from 22cm to 42cm.
It is intended for adult indoor use only.
2. The device is not suitable for use on patients with implanted, electrical
devices, such as cardiac pacemakers, defibrillators.
Support
Measurement Principle
Contraindications
General Description
Indications for Use
Thank you for selecting Kinetik arm type blood pressure monitor (WBP2).
The monitor features blood pressure measurement, pulse rate measurement
and the result storage. The design provides you with three years warranty.
Readings taken by the WBP2 are equivalent to those obtained by a trained
observer using the cuff and stethoscope auscultation method.
This manual contains important safety and care information, and provides
step by step instructions for using the product.
Read the manual thoroughly before using the product.
1. The device should not be used by any person who may be suspected of, or
is pregnant.
This product uses the Oscillometric Measuring method to detect blood pressure.
Before every measurement, the unit establishes a “zero pressure” equivalent to
the atmospheric pressure. Then it starts inflating the arm cuff, meanwhile, the
unit detects pressure oscillations generated by beat-to-beat pulsatile, which is
used to determine the systolic and diastolic pressure, and also pulse rate.
Our manual should provide you with all the information you need
to set up and use this product.
If you have a question, have a look at our Troubleshooting page!
For further assistance, why not contact our Customer Care team
directly? We’re here to help!
Our Customer Care team are available from 9am-5pm, Monday to
Friday (excluding bank holidays).
We promise to respond to all queries and will ensure to resolve any
issue you may be having.
You can reach us by…
Live Chat:
Simply visit www.kinetikwellbeing.com and send us a message.
Email:
[email protected]
Phone (UK):
[phone]
Post (UK):
Kinetik Medical Devices Limited
Unit 3, Perrywood Business Park, Honeycrock Lane,
Salfords, Redhill. RH1 5DZ
Phone (NZ):
[phone]
Post (NZ):
Kinetik Wellbeing NZ
44 John Brian Drive, 0794 Redvale, Albany,
Auckland, NewZealand

INTRODUCTIONINTRODUCTION
4 5
CAUTION
* Do not take any therapeutic measures on the basis of a self measurement. Never alter the dose of a
medicine prescribed by a doctor. Consult your doctor if you have any question about your blood pressure.
* When the device was used to measure patients who have common arrhythmias such as atrial or
ventricular premature beats or atrial fibrillation, the best result may occur with deviation. Please consult
your physician about the result.
* Don't kink the connection tube during use, otherwise, the cuff pressure may continuously increase
which can prevent blood flow and result in harmful injury to the PATIENT.
CAUTION
* This device is intended for adult use in homes only.
* The device is not suitable for use on neonatal patients, pregnant women,patients with implanted,
electronical devices, patients with pre-eclampsia, premature ventricular beats, atrial fibrillation,
peripheral, arterial disease and patients undergoing intravascular therapy or arterio-venous shunt or
people who received a mastectomy. Please consult your doctor prior to using the unit if you suffer from
illnesses.
* The device is not suitable for measuring the blood pressure of children. Ask your doctor before using it
on older children.
* The device is not intended for patient transport outside a healthcare facility.
* The device is not intended for public use.
* This device is intended for no-invasive measuring and monitoring of arterial blood pressure.It is not
intended for use on extremities other than the arm or for functions other than obtaining a blood pressure
measurement.
* Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood
pressure.Do not begin or end medical treatment without asking a physician for treatment advice.
* If you are taking medication,consult your physician to determine the most appropriate time to measure
your blood pressure. Never change a prescribed medication without consulting your physician.
The signs below might be in the user manual, labeling or other component.
They are the requirement of standard and using.
Safety Information
* When using this device, please pay attention to the following situation which may interrupt blood flow and
influence blood circulation of the patient, thus cause harmful injury to the patient: connection tubing kinking
too frequent and consecutive multiple measurements; the application of the cuff and its pressurization on
any arm where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; inflating the
cuff on the side of a mastectomy.
* Warning: Do not apply the cuff over a wound;otherwise it can cause further injury.
*Do not inflate the cuff on the same limb which other monitoring ME equipment is applied around
simultaneously, because this could cause temporary loss of function of those simultaneously-used
monitoring ME equipment.
*On the rare occasion of a fault causing the cuff to remain fully inflated during measurement, open the cuff
immediately. Prolonged high pressure (cuff pressure ＞300mmHg or constant pressure ＞15mmHg for
more than 3 minutes) applied to the arm may lead to an ecchymosis.
*Please check that operation of the device does not result in prolonged impairment of patient blood
circulation.
* When measurement, please avoid compression or restriction of the connection tubing.
* The device cannot be used with HF surgical equipment at the same time.
* The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER was clinically
investigated according to the requirements of ISO 81060-2:2013.
* To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the manufacturer.
* This device is contraindicated for any female who may be suspected of, or is pregnant. Besides providing
inaccurate readings, the effects of this device on the fetus are unknown.
* Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.
* This unit is not suitable for continuous monitoring during medical emergencies or operations.Otherwise,
the patient’s arm and fingers will become anaesthetic, swollen and even purple due to a lack of blood.
* When not in use, store the device with the adapter in a dry room and protect it against extreme moisture,
heat, lint, dust and direct sunlight. Never place any heavy objects on the storage case.
* This device may be used only for the purpose described in this booklet. The manufacturer cannot be held
liable for damage caused by incorrect application.
*This device comprises sensitive components and must be treated with caution. Observe the storage and
operating conditions described in this booklet.
* The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable
anesthetic mixture with air of with oxygen or nitrous oxide.
* Warning: No servicing/maintenance while the ME equipment is in use.
* The patient is an intended operator.
* The patient can measure data and change battery under normal circumstances and maintain the device
and its accessories according to the user manual.
* To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated
interference signal or electrical fast transient/burst signal.
* The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient environment.
If you are allergic to polyester, nylon or plastic, please don't use this device.
* During use, the patient will be in contact with the cuff. The materials of the cuff have been tested and
found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause any
potential sensization or irritation reaction.
* Adaptor is specified as a part of ME EQUIPMENT.
Classification for water ingress
and particulate matter
Read the instructions (actual
symbol colours are white on a
blue background).
Symbol for “MANUFACTURER”
Symbol for “SERIAL NUMBER”
Symbol for “TYPE BF APPLIED
PARTS”
Symbol for “DIRECT CURRENT”
Symbol for “RECYCLE”
Symbol for “ENVIRONMENT
PROTECTION - Electrical waste
products should not be disposed of
with household waste. Please recycle
where facilities exist. Check with your
local authority or retailer for recycling
advice”
Symbol for “Authorised Representative
in the European Community”
EC REP
Symbol for “MANUFACTURE
DATE”
Caution: These notes must be
observed to prevent any damage
to the device.
SN
0197
Symbol for “COMPLIES WITH
MDD 93/42/EEC
REQUIREMENTS”

INTRODUCTION
INTRODUCTION
76
CAUTION
* If you experience discomfort during a measurement, such as pain in the arm or other complaints, press
the START/STOP button to release the air immediately from the cuff. Loosen the cuff and remove it from
your arm.
* If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff not
deflate when pressures reaches 40 kPa (300 mmHg), detach the cuff from the arm and press the
START/STOP button to stop inflation.
* Before use, make sure the device functions safely and is in proper working condition. Check the device,
do not use the device if it is damaged in any way. The continuous use of a damaged unit may cause
injury, improper results, or serious danger.
* Do not wash the cuff in a washing machine or dishwasher!
* The service life of the cuff may vary by the frequency of washing, skin condition, and storage state. The
typical service life is 10000 times.
* It is recommended that the performance should be checked every 2 years and after maintenance and
repair, by retesting at least the requirements in limits of the error of the cuff pressure indication and air
leakage (testing at least at 50mmHg and 200mmHg).
* Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local
guidelines.
* Manufacturer will make available on request circuit diagrams, component part lists, descriptions,
calibration instructions,etc., to assist to service personnel in parts repair.
* Cleaning :Dust environment may affect the performance of the unit. Please use the soft cloth to clean
the whole unit before and after use. Don’t use any abrasive or volatile cleaners.
* The device doesn’t need to be calibrated within three years warranty.
* If you have any problems with this device, such as setting up, maintaining or using, please contact the
SERVICE PERSONNEL of Harvard Medical Devices. Don’t open or repair the device by yourself in the
event of malfunctions. The device must only be serviced, repaired and opened by individuals at
authorized sales/service centers.
* Please report to Harvard Medical Devices if any unexpected operation or events occur.
* Keep the unit out of reach of infants, young children or pets to avoid inhalation or swallowing of small
parts. It is dangerous or even fatal.
* Be careful to strangulation due to cables and hoses, particularly due to excessive length.
* At least 30 min required for ME equipment to warm from the minimum storage temperature between
uses until it is ready for intended use. At least 30 min required for ME equipment to cool from the
maximum storage temperature between uses until it is ready for intended use.
* This equipment needs to be installed and put into service in accordance with the information provided in
the ACCOMPANYING DOCUMENTS;
* 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 away from the equipment. The distance d is calculated by the MANUFACTURER from the 80
MHz to 5.8 GHz column of Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.
* Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE.
Otherwise, it may cause damage to the unit or danger to the user/patients.
* There is no luer lock connectors are used in the construction of tubing, there is a possibility that they
might be inadvertently connected to intravascular fluid systems, allowing air to be pumped into a blood
vessel.
* Please use the device under the environment which was provided in the user manual. Otherwise, the
performance and lifetime of the device will be impacted and reduced.
SYMBOL DESCRIPTION
Systolic pressure High blood pressure
Diastolic pressure Low blood pressure
EXPLANATION
mmHg Measurement Unit of the blood pressure
Low battery Batteries are low and need to be replaced
Current Time Year/Month/Day, Hour : Minute
(1mmHg=0.133kPa)
Heartbeat
Irregular heartbeat
Average value The average value of blood pressure
Pulse in beats per minute
Pulse display
Blood pressure monitor is detecting an
irregular heartbeat during measurement.
Blood pressure monitor is detecting a
heartbeat during measurement.
LCD display signal
* The plug/adapter plug pins insulates the device from the main supply. Do not position the device in a
position where it is difficult to disconnect from the supply mains to safely terminate operation of ME
equipment.
* The operator shall not touch output of batteries /adapter and the patient simultaneously.
User 1/User 2 Start measurement and save the
measuring results for User 1/User 2
/

INTRODUCTION BEFORE YOU START
98
1. Blood Pressure Monitor
(WBP2)
4. User manual
2. Cuff (Type BF applied part)
3. Bag
(Please use Kinetik
authorized cuff. The size
of the actual cuff please
refer to the label on the
attached cuff.)
(22cm~42cm)
In order to get the best effect and protect your monitor, please use the right
•Open the battery cover.
•Install the batteries by matching
the correct polarity, as shown.
•Replace the battery cover.
CAUTION
CAUTION
Replace the batteries whenever the below happens
The shows
The display is dim
The display does not light up.
1Battery powered mode:
6VDC 4×AA batteries
2AC adaptor powered mode:
6V 1A (not included)
Do not use new and used batteries together.
Do not use different types of batteries together.
Do not dispose the batteries in fire. Batteries may explode or leak.
Remove batteries if the device is not likely to be used for some time.
Worn batteries are harmful to the environment. Do not dispose with daily garbage.
Remove the old batteries from the device following your local recycling guidelines.
Monitor Components The Choice of Power Supply
Installing and Replacing the Batteries
List
Component list of
pressure measuring system
1. Cuff
2. Air pipe
3. PCBA
4. Pump
5. Valve
MEMORY BUTTON
USER BUTTON
START/STOP BUTTON
BATTERY COMPARTMENT
LCD DISPLAY
(Please only use the recommended
AC adaptor model).
Please unplug the adaptor to depart
from the using utility power.
DC POWER SOCKET
CUFF
AIR HOSE
AIR CONNECTOR PLUG
battery and special power adaptor which complies with local safety standard.
AC adaptor
(not included)

BEFORE YOU START BEFORE YOU START
1110
1. When the monitor is off, hold pressing “ ” button
It is important to set the clock before using your blood pressure
monitor, so that a time stamp can be assigned to each record that is
stored in the memory. (The setting range of the year :2017—2057;
Time format:24H)
for 3 seconds to enter the mode for year setting.
3. Press “ ” button to confirm [YEAR]. Then the monitor
4. Repeat steps 2 and 3 to set the [MONTH] and [DAY].
enter into [MONTH] and [DAY] setting.
Setting Date and Time.
2. Press “ ” button to
increase one year.
Press “ ” button to
decrease one year.

BEFORE YOU START
1312
5. Repeat steps 2 and 3 to set the [HOUR] and [MINUTE].
6. After hour and minute is set, the LCD will display “donE”
and then turn off.
BEFORE YOU START
Select the User ID
1. When the blood pressure monitor is off, press “ ” button the
user ID will be shown. Then press “ ” button to change the
user ID between user 1 and user 2.
2. Confirm the user ID by pressing the “ ” button to recall the records;
or pressing the “ ” button to start the measurement.
Before you start the measurement, please select the desired user ID first.

1514
TAKING A MEASUREMENT
1.
Adjust the zero.
Inflating and measuring.
LCD display
Display and save the
measurement result.
2. Press the “ ” button to power off,
otherwise it will turn off within 1 minute.
Start the Measurement
TAKING A MEASUREMENT
cuff on your upper arm, then position the tube off-center
toward the inner side of arm in line with the little finger.
Or position the artery mark over the main artery (on
the inside of your arm). Note: Locate the main artery
by pressing with 2 fingers approximately 2 cm
above the bend of your elbow on the inside
of your left arm. Identify where the pulse can be
felt the strongest. This is your main artery.
should be able to insert one finger between the cuff
and your arm.
bracelets from your left arm.
Note: If your doctor has diagnosed you with
poor circulation in your left arm, use your right arm.
Make sure your sleeve is not too tight.
Place your elbow on a table so that the cuff is at the same level as your heart.
Turn your palm upwards. Sit upright in a chair, and take 5-6 deep breaths.
Rest for 5 minutes before first measuring.
Wait at least 3 minutes between measurements.
This allows your blood circulation to recover.
The patient must relax as much as possible and do not
move and talk during the measurement procedure.
For a meaningful comparison, try to measure
under similar conditions. For example,
take daily measurements at approximately
the same time, on the same arm, or as
directed by a physician.
Take the measurement in a silent room.
The cuff should maintain at the same level as the
right atrium of the heart.
Please sit comfortably. Do not cross your legs
and keep your feet flat on the ground.
Keep your back against the backrest of the chair.
2~3cm
Tie the cuff
3. Hold your arm with your palm facing up and tie the
4. The cuff should be snug but not too tight. You
1. Remove all Jewellery, such as watches and
5. Sit comfortably with your tested arm resting on a flat surface.
6. Helpful tips for Patients, especially for Patients with Hypertension:
2. Roll or push up your sleeve to expose the skin.
When the monitor is off, press “ ” button to turn on the
monitor, and it will finish the whole measurement.
(Take user 1 for example.)

17
16
DATA MANAGEMENT
1. When the monitor is off, please press “ ” button to show the
average value of the latest three records. If the records are less than
3 groups, it will display the latest record instead.
2. Press the “ ” button to get the record you want.
The current No. is No 1.
Five records in total.
The corresponding
time is 6:00.
The corresponding
date is January 1st
2017.
The current No.,
date and time
of the record
will be shown
alternately.
Recall the Records
DATA MANAGEMENT
If you did not get the correct measurement, you can delete the
result for the selected user by following steps below.
for 3 seconds when the monitor
is in the memory recall mode,
the display will show “dEL y”.
2. Press “ ” or “ ”
button to switch the display
between “dEL n” or “dEL y”.
to confirm deleting this group
result when it shows “dEL y”
then the display will show
“User + donE”, and then the
average value of the latest
three records will show.
(If the records are less than 3
groups, it will display the latest
record instead).
Delete the Records
1. Hold pressing “ ” button
3. Press “ ” button

1918
INFORMATION FOR USER
1. Hold pressing both “ ”
button and “ ” botton
for 3 second when the monitor
is in the memory recall mode,
the “dEL y + U5 Er” will show
the display.
DATA MANAGEMENT
2. Press “ ” or “ ”
button to switch
“dEL n” or “dEL y”.
to confirm deleting when it
shows “dEL y”, then the
monitor will turn off when it
shows “User + donE”.
3. Press “ ” button
Tips: Press “ ” button
when it shows “dEL n”.
it will drop out.
4. If there is no record,
press “ ” button,
the right display will show.
Tips for Measurement
Measurements may be inaccurate if taken in the following
circumstances.
1. Within 1 hour after drinking or eating.
2. Immediate measurement after tea, coffee or smoking
3. Within 20 minutes after taking a bath
4. When talking or moving your fingers
5. In a very cold Environment
6. When you need the bathroom
Maintenance
In order to get the best performance, please follow the
instructions below.
1. Put in a dry place and avoid the sunshine
2. Avoid touching water, clean it with a dry cloth in case.
3. Avoid intense shaking and collisions
4. Avoid dusty and unstable temperature environment
5. Using wet cloths to remove dirt
6. Do not attempt to clean the reusable cuff with water and
never immerse the cuff in water.

2120
ABOUT BLOOD PRESSURE
Only a physician can tell your normal BP
range. Please contact a physician if your
measuring result falls out of the range.
Please note that only a physician can tell
whether your blood pressure value has
reached a dangerous point.
press
artery vein
blood discharging
Systolic
relax
blood entering
Diastolic
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.
The blood pressure classification published
by World Health Organization (WHO) and
International Society of Hypertension (ISH)
in 1999 is as follows:
CAUTION
The appearance of the IHB icon indicates that a pulse irregularity consistent with an
irregular heart-beat 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.
CAUTION
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
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Irregular Heartbeat Detector
ABOUT BLOOD PRESSURE
The blood pressure is different even
throughout the day due to weather,
emotion, exercise etc, Also, there is the
“white coat” effect, which means blood
pressure usually increases in clinical
settings.
What you need to pay
attention to when you measure
your blood pressure at home:
If the cuff is tied properly.
If the cuff is too tight or too loose.
If the cuff is tied on the upper arm.
If you feel anxious.
Taking 2-3 deep breaths before
beginning will be better for measuring.
Advice: Relax yourself for 4-5
minutes until you calm down.
It is ok for both arms, but there
will be some different results for
different people. We suggest you
measure the same arm every time.
Why does my blood pressure
fluctuate throughout the day?
Why do I get a different
blood pressure at home
compared to the hospital?
Is the result the same
if measuring on the
right arm?
An irregular heartbeat is detected when a heartbeat rhythm varies while the device is
measuring systolic pressure and diastolic pressure. During each measurement, blood
pressure monitor will keep a record of all the pulse intervals and calculate the average
value of them. If there are two or more pulse intervals , the difference between each
interval and the average is more than the average value of ±25% , or there are four or
more pulse intervals ,the difference between each interval and the average is more
than the average value of ±15%, then the irregular heartbeat symbol will appear on
the display with the measurement result.
1. Individual blood pressure varies
multiple times everyday. It is also affected
by the way you tie your cuff and your
measurement position, so please take the
measurement under the same conditions.
2.If the person takes medicine, the
pressure will vary more.
3.Wait at least 3 minutes for another
measurement.

2322
TROUBLE SHOOTING
PROBLEM SYMPTOM CHECK THIS REMEDY
No power
Low
batteries
Error
message
Display will not
light up.
Batteries are exhausted. Replace with new batteries
Insert the batteries
correctly
Replace with new batteries
Batteries are inserted
incorrectly.
Display is dim or
show Batteries are low.
E 01 shows
E 03 shows
E 04 shows
EExx, shows on
the display.
A calibration error
occurred. (XX can
be some digital symbol,
such as 01, 02,etc., if
this similar situation
appear, all belong to
calibration error.)
Retake the measurement.
If the problem persists,
contact the retailer or our
customer service
department for further
assistance. Refer to the
warranty for contact
information and return
instructions.
Measurement failed.
E 02 shows
The cuff is too tight
or too loose.
Refasten the cuff and then
measure again.
Movement can affect the
measurement. Relax for a
moment and then
measure again.
Relax for a moment and
then measure again.
The measurement
process does not
detect the pulse
signal.
Loosen the clothing on
the arm and then
measure again.
Warning
message
Relax for a moment.
Refasten the cuff and then
measure again. If the
problem persists, contact
your physician.
“OUt ” shows Out of measurement
range
This section includes a list of error messages and frequently
asked questions for problems you may encounter with your blood
pressure monitor. If the products not operating as you think it
should, check here before arranging for servicing.
SPECIFICATIONS
Type BF applied part
WARNING: No modification of this equipment is allowed.
Power supply
Battery powered mode:
6VDC 4×AA batteries
AC adaptor powered mode: 6V 1A (not included)
(Please only use the recommended AC adaptor model).
Display mode
Measurement mode Oscillographic testing mode
Measurement range
Measurement perimeter
of the upper arm
Weight Approx.254g(Excluding the batteries and cuff)
External dimensions
Attachment
Mode of operation Continuous operation
Degree of protection
Protection against
ingress of water
Accuracy
Normal working condition
Storage & transportation
condition
Software Version A04
Pressure:
5°C - 40°C within±3mmHg(0.4kPa)
Pulse value:±5%
Digital LCD display V.A.80mm×58.5mm
Approx.140.4mm×110.4mm×64.8mm
user manual, bag
Rated cuff pressure:
0mmHg~299mmHg (0kPa~39.9kPa)
Measurement pressure:
SYS: 60mmHg~230mmHg (8.0kPa~30.7kPa)
DIA: 40mmHg~130mmHg (5.3kPa~17.3kPa)
Pulse value: (40-199) beats/minute
IP21 It means the device could protected against
solid foreign objects of 12.5mm and greater, and
protect against vertically falling water drops.
Device Classification
Battery Powered Mode:
Internally Powered ME Equipment
AC Adaptor Powered Mode: Class II ME Equipment
A temperature range of :+5°C to +40°C
A relative humidity range of 15% to 90%,
non-condensing, but not requiring a water vapour
partial pressure greater than 50 hPa
An atmospheric pressure range of :
700 hPa to 1060 hPa
Temperature:-20°C to +60°C
A relative humidity range of ≤93%, non-condensing,
at a water vapour pressure up to 50hPa
About 22cm~42cm
The monitor detected
motion or talking
during measuring.

24 25
AUTHORISED COMPONENTS COMPLIED STANDARDS LIST AND EMC GUIDANCE
EN ISO 14971:2012 / ISO 14971:2007 Medical devices -
Application of risk management to medical devices
EN ISO 15223-1:2016 / ISO 15223-1:2016 Medical devices.
Symbols to be used with medical device labels, labelling and
information to be supplied. Part 1 : General requirements
EN 1041:2008+A1:2013 Information supplied by the manufacturer of
medical devices
EN 60601-1-2:2015/ IEC 60601-1-2:2014 Medical electrical
equipment - Part 1-2: General requirements for basic safety and
essential performance - Collateral standard: Electromagnetic
compatibility - Requirements and tests
EN ISO 81060-1:2012 Non-invasive sphygmomanometers - Part 1:
Requirements and test methods for non-automated measurement type
EN 1060-3:1997+A2:2009 Non-invasive sphygmomanometers -
Part 3: Supplementary requirements for electro-mechanical blood
pressure measuring systems
EN 1060-4:2004 Non-invasive sphygmomanometers - Part 4: Test
procedures to determine the overall system accuracy of automated
non-invasive sphygmomanometers
EN 60601-1-6:2010+A1:2015/IEC 60601-1-6:2010+A1:2013
Medical electrical equipment - Part 1-6: General requirements for basic
safety and essential performance - Collateral standard: Usability
IEC 62366-1:2015 Medical devices - Part 1: Application of usability
engineering to medical devices
EN 62304:2006/AC: 2008 / IEC 62304: 2006+A1:2015 Medical device
software - Software life-cycle processes
Risk management
Labeling
User manual
General Requirements
for Safety
Electromagnetic
compatibility
Performance
requirements
Clinical investigation
Usability
Software life-cycle
processes
Bio-compatibility
ISO 10993-1:2009 Biological evaluation of medical devices-
Part 1: Evaluation and testing within a risk management process
ISO 10993-5:2009 Biological evaluation of medical devices -
Part 5: Tests for in vitro cytotoxicity
ISO 10993-10:2010 Biological evaluation of medical devices -
Part 10: Tests for irritation and skin sensitization
IEC 80601-2-30:2018 Medical electrical equipment- Part 2-30:
Particular requirements for the basic safety and essential performance of
automated non-invasive sphygmomanometers
ISO 81060-2:2018 Non-invasive sphygmomanometers - Part 2:
Clinical validation of automated measurement type
EN 60601-1:2006+A1:2013/ IEC 60601-1:2005+A1:2012 Medical
electrical equipment - Part 1: General requirements for basic safety and
essential performance
EN 60601-1-11:2015/ IEC 60601-1-11:2015 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
Complied Standards List
MANUFACTURER INFORMATION
Authorized European Representative:
Manufactured by:
Company:
Address:
Company: Share Info Consultant Service LLC Repräsentanzbüro
Address: Heerdter Lohweg 83, 40549 Düsseldorf
Harvard Medical Devices Ltd. HK
1002, Railway Plaza, TST, HK
Harvard Medical Devices Ltd. HK
Manufacturer Information
RETURN POLICY
Product may be returned if faulty, please contact the Retailer or
Kinetik directly if you're experiencing issues with your product.
This does not affect your statutory rights. Please note the retailer's
own return policy may still be valid, contact the retailer for more
information.
Authorised Components
1. please use the Kinetik authorised adapter. (not included)

2726
COMPLIED STANDARDS LIST AND EMC GUIDANCE
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments
Warning: Don’t near active HF surgical equipment and the RF shielded room of an ME
system for magnetic resonance imaging, where the intensity of EM disturbances is high.
Warning: Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this
equipment and the other equipment should be observed to verify that they are operating
normally.
Warning: Use of accessories, transducers and cables other than those specified or provided
by the manufacturer of this equipment could result in increased electromagnetic emissions
or decreased electromagnetic immunity of this equipment and result in improper operation.”
Warning: Portable RF communications equipment (including peripherals such as antenna
cables and external antennas) should be used no closer than 30 cm (12 inches) to any part
of the equipment WBP2, including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
Technical description:
Table 1
Group 1
Class [B]
Class A
Comply
1. all necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFOR-
MANCE with regard to electromagnetic disturbances for the excepted service life.
2. Guidance and manufacturer’s declaration-electromagnetic emissions and Immunity
RF emissions
CISPR 11
RF emissions
CISPR 11
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Harmonic emissions
IEC 61000-3-2
EMC Guidance
Guidance and manufacturer’s declaration - electromagnetic emissions
Emissions test Compliance
COMPLIED STANDARDS LIST AND EMC GUIDANCE
Immunity Test
±8 kV contact
±2 kV, ±4kV, ±8 kV, ±15 kV air
Table 2
Compliance level
Electrostatic
discharge (ESD)
IEC 61000-4-2
30 A/m
50Hz/60Hz
Power frequency
magnetic field
IEC 61000-4-8
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC61000-4-5
IEC 60601-1-2 Test level
±8 kV contact
±2 kV, ±4kV, ±8 kV,
±15 kV air
Conduced RF
IEC61000-4-6
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
Radiated RF
IEC61000-4-3
±2kV for power supply lines
±1 kV signal input/output
100 kHz repetition frequency
±2 kV for power supply lines
±1 kV signal input/output
100 kHz repetition frequency
±0.5 kV, ±1 kV differential mode
±0.5 kV, ±1 kV, ±2 kV common
mode
±0.5 kV, ±1 kV differential mode
±0.5 kV, ±1 kV, ±2 kV common
mode
0 % UT; 0,5 cycle. At 0°, 45°, 90°,
135°, 180°, 225°, 270° and 315°.
0 % UT; 1 cycle and 70 % UT;
25/30 cycles;
Single phase: at 0°.0 % UT;
250/300 cycle
0 % UT; 0,5 cycle. At 0°, 45°, 90°,
135°, 180°, 225°, 270° and 315°.
0 % UT; 1 cycle and 70 % UT;
25/30 cycles; Single phase: at 0°.
0 % UT; 250/300 cycle
3 V
0,15 MHz – 80 MHz
6 V in ISM and amateur radio
bands between 0,15 MHz and
80 MHz 80 % AM at 1 kHz
3 V
0,15 MHz – 80 MHz
6 V in ISM and amateur radio
bands between 0,15 MHz and
80 MHz 80 % AM at 1 kHz
Guidance and manufacturer’s declaration – electromagnetic Immunity
NOTE U
T
is the a.c. mains voltage prior to application of the test level.
30 A/m
50Hz/60Hz

0197
Share Info Consultant Service LLC Repräsentanzbüro
Heerdter Lohweg 83, 40549 Düsseldorf
Harvard Medical Devices Ltd. HK
1002, Railway Plaza, TST, HK
Manufactured by Harvard Medical Devices Ltd. HK
Made in China
Kinetik WBP2 NZ IB(EN) 20210720
28
COMPLIED STANDARDS LIST AND EMC GUIDANCE
Table 3
385 0.3 27
Band
(MHz)
Service Modulation Modulation
(W)
Distance (m) IMMUNITY
TEST
LEVEL
(V/m)
380-
390
TETRA
400
Pulse
modulation b)
18Hz
1.8
450 430-
470
FM c) ±5kHz
deviation 1kHz
sine
20.3 28
710 704-
787
745
780
LTE Band
13,
17
Pulse
modulation b)
217Hz
0.2 0.3 9
810
870
930
800-
960
GSM
800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse
modulation b)
18Hz
20.3 28
1720
1845
1970
1700-
1990
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1,
3,
4,25; UMTS
Pulse
modulation b)
217Hz
20.3 28
20.3 282450 2400-
2570
Bluetooth,
WLAN,
802.11
b/g/n, RFID
2450, LTE
Band 7
Pulse
modulation
217 Hz
5240
5500
5785
5100-
5800
WLAN
802.11
a/n
Pulse
modulation
217 Hz
0.2 0.3 9
Guidance and manufacturer’s declaration - electromagnetic Immunity
Test
Frequency
(MHz)
GMRS 460,
FRS 460
Radiated RF
IEC61000-4-3
(Test
specifications
for
ENCLOSURE
PORT
IMMUNITY to
RF wireless
communica-
tions
equipment)