Polygreen KP-6650 User manual

Automatic Arm Type
Blood Pressure Monitor
KP-6650
INSTRUCTION MANUAL
Precautions for Use..................................................1
Product Description and Intended Use.....................3
About Blood Pressure...............................................3
Device and Display Overview....................................5
Explanation of Symbols............................................5
Battery Installation..............................................7
Setting the Clock.....................................................7
Attaching the Cuff and Measuring Posture...............7
Taking a Measurement............................................8
Memory Function....................................................8
Care and Maintenance...........................................9
Clean / Disinfection.................................................9
Troubleshooting....................................................10
Product Specifications...........................................10
Compliance Statement ...........................................11
Warranty Information..............................................12
Table of Contents
Manufacturer:
K-Jump Health Co., Ltd.
No. 56, Wu Kung 5th Rd. , New Taipei
Industrial Park, New Taipei City 24890, Taiwan
www.kjump.com
EU Authorized Representative:
Polygreen Germany GmbH
Ruhlsdorfer Straβe 95, D-14532, Stahnsdorf,
Germany
[phone]

1 2
17.I f y ou suff e r f r o m a c ardio v as cula r d i s ea se ( su c h a s
atherosclerosis), diabetes, a liver or kidney disease, severe
hypertension or peripheral circulatory disorders, etc., please
consult your doctor before using this unit.
18.The performance of this device can be influenced as severe
arrhythmias such as atrial or ventricular premature beats or atrial
19.The blood pressure measurements conducted with this unit are
equivalent to measurements obtained by a trained observer in
accordance with the values achieved using the cuff/stethoscope
auscultation method and are within the specified EN 1060-4
standard limits.
20.Do not use this appliance on infants, children or persons who
cannot express their own intentions.
21.Measuring too frequently may result in circulatory disorders, which
can cause unpleasant sensations such as localized bleeding under
the skin or temporary numbness in your arm. These symptoms
do not usually last long. However, if you have not recovered after
some time, please consult your doctor.
22.To avoid accidental strangulation, keep the product away from
children and do not place the hose around the neck.
23.Please take into consideration the electromagnetic compatibility
of the unit (e.g. disruptions to the power supply, radio frequency
interference, etc.) Please only use the unit indoors. To avoid
inaccurate results due to electromagnetic interference between
electrical and electronic equipment, please do not use the unit
near mobile phones or microwave ovens. In the case of devices
whose maximum power exceeds 2 W, the minimum distance from
your blood pressure monitor should be 3.3 meters.
24.The unit is not waterproof. Never immerse this instrument in any
liquids.
25.Do not use the instrument if you think it is damaged or if you notice
anything unusual.
26.Any known restrictions on use or contra-indication(s): Consult your
doctor prior to using in pregnancy or if diagnosed with arrhythmia
or arteriosclerosis.
27.Do not modify this device or cuff without authorization of the
manufacturer.
Precau t ions fo r U se
※WARNINGS:
1. Avoid prolonged over-inflation of the bladder to prevent harmful
physical injury.
2. If the cuff causes any discomfort during measurement, press the
POWER button to turn off the device immediately.
3. Pull off the Velcro strap to detach the cuff if the cuff pressure
exceeds 300mmHg without an automatic rapid exhaust.
4. Keep blood pressure monitor away from children to avoid misusing.
Children should not use the device without the supervision of an
adult.
5. This manual and the product are not substitutes for visiting the
doctor. Neither the information contained herein nor this product
may be used to diagnose or treat health problems, or to prescribe
drugs. If you have or suspect that you have a medical problem,
please seek immediate advice from your doctor.
6. Do not conduct any measurements if the temperature is low (below
+5 °C) or high (over +40 °C), or if the relative humidity is beyond
the range of 15 % to 90 %, as this can lead to inaccurate readings.
7. Wait 30 to 45 minutes, before taking a measurement if you have
just had a caffeinated drink or a cigarette.
8. Relax for at least 5 to 10 minutes before taking a measurement.
9. Please wait 3 to 5 minutes between measurements, so that
your blood vessels can return to the state they were in prior to
measurement. You may have to adapt the waiting time to your
personal physiology.
10.It is recommended that you use the same arm for each
measurement (preferably the left) and take the measurement at
about the same time every day.
11.Sit down comfortably with your elbows placed on the table and
both feet on the ground. Please do not interlock your legs during
the measurement.
12.Place the unit at the level of the heart. Relax your hand. Your palm
should be facing up.
13.Take the measurement at room temperature in a quiet and stress-
free environment.
14.The unit should not be moved or shaken during the measurement.
Please do not speak during the measurement.
15.Please keep in mind that blood pressure naturally varies
depending on the time of day and is affected by many different
factors. Blood pressure is usually highest at work and reaches its
lowest level during the sleep phase.
16.Blood pressure measurements should be assessed by a doctor or
trained healthcare professional who is familiar with your medical
history. If you use the unit and regularly record the results, please
keep your doctor informed with regard to the ongoing changes in
your blood pressure.
28. FCC § 15.21 Information to user.
The users manual or instruction manual for an intentional or uninten-
tional radiator shall caution the user that changes or modifications not
expressly approved by the party responsible for compliance could
void the user's authority to operate the equipment. In cases where the
manual is provided only in a form other than paper, such as on a
computer disk or over the Internet, the information required by this
section may be included in the manual in that alternative form, provid-
ed the user can reasonably be expected to have the capability to
access information in that form.

3 4
4. Do not press the measurement icon from application software
either if the cuff has not been properly wrapped.
5. For long-term storage, be sure to place the device at a proper
environment and make sure to recharge the battery regularly
every 3-6 month in order to prevent the damage caused by deep
discharge.
6. Do not use the unit when charging battery.
7. The accuracy of the blood pressure monitor is recommended to be
inspection/calibration service.
Product Descri p tion and In t ended Use
The Blood Pressure Monitor is an electronic device intended to make
human blood pressure and pulse rate at upper arm of adult population
utilizing non-invasive oscillometric method in household environment.
The BPM for measuring human blood pressure and pulse rate with
the following characteristics:
* The users: the device can be used by adults.
* To be used in room temperature.
* To be used (Installed) by the user, with the exception of
handicapped persons.
* Handicapped persons need assistance by another person to use
the device.
* Contact type: skin contact
About Blood P ress ure
●What is blood pressure?
artery walls after the heart ejects blood into vessel system.
●What are systolic and diastolic pressures?
Systolic pressure represents the highest pressure during heart
contraction and diastolic pressure is the lowest pressure while
heart is resting.
●What is MOMI?
MOMI (Measurement on Multiple Intelligence) is a new blood-
pressure-measuring technology. MOMI, unlike the general
then output a weighted value.
You can select this function by adjusting the "dU."
Your blood pressure measurement can be compared with
– International Society of Hypertension Guidelines for Management
of Hypertension for preliminary evaluation. Please consult your
physician for interpretation of blood pressure measurement and
follow their directions.
●What about low blood pressure?
In general, lower blood pressure reading is better unless it causes
some uncomfortable symptoms such as fainting and/or light
headedness.
● Fluctuation and variation of blood pressure
24 hours a day. Blood pressure measurement can be affected by
the measurement position, posture, physiologic condition as well
as factors such as eating, bathing, exercising, smoking, drinking
alcohol, stress, mental tension, breathing, conversation, movement,
temperature or humidity change, etc.
● How to obtain reliable measurements?
In order to obtain reliable measurements, please follow
recommendations below:
1. Keep taking and recording blood pressure measurement at the
same time every day for consistency to establish your blood
pressure pattern.
2. Avoid eating, bathing, smoking, exercising, or ingest caffeine and
alcohol at least 30 minutes prior to take measurement.
3. Remove constricting clothing or ornaments from your arm and
make sure that the range of cuff circumference is applicable to
you.
Indicates a potentially hazardous situation which, if not avoided,
could result in death or serious injury.
※CAUTIONS:
1. Read and follow the entire instruction manual before operating
blood pressure monitor.
2. Do not press the POWER button on blood pressure monitor if the
cuff has not been properly wrapped.
3. The malfunctions of display can be determined by pressing and
holding the POWER button under power-off mode.

5 6
Device and Display O vervi ew
This retail product includes device, cuff, batteries, instruction manual
and a storage bag or case. Micro USB cable is optional.
Explan ation o f Symbols
SYS Systolic Pressure
DIA Diastolic Pressure
Direct Current
Type BF Applied Part
Caution & Attention, consult accompanying documents
MMYY Lot Number composed by month(M) and year(Y) of
manufacture.
Manufacturer
Serial Number
Authorized Representative in the European
Community
Irregular Pulse Detection
Atrial Fibrilation
Change all batteries
Keep dry
Do not dispose of the device and batteries with
household waste.
Follow operating instructions
Pumping
Pumping failure
Excessive body movement is detected during
measurement.
SYS and DIA readings detected are not reasonable.
Cuff pressure is over 300 mmHg.
Interference may occur in the vicinity of equipment
Temperature Limit
Humidity Limitation
Battery recycling symbol
Restriction of Hazardous Substances
The CE marking with the Registration Number of
European Medical Directive 93/42/EEC.
REACH symbol- Registration, Evaluation,
Authorisation and Restriction of Chemicals (REACH)
is a European Union regulation.
Power "ON" / "OFF"
4. Be seated and relax for at least 5 minutes in a quiet and
comfortable place prior to take measurement
5. To make repeated measurements, the rest interval between
measurements shall be no less than 30 sec and the rest interval
may need to be extended according to individual physiological
conditions.

7 8
Battery Installation
1. Remove the battery cover and insert three AAA alkaline batteries
into the battery compartment with polarities “+” and “-“ are matched
with correct polarity indicator. Replace the battery cover.
2. Using only same type of alkaline batteries is recommended to
avoid incompatibility.
3. If the low battery indicator appears frequently, replace all batteries
at the same time.
4. Built-in clock may need to be reset and reading memories may be
erased after battery replacement.
Setting the Clock
1. To have correct date and time for memory storage, the built-in
clock needs to be set prior to start rst measurement.
2. Under power-off mode, press and hold the MEMORY button until
the display shows a blinking year and press the POWER button for
adjustment. After current year is selected, set the year by pressing
the MEMORY button and switch to next adjustment.
3. Repeat previous steps to adjust and set current month, day, hour,
and minute one by one while they are blinking.
4. Following the date and time setting, the clock display function can
be set by pressing POWER button for adjusting ON/ OFF in “CL”
show status and conrmed by MEMORY button.
5. Following clock function enabled, the alarm function can be set
by pressing POWER button for adjusting ON/ OFF in “AL1” show
status. Conrmed ON by MEMORY button and adjusted Hour by
POWER button and then same procedure set for minute.
6. As last, press MEMORY button again to nish setting.
Attaching the Cuff and Measuring Posture
1. Make sure the circumference of your upper arm is within applicable
cuff range.
2. Plug the tube connector into the cuff socket securely.
3. Put bare-skinned left arm through the cuff with tube located
at middle of your inner arm and aligned to your middle finger.
Measuring with thin clothing is allowed.
4. Fasten the cuff with its bottom edge should be approximately 2~3
cm above your elbow and make sure it is not wrapped too tight.
5. Sit upright in a chair with your feet at on the oor and relax in a
natural position.
6. Steadily rest your forearm on a table and make sure the cuff is at
heart level.
7. Hold still and do not talk during measurement.
8. If it is not possible to take measurement with left arm, use right arm
instead.
Taking a Measurement
1. Press the USER button to choose user number for memory
storage. User selection can also be made by pressing the
USER button while readings are displayed after measurement is
completed.
2. Press the POWER button to start automatic measurement. The
measurement can be interrupted anytime by pressing the POWER
button again.
3. Select preferred measuring mode MOMI or Fuzzy Logic by using
the Mode Switch.
4. Press the POWER button to start automatic measurement. The
measurement can be interrupted anytime by pressing the POWER
button again.
5. When the measurement is completed, the systolic pressure,
diastolic pressure and pulse rate will be displayed.
6. The display will also indicate which category your blood pressure
reading belongs to according to classification defined in 1999
WHO-ISH Guidelines for Management of Hypertension.
7. IPD (Irregular Pulse Detection): The device can detect irregular
pulse which is dened as a pulse interval is longer than 5/3 times
the average pulse interval during measurement.
The IPD indicator will appear when more than three irregular pulses
were detected during measurement.
8. The device can detect A-fib (Atrial Fibrillation), which is also a
type of arrhythmia as IPD, but A-b detects different scale of the
irregularity of pulse time interval. If the A-b indicator is displayed
with measurement readings frequently, please consult a qualied
Physician for further directions.
9. The device also provides the PP(Pulse Pressure) function that is
equal to systolic minus diastolic. If systolic is higher than diastolic
60 mmHg, LCD will display “PP” and differentiation value. If PP
indicator is displayed with measurement readings frequently,
please consult a qualied physician for further directions.
10. Press the POWER button to turn off the device or it will turn off
automatically after 150 seconds non-operation. Readings will be
saved into memory automatically while power-off.
Memory Function
1. Press the USER button to select desired user number for recalling
memories.
2. Press the MEMORY button to recall the last reading stored in the
memory.
3. Next set of previous readings can be recalled by pressing the
MEMORY button repetitively.
4. To delete a reading from the memory: repeat step 1-3 and select
a reading which need to be deleted. Press and hold the POWER

910
Troubleshooting
Pumping failure. Refasten the cuff.
The upper edge of cuff should be approximately
1~2 cm away from your palm line.Excessive body movement is detected during
measurement. Refasten the cuff and measure
again.
No sufcient pulses are detected for measurement.
Refasten the cuff and measure again.
Detected SYS and DIA readings are not reasonable
may due to too much interference around. Do not
keep the unit close to mobile phones or microwave
ovens. Refasten the cuff and measure again.
The pumping pressure is over 300 mmHg. The
cuff might be blocked due to improper wrapping.
Refasten the cuff and measure again.
Change all batteries.
Product Specifications
Measuring Range Pressure: 20~300 mmHg
Pulse Rate: 40~200 pulse/min
Accuracy Pressure: ± 3 mmHg
Pulse Rate: ± 5 % of reading
Measuring Method Oscillometric method
Ination Method Electrical rolling pump
Deation Method Mechanical release valve
Rapid Exhaust Electrical solenoid valve
Display Digital liquid crystal display
Memory 2x100 sets
Operation Condition 5 ~ 40 ˚C (41 ~ 104˚F), 15 ~ 90 % RH
Storage condition -20 ~ 55 ˚C (-4 ~ 131˚F) , < 93 % RH
button for at least 3 seconds until “dEL” with the memory number
appear, and press the POWER button again to delete the selected
reading.
5. To erase all readings in memory, please finish above 1~3 steps
first. Press and hold the POWER button under memory mode
until the display shows "dEL" and press the MEMORY button to
show “dEL ALL” on the display. Then press the POWER button, all
readings in memory are erased after three beeps are sound.
6. As last, press POWER button to exit memory function.Care and Maintenance
1. Do not drop the device. It is not shock proof.
2. Do not disassemble or modify the device and cuff.
3. Do not twist the cuff or fully bend the tube.
4. Do not store the device and cuff in environments with direct
sunlight, high temperature or moisture, and severe dust.
5. Do not use thinner, benzene, and other harsh cleaners to clean the
device (exclude alcohol).
6. Do not wash or immerse the cuff.
7. Remove all batteries if the device is not likely to be used for a long
period of time.
8. For long-term storage, be sure to place the device at a proper
environment and make sure to recharge the battery regularly
every 3-6 month in order to prevent the damage caused by deep
discharge.
Clean / Disinfection
Cleaning process:
1. Use a cloth moistened with water or neutral detergent to clean the
device, with a solution of 5-10% mild detergent.
2. The cleaning operation with cold water to avoid the chemical
residues remaining on the device.
3. If necessary, repeat step 1 to step 2 in order to make sure the
device was clean.
4. A final wipe down by a clean wiper is necessary to avoid water
stains.
Disinfection process:
1. To disinfect the device when completed the cleaning process.
2. Use 70 to 75% alcohol; Put alcohol into a spray bottle and spray
both sides of the cuff with it.
Drying process:
1. After cleaning and disinfection process.
2. Put the device to air-dry in the room temperature.

11 12
2) For portable operation, this device has been tested and meets
FCC RF exposure guidelines. When used with an accessory that
contains metal may not ensure compliance with FCC RF exposure
guidelines.
Warranty Info rmation
Warranty:
The device itself (battery and accessories excluded) comes with a
year warranty if it is operated under normal circumstances without
evidence of tampering. See exclusions below.
Warranty exclusions:
1. If user does not properly operate the device according to the
instructions as described in this manual.
2.
3. Improper handing, such as dropping, liquid or cleaner damage.
4. Natural disasters (such as fire, flood, earthquake and thunder
strike).
5. If you do not have a receipt or proof of purchase showing date of
purchase.
IP20 (Protection against solid foreign objects
> 12.5mm Ø and no water-proof test)
Power Source AAA alkaline battery x 3
Battery Life Around 250 (for New Battery) measurements
Power Saving Auto-off after 150 sec non-operation
Size 152 x 97 x 27.2 mm
Weight Approx. 224 g including batteries
Cuff Range 20~35 cm
Complian ce Statemen t
●This device complies with Part 15 of the FCC Rules.
Operation is subject to the following two conditions:
1) this device may not cause harmful interference and
gnidulcni,deviecerecnerefretniynatpeccatsumecivedsiht)2
interference that may cause undesired operation.
●Federal Communications Commission (FCC) Statement
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 RF Radiation Exposure Statement:
1) This Transmitter must not be co-located or operating in conjunction
with any other antenna or transmitter. REV.20220610 PN.826650XXXX