Recalling Values from Memory
1. T he monitor has two memory zones (1 and 2). Each zone can store up to 60 measurements.
2. To read memory values from a selected memory zone, use the User-Switching key to
select a memory zone (1 or 2) from which you want to recall values. Press the Memory
key. The first reading displayed is the average of all morning readings from the last 7
3. Continue to press the Memory key to view the average of all nighttime readings from
the last 7 days.
4. Press the Memory key again to view the average of the last 3 measurements stored
in memory, and the last previously stored measurement. Every measurement comes
with an assigned memory sequence number.
Note: The memory bank can store up to 60 readings per memory zone. When the number of readings exceeds 60, the oldest data will be replaced with the new record.
Note: AM is defined as 4:00 AM – 11:59 AM
Note: PM is defined as 6:00 PM – 2:00 AM
Clearing Values from Memory
1. Press the User-Switching key to select memory zone 1 or memory zone 2.
2. Press and hold the Memory key for approximately 5 seconds, then the data in the
memory zone can be erased automatically.
Time and Bluetooth® Adjustment
1. To adjust the date/time/Bluetooth® in the monitor after installing or replacing batteries. The display will show a blinking number showing the year.
2. Change the year by pressing the Memory key, each press will increase the number.
Press the ON/OFF/START key to confirm the entry and the screen will show a blinking
number representing the date.
3. Change the date, the hour and the minute as described in Step 2 above, using the
Memory key to change and the ON/OFF/START key to confirm the entries.
4. After adjusting the date/time, the Bluetooth® symbol ( ) and the blinking icon “
” will be shown on the display simultaneously. Use the Memory key to choose whether automatic Bluetooth® data transfer is activated (Bluetooth® symbol ( )+
) or
deactivated (Bluetooth® symbol ( )+
) and confirm with the ON/OFF/START key.
5. Press the ON/OFF/START key again, “0” will reappear as the Blood Pressure Monitor is
ready for measurement.
Data Transfer via Bluetooth®
Pairing the Blood Pressure Monitor with your
To begin using Bluetooth® for the first time, please visit
the website at for the initial
set-up instructions.
1. Download and install the free APP onto your smartphone.
2. To pair this device with your smartphone, turn on the
device, Bluetooth® and the App of smartphone, and
follow set-up and pairing instructions.
3. The Bluetooth® symbol ( ) will flash on the display
that indicates the pairing is proceeding.
- If the pairing is successful, the Bluetooth® symbol ( ) will stop flashing and appear
on the display, the device will start the measurement automatically. The current
measured reading (Systolic, Diastolic and Pulse) will automatically be transferred to
the App.
- If the pairing has failed, the Bluetooth® symbol ( ) will continue flashing until the
device shuts off automatically after 1 minute. Please re-pair this device with your
Notes: 1. You can pair up to 2 destination devices with the monitor
2. Unpairing your device will not delete the information on the phone App.
3. If you re-pair your smartphone with your blood pressure monitor, all prior reading history stored on the phone App will be retained.
4. Bluetooth® data transfer will reduce the battery capacity.
Data Transfer to PC
Rossmax provides a free, integrated and user-friendly
blood pressure management softBP Manager
which can be downloaded and installed on your computer. You may purchase a
special designed USB cable in order to connect Rossmax’s blood pressure monitor and
your PC. Please visit the website at for proceeding the downloading and installation process.
BP Manager
If any abnormality will arise during use, please check the following points.
Check Points
No display when the
EE mark shown on display or the blood pressure value is displayed
excessively low (high)
Replace them with four new
Have the batteries run down?
Have the batteries' polarities been Re-insert the batteries in the
positioned incorrectly?
correct positions.
Wrap the cuff properly so that
Is the cuff placed correctly?
it is positioned correctly.
Did you talk or move during
Measure again. Keep wrist
Did you vigorously shake the cuff steady during measurement.
during measurement?
Note: If the unit still does not work, return it to your dealer. Under no circumstance should
you disassemble and repair the unit by yourself.
Cautionary Notes
1. T he unit contains high-precision assemblies. Therefore, avoid extreme temperatures, humidity, and direct sunlight. Avoid dropping or strongly shocking the main unit, and protect it from dust.
2. Clean the blood pressure monitor body and the cuff carefully with a slightly damp, soft
cloth. Do not press. Do not wash the cuff or use chemical cleaner on it. Never use thinner,
alcohol or petrol (gasoline) as cleaner.
3. Leaky batteries can damage the unit. Remove the batteries when the unit is not used for
a long time.
4. The unit should not be operated by children so to avoid hazardous situations.
5. If the unit is stored near freezing, allow it to acclimate at room temperature before use.
6. This unit is not field serviceable. You should not use any tool to open the device nor should
you attempt to adjust anything inside the device. If you have any problems, please contact
the store or the doctor from whom you purchased this unit or please contact Rossmax
International Ltd.
7. As a common issue for all blood pressure monitors using the oscillometric measurement
function, the device may have difficulty in determining the proper blood pressure for us120
diagnosed with diabetes, poor circulation of blood, kidney problems, or for users suffered from stroke, or for unconscious users.
8. This unit is able to detect common arrhythmia (atrial or ventricular premature beats or
atrial fibrillation). The ARR, AFib and PC icons are displayed after the measurement if Atrial
Fibrillation and Premature Contraction was detected during the measurement. If ARR,
AFib or PC icons are displayed, you are advised to wait for a while and take another measurement. It is strongly recommended that you consult your physician if the ARR, AFib or
PC icons appear often.
9. While the given device is able to detect specific pulse arrhythmia, the measurement acBP be
curacy of the blood pressure meter may
impaired with the occurrence of pulse arrhythmia.
10. To stop operation at any time, press the ON/OFF/START key, and the air in the cuff will be
rapidly exhausted.
11. Once the inflation reaches 300 mmHg, the unit will start deflating rapidly for safety reasons.
12. Please note that this unit can be a home healthcare product, but it is not intended to
serve as a substitute for the advice of a physician or medical professional.
13. Do not use this device for diagnosis or treatment of any health problem or disease. Measurement results are for reference only. Consult a healthcare professional for interpretation of pressure measurements. Contact your physician if you have or suspect any medical problem. Do not change your medications without the advice of your physician or
healthcare professional.
14. Electromagnetic interference: The device contains sensitive electronic components.
Avoid strong electrical or electromagnetic fields in the direct vicinity of the device (e.g.
mobile telephones, microwave ovens). These may lead to temporary impairment of
measurement accuracy.
15. Dispose of device, batteries, components and accessories according to local regulations.
16. This monitor may not meet its performance specification if stored or used outside temperature and humidity ranges specified in Specifications.
17. Please note that when inflating, the functions of the limb in question may be impaired.
18. During the blood pressure measurement, blood circulation must not be stopped for an
unnecessarily long time. If the device malfunctions, remove the cuff from the arm.
19. Avoid any mechanical restriction, compression or bending of the cuff line.
20. Do not allow sustained pressure in the cuff or frequent measurements. The resulting restriction of the blood flow may cause injury.
21. Ensure that the cuff is not placed on an arm in which the arteries or veins are undergoing
medical treatment, e.g. intravascular access or therapy, or an arteriovenous (AV) shunt.
22. Do not apply the cuff on the side, where a mastectomy has been performed in your
patient history.
23. Do not place the cuff over wounds as this may cause further injury.
24. Only ever use the cuffs provided with the monitor or original replacement cuffs. Otherwise erroneous results will be recorded.
25. Batteries can be fatal if swallowed. You should therefore store the batteries and products
where they are inaccessible to small children. If a battery has been swallowed, call a doctor immediately.
Measurement Method
Measurement Range
Pressure: 30~260 mmHg; Pulse: 40~199 beats/
Pressure Sensor
Semi conductor
Pressure: ± 3 mmHg; Pulse: ± 5% of reading
Pump Driven
Automatic Air Release Valve
Memory capacity
60 memories for each zone x 2 zones
1 minute after last key operation
Permissible Operating Temperature 10°C~40°C (50°F~104°F); 15%~85% RH; 700~1060
and Humidity
Permissible Transport and Storage -10°C~60°C (14°F~140°F); 10%~90% RH; 700~1060
Temperature and Humidity
DC Power Source
DC 6V four AAA Batteries
AC Power Source
DC 6V, ≥600mA (Plug size: outer(-) is Ø4.0, inner(+) is Ø1.7)
96 (L) X 139.7 (W) X 63.2 (H) mm
248.6g (G.W.) (w/o Batteries)
Arm circumference
Adult: 24~40 cm (9.4”~15.7”)
Limited Users
Adult users
Type BF: Device and cuff are designed to provide
special protection against electrical shocks.
IP Classification
IP21: Protection against harmful ingress of water
and particulate matter
*Specifications are subject to change without notice.
EMC guidance and manufacturer’s declaration
Guidance and manufacturer’s declaration-electromagnetic emissions
The X5 is intended for use in the electromagnetic environment specified below. The customer or the user of the X5 should assure that it is used in such an environment.
Emission test
Electromagnetic environment-guidance
RF emissions CISPR 11
Group 1 The X5 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.
RF emissions CISPR 11
Class B
The X5 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.
Harmonic emissions IEC 61000-3-2
Class A
Voltage fluctuations/flicker emissions IEC 61000-3-3 Compliance
Guidance and manufacturer’s declaration-electromagnetic immunity. The X5 is intended for use in the electromagnetic environment specified below. The customer or the user of the
X5 should assure that it is used in such an environment.
Immunity test
IEC 60601 test level
Compliance level
Electromagnetic environment-guidance
Electrostatic discharge (ESD) ± 6 kV contact
± 6 kV contact
Floors should be wood, concrete or ceramic tile. If floors are covered
IEC 61000-4-2
± 8 kV air
± 8 kV air
with synthetic material, the relative humidity should be at least 30%
Electrical fast transient/burst ± 2kV for power supply lines
± 2kV for power supply lines
Mains power quality should be that of a typical commercial or hosIEC 61000-4-4
± 1kV for input / output lines
Not applicable
pital environment.
Surge IEC 61000-4-5
± 1kV line(s) to line(s)
± 1kV differential mode
Mains power quality should be that of a typical commercial or hos± 2kV line(s) to earth
Not applicable
pital environment.
Voltage Dips, short interrup- <5% UT(>95% dip in UT) for 0,5 cycle <5% UT(>95% dip in UT) for 0,5 cycle Mains power quality should be that of a typical commercial or hostions and voltage variations 40% UT(60% dip in UT) for 5 cycles 40% UT(60% dip in UT) for 5 cycles pital environment. If the user of the X5 requires continued operation
on power supply input lines 70% UT(30% dip in UT) for 25 cycles 70% UT(30% dip in UT) for 25 cycles during power mains interruptions, it is recommended that the X5 be
IEC 61000-4-11
<5% UT(>95% dip in UT) for 5 s
<5% UT(>95% dip in UT) for 5 s
powered from an uninterruptible power supply or a battery.
Power frequency (50/60 Hz) 3 A/m
3 A/m
Power frequency magnetic fields should be at levels characteristics of
magnetic field IEC 61000-4-8
a typical location in a typical commercial or hospital environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration-electromagnetic immunity
The X5 is intended for use in the electromagnetic environment specified below. The customer or the user of the X5 should assure that is used in such and environment.
Immunity test IEC 60601 test level Compliance level
Electromagnetic environment-guidance
Portable and mobile RF communications equipment should be used no closer to any part of the X5 including cables, than
the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. RecomConducted RF 3 Vrms
mended separation distance:
IEC 61000-4-6 150 KHz to 80 MHz 3 Vrms
d = 1,2 √P; d = 1,2 √P 80MHz to 800 MHz; d = 2,3 √P 800MHz to 2,5 GHz
Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and
Radiated RF IEC 3 V/m
3 V/m
d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an
61000-4-3 80MHz to 2,5 GHz
electromagnetic site survey, a should be less than the compliance level in each frequency range. b Interference may occur in the
vicinity of equipment marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Model: X5
Data Transfer via
Please download and install the
free APP onto your smartphone
Blood Pressure Monitor
a: F ield strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV
broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the X5 is used exceeds the applicable RF compliance level above, the X5 should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the X5.
b: O ver the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distance between portable and mobile RF communications equipment and the X5
The X5 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the X5 can help prevent electromagnetic
interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the X5 as recommended below, according to the
maximum output power of the communications equipment.
Separation distance according to frequency of transmitter / m
Rated maximum output power
of transmitter / W
150 kHz to 80 MHz / d=1,2√P
80 MHz to 800 MHz / d=1,2√P
800 MHz to 2,5 GHz / d=2,3√P
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the
frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1: A t 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Warranty Card
This instrument is covered by a 5 year guarantee from the date of purchase. The guarantee is valid only on presentation of the warranty card completed or stamped by the
seller/dealer confirming date of purchase or the receipt. Batteries, cuff and accessories
are not included. Opening or altering the instrument invalidates the guarantee. The
guarantee does not cover damage, accidents or non-compliance with the instruction
manual. Please contact your local seller/dealer or
Customer Name: _____________________________________________________
Address: ____________________________________________________________
E-mail address: _______________________________________________________
Female Age: _____
Product Information
Date of purchase: ____________________________________________________
Store where purchased: _______________________________________________
WARNING: The symbol on this product means that it's an electronic product and following the European directive
2012/19/EU the electronic products have to be dispose on your local recycling centre for safe treatment.
- The Bluetooth® word mark and logos are registered trademarks owned by the Bluetooth SIG, Inc. and any use of such marks by Rossmax International Ltd. is under
license. Other trademarks and trade names are those of their respective owners.
- The blood pressure monitor uses Bluetooth®(Bluetooth® low energy technology)
- A pple and the Apple logo are trademarks of Apple Inc., registered in the U.S. and other countries. App Store is a service mark of Apple Inc.
- G oogle Play and the Google Play logo are trademarks of Google Inc.
Rossmax Swiss GmbH,
Tramstrasse 16, CH-9442 Berneck, Switzerland
it can start measurement in the chosen memory zone.
2. Press the ON/OFF/START key. All digits will light up, checking the display functions.
The checking procedure will be completed in 2 seconds.
3. After all symbols appear, the display will show a blinking “0”. The monitor is ready to
measure and will automatically inflate the cuff slowly to start measurement.
4. Bluetooth® will automatically be activated on the device, please see Data Transfer
via Bluetooth®. You can also start measurement directly by pressing the ON/OFF/
START key again, but the current measured reading (Systolic, Diastolic and Pulse) will
not automatically be transferred to the App.
5. When the measurement is completed, the cuff will exhaust the pressure inside. Systolic pressure, diastolic pressure and pulse will be shown simultaneously on the LCD
screen. The measurement is then automatically stored into the pre-designated memory zone.
6. In order to enhance the probability of pulse arrhythmia detection by the PARR
nology, measurement repetitions are recommended.
This monitor will re-inflate automatically to approximately 220 mmHg if the system detects that your body needs more pressure to measure your blood pressure.
Note: 1. This monitor automatically switches off approximately 1 minute after last key
2. To interrupt the measurement, simply press the ON/OFF/START key; the cuff will deflate immediately.
3. During the measurement, do not talk or move your arm or hand muscles.
Blood pressure measurements determined with X5 are equivalent to those obtained by
a trained observer using cuff/stethoscope auscultation method, within the limits prescribed by the American National Standard, Electronic or Automated Sphygmomanometers. This unit is to be used by adult consumers in a home environment. Do not use
this device on infants or neonates. X5 is protected against manufacturing defects by an
established International Warranty Program. For warranty information, you can contact
the manufacturer, Rossmax International Ltd.
Attention: Consult the accompanying documents. Please read this manual carefully before use. For specific information on your own blood pressure, contact
your physician. Please be sure to keep this manual.
Note: It is strongly recommended, that you consult your physician, if either the ARR icon occurs
newly for several times, or, if your ARR is known to your doctor, but the incidence of ARR
readings changes over time. This is independent whether the ARR icon is specified by another pulse arrhythmia icon or not. Your doctor will then be able to provide all required
medical test and possible therapeutic procedures.
The PARR technology is able to detect and display combined pulse arrhythmia findings.
Normal finding
Pulse Arrhythmia without type-specific detection
Pulse Arrhythmia-Premature ventricular, atrial or nodal beat detection
Pulse Arrhythmia-Atrial fibrillation detection
Combined Pulse Arrhythmia: Atrial fibrillation & Premature beats detection
PARR(Pulse Arrhythmia) Technology
Real Fuzzy Measuring Technology
Pulse Arrhythmia (PARR) technology specifically detects the existence of pulse arrhythmia, including atrial fibrillation (AF, AFib), Atrial and / or Ventricular Premature Contractions (PC). Pulse Arrhythmia may be related to cardiac disorders, needs medical attention and thus early diagnosis is of paramount importance. The PARR technology detects
arrhythmia during regular blood pressure checks without any additional user skills, user
interaction and measurement prolongation. Beside the blood pressure diagnosis a specific pulse arrhythmia diagnosis is provided with PARR.
Note: The PARR detection of AFib and PC is provided with a clinically proven high detection probability [1]. However, the sensitivity and specificity is limited, thus most,
but not all pulse arrhythmia will be detected and displayed. In certain patients
with uncommon clinical conditions the PARR technology may not be able to detect pulse arrhythmia. This partly comes from the fact that some arrhythmia can
only be found with an ECG diagnosis, but not with a pulse diagnosis. Thus PARR
is not meant to replace any medical ECG diagnosis by your doctor. PARR provides
an early detection of certain pulse arrhythmia, which inevitably need to be presented to your doctor in charge.
Remark: [1] Clinical Investigation of PARR - A new Oscillometric Pulse Arrhythmia Type
Discriminating Detection Technology.
This unit uses the oscillometric method to detect your blood pressure. Before the cuff
starts inflating, the device will establish a baseline cuff pressure equivalent to the air pressure. This unit will automatically determine the appropriate inflation level based on pressure oscillations, followed by cuff deflation.
During the deflation, the device will detect the amplitude and slope of the pressure oscillations and thereby determine your actual the systolic blood pressure, diastolic blood
pressure, and pulse rate.
Atrial Fibrillation Detection (AFib)
The upper chambers of the heart (the atria) do not contract, but quiver and thus blood
is driven irregularly and with lower efficiency into the ventricles. Subsequently irregular
heartbeats occurs, which mostly are associated with a fast, yet highly instable heart rate.
This condition is associated with a higher risk for the formation of cardiac blood clots.
Amongst others, they may elevate the risk of brain strokes. Beside this atrial fibrillation
may contribute to the severity of a chronic or acute heart failure condition and may be
associated with other heart-related complications. Age dependent, about 10 %- 20 %
percent of patients who suffer from an ischemic stroke also suffer from atrial fibrillation.
Atrial fibrillation most often initially occurs with temporary periods of arrhythmia and
may progress to a permanent state of this disorder in the course of time. No matter,
whether you intent to safeguard yourself from an undetected AFib state, or you measure during an ongoing period of active atrial fibrillation, or you measure in between periods of AFib, the PARR technology can be applied at any of these conditions. This unit
) are displayed
is able to detect Atrial fibrillation (AFib). The ARR and AFib icons (
right after the measurement if Atrial Fibrillation was detected.
Note: It is strongly recommended, that you consult your physician, if either the AFib icon
occurs newly for several times, or, if your AFib is known to your doctor, but the
incidence of AFib readings changes over time. Your doctor will then be able to
provide all required medical test and possible therapeutic procedures.
Note: T he presence of a cardiac pacemaker may impair the AFib detection by PARR.
Preliminary Remarks
This Blood Pressure Monitor complies with the European regulations and bears the CE
mark “CE 0120”. The quality of the device has been verified and conforms to the provisions of the EC council directive 93/42/EEC (Medical Device Directive), Annex I essential
requirements and applied harmonized standards.
EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanometers - Part 1 - General requirements
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.
This blood pressure monitor was designed for long service periods. In order to ensure
continued accuracy, it’s recommended that all digital blood pressure monitors require
re-calibration. This monitor (under normal usage with approx. 3 measurements a day)
does not require re-calibration for 2 years. Once the unit should be re-calibrated the device will display . The unit should also be re-calibrated if the monitor sustains damage
due to blunt force (such as dropping) or exposure to fluids and / or extreme hot or cold
temperature / humidity changes. When
appears, simply return your device to your
nearest dealer for re-calibration service.
Blood Pressure Standard
Refer to the definitions of the World Health Organization, the blood pressure ranges
can be classified into 6 grades. (Ref. 1999 WHO-International Society of Hypertension
Guidelines for the management of Hypertension). This blood pressure classification are
based on statistical data, and may not be directly applicable to any particular patient. It
is important that you consult with your physician regularly. Your physician will tell you
your normal blood pressure range as well as the point at which you will be considered
at risk. For reliable monitoring and reference of your blood pressure, keeping long-term
records is recommended. Please download the blood pressure log at our website www.
Blood Pressure Standard World Health Organization (WHO) : 1999
Premature Contraction Detection (PC)
Extra abnormal heartbeats generated in irregular excitation sites of your heart, either in
the atria (PAC), the ventricle (PVC) or the cardiac conduction nodes (PNC). These extra
beats may disrupt your regular rhythm, they may come in early or cause a significant
pauses regarding your perceivable pulse. This is called palpitations, which can be felt in
your chest. They may occur as isolated, single events, as a series of irregular pulses or can
be distributed all over your pulse beats. If they are not related to mental stress, or acute
demanding physical load, they may be a marker for a multitude of cardiac disorders.
Some of these disorders go along with an elevated risk profile for ischemic events, either
in the heart (e,g, coronary heart disease) or outside the heart, e.g. an elevated risk for a
stroke. Some PCs may indicate on valvular or myocardial disorders and become very
important if a myocarditis (infection of the heart muscle) is suspected. This unit is able
to detect premature contractions (
). The ARR and PC icons are displayed right after
the measurement if premature contractions have been detected.
Note: It is strongly recommended, that you consult your physician, if either the PC icon
occurs newly for several times, or, if your PC is known to your doctor, but the incidence of PC readings changes over time. Your doctor will then be able to provide
all required medical test and possible therapeutic procedures.
Systolic Pressure
Grade 1 hypertension (mild)
Grade 2 hypertension (moderate)
Grade 3 hypertension
Name/Function of Each Part
Pulse Arrhythmia Detection (ARR)
Once the occurrence of pulse arrhythmia has been detected in the course of your blood pressure measurement, the icon ARR is displayed. In the case, that the found pulse arrhythmia
can be specified by the PARR technology, the ARR icon is accompanied by the specifically
detected type of arrhythmia, e.g. PC or AFib. Once the kind of found pulse arrhythmia cannot
be safely determined by PARR, the device is displaying ARR without any additional pulse arrhythmia type icon.
Diastolic Pressure
1. Arm Cuff
2. LCD Display
3. Air Tube and
4. Memory Key
6. User-Switching key
7. Battery Cover
8. Data Link Socket
9. AC Adaptor Jack
10. Cuff Holder Design
Name/Function of Each Part
1. Arrhythmia Detection (ARR)
2. A
trial Fibrillation Detection (AFib)
3. P
remature Contraction Detection (PC)
4. Date/Time Indication
5. Weak Battery Mark
6. Movement Mark
7. Loose Cuff Detection
8. H
ypertension Risk Indication
9. M
orning and Nighttime Mark
10. Memory/Date Mark
11. Memory Average Mark
12. Bluetooth® Mark
13. Systolic Pressure
14. Diastolic Pressure
15. Pulse Rate
16. Pulse Mark
17. M
emory Zone
Loose Cuff Detection
If the cuff was applied too loosely, it may cause unreliable measurement results or measurements can fail to start. The “Loose Cuff Detection” can help to determine if the cuff is
appears once a “loosen cuff” has been
wrapped snugly enough. The specified icon
appears if the cuff is
detected during measurement. Otherwise the specified icon
wrapped correctly during measurement.
Movement Detection
The “Movement Detection” helps reminding the user to remain still and is indicating any
adverse body movement during measurement. The specified icon appears once a “body
movement” has been detected during and after such a measurement.
Note: It’s highly recommended that you measure again if the icon
Guest Mode
4. Use only the authorized AC Adaptor with this blood pressure monitor. Information for
the authorized AC adaptor, please refer to APPENDIX 1.
Installing Batteries
1. Press down and lift the battery cover in the direction of the arrow to open the battery
2. Install or replace 4 “AAA” sized batteries in the battery compartment according to the
indications inside the compartment.
3. Replace the battery cover by clicking in the bottom hooks first, then push in the top
end of the battery cover.
4. Replace the batteries in pairs. Remove batteries when unit is not in use for extended
periods of time.
You need to replace the batteries when
1. low battery icon appears on display.
2. the ON/OFF/START key is pressed and nothing appears on display.
1. Batteries are hazardous waste. Do not dispose them together with the household
2. There are no user serviceable parts inside. Batteries or damage from old batteries are
not covered by warranty.
3. Use exclusively brand batteries. Always replace with new batteries together. Use batteries of the same brand and same type.
Applying the Cuff
1. Unwrap the arm cuff, leaving the end of the cuff through the D-ring of the cuff.
2. Put your left arm through the cuff loop. The color strip indication should be positioned closer to you with the tube pointing in the direction of your arm (Fig. ). Turn
your left palm upward and place the edge of the arm cuff at approximately 1.5 to 2.5
cm above the inner side of the elbow joint (Fig. ). Tighten the cuff by pulling the
end of the cuff.
3. Center the tube over the middle of the arm. Press the hook and loop material together securely. Allow room for 2 fingers to fit between the cuff and your arm. Position
the artery mark (Ø) over the main artery (on the inside of your arm) (Fig. ,). 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.
4. P
lug in the cuff connecting tube into the unit (Fig. ).
5. Lay your arm on a table (palm upward) so the cuff is at the same height as your heart.
Make sure the tube is not kinked (Fig. ).
6. This cuff is suitable for your use if the arrow falls within the solid color line as shown on
the right (Fig. ). If the arrow falls outside the solid color line, you will need a cuff with
other circumferences. Contact your local dealer for additional size cuffs.
This monitor has a non-stored single measurement function. Press the User-Switching
, and follow the Measurement Procedure to
key to select the memory zone of guest
take a measurement correctly. When the measurement is completed, the measurement
value will not be stored in memory zone.
Hypertension Risk Indication (HRI)
The World Health Organization, classifying blood pressure ranges into 6 grades. This unit
is equipped with an innovative blood pressure risk indication, which visually indicates
the assumed risk level (optimal / normal / high-normal/ grade1 hypertension / grade 2
hypertension / grade 3 hypertension) of your result, making the meaning of your findings comprehensive.
Error Codes for your reference
EE / Measurement Error: Make sure the L-plug is securely connected to the air socket
and calmly measure again. Wrap the cuff correctly around your arm and keep arm steady
during measurement. If the error keeps occurring, return the device to your local distributor or service centre.
E1 / Air Circuit Abnormality: Make sure the L-Plug is securely connected to the air
socket on the side of the unit and calmly measure again. If the errors still occur, return the
device to your local distributor or service centre for help.
E2 / Pressure Exceeding 300 mmHg: Switch the unit off and measure again quietly.
If the error keeps occurring, return the device to your local distributor or service centre.
E3 / Data Error: Remove the batteries, wait for 60 seconds, and reload. If the error keeps
occurring, return the device to your local distributor or service centre.
Er / Exceeding Measurement Range: Measure again quietly. If the error keeps occurring, return the device to your local distributor or service centre.
Using the AC Adaptor (Optional)
1.Connect the AC adaptor with the AC adaptor jack on the right side of the unit.
2.Plug the AC adaptor into the socket. (AC adaptors with required voltage and current
indicated near the AC adaptor jack.)
1. Please unload the batteries when operating with the AC mode for a longer period
of time . Leaving the batteries in the compartment for a long time may cause leakage,
which may lead to damage of the unit.
2. No batteries are needed when operating with the AC mode.
3. AC adaptors are optional. Please contact the distributor for the compatible AC adaptors.
Center tube over
middle of arm
Measurement Procedures
Here are a few helpful tips to help you obtain more accurate readings:
• Blood pressure changes with every heartbeat and is in constant fluctuation throughout the day.
• Blood pressure recording can be affected by the position of the user, his or her physiological condition and other factors. For greatest accuracy, wait one hour after exercising, bathing, eating, drinking beverages with alcohol or caffeine, or smoking to measure blood pressure.
• Before measurement, it’s suggested that you sit quietly for at least 5 minutes as measurement taken during a relaxed state will have greater accuracy. You should not be
physically tired or exhausted while taking a measurement.
• Do not take measurements if you are under stress or tension.
• During measurement, do not talk or move your arm or hand muscles.
• Take your blood pressure at normal body temperature. If you are feeling cold or hot,
wait a while before taking a measurement.
• If the monitor is stored at very low temperature (near freezing), have it placed at a
warm location for at least one hour before using it.
• Wait 5 minutes before taking the next measurement.
1. Press the User-Switching key to select memory zone 1, memory zone 2 or guest mode.
After a memory zone is selected, press the ON/OFF/START key to reset the monitor so
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