www
Instruction Manual
EN
Model: MW821 f
The National High Blood Pressure Education Pr
Committee has developed a blood pressure standar
pressure ranges into 4 stages. (Ref. The Sev-
enth Report of the Joint National Committee
on Prevention, Detection, Evaluation, and
T
Report JNC-7, 2003).This blood pressure
classification are based on historical data,
and may not be directly applicable to any
particular patient. It is important that you
consult with your physician regularly
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 blood pr
keeping long- term records is r
Please download the blood pressure log at
www
Attention: Consult the accompanying documents. Please read this
manual carefully
own blood pressure, contact your physician. Please be sure
to keep this manual.
Blood pressure measurements determined with MW821f 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. MW821f is protected against manufacturing defects by an
established International Warranty Program. For warranty information,
you can contact the manufacturer, Rossmax International Ltd.
1. Introduction
3. Real Fuzzy Measuring Technology
4. Preliminary Remarks
This unit uses the oscillometric method to detect your blood pressure. Be-
fore the -
sure equivalent to the air pressure. This unit will determine the appropriate
ination level based on pressure oscillations, followed by cuff deation.
During the deation, the device will detect the amplitude and slope of
the pressure oscillations and thereby determine for you the systolic blood
pressure, diastolic blood pressure, and pulse.
This Blood Pressure Monitor complies with the European regulations and
bears the CE mark “CE 0120”. The quality of the device has been veri-
ed 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 - -
sure measuring systems
EN 1060-4: 2004 Non-invasive sphygmomanometers
- Part
mated non-invasive sphygmomanometers.
This blood pressure monitor was designed for long service time. To en-
sure continued accuracy, it’s recommended that all digital blood pressure
monitors require re-calibration. This monitor (under normal usage with
approx. 3 -
tion 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 uids and /
temperature / humidity changes. When appears, simply
return to your nearest dealer for re-calibration service.
7. Display Explanations
Blood pressure -
tuates all the time!
You should not be
overly worried if you
encountered two or
three measurements
at high levels. Blood
pressure changes over
the month and even
throughout the day.
It is also inuenced
by season and tem-
perature.
5. Blood Pressure Standard
6. Blood Pressure Fluctuation 11. Installing Batteries
11. Using the Talking Function
1.
the direction of the arrow to open the
battery compartment.
2.
in the battery compartment according
to the indications inside the compart-
ment.
3. the battery cover by clicking
in the bottom hooks rst, then
the top end of the battery cover.
4.
extended periods of time.
You need to replace the batteries when
1.
2.
Caution
1.
hold garbage.
2.
teries are not covered by warranty.
3.
Use batteries of the same brand and same type.
1.
Selection key labelled with an “L” and located on
the back of the unit.
•”L1” will appear on the display for English.
•”L2” will appear on the display for Spanish.
2.
Speaker ON/OFF key located on the front of the unit.
2. Name/Function of Each Part
1.
of the cuff.
2.
should be positioned closer to you with the tube pointing in the direc-
tion of your arm (Fig. 1). T
edge
side of the elbow joint (Fig. 2). Tighten the cuff by pulling the end of
the cuff.
3.
material together securely
cuff and your arm. Position the artery mark (Ø) over the main artery (on
the inside
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
The National High Blood Pressure Educa-
tion Program Coordinating Committee
has developed a blood pressure stand-
ard, classifying blood pressure ranges
into 4 stages. This unit is equipped with
innovative blood pressure risk indicator,
which visually indicates the assumed risk
level (prehypertension / stage 1 hyper-
tension / stage 2 hypertension) of the
result after each measurement.
This unit is equipped with an Irregular Heart-
beat Detector (IHB) which allows those who
have an irregular heartbeat to obtain accurate
measurements alerting the user of the pres-
ence of an irregular heart beat during the
measurement.
Note:
consult your physician if the IHB icon
() appears often.
12. Applying the Cuff
8. Hypertension Risk Indicator
9. Irregular Heartbeat Detector (IHB)
1. Hypertension Risk Indicator
2. Memory Zones
3. Speaker Mark
4. Memory Average
5. Weak Battery Mark
6. Date/Time Indicator
7. Irregular Heartbeat (IHB) Detector
8. Systolic Pressure
9. Diastolic Pressure
10. Pulse Rate
11. Pulse Mark
Fig.1
Fig.3
Fig.2
Fig.4
Fig.5
Fig.7
Fig.6
4“AA”(R06) size,
1.5V batteries.
1.
er jack in the back of the unit.
2.
adapters with required voltage and current
indicated near the AC adapter jack.)
Caution:
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.
3. optional.
the compatible AC adapters.
4.
monitor. Information for the authorized AC adaptor, please
refer to APPENDIX 1.
10. Using the AC Adapter (Optional)
AC Adapter
(Ø4.0/Ø1.7)
Arm Cuff
Date/Time
Set Key
LCD Display
User
ON/OFF/ST
Memory Key
Air T
Connector
Battery Cover
(Located on
back of unit)
Data Link Socket
AC Adapter
Jack
Speaker
ON/OFF key Speaker
Language
Selection key
8
9
10
11
7
2
3
6
1
4
5
Language Selection key
"L1" is English "L2" is Spanish Speaker ON/OFF key
Measurement Err Make sure the L-plug is securely con-
nected to the air socket and measure again quietly
cuff corr
error keeps occurring, r
tor or service center
Air Circuit Abnormality: Make sure the L-Plug is secur
connected to the air socket on the side of the unit and meas-
ure again quietly
your local distributor or service center for help.
Pressure Exceeding 300 mmHg: Switch the unit of
measure again quietly
device to your local distributor or service center
Data Error: Remove the batteries, wait for 60 seconds, and
reload. If the err
local distributor or service center
Exceeding Measurement Range: Measur
the error keeps occurring, r
tributor or service center
