The
National High Blood Pressure Education Program Coordinating
Committee
has developed a blood pressure standard, classifying blood
pressure ranges into 4 stages.
(Ref. The Seventh Report of the Joint Na-
tional Committee on Prevention, Detection,
Evaluation, and Treatment of High Blood
Pressure-Complete Report JNC-7, 2004).
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 physi-
cian 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 refer-
ence of blood pressure, keeping long- term
records is recommended. Please download
the blood pressure log at
www.rossmaxhealth.com.
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.
Blood pressure measurements determined with MJ701f are equivalent to
those obtained by a trained observer using cuff/stethoscope auscultation
method, within the limits prescribed by the American National Standard, Elec-
tronic or Automated Sphygmomanometers. This unit is to be used by adult
consumers in a home environment. Do not use this device on infants or neo-
nates. MJ701f 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 cuff starts inflating, the device will establish a baseline cuff pres
-
sure equivalent to the air pressure. This unit will 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 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 0366”. The quality of the device has been veri-
fied and conforms to the provisions of the EC council directive 93/42/EEC
dated 14 June 1993 concerning medical devices:
EN 1060-1: 1995/A1: 2002 Non-invasive sphygmomanometers
- Part 1 - General requirements
EN 1060-3: 1997/A2: 2009 Non-invasive sphygmomanometers
- Part 3 - Supplementary requirements for electro-mechanical blood pres-
sure measuring systems
EN 1060-4: 2004 Non-invasive sphygmomanometers
- Part 4: Test Procedures to determine the overall system accuracy of auto
-
mated non-invasive sphygmomanometers.
This blood pressure monitor was designed for long service time. To ensure
continued accuracy, it’s recommended that all digital blood pressure mon-
itors require re-calibration. This monitor (under normal usage
with approx. 3 measurements a day) does not require re-cali-
bration 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
7. Display Explanations
Blood pressure fluctu
-
ates all the time!
You should not be overly
worried if you encoun-
tered two or three meas-
urements at high levels.
Blood pressure changes
over the month and even
throughout the day. It is
also influenced by season
and temperature.
5. Blood Pressure Standard
6. Blood Pressure Fluctuation
11. Installing Batteries
1. Press down and lift the battery cover in the direction of the arrow to open
the battery compartment.
2. Install or replace 4 “AA” sized batteries in the battery compartment accord
-
ing 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 START/STOP key is pressed and nothing appears on display.
Caution
1. Batteries are hazardous waste. Do not dispose them together with the
household garbage.
2. There are no user serviceable parts inside. Batteries or damage from old bat
-
teries 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.
www.rossmaxhealth.com
2. Name/Function of Each Part
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. 1). 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. 2).
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. 3,4).
The National High Blood Pressure Education Program Coordinating Com-
mittee has developed a blood pres-
sure standard, classifying blood
pressure ranges into 4 stages.
This unit is equipped with innova-
tive blood pressure risk indicator,
which visually indicates the as-
sumed risk level (prehypertension /
stage 1 hypertension / stage 2 hy
-
pertension) 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:
It is strongly recommended that you
consult your physician if the IHB icon (
) appears often.
12. Applying the Cuff
8. Hypertension Risk Indicator
9. Irregular Heartbeat Detector (IHB)
1.
Date/Time Indicator
2.
Hypertension Risk Indicator
3.
Memory Zones
4.
Memory Average
5.
Memory Sequence Number
6.
Weak Battery Mark
7.
Irregular Heartbeat Detector (IHB)
Fig.1
Fig.3
Fig.2
Fig.4
Fig.5
Fig.7
Fig.6
Arm Cuff
Date/Time Set key
LCD Display
User-Switching key
START/STOP key
Memory key
Air Tube and
Connector
Battery Cover
(Located on
back of unit)
4“AA”(R06) size,
1.5V batteries.
Data Link
Socket
AC Adapter
Jack
temperature / humidity changes. When
appears, simply return to your
nearest dealer for re-calibration service.
2
3
6
1
8
9
10
11
7
4
5
8.
Systolic Pressure
9.
Diastolic Pressure
10.
Pulse Rate
11.
Pulse Mark
1. Connect the AC adapter with the AC adapter jack in the
back of the unit.
2. Plug the AC adapter into the socket. (AC adapters with re
-
quired voltage and current indicated near the AC adapter
jack.)
Caution:
1. Please unload the batteries when op-
erating 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 adapters are optional. Please contact the distributor for the
compatible AC adapters.
4. Use only the authorized AC Adaptor with this blood pressure
monitor.
10. Using the AC Adapter (Optional)
AC Adapter
(Ø3.8/Ø1.3)
Instruction
Manual
Model:
MJ701 f
EN
