EN - 2
3 - EN
Introduction
Blood pressure measurements determined with MG40 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.
MG40 is protected against manufacturing defects by an established International Warranty Pro-
gram. For warranty information, you can contact the manufacturer, Rossmax International Ltd. or
your local distributors.
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.
Name/Function of Each Part
Preliminary Remarks
This Blood Pressure Monitor complies with the European regulations and bears the CE mark "CE
0366". The quality of the device has been verified and conforms to the provisions of the EC coun-
cil directive 93/42/EEC (Medical Device Directive), Annex I essential requirements and applied
harmonized standards.
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 require-
ments 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 time. To ensure accurate measure-
ments, it is recommended that calibration be completed every two years.
Blood Pressure Standard
The National High Blood Pressure Education Program Coordinating Committee has developed
a blood pressure standard, according to which areas of low- and high-risk blood pressure are
identified. This standard, however, is a general guideline as individual's blood pressure varies
among different people and different age groups...etc.
(Ref. The Seventh Report of the Joint National 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 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.
The
National High Blood Pressure Education Program
Coordinating Committee
has developed a blood pressure
standard, classifying blood pressure ranges into 4 stages. This
unit is equipped with innovative blood pressure risk indicator,
which visually indicates the assumed risk level (prehyperten-
sion / stage 1 hypertension / stage 2 hypertension) of the
result after each measurement. (Please note below.)
Display Explanations
1. Hypertension Risk Indicator
2. Inflation / Deflation Marks
3. Memory Mark
4. Weak Battery Mark
5. Systolic Pressure
6. Diastolic Pressure
7. Pulse Rate
8. Pulse Mark
4“AA”(R06) size,
1.5V batteries.
Arm Cuff
LCD Display
Air Tube and
Connector
Battery Cover
(Located on
back of unit)
Memory Key
ON/OFF Key
Inflating
Bulb
4
5
6
3
8
7
1
2
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 ac-
cording 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. As the supplied batteries are for test only, they may be discharged earlier than batteries you
buy in stores. Replace the batteries in pairs. Remove batteries when unit is not in use for ex-
tended periods of time.
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