EN -
- EN
Introduction
Blood pressure measurements determined with this unit are equivalent to those obtained by a
trained observer using cuff/stethoscope auscultation method, within the limits prescribed by the
American National Standard Manual, 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.
This unit is protected against manufacturing defects by an established International Warranty
Program. 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
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 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 continued accuracy,
it's recommended that all digital blood pressure monitors require re-calibration. This monitor
does not require re-calibration for 2 years under normal usage with approximately 3 times a
day, until, at which time your monitor displays CA . The unit should also be re-calibrated if the
monitor sustains damange due to blunt force (such as dropping) or exposure to fluids and / or
extreme hot or cold temperature / humidity changes. When CA appears, simply return to your
nearest dealer for re-calibration service.
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. Memory Zones
3. Memory Average
4. Weak Battery Mark
5. Date/Time Indicator
6. Irregular Heartbeat (IHB) Detector
7. Systolic Pressure
8. Diastolic Pressure
9. Pulse Rate
10. Pulse Mark
Date/Time Set key
M
Arm Cuff
LCD Display
User-Switching key
ON/OFF/START 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
1
2
4
5
7
8
9
10
6
3
