EN - 2
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 War-
ranty Program. For warranty information, you can contact the manufacturer, Rossmax Inter-
national 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.
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
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
www.hiperfarma.lt
www.hiperfarma.lt