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This unit uses the oscillometric method to detect your blood
pressure. Before the cuff starts inflating, the device will establish
a baseline cuff pressure equivalent to the air pressure.
This unit will automatically 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 your
actual the systolic blood pressure, diastolic blood pressure, and
pulse rate.
This Blood Pressure Monitor complies with the European reg-
ulations and bears the CE mark “CE 0120”. The quality of the
device has been verified and conforms to the provisions of the
EC council directive 93/42/EEC (Medical Device Directive), An-
nex I essential requirements and applied harmonized standards.
EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanome-
ters - 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 accura-
cy of automated non-invasive sphygmomanometers.
This blood pressure monitor was designed for long service pe-
riods. In order to ensure continued accuracy, it’s recommended
that all digital blood pressure monitors require re-calibration.
This monitor (under normal usage with approx. 3 measurements
a day) does not require re-calibration 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 temperature / humidity changes. When
appears, simply return your device to your nearest dealer for
re-calibration service.
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