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Measurement accuracy
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Technical data EW 3036
Warning function Flashing figures on the display and
3 color LED
Method of measurement: Intelligent measuring technology
(oscillometric) (FUZZY LOGIC)
Measuring range: Pressure: 0–280 mmHg
The device is vented automatically at
pressures exceeding 280 mmHg and
an error message is shown.
Pulse: 30–160 beats per minute
Measuring accuracy: Pressure ± 3 mmHg
Pulse rate: ± 5 %
Leakage of pneumatic system: ≤ 6 mmHg/min
Inflation/deflation system: Automatic measurement during
inflation, and rapid deflation
Wrist circumference: 12.5–22.0 cm (4 7/8–8 5/8 inches)
Batteries: 2#1.5 V alkaline (LR03/AAA/Micro)
(Control sign for battery change) Battery symbol appears when the
batteries have to be replaced.
Automatic switch-off: Approx. 5 minutes after measurement
Reference method for clinical trials: Auscultatory measurement
Weight: 90 g (without batteries)
Storage and transport conditions: – 10˚C to + 60˚C, 10% to 95% RH
Operating conditions: + 10˚C to + 40˚C, 30% to 85% RH
EW3036 was proven clinically by sequential comparison with auscultatory
measurement. The waiting period before EW3036 evaluation requires 1.5-2
minutes, and before auscultatory measurement of 0.5-1 minute.
General
This blood pressure measurement device complies with the European
regulations (EU council directive 93/42/EEC dated June 14, 1993) and
bears the CE mark “CE 0197”. The quality of the device has been verified
and it conforms to the following standards:
EN 1060-1 (Dec. 1995) Non-invasive blood pressure measuring
equipment
General requirement
EN 1060-3 (Sep. 1997) Non-invasive blood pressure measuring
equipment
Supplementary requirements for
electromechanical blood pressure measuring
systems
ANSI/AAMI SP10 (1992) Electronic or automated sphygmomanometers
Overall system efficacy
Auscultatory method as the reference standard
EN 60601-1-2 (Nov. 2001) Electromagnetic compatibility and safety for
medical electrical equipment
The CE mark serves to facilitate the free movement of goods between the
member countries of the EU.
Panasonic ensures accurate measurement
The seal confirms that each Diagnostec has been checked for
accurate measurement at the Matsushita plant. It is
recommended that the device be recalibrated every 3 years
starting with the year printed on the seal.
When the device has been repaired or the seal has been rendered illegible,
the accuracy of the device should be assumed to be inaccurate. In such
cases, it is recommended that the device be submitted for recalibration.
