Operation Manual

6
Accuracy test
We recommend this instrument is tested for accuracy every
2 years or after mechanical impact (e.g. being dropped). Please
contact Microlife-Service to arrange the test (see foreword).
Disposal
Batteries and electronic instruments must be disposed of in
accordance with the locally applicable regulations, not with
domestic waste.
11.Guarantee
This instrument is covered by a 5 year guarantee from the date of
purchase. The guarantee is valid only on presentation of the guar-
antee card completed by the dealer (see back) confirming date of
purchase or the receipt.
 Batteries, cuff and wearing parts are not included.
 Opening or altering the instrument invalidates the guarantee.
 The guarantee does not cover damage caused by improper
handling, discharged batteries, accidents or non-compliance
with the operating instructions.
Please contact Microlife-Service (see foreword).
12.Technical Specifications
This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Technical alterations reserved.
Operating tempera-
ture:
10 - 40 °C / 50 - 104 °F
15 - 95 % relative maximum humidity
Storage temperature: -20 - +55 °C / -4 - +131 °F
15 - 95 % relative maximum humidity
Weight: 610 g (including batteries)
Dimensions: 160 x 125 x 98 mm
Measuring procedure: oscillometric, corresponding to Korotkoff
method: Phase I systolic, Phase V
diastolic
Measurement range: 20 - 280 mmHg – blood pressure
40 - 200 beats per minute – pulse
Cuff pressure display
range: 0 - 299 mmHg
Resolution: 1 mmHg
Static accuracy: pressure within ± 3 mmHg
Pulse accuracy: ± 5 % of the readout value
Voltage source:
4 x 1.5 V Batteries; size AA
Mains adapter DC 6V, 600 mA (optional)
Reference to
standards:
EN 1060-1 /-3 /-4; IEC 60601-1;
IEC 60601-1-2 (EMC)