Technical Specifications - Microlife BP A1 Basic Manual

• The measurement results given by this device is not a diagnosis.
It is not replacing the need for the consultation of a physician,
especially if not matching the patient's symptoms. Do not rely on
the measurement result only, always consider other potentially
occurring symptoms and the patient's feedback. Calling a doctor
or an ambulance is advised if needed.
Ensure that children do not use this device unsupervised;
some parts are small enough to be swallowed. Be aware of
the risk of strangulation in case this device is supplied with
cables or tubes.
Device care
Clean the device only with a soft, dry cloth.
Cleaning the cuff
Carefully remove spots on the cuff with a damp cloth and soapsuds.
WARNING: Do not wash the cuff in a washing machine or
dishwasher!
Accuracy test
We recommend this device is tested for accuracy every 2 years or
after mechanical impact (e.g. being dropped). Please contact your
local Microlife-Service to arrange the test (see foreword).
Disposal
Batteries and electronic devices must be disposed of in
accordance with the locally applicable regulations, not with
domestic waste.
10. Guarantee
This device 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 and parts that become worn with use are not included.
• Opening or altering the device invalidates the guarantee.
• The guarantee does not cover damage caused by improper
handling, discharged batteries, accidents or non-compliance
with the operating instructions.
• The cuff has a functional guarantee (bladder tightness) for 2 years.
Please contact your local Microlife-Service (see foreword).
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11. Technical Specifications

Operating conditions: 10 - 40 °C / 50 - 104 °F
15 - 95 % relative maximum humidity
Storage conditions: -20 - +55 °C / -4 - +131 °F
15 - 95 % relative maximum humidity
Weight: 319 g (including batteries)
Dimensions: 146 x 65 x 46 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 alkaline batteries; size AA
Mains adapter DC 6V, 600 mA (optional)
Battery lifetime: approx. 920 measurements
(using new batteries)
IP Class: IP20
Reference to EN 1060-1 /-3 /-4; IEC 60601-1;
standards: IEC 60601-1-2 (EMC); IEC 60601-1-11
Expected service life: Device: 5 years or 10000 measurements
Accessories: 2 years
This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Technical alterations reserved.