Accuracy Test; Disposal; Guarantee; Technical Specifications - Microlife BP A2 Classic Manual

Accuracy test

We recommend this device is tested for accuracy every once a year
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 1 year.
Please contact your local Microlife-Service (see foreword).

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
Electronic unit
weight: not more than 400 g (including batteries)
Overall dimensions of
the electronic unit: no more than 120 x 87 x 59 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
6
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
This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Technical alterations reserved.
Date of production: first 8 digits of the serial number of the device.
First 4 digits: year / 5th and 6th digit: month / 7th and 8th digit: day
of production.