Microlife BP A2 Standard Manual page 8

 mechanically damaged goods
 cases of radioactive contamination
 cases of damage due to non-observance of the operating
rules, described in the manual
 cases of damage caused by intentional or erroneous actions
of the consumer
 cases of damage caused by ingress of foreign liquids and
solids, insects, hair, pile, litter, other pollutants from the envi-
ronment, etc.
 cases of damage due to battery leak
 goods with traces of interference or repair by an unauthor-
ized person
 goods that underwent unauthorized changes in design
 failures caused by using network adapters, others than
recommended by the manufacturer of goods indicated by
the Microlife trademark
 failures caused by self-use of spare parts and components
from other manufacturers
 events of force majeure (accident, fire, flood, malfunction of
the electrical network, etc.)
5. This guarantee does not infringe upon the legitimate rights of
the consumers that are granted by the current legislation of the
Republic of Belarus, neither upon the consumer-seller rights
that arise from the contract of sale made between them.
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: 375 g (including batteries)
Dimensions: 120 x 87 x 59 mm
Measuring procedure: oscillometric
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
6
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)
Included: blood pressure monitor, bag (optional),
cuff, adapter (optional), 4 x AA batteries,
instruction manual, guarantee card,
blood pressure diary, cuff-marker
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: 12 years or 10000 measurements
Accessories: 2 years
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.