Traonsport csts and risks of transport.
Damage caused by incorrect application or non-compliance
with the instructions for use.
Damage caused by leaking batteries.
Damage caused by accident or misuse.
Packaging/storage material and instructions for use.
Regular checks and maintenance (calibration).
Accessories and wearing parts: Batteries, power adapter
(optional).
The cuff is covered by a functional guarantee (bladder tightness)
for 2 years.
Should guarantee service be required, please contact the dealer
from where the product was purchased, or your local Microlife
service. You may contact your local Microlife service through our
website:
www.microlife.com/support
Compensation is limited to the value of the product. The guarantee
will be granted if the complete product is returned with the original
invoice. Repair or replacement within guarantee does not prolong
or renew the guarantee period. The legal claims and rights of
consumers are not limited by this guarantee.
10. Technical specifications
Operating condi-
10 - 40 °C / 50 - 104 °F
tions:
15-90 % relative maximum humidity
Storage conditions: -20 - +55 °C / -4 - +131 °F
15-90 % relative maximum humidity
Weight:
277 g (including batteries)
Dimensions:
131 x 90 x 60.5 mm
Cuff size:
from 17-52 cm according to the cuff sizes
(see «Selecting the correct cuff»)
Measuring proce-
oscillometric, corresponding to Korotkoff
dure:
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:
within ± 3 mmHg
Microlife BP B2 Easy
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:
IP 20
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,
whichever comes first
Accessories: 2 years or 5000 measure-
ments, whichever comes first
This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Technical alterations reserved.
EN
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