Andon KD-5905 Manual de instrucciones - Página 5
Navegue en línea o descargue pdf Manual de instrucciones para Tensiómetro Andon KD-5905. Andon KD-5905 16 páginas. Fully automatic arm cuff blood pressure monitor
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limits prescribed by the American National Standard Institute, Electronic or automated
sphygmomanometers.
11. Information regarding potential electromagnetic or other interference between the blood
pressure monitor and other devices together with advice regarding avoidance of such
interference please see part ELECTROMAGNETIC COMPATIBILITY INFORMATION.
12. If Irregular Heartbeat (IHB) brought by common arrhythmias is detected in the procedure
of blood pressure measurement, a signal of
the Electronic Sphygmomanometers can keep function, but the results may not be
accurate, it's suggested that you consult with your physician for accurate assessment.
There are 2 conditions under which the signal of IHB will be displayed:
1) The coefficient of variation (CV) of pulse period >25%.
2) The difference of adjacent pulse period≥0.14s, and the number of such pulse takes
more than 53 percentage of the total number of pulse.
13. Please do not use the cuff other than supplied by the manufacturer, otherwise it may bring
biocompatible hazard and might result in measurement error.
14.
The monitor might not meet its performance specifications or cause safety hazard if
stored or used outside the specified temperature and humidity ranges in specifications.
15.
Please do not share the cuff with other infective person to avoid cross-infection.
16. Medical AC adapter which output is DC 6.0V 600mA and complied with IEC 60601-1/EN
60601-1/UL 60601-1 and IEC 60601-1-2/EN 60601-1-2/UL 60601-1-2 is suitable for this
monitor. Please note that the monitor jack size: hole Φ5.5mm, center pin Φ2.0mm. Please
pay attention to polarity.
17. This equipment has been tested and found to comply with the limits for a Class B digital
device, pursuant to part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference in a residential installation. This
equipment generates, uses and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to radio
communications. However, there is no guarantee that interference will not occur in a
particular installation. If this equipment does cause harmful interference to radio or
television reception, which can be determined by turning the equipment off and on, the
user is encouraged to try to correct the interference by one or more of the following
measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected.
—Consult the dealer or an experienced radio/TV technician for help.
18. This blood pressure monitor is verified by auscultatory method. It is recommended that
you check annex B of ANSI/AAMI SP-10:2002+A1:2003+A2:2006 for details of verification
method if you need.
will be displayed. Under this condition,
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Operation Guide
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