Andon KD-5917 Operation Manual - Page 5
Browse online or download pdf Operation Manual for Blood Pressure Monitor Andon KD-5917. Andon KD-5917 15 pages.
Print PageDN:KD-5917-SMSY01 V3.0
7. Consult your physician if you have any doubt about below cases:
1) The application of the cuff over a wound or inflammation diseases;
2) The application of the cuff on any limb where intravascular access or therapy, or an
arterio-venous (A-V) shunt, is present;
3) The application of the cuff on the arm on the side of a mastectomy;
4) Simultaneously used with other monitoring medical equipments on the same limb;
5) Need to check the blood circulation of the user.
8.
This Electronic Blood Pressure Monitor s is designed for adults and should never be
used on infants or young children. Consult your physician or other health care
professionals before use on older children.
9. Do not use this unit in a moving vehicle, This may result in erroneous measurement.
10. Blood pressure measurements determined by this monitor are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultation method, within the
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) is detected in the procedure of blood pressure measurement, a
signal of
will be displayed. Under this condition, the Electronic Blood Pressure
Monitors 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
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Operation Guide
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