Andon KD-5904 Bedieningshandleiding - Pagina 5

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1. Voice Setting

DN:KD-5904-SMSY01 V3.0

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.

This Electronic Sphygmomanometers 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) 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 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.

18. 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

will be displayed. Under this condition,

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Operation Guide

JS-KD5904-03-V2.0