Bedienungsanleitung Lanaform LA090207 (Seite 6 von 64) (Deutsch, Englisch, Holländisch, Französisch)

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Under this condition, 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:

a The coecient of variation

(CV) of pulse period >25%.

b The dierence 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 cu other than

supplied by the manufacturer, otherwise

it may bring biocompatible hazard and

might result in measurement error.



The monitor might not meet

its performance specications or

cause safety hazard if stored or used

outside the specied temperature and

humidity ranges in specications.



Please do not share the cu with other

infective person to avoid cross-infection.

16 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 reason-

able protection against harmful interference

in a residential installation. This equipment

generates, uses and can radiate radio fre-

quency energy and, if not installed and used

in accordance with the instructions, may

cause harmful interference to radio commu-

nications. However, there is no guarantee

that interference will not occur in a particu-

lar installation. If this equipment does cause

harmful interference to radio or television

reception, which can be determined by

turning the equipment o and on, the user is

encouraged to try to correct the interference

by one or more of the following measures:

a Reorient or relocate the receiving antenna.

b Increase the separation between

the equipment and receiver.

c Connect the equipment into an

outlet on a circuit dierent from that

to which the receiver is connected.

d Consult the dealer or an experienced

radio/TV technician for help.

17 Measurements are not possible in patients

with a high frequency of arrhythmias.

18 The device is not intended for use on

neonates, children or pregnant women.

(Clinical testing has not been conducted on

neonates, children or pregnant women.)

19 Motion, trembling, shivering may

aect the measurement reading.

20 The device would not apply to the

patients with poor peripheral circulation,

noticeably low blood pressure, or low

body temperature (there will be low blood

ow to the measurement position).

21 The device would not apply to the

patients who use an articial heart

and lung (there will be no pulse)

22 Consult your physician before using the

device for any of the following conditions:

common arrhythmias such as atrial or

ventricular premature beats or atrial

brillation, arterial sclerosis, poor perfusion,

diabetes, pre-eclampsia, enal diseases.

23 The patient can be an intended operator.

24 This device complies with part 15 of the

FCC Rules. Operation is subject to the

following two conditions: (1) This device

may not cause harmful interference, and

(2) this device must accept any interference

received, including interference that

may cause undesired operation.

25 Attention that changes or modication

not expressly approved by the party

responsible for compliance could void the

user’s authority to operate the equipment.

26 Swallowing batteries and/or battery uid

can be extremely dangerous. Keep the

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