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Lanaform LA090207 Manual

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6 / 64 WB PM -110
EN FR NL DE
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.
14
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.
15
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
… 6 …


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