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and lifetime of the device will be
impacted and reduced.
•
During
using,
will contact with the cuff. The
materials of the cuff have been
tested and found to comply
with requirements of ISO 10993-
5:2009 and ISO 10993-10:2010.
It will not cause any potential
allergic reaction or contact injury.
• The device doesn't need to be
calibrated in two years of reliable
service.
• Please dispose of ACCESSORIES,
detachable parts, and the ME
EQUIPMENT according to the
local guidelines.
• When the device was used
to measure patients who have
common arrhythmias such as
atrial or ventricular premature
beats or arterial fibrillation, the
best result may occur deviation.
Please consult your physician
about the result.
• The device is contraindicated
for any female subject who may
be suspected of, or is pregnant.
Besides
provided
readings, the effects of this
device on the fetus are unknown.
• When using this device, please
pay attention to the following
situation which may interrupt
blood flow and influence blood
circulation
of
thus cause harmful injury to
the patient: Too frequent and
consecutive multiple
the
patient
inaccurate
the
patient,
measurements; The application
of the cuff and its pressurization
on any arm where intravascular
access or therapy, or an arterio-
venous (A-V) shunt, is present;
Inflating the cuff on the arm on
the side of a mastectomy.
• Do not apply the cuff over a
wound, otherwise it can cause
further injury.
• Do not inflate the cuff on the
same limb which other monitoring
ME EQUIPMENT is applied around
simultaneously,
could cause temporary loss of
function of those simultaneously-
used monitoring ME EQUIPMENT.
Using it in case to result in
prolonged impairment of the
circulation of the blood of the
PATIENT.
• Don't kink the connection tube,
otherwise, the cuff pressure may
continuously increase which can
prevent blood flow and result in
harmful injury to the PATIENT.
• The device has been evaluated
clinically
used
stethoscope auscultations the
reference.
measurements determined with
this device are equivalent to those
obtained by a trained observer
using
the
auscultatory
the limits prescribed by the
"American National Standard,
Manual, electronic or automated
sphygmomanometers".
5
because
manual
cuff/
Blood
pressure
cuff/stethoscope
method,
within
this
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