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iHerz iCare
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7
EN
scribed medication without consulting your physician.
* Do not take any therapeutic measures on the basis of a self measure-
ment. Never alter the dose of a medicine prescribed by a doctor. Consult
your doctor if you have any question about your blood pressure.
* When the device was used to measure patients who have common ar-
rhythmias such as atrial or ventricular premature beats or atrial brillation,
the best result may occur with
deviation. Please consult your physician about the result.
* Don’t kink the connection tube during use, otherwise, the cu󰀨 pressure
may continuously increase which can prevent blood ow and result in
harmful injury to the PATIENT.
* When using this device, please pay attention to the following situation
which may interrupt blood ow and inuence blood circulation of the pa-
tient, thus cause harmful injury to the patient: connection tubing kinking
too frequent and consecutive multiple measurements; the application of
the cu󰀨 and its pressurization on any arm where intravascular access or
therapy, or an arterio-venous (A-V) shunt, is present; inating the cu󰀨 on
the side of a mastectomy.
* Warning: Do not apply the cu󰀨 over a wound;otherwise it can cause
further injury.
*Do not inate the cu󰀨 on the same limb which other monitoring ME
equipment is applied around simultaneously, because this could cause
temporary loss of function of those simultaneously-used monitoring ME
equipment.
*On the rare occasion of a fault causing the cu󰀨 to remain fully inated
during measurement, open the cu󰀨 immediately. Prolonged high pressure
(cu󰀨 pressure > 300mmHg or constant pressure > 15mmHg for more than
3 minutes) applied to the arm may lead to an ecchymosis.
*Please check that operation of the device does not result in prolonged
impairment of patient blood circulation.
* When measurement, please avoid compression or restriction of the con-
nection tubing.
* The device cannot be used with HF surgical equipment at the same time.
* The ACCOMPANYING DOCUMENT shall disclose that the SPHYG-
MOMANOMETER
was clinically investigated according to the requirements of ISO 81060-
2:2013.