Bedienungsanleitung Salter BPA-9201 (Seite 3 von 20) (Englisch)

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CAUTION

• This device is intended for adult use in homes only.

• The device is not suitable for use on neonatal patients,

pregnant women, patients with implanted, electronical

devices, patients with pre-eclampsia, premature ventricular

beats, atrial ﬁbrillation, peripheral, arterial disease and

patients undergoing intravascular therapy or arterio-

venous shunt or people who received a mastectomy. Please

consult your doctor prior to using the unit if you suer

from illnesses.

• The device is not suitable for measuring the blood

pressure of children. Ask your doctor before using it on

older children.

• The device is not intended for patient transport outside

a healthcare facility.

• The device is not intended for professional use.

• This device is intended for no-invasive measuring and

monitoring of arterial blood pressure.

It is not intended for use on extremities other than the

arm or for functions other than obtaining a blood pressure

measurement.

• Do not confuse self-monitoring with self-diagnosis. This

unit allows you to monitor your blood pressure. Do not

begin or end medical treatment without asking a physician

for treatment advice.

• If you are taking medication,consult your physician to

determine the most appropriate time to measure your

blood pressure. Never change a prescribed medication

without consulting your physician.

• Do not take any therapeutic measures on the basis of

a self measurement. 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 arrhythmias such as atrial or ventricular

premature beats or atrial ﬁbrillation, 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 ﬂow and result in harmful injury to the PATIENT.

• When using this device, please pay attention to the

following situation which may interrupt blood ﬂow and

inﬂuence blood circulation of the patient, 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; inﬂating 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 inﬂate 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 inﬂated 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 connection tubing.

• The device cannot be used with HF surgical equipment

at the same time.

• The ACCOMPANYING DOCUMENT shall disclose that the

SPHYGMOMANOMETER was clinically investigated according

to the requirements of ISO 81060-2:2013.

• To verify the calibration of the AUTOMATED

SPHYGMOMANOMETER, please contact the manufacturer.

• This device is contraindicated for any female who

may be suspected of, or is pregnant. Besides providing

inaccurate readings, the eects of this device on the fetus

are unknown.

• Too frequent and consecutive measurements could cause

disturbances in blood circulation and injuries.

• This unit is not suitable for continuous monitoring during

medical emergencies or operations.Otherwise, the patient’s

arm and ﬁngers will become anaesthetic, swollen and even

purple due to a lack of blood.

• When not in use, store the device in a dry room and

protect it against extreme moisture, heat, lint, dust and

direct sunlight. Never place any heavy objects on the

storage case.

• This device may be used only for the purpose described

in this booklet. The manufacturer cannot be held liable for

damage caused by incorrect application.

• This device comprises sensitive components and must

be treated with caution. Observe the storage and operating

conditions described in this booklet.

• The equipment is not AP/APG equipment and not suitable

for use in the presence of a ﬂammable anesthetic mixture

with air of with oxygen or nitrous oxide.

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