HoMedics BPW-3010-EU Bedienungsanleitung Seite 4

application of the cuff and its pressurization on any
wrist where intravascular access or therapy, or an
arterio-venous (A-V) shunt, is present; inflating the
cuff on the side of a mastectomy.
• Warning: 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, because this could cause temporary
loss of function of those simultaneously-used
monitoring ME equipment.
•On the rare occasion of a fault causing the cuff
to remain fully inflated during measurement, open
the cuff immediately. Prolonged high pressure
(cuff pressure > 300mmHg or constant pressure >
15mmHg for more than 3 minutes) applied to the
wrist 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 effects 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 wrist 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 maximum temperature that the applied part
can be achieved is 42.5ºC while the
environmental temperature is 40ºC.
• 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.
• Warning: No servicing/maintenance while the ME
equipment is in use.
• The patient is an intended operator.
• The patient can measure data and change
batteries under normal circumstances and maintain
the device and its accessories according to the
user manual.
• To avoid measurement errors, please avoid the
condition of strong electromagnetic field radiated
interference signal or electrical fast transient/
burst signal.
• The blood pressure monitor and the cuff are
suitable for use within the patient environment. If
you are allergic to polyester, nylon or plastic, please
don't use this device.
• During use, the patient will be in 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
sensization or irritation reaction.
• If you experience discomfort during a
measurement, such as pain in the wrist or other
4 I GB