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Safety Information (Cont.)
- Using the cuff on any arm 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, as it can cause further injury.
•
If a limb has other monitoring ME equipment
applied to it, do not inflate the cuff on that
limb. This could cause the other monitoring ME
equipment to temporarily lose function.
•
Rarely, a fault may cause the cuff to remain fully
inflated during measurement. In this case, open
the cuff immediately. Prolonged high pressure
(cuff pressure > 300 mmHg or constant
pressure > 15 mmHg for more than 3 minutes)
applied to the arm may lead to an ecchymosis
(bruising).
•
Always check to make sure that operating
this monitor does not result in prolonged
impairment of patient blood circulation.
8
•
When measuring, please avoid compression or
restriction of the connection tubing.
•
The monitor cannot be used with HF surgical
equipment.
•
The ACCOMPANYING DOCUMENT (see
Complied Standards List, page 44) shall
disclose that the SPHYGMOMANOMETER
is clinically investigated according to the
requirements of ISO 81060-2:2013.
•
To verify the calibration of the AUTOMATED
SPHYGMOMANOMETER, please contact the
manufacturer.
•
Too frequent and consecutive measurements
could cause disturbances in blood circulation
and injuries.
•
This monitor is not suitable for continuous
monitoring of blood pressure during medical
emergencies or operations. The patient's arm
Safety Information (Cont.)
and fingers will become anaesthetic, swollen,
and even purple due to a lack of blood.
•
When not in use, store the monitor with the
adapter 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 monitor may be used only for the purpose
described in this booklet. The manufacturer
cannot be held liable for damage caused by
incorrect application.
•
This monitor contains sensitive components
and must be treated with caution. Observe the
storage and operating conditions described in
this booklet.
•
This monitor is not AP/APG equipment and
is not suitable for use in the presence of a
flammable anesthetic mixture with air or with
oxygen or nitrous oxide.
•
WARNING: No servicing/maintenance while
the ME equipment is in use.
•
The patient is an intended operator of this
monitor. The patient can measure, transmit
data, and change batteries under normal
circumstances and maintain the monitor and its
accessories according to the user manual.
•
To avoid measurement errors, please
avoid using in the presence of a strong
electromagnetic field radiated interference
signal or an electrical fast transient/burst
signal.
•
The blood pressure monitor, its adapter, 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 monitor
or cuff.
•
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
9
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