Archos Blood Pressure Monitor Mode D'emploi page 6

MANUFACTURER. Otherwise, it may cause damage to the unit or danger to the user
/ patient.
Manufacturer will make available on request circuit diagrams, component parts
listed.
Sensitive people, including pregnant women and those who implanted medical
electronic
Instrument, should avoid using the unit whenever possible.
This unit is not suitable for continuous monitoring during medical emergencies or
operations.
After the cuff inflated long time, the patient's wrist and fingers will is insufficient,
anesthesia, distending pain and ecchymosis.
Please use the device under the environment which was provided in the user
manual.
Otherwise, the performance and lifetime of the device will been impacted and
reduced.
During using, the patient 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 has been evaluated clinically used manual cuff/ stethoscope auscultation
as the reference.
The device doesn't need to be calibrated in two years of reliable service.
When the device was used to measure patients who have common arrhythmias such
as atrial or ventricular premature beats or atrial fibrillation, the test result may occur
deviation. Please consult your physician about the result.
This device is contraindicated for any female subject who may be suspected of, or is
pregnant.
Besides provided inaccurate readings, the effects of this device on the fetus are
unknown.
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