Terraillon Tensio Instruction Manual page 14

EN
BLOOD PRESSURE MONITOR – INSTRUCTION MANUAL
CAUTION MO
This device is intended for adult use only. 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 wrist 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.
When the device was used to measure patients who have common arrhythmias such as atrial or ventricular
premature beats or arterial fibrillation, the best result may occur with deviation. Please consult your physician
about the result. If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should
the cuff not deflate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and press the
START/STOP button to stop inflation. 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. The operator shall not
touch output of batteries /adapter and the patient simultaneously. To avoid measurement errors, please avoid
the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst
signal. The user must check that the equipment functions safely and see that it is in proper working condition
before being used. This device is contraindicated for any female who may be suspected of, or is pregnant.
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. Please
use the device under the environment which was provided in the user manual. Otherwise, the performance
and lifetime of the device will be impacted and reduced. 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. Please use ACCESSORIES
and detachable partes specified/ authorised by MANUFACTURE. Otherwise, it may cause damage to the
unit or danger to the user/patients. The device doesn't need to be calibrated within the two years of reliable
co
service. Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local
guidelines. If you have any problems with this device, such as setting up, maintaining or using, please contact
the after-sales service. Don't open or repair the device by yourself.
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