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Terraillon TensioSmart Seite 33

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Safety Information
The below signs might be in the user manual, labeling or other components.
They are the requirement of standard and using.
CAUTION
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 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. When the device was used to measure patients who have common
arrhythmias such as atrial or ventricular premature beats or atrial brillation, 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
deate. Should the cuff not deate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and
press the corresponding user button to stop ination. The equipment is not AP/APG equipment and not suitable for use
in the presence of a ammable anesthetic mixture with air of with oxygen or nitrous oxide. The operator shall not touch
output of adapter and the patient simultaneously. To avoid measurement errors, please avoid the condition of strong
electromagnetic eld 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. Besides providing inaccurate readings, the effects of this device
on the fetus are unknown. Manufacturer will make available on request circuit diagrams, component parts list etc. This unit is
not suitable for continuous monitoring during medical emergencies or operations. Otherwise, the patient’s arm and ngers
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 specied/ 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 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 SERVICE
PERSONNEL of TERRAILLON. Don’t open or repair the device by yourself. Please report to TERRAILLON if any unexpected
operation or events occur. Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners.
Symbol for “THE OPERATION GUIDE
MUST BE READ”
Symbol for “TYPE BF APPLIED PARTS”
Symbol for “COMPLIES WITH
MDD93/42/EEC REQUIREMENTS”
Symbol for “ENVIRONMENT PROTECTION
- Electrical waste products should not
be disposed of with household waste.
Please recycle where facilities exist.
Check with your local authority
or retailer for recycling advice”
Symbol for “MANUFACTURER”
Symbol for “DIRECT CURRENT”
Symbol for “SERIAL NUMBER”
EC REP
Symbol for “Authorised Representative
in the European Community”
The Bluetooth Combination Mark
T1A/250V 3.6*10CCC
Symbol for “MANUFACTURE DATE For indoor use only
Symbol for “Class II Equipment”
Caution: These notes must be
observed to prevent any damage
to the device.
Symbol for “Including RF transmitter”
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