19
Safety Information
The below signs might be in the user manual, labeling or other component.
they are the requirement of standard and using.
Symbol for ”THE OPERATION
GUIDE MUST BE READ“
Symbol for ”COMPLIES WITH
MDD 93/42/EEC REQUIREMENTS“
Symbol for ”MANUFACTURER“
Symbol for ”SERIAL NUMBER“
Symbol for ”TYPE BF APPLIED
PARTS“
Symbol for ”DIRECT CURRENT“
Symbol for ”ENVIRONMENT
PROTECTION - Wast electrical
products should not be disposed of
CAUTION
This device is intended for adult use only.
This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is not
intended for use on extremities other than the upper 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. Please start or end medical treatment basing solely on physician’s treatment advice.
If you are taking medication, consult your physician to determine the most appropriate time for your
measurement. Never change a prescribed medication without your physician’s consent.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
If the pressure of the cuff exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when its pressure exceeds 40 kPa (300 mmHg), detach the cuff from the upper arm
and press the homologous button to stop inflation.
Please do read this user manual carefully and thoroughly before use.
The device is not AP/APG equipment. It is not suitable for use in the presence of a flammable
anesthetic mixture with air (or oxygen, nitrous oxide).
Do not use the monitor under the conditions of strong electromagnetic field (e.g. mobile) that radiates
interference signal or electrical fast transient / burst signal.
Please keep the unit out of reach of infants or children, since inhalation or swallowing of small parts
is dangerous or even fatal.
Please use ACCESSORIES and detachable parts specified / authorised by MANUFACTURER.
Otherwise, it may cause damage to the unit or danger to the user / patient.
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 alergic reaction or contact injury.
Please make sure the unit functions safely and it is in proper working conditions before use.