•
Too frequent and consecutive measurements could cause disturbances in blood cir-
culation and injuries.
•
Do not wrap the cuff on the same arm which other monitoring ME EQUIPMENT is ap-
plied simultaneously, because this could cause temporary loss of function of those
simultaneously-used monitoring ME EQUIPMENT.
•
Don't kink the connection tube during use, otherwise, the cuff pressure may con-
tinuouslyincreasewhichcanpreventbloodflowandresultinharmfulinjurytothe
PATIENT.
•
The equipment is not AP/APG equipment and not suitable for use in the presence of
aflammableanestheticmixturewithairofwithoxygenornitrousoxide.
•
This unit is not suitable for continuous monitoring during medical emergencies or
operations.
•
This device cannot be used with HF surgical equipment at the same time.
•
This device is not intended for patient transports outside a healthcare facility.
•
To avoid measurement errors, please avoid the condition of strong electromagnetic
fieldradiatedinterferencesignalorelectricalfasttransient/burstsignal.
•
The operator shall not touch output of batteries/adapter and the patient simultane-
ously.
•
Manufacturer will make available on request circuit diagrams, component parts list
etc.
•
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 sensitization or irritation reaction. Never apply the
cuff over hurt skin.
•
Do not use the unit in case of existing polyester resp. synthetic allergies.
•
Be careful to strangulation due to cables and hoses, particularly due to excessive
length.
•
Do not connect the air hose to other medical equipment, as this could cause air to
be pumped into intravascular systems or high pressure, what could lead to dangerous
injuries.
38