HMM Diagnostics smartLAB Manual De Instrucciones página 39

• If you experience discomfort during a measurement, such as pain in the arm or other
complaints, press the START/STOP button to release the air immediately from the
cuff. Loosen the cuff and remove it from your arm.
• On the rare occasion of a fault causing the cuff to remain fully inflated during
measurement, open the cuff immediately. Prolonged high pressure (cuff pressure
>300mmHg or constant pressure >15mmHg for more than 3 minutes) applied to the
arm may lead to an ecchymosis.
• 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.
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