8
• To avoid measurement errors, please avoid using the device in areas with
a strong electromagnetic eld radiated interference signal or electrical fast
transient/ burst signals.
• The user must check that the equipment functions safely and see that it is in
proper working condition before being used.
• This device is not suitable for continuous monitoring during medical
emergencies or operations. Otherwise, the patient’s arm and ngers can
become numb, swollen and even purple due to a lack of blood.
• Please use the device as instructed in this user manual. If you do not do
so, the performance and lifetime usage of the device will be impacted and
reduced.
• During use, the user/patient will be in contact with the cuff. The materials
of the cuff have been tested and found to comply with the requirements of
ISO 10993-5:2009 and ISO 10993-10:2010, therefore should not cause any
irritation.
• Use only Duronic authorised parts and accessories. Parts and accessories
not approved for use with the device may result in operational failure.
• The device should not need to be calibrated within the rst two years of use.
• If you have any problems with this device, such as setting up, maintaining
or using the device, please contact the Duronic Customer Care Team for
assistance.
• Do not open or repair the device by yourself. If you experience any problems
with your device, contact Duronic for assistance.
• When cleaning the device, please use a soft cloth to clean the whole unit. Do
not submerge it in water or any other liquid, and do not use any abrasive or
volatile cleaners.
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