HMM Diagnostics smartLAB easy nG Benutzerhandbuch Seite 61

• Please use the device under the environment which is provided in the
user manual. Otherwise, the performance and lifetime of the device will
be impacted and reduced
• During the 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
alergic reaction or contact injury
• When the device was used to measure patients who have common arrhyth-
mias such as arterial or ventricular premature beats or arterial liberation,
the test result may cause deviation. Please consult your physician about
the result
• Please use accessories and detachable parts specified/ authorised by
manufacturer. Otherwise, it may cause damage to the unit or danger to
the user/patient
• This device is contraindicated for any female subject who may be suspect-
ed of, or is pregnant. Besides provided inaccurate readings, the affects of
this device on the fetus are unknown
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