of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause any potential allergic reaction or contact injury.
• The device doesn’t need to be calibrated during two years of reliable service.
• Please dispose of the ACCESSORIES, detachable parts and the ME EQUIPMENT according to the local guidelines.
• When the device was used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or atrial
fibrillation, the best result may occur with a deviation. Please consult your physician about the result.
• This device is contraindicated for any female subject who may be suspected of being, or is, pregnant. Besides providing inaccurate
readings, the effects of this device on the foetus are unknown.
• Please keep the unit out of reach of infants, children or pets, since inhalation or swallowing of small parts is dangerous or even fatal.
• Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.
• When using this device, please pay attention to the following situation which may interrupt blood flow and influence blood circulation of
the patient, thus cause harmful injury to the patient: too frequent and consecutive multiple measurements; the application of the CUFF
and its pressurisation on any wrist where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; inflating the cuff on
the wrist on the side of a mastectomy.
• Do not apply the cuff over a wound; otherwise, it can cause further injury.
• Do not inflate the cuff on the same limb which other monitoring ME EQUIPMENT is applied around simultaneously, because this could
cause temporary loss of function of those simultaneously-used monitoring ME EQUIPMENT.
• Using it in this case can result in prolonged impairment of the circulation of the blood of the PATIENT.
• Don’t kink the connection tube; otherwise, the cuff pressure may continuously increase which can prevent blood flow and result in
harmful injury to the PATIENT.
28 • English
