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• Please check that operation of the device does not result in prolonged impairment of patient
blood circulation.
• When measurement, please avoid compression or restriction of the connection tubing.
• The device cannot be used with HF surgical equipment at the same time.
• The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER was clin-
ically investigated according to the requirements of ISO 81060-2:2013.
• To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the
manufacturer.
• This device is contraindicated for any female who may be suspected of, or is pregnant.
Besides providing inaccurate readings, the effects of this device on the fetus are unknown.
• Too frequent and consecutive measurements could cause disturbances in blood circulation and
injuries.
• This unit is not suitable for continuous monitoring during medical emergencies or operations.
Otherwise, the patient’s arm and fingers will become anaesthetic, swollen and even purple due
to a lack of blood.
• When not in use, store the device with the adapter in a dry room and protect it against extreme
moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the storage
case.
• This device may be used only for the purpose described in this booklet. The manufacturer
cannot be held liable for damage caused by incorrect application.
* This device comprises sensitive components and must be treated with caution. Observe the
storage and operating conditions described in this booklet.
• The maximum temperature that the applied part can be achieved is 42.8℃ while the environ-
mental temperature is 40℃.
• The equipment is not AP/APG equipment and not suitable for use in the presence of a flamma-
ble anesthetic mixture with air of with oxygen or nitrous oxide.
• Warning: No servicing/maintenance while the ME equipment is in use.
• The patient is an intended operator.
• The patient can measure,transmit data and charge power under normal circumstances and
maintain the device and its accessories according to the user manual.
• To avoid measurement errors, please avoid the condition of strong electromagnetic field radiat-
ed interference signal or electrical fast transient/burst signal.
• The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient
environment. If you are allergic to polyester, nylon or plastic, please don’t use this device.
• During 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 sensation or irritation reaction.
• Adaptor is specified as a part of ME EQUIPMENT.
• If you experience discomfort during a measurement, such as pain in the arm or other com-
plaints, press any button to release the air immediately from the cuff. Loosen the cuff and
remove it from your arm.
• If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when pressure reaches 40 kPa (300 mmHg), detach the cuff from the arm and
press any button to stop inflation.
• Before use, make sure the device functions safely and is in proper working condition.
Check the device, do not use the device if it is damaged in any way. The continuous use of a
damaged unit may cause injury, improper results, or serious danger.
• Do not wash the cuff in a washing machine or dishwasher!
The service life of the cuff may vary by the frequency of washing, skin condition, and storage
state. The typical service life is 10000 times.
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