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IMPORTANT PRODUCT NOTICES AND SAFETY
INSTRUCTIONS
When using your blood pressure monitor, basic pre-
cautions should always be followed. Please read and
follow all instructions and warnings before using this
product. Save these instructions for future reference.
• Please note that this is a home healthcare product
only and it is not intended to serve as a substitute
for the advice of a physician or medical professional.
• Do not use this device for diagnosis or treatment of any
health problem or disease. Measurement results are for
reference only. Consult a healthcare professional for
interpretation of pressure measurements. Contact your
physician if you have or suspect any medical problem.
Do not change your medications without the advice of
your physician or healthcare professional.
• Proper cuff size is critical for accurate measurements. If
the arrow on the cuff falls outside of the solid color line
when applied to the user’s arm, contact HoMedics
Consumer Relations regarding additional cuff sizes.
• This product is not suitable for people with arrythmias.
This device may have difficulty determining the proper
blood pressure for individuals with diabetes, poor
circulation of blood, kidney problems or for users
who have suffered from a stroke.
• The pulse display is not suitable for checking the
frequency of heart pacemakers.
• Electromagnetic interference: The device contains
sensitive electronic components. Avoid strong
electrical or electromagnetic fields in the direct vicinity
of the device (e.g. mobile telephones, microwave
ovens). These may lead to temporary impairment of
measurement accuracy.
• Use blood pressure monitor only for its intended use.
• Do not wrap the cuff around body parts other than
your arm.
• This unit is intended for use in measuring the blood
pressure and pulse rate of adults. Do not use this device
on infants or those who cannot express their own
consent. This unit should not be operated by children.
• Do not plug or unplug the adapter power cord with
wet hands.
Blood pressure measurements determined with this
device are equivalent to those obtained by a trained
observer using the cuff/stethoscope ausculatory
method, within the limits prescribed by the American
National Standard,
Manual, electronic, or automated
sphygmomanometers
.
