INTRODUCTION
1
• Measures Systolic Blood Pressure
• Measures Diastolic Blood Pressure
• Measures Pulse Rate
• Retains historic records of up to 60
previous measurements
• Large 5.5” x 1.5” bright LCD display
The following symbols may be used in the user manual, product labeling, or on
other components. They are the requirement of standard and use.
♥
Features
♥
Safety Information
Type B applied part
Direct current
Follow instructions/
directions for use -
mandatory action
Specifies serial
number
DISPOSAL: Do not
dispose this product as
unsorted municipal waste.
Collection of such waste
separately for special
treatment is necessary.
Manufacture Date
!
Caution: These notes
must be observed to
prevent any damage
to the device.
• This device is for adult use only.
• To avoid measurement errors, carefully read this manual before using
this device.
• This device is intended for non-invasive measuring and monitoring of
arterial blood pressure. It is not intended for use on extremities other
than the arm or for functions other than obtaining a blood pressure
measurement and pulse rate.
• Do not confuse self-monitoring with self-diagnosis. This unit allows you
to monitor your blood pressure. Do not begin or end medical treatment
based solely on self-monitoring, consult a physician for treatment
advice.
• If you are taking medication, consult your physician to determine the
most appropriate time to measure your blood pressure. Never change
a prescribed medication without consulting your physician. This unit
is not suitable for continuous monitoring during medical emergencies
or operations.
• Sensitive people, including pregnant women pre-eclamptic patients,
patients who have implanted medical electronic instruments and have
atrial fibrillation (AF), premature ventricular beats and peripheral arterial
disease (PAD), should avoid using the unit whenever possible.
• This device has been evaluated clinically with a manual cuff/
stethoscope auscultation as a reference. Blood pressure
measurements determined with this device are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultatory
method within the limits prescribed by the American National Standard
for manual, electronic, or automated sphygmomanometers.
• If the cuff pressure exceeds (300 mmHg), the unit will automatically
deflate. Should the cuff not deflate when pressures exceeds (300
mmHg), detach the cuff from the arm and press the START/STOP
button to stop inflation.
• This device is not AP/APG equipment and not suitable for use in the
presence of a flammable anesthetic mixture with air, or with oxygen,
or nitrous oxide.
• This unit is not suitable for continuous monitoring during
medical emergencies or operations. This device cannot be used
simultaneously with HF surgical equipment.
• This device is not intended for patient transports outside a healthcare
facility.
• To avoid measurement errors, please avoid strong electromagnetic
field radiated interference signals or electrical fast transient/burst
signals.
• The manufacturer will make available on request circuit diagrams,
component parts list etc. 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 sensitization or irritation
reaction. Never apply the cuff over damaged skin.
• Please dispose of any accessories, detachable parts, and the ME
EQUIPMENT itself according to your local guidelines.
• Please do not attempt to repair the unit yourself in the event of
malfunctions. Only have repairs carried out by authorized service
centers.
• Please report to Hopkins Medical Products if any unexpected
operation or events occur.
• We recommend that you have your device calibrated after every two
years of use. Please contact Hopkins Medical Products to have your
device calibrated.
• Please use only a soft cloth to clean the entire unit. Don’t use any
abrasive or volatile cleaners.
• Always check this device to make sure that it is in proper working
condition before use.
CAUTION
!
