IMPORTANT
¨
Change the electrodes
every 3 days
or when they no longer adhere to your
skin.
¨
Charge monitor daily for
at least two hours
or as needed using
only
the
monitor charger provided in the box.
Preventice Solutions
1717 N. Sam Houston Parkway West
Suite 100 Houston, TX 77038
www.preventicesolutions.com
888.747.1442
PAT-014 APR2017
Record Your Symptoms and Activities
3
¨
Push and hold the Event button until the symptom screen displays on the
screen.
¨
Touch the up or down arrows to scroll through the selections until the
symptom of your choosing is highlighted in the
CENTER
of the screen.
¨
Push the center button to select the highlighted entry. The activity screen
will display next.
¨
Using the arrows, scroll until the activity of your choosing is in the
CENTER
of the screen and select the highlighted entry.
¨
The “Event recorded successfully” screen will display briefly, then the
“Monitoring”
screen will appear.
Event
button
You have
20 seconds
to select the appropriate symptom and
20 seconds
to select the appropriate activity.
Keep the monitor away from water. Remove the monitor and the lead wires
when you bathe, swim or perform other similar activities.
IMPORTANT SAFETY INFORMATION
The BodyGuardian Verité is intended for acquiring ambulatory ECG signals from patients with coronary
problems or suspected coronary problems. Indications for conducting ambulatory recording include: 1)
Patients presenting symptoms such as shortness of breath, syncope of unknown origin, or dizziness which
may be due to arrhythmia or need to be excluded as cause 2) Monitoring the effect of drugs prescribed
as remediation for various atrial arrhythmias and ventricular rate 3) Post cardiac surgery 4) Diagnosed
sleep apnea patients to evaluate possible nighttime arrhythmias 5) Evaluating arrhythmias possibly due
to stroke or transient cerebral ischemia 6) Patients requiring rhythm correction due to palpitation or
other unknown arrhythmic disorder 7) Evaluation of bradycardia, tachycardia, atrial fibrillation and pause
8) Assessment of post myocardial infarction, hypertension and chronic lung disease. The BodyGuardian
Verité is not for use with patients with potentially life-threatening arrhythmias who require inpatient
monitoring or patients who the attending physician thinks should be hospitalized. The BodyGuardian Verité
does not provide interpretive or diagnostic statements. Interpretation and diagnosis is the responsibility
of a trained healthcare professional or physician. The BodyGuardian Verité is not intended for use for
monitoring infants weighing less than 10 kg. (22 lbs.). Only certified microSD memory card for recording
may be used. Do not connect anything other than a battery charger provided to the charge port on the
BodyGuardian Verité. Use only patient cables provided by TZ Medical, Inc. with the BodyGuardian Verité.
Failure to observe the procedures for early recording cessation may result in the loss of recorded data.
Disconnect patient leads before defibrillation. False positive and false negative pacer pulse detects may
occur when using Pacemaker Pulse Detection. False positives – may result from poor electrode connection
to the patient or a large amount of electrical interference from nearby source. False negatives – may occur
with pacemakers that are bipolar because of a weak pacemaker pulse signal at the patient’s skin. When
viewing the ECG data, the presence of pacemaker signals in the ECG trace should not be considered
true representations of the actual pacemaker stimulus amplitude. To avoid unintended battery discharge,
do not leave batteries in the recorder when it is not in use. To receive the best recording results, instruct
patients to stay away from heavy electrical equipment or other sources of electromagnetic interference.
This includes equipment such as electric blankets and heating pads. Avoid device contact with water. Do
not expose device to extreme temperatures (beyond the limits shown in the environmental specifications).
4
Daily Usage
