User Manual - R.Test Evolution 4 EN V2019-12/06/2019 Page 5
2 Introduction
2.1 Description of the device
The R.Test Evolution 4 is a miniature automatic ECG arrhythmia detection device; it is
quick and easy to fit to the patient. It is designed to detect and store the most
important pathologic events (symptomatic or asymptomatic) as well as the patient’s
continuous heart rate, and is capable of up to 32 days of ambulatory monitoring.
The system consists of a unit weighing approximately 40 grams that can be worn by
the patient unobtrusively and without any discomfort. The R.Test Evolution 4 is
connected to the patient by a system of electrodes and a neck cable. Events stored
by the R.Test Evolution 4 are then transferred to a computer for interpretation via a
USB cable.
The use of a computer will allow:
- the programming of the conditions and criteria for each recording made by the
R.Test Evolution 4.
- in addition, to select, organize and store the results of the examinations, then to
print a customised report according to your needs.
2.2 This manual
This manual describes the physical operation, instructions, characteristics, technical
specifications and the particular recommendations of use of the R.Test Evolution 4
and its accessories.
Although the greatest care was taken in its drafting, in order to make it as complete
as possible, NOVACOR does not accept any responsibility for any errors, omissions or
inaccuracies which it may contain.
The functionalities of the device and the accessories, as well as the contents of the
manual, can be modified by NOVACOR without notice.
2.3 Safety information
Intended Users:
The R.Test Evolution 4 is intended for use by a licensed physician, or a person
working under their supervision, after having read the R.Test 4 and RTSoft Ultima
user manuals. No further training is necessary to use the equipment.
The patient is required to wear the device and should trigger recordings manually,
the physician should ensure that the mental and physical condition of the patient is
compatible with an R.Test procedure. The physician should inform the patient of the
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