Operating Manual Version 7.3-03 of 28.07.20
6
1 PURPOSE
RITMSCENAR
Super
Pro
v.2
transdermal
electroneurostimulator
–
(hereinafter – the device or SCENAR) – is
intended for delivering general therapeutic non-invasive treatment to the
physiological systems of the body via human skin areas in order to treat
various pathologies.
The device is intended to treat and rehabilitate people and can be
used by medical professionals in medical-prophylactic institutions, hospi-
tals, emergency care units as well as at home according to the doctor’s
prescription.
The device should be used under temperatures between 10 C and
35 C with relative humidity not to exceed 80 % at a temperature of 25 C.
Potential risk from the device usage refers to Class IIa (2a)
DIRECTIVE 93/42/EEC (GOST R 31508).
The device complies with the standards EN 60601-1 (GOST R
50267.0) and EN 60601-2-10 (GOST R 50267.10) for internally powered
equipment, type BF, which classifies it as a safe device for personal use.
2 SPECIFICATIONS
2.1 Supply voltage – from 4 up to 6.4 V (four 1.5 V alkaline batteries).
2.2 Maximum supply current – not greater than 650 mA.
2.3 At a load as shown in Fig.1 SCENAR provides:
2.3.1 two-phase stimuli without a DC-component (see Fig.2) with a
waveform depending on the skin impedance under the electrode
(see Fig.3 through 5) generated at a fixed frequency that can be
controlled within 15 to 350 Hz ± 5 %.
2.3.2 control of the stimulus’ 1
st
phase duration (see Fig.2) within
(4 ± 2) to (500 ± 50) µsec, and the amplitude of the first pulse of
the stimulus 2
nd
phase at L1 load as shown in Fig.1 varies from
(1.7…2.5) V to (100…150) V;
