Operating Manual Version 6.3-04 of 10.10.18
7
1 PURPOSE
SCENAR Home
biofeedback transcutaneous electrostimulator
with individual dosing of reflex zone stimulation;
SCENAR Sport
transcutaneous three-mode electrostimulator with
individual dosing of reflex zone stimulation;
SCENAR Basic
transcutaneous dual-mode electrostimulator with
individual dosing of reflex zone stimulation.
SCENAR Home, SCENAR Sport, SCENAR Basic transcutaneous
electrostimulators
(hereinafter called the SCENAR device or the device or
SCENAR) are intended for general therapeutic non-invasive treatment of
the human skin in order to remove pain of different etiology, alleviate dis-
eases, and speed up the recovery process of the organs and systems in the
course of combined therapy of different diseases.
The SCENAR device can be used:
by home users and in medical and prophylactic institutions to re-
move or reduce pain syndromes of various genesis, swelling, to
speed up the recovery process and prevent complications after
traumas of any kind and also to restore dysfunctions of the body in
various diseases;
only in medical and prophylactic institutions
– as a stand-alone
treatment or alongside other therapies to remove postsurgical pain
syndrome and acute pain (including renal colic).
The SCENAR device is intended for use over a temperature range of
10 C to 35 C, and relative humidity up to 80 % at 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.
