Be
your own Doctor. Trust treatment to your own body.
Corporation "DENAS
MS" present the high quality devices for DENS-therapy such
as DENAS and DiaDENS.
We made DENS - technology affordable for many thousand people.
Buy now!
The
main principle of DENAS-family devices:
The device recover lost connections
between central nervous system and internal organs, launching process of
self-recovery in the human body. |
Advantages
of DENAS and DiaDENS devices.
1. The impulses of the device are built in such a way that they are close by their characteristics to neurological impulses. That's why they are interpreted as native neurological impulses by the human body. It makes recovery easier and more effective.
2. Devices has improved biological feedback which makes treatment more individual.
3. Devices can be apply at any age in domestic conditions.
4. Application at any stage of disease - during the acute period, at urgent conditions, and as/or supporting therapy.
5. Vast spectrum of indications and relatively small number of incompatibilities (individual intolerance of an electric current, presence of the cardiac pacemaker, the first trimester of pregnancy)
6.
Compatibility with other kinds of treatment
Acting in a natural way by supporting the regenerative capacity of the body and therefore helps the body to release its own healing potential, DENS-Therapy has become accepted as a new form of treatment in prevention, therapy and rehabilitation worldwide.
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These
devices are allowed to be used in medical practice by
the order of Ministry of Health of the Russian Federation,
Registered Certificate 29, No. 199/40-5, August, 23,
1993. Safety of the device is guaranteed by the State
license of Ministry of Health and the Medical Industry
of the Russian Federation and certificates of conformity.
Russian
Federal Service of control the public health and social
development sphere has granted “DENAS MS” Corporation
with Registration certificate ¹ FS-2005/004 for “Dynamic
electric stimulation” method on the 4-th of March,
2005.
The previous version of Scenar is regulated by the United States Food and Drug
Administration, under 21 CFR 882.5050. Generic name:
device, biofeedback, Product Code HCC, Class II exempt
from 510 (k) pre-market notification according to FDA
Notice FR21ja98-84 as a battery powered, professional
use device for relaxation training and muscle reeducation.
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