|
DiaDENS.
Advanced SCENAR-technology. |
Devices DiaDENS-T -
best choice to cure chronic diseases. Leader of
sales.
-
Biological feedback
-
Six modes of operations
-
No contra-indications*
- "Screening" mode for fast diagnose of trigger zones.
-
High reliability in use
- Multipurpose liquid crystal display
- 9 volt battery
|
Devices DiaDENS-DT -
more opportunities for diagnostics and treatment.
-
Biological feedback
-
Equipped with electro-punctual
diagnostics "BYOREPER" and "Voll method"
- Six modes
of operations
-
No contra-indications*
- "Screening" mode for fast diagnose of
trigger zones.
-
High reliability in use
- Multipurpose liquid crystal display
-
9 volt battery |
Devices of series DiaDENS - a new stage of DENS-THERAPY.
Within the DENAS family of devices,there are three devices within the series
called DiaDENS. These are: DiaDENS-T, DiaDENS-DT and DiaDENS-PC. (The DiaDENS-PC has all the features of the DiaDENS-DT plus features that are unique and are described seperately).
All of these DiaDENS devices represent a major advancement in the development of
non-invasive and highly effective medical techniques that are outstanding for applying DENS-THERAPY.
The distinctive features of DiaDENS as applied to DENS (Dynamic TENS)-therapy
include:
- The DiaDENS devices are equipped with advanced
diagnostic modes for fast search of the zones demanding further
hardware influence.
The advanced mode of diagnostics is referred
to as "Screening".
- The upgraded DiaDENS-DT is equipped with electro-punctual
diagnostics BYOREPER* and Voll method**, which estimates
the
immediate functional
condition of internal organs and meridians, here and now.
- All the DiaDENS devices offer a wide range of frequencies from 10 up to 200 Hz for a powerful therapeutic
influence a maximum of diseases, conditions and chronic pain syndromes.
- The DiaDENS microcomputer program called MED (Minimal Effective
Doze of influence) allows the device to generate signals that are designed to prevent the development
of many diseases and conditions. These also raise the awareness or perception of a human body to
DENS-influence that involve chronic diseases.
- A remote electrode is included with the complete set of the DiaDENS device and can be
applied as an influence on the auricular and others biologically active points.
- The DiaDENS provides a convenient individual adjustment that controls the level of power capacity of the signal. This is
for people of any age and with various degrees of skin sensitivity.
- The DiaDENS systems maintain a very high reliability factor in usage.
- A multipurpose liquid crystal display is provided for ease of monitoring and visual control.
* BIOREPER program - a method of electropuncture auriculodiagnostics (diagnostics relating to the auricle) to assess the functional state of all internal organs and systems, unique to DiaDENS-DT and PC devices.
** FOLL program - method of electropuncture assessment of the state of energy meridians and internal organs and systems in the human body. Can be used for TESTing and selection of homeopathic and allopathic remedies and food supplements, unique to DiaDENS-DT & PC devices.
*Devices
have no contraindications except for:
- built-in cardiostimulator (heart pacemaker)
- first trimester of pregnancy
- serious disease of mind
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
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.
|
