CHANS-SCENAR is a particular version of the device that can be used at home and in any other conditions (on a business trip or a journey, in a car, in a plane, etc.) to alleviate the pain, to treat respiratory diseases, relieve from problems at traumas, burns, frostbite
Medical personnel can use this device to treat any diseases.
CHANS-02- "SCENAR" - a budget model of series devices CHANS "SCENAR" with an additional mode dosed, which implemented the amplitude modulation of 3: 1. Indispensable in the home, and any other conditions for the treatment of pain, the treatment of respiratory diseases, injuries, burns, frostbite, etc. The indication mode setting and displaying of exposure by using LEDs.
CHANS-02-Scenar - is the easiest to use of all the production devices for home use. Designed to provide emergency assistance and treatments of various diseases. This device be usable by all, regardless of age.
In this device two operating modes. F1 - is a constant mode of action (subjectively dosed) and F2- Diagnostic (objectively dosed) in acute conditions recommended mode F1. To carry out a course of treatment for chronic diseases using F2 mode.
Each of our devices has a unique SCENAR impulse, which is effective in any modification.
- Support, maintenance, repair, accelerating the treatment at any age.
- Elimination of any type of pain, edema, acute conditions.
- Comfort of life with different diseases.
- Treating "household" disease (trauma, burns, cuts, etc.).
- Smart home device
- It is used as a substitute for allergic reactions to medications
- "ER" in acute conditions yourself and loved ones at home and travel.
Individually-dozed mode: Yes - only at 60Hz
Amplitude modulation: 3:1 only at 60Hz
Frequency modulation: No
Frequency of the impulses: 90Hz, 60Hz
Dozed mode : Yes - only at 60Hz
External electrodes port: Yes
Power supply: 9V battery
Manual in English and Russian
The effectiveness of Device Scenar increases significantly, if you use healing Blanket ULM or ULM Clothes.
USA (FDA code of Federal Regulations): The SCENAR device, Biofeedback-controlled electro-stimulator, 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 (Federal Register), Jan. 21, 1998, p. 84) as a battery-powered, professional use device . www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?FR=882.5050
EUROPE: The SCENAR device has received a CE-mark in Europe (CE 60906 BSI).
AUSTRALIA: The SCENAR device listed on the Australian Register of Australian Goods (ARTG). The registration listing number is 101783