RITM CHANS-Scenar Base Model

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-Scenar - "base model" of a personal device has a set of functions sufficient to support yourself and your family at home including in an emergency until medical help arrives. Compared with the version of CHANS-02-Scenar functional of device is supplemented "Swinging frequency" mode and the possibility of a combination of several modes of action.

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 90Hz
Frequency modulation: 30 Hz - 120 Hz
Frequency of the impulses: 90Hz
Dozed mode : Yes
Dynamic screening: Yes
External electrodes port: Yes
Power supply: 9V battery
Warranty:  24m.

Manual in English and Russian

The effectiveness of Device Scenar increases significantly,  if you use healing Blanket ULM or ULM Clothes.

Certifications:
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