The electromedical device generates controlled electromagnetic waves at high frequencies (2, 4 or 8 MHz), that overcome the biological barriers of tissues.
The technology has been developed specifically for skin lesions: the safety devices, present inside our devices, prevent any stress harmful to the patient in the treatment site. In addition, Rinovacell® does not require creams, conductive gels or anesthetics.
It is a portable medical device, designed specifically for health professionals working in the field of vulnology and dermatology and certified for the treatment of skin lesions of different etiology, both at the outpatient and at home.
How do high frequencies work therapeutically?
The high frequencies of Rinovacell® cause a significantly dilation of arterioles and capillaries, hence enhancing the local blood flow and allowing the repaerfusion of previously ischemic areas.
The local microenvironment, thanks to the additional blood flow, is replenished with metabolites and nutrients necessary for the physiological regeneration of the tissues. In addition, increased blood flow facilitates effective lymphatic drainage and reduces the amount of pro-pain and pro-inflammatory chemokines present in the context of the lesion.
Also the immune system is favored by high frequencies: the blood hyperinflux leads more white blood cells to the ulcerated site, thus speeding up the elimination of bacteria, and the reperfusion of the previously ischemic and damaged districts favors a rebalancing of the local inflammatory state: as an example, the macrophages are able to modify own phenotype, in proinflammatory or proregenerative direction, also based on the amount of oxygen present in the tissues.
Thanks to its dynamic action, Rinovacell® allows to:
Difficult skin wounds that respond well to treatment with Rinovacell®:
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Legislative Decree of 24 February 1997, No 46 Article 21
1. It is forbidden to advertise to the public devices that, according to provisions adopted by decree of the Minister of Health, may be sold only on prescription or may be used with the assistance of a doctor or other healthcare professional.
2. Advertising to the public of devices other than those referred to in paragraph 1 is subject to authorization by the Ministry of Health. On the requests for authorization expresses opinion the Commission of experts provided for by article 6, paragraph 3, of the legislative decree 30 December 1992, n. 541, which for this purpose is supplemented by a representative of the Department of the Ministry of Health responsible for medical devices and one of the Ministry of Industry, Commerce and Crafts.