"Rehab and Sanatorium Treatment Congress”, congress held in Moscow from 24 September to 25, has represented for ASAlaser something more than a meeting dedicated to doctors and physiotherapists. The two days of meetings and insights that has taken place at the Moscow Government Information Center has been to Hilterapia®, MLS® Laser therapy and Magneto Therapy an important showcase, thanks also to thousand professionals expected to the Congress and to the numerous visitors to the stand. Beka, ASAlaser's dealer for Russia, has given wide space to Company therapies and devices, also promoting them through an unusual but attractive travelling kart with a monitor for video transmission. The feedbacks obtained confirmed the effectiveness of this double action, also signed by the success achieved by the report devoted to Hilterapia® held by Lucio Zaghetto (CEO ASAlaser ), referred as official speaker in the "Innovation Technologies" section of the scientific program of the meeting. «The courtroom reserved for exhibitions - confirms Giacomo Granozio, ASAlaser Area Manager - was crowded beyond the expectations of the organizers, confirming that the interest of the Russian market for our therapies is rising». Maximum attention manifested by the participants too: after having learned the uniqueness, the application directions, the results obtained in short time and the possibility of combination with other therapeutic techniques of the HILT® pulse, they showed a tangible desire for further study. «The Russian market shows a special care on our therapeutic proposals, already in force in some of the most prestigious local structures and object of interest by major institutions. Feedback from the field make us thinking that there is margin for further penetration of our solutions: therefore we will work in this direction also during 2014» concludes Zaghetto.
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Decreto Legislativo 24 febbraio 1997, n°46 Articolo 21
1. E' vietata la pubblicità verso il pubblico dei dispositivi che, secondo disposizioni adottate con decreto del Ministro della Sanità, possono essere venduti soltanto su prescrizione medica o essere impiegati eventualmente con l'assistenza di un medico o di altro professionista sanitario.
2. La pubblicità presso il pubblico dei dispositivi diversi da quelli di cui al comma 1 è soggetta ad autorizzazione del Ministero della Sanità. Sulle domande di autorizzazione esprime parere la Commissione di esperti prevista dall'articolo 6, comma 3, del decreto legislativo
30 dicembre 1992, n. 541, che a tal fine è integrata da un rappresentante del Dipartimento del Ministero della Sanità competente in materia di dispositivi medici e da uno del Ministero dell'Industria, del commercio e dell'artigianato.
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