The promotional activities of our partner in USA, Cutting Edge Laser Technologies, continue in full swing. The company took part in two top events of the therapeutic scene within a few days of each other, finding keen interest in the ASAlaser solutions by many new interlocutors.
‘The Parker Experience 2017’
The Paris Hotel and Casino in Las Vegas hosted, from 23th to 25th February, the training event of the Parker Seminars, known worldwide and aimed at chiropractors and professionals looking for innovation and new therapeutic approaches. Our dealer obviously couldn’t miss ‘The Parker Experience 2017’: there with a stand dedicated to the MLS® Laser Therapy, it exhibited the M6 device. The turnout was good and numerous were the new interlocutors who wanted to explore the therapeutic solution ASAlaser. The staff of Cutting Edge Laser Technologies was visited by several clients who took advantage of the occasion to reiterate their satisfaction with the equipment for MLS® Laser Therapy.
‘Scientific Conference ACFAS 2017’
On 27th February, it was the turn of another major conference organized by the American College of Foot and Ankle Surgeons, at its 75th anniversary. In the environments of the prestigious Mirage Hotel and Casino in Las Vegas, the event brought together about 1,500 ACFAS members. Even during this event, in which our dealer exhibited the devices for MLS® Laser Therapy M6 and Mphi 5, many new contacts were registered, and several clients visited to convey their satisfaction with the results they are getting with the ASAlaser systems.
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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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