This year too, ASAlaser could not be missing at MEDICA, the most important international event in the medical sector, attended by professionals, buyers, and specialists from all over the world, which was held from the 14th to the 17th of November in Düsseldorf. The event is an excellent showcase for the equipment and applicative technologies created by ASAlaser, other than being an important opportunity to acquire new international contacts, implement the already existing ones, and consider the building of new partnerships for research.
With the aim of giving more visibility to its products, ASAlaser’s staff presented, in its exhibition space, the entire range of devices for the application of MLS® Laser Therapy, Hilterapia®, and Qs Magnetotherapy, an area that was very crowded by the numerous meetings that occurred throughout the event.
‘We had the pleasure of meeting - said Leonardo Turolla, ASA Sales & Marketing Director - an important number of distributors and customers coming from all continents, with whom we discussed and fine-tuned the program for 2017, and laid the foundation for an even stronger medical-scientific collaboration. Also thanks to the many new contacts, in particular from China, Middle East, and Latin America, interested in receiving information on the areas of application and the technology itself, MEDICA ends with a feeling of optimism for ASAlaser, opening up prospects for a consolidated future of international scope. Many visitors, willing to establish a possible relationship of collaboration, already knew ASAlaser, confirming the excellent advertisement work of the company's know-how by the distribution network, combined with the growth of the brand around the world.’
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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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