The partnership between ASAlaser and Eickemeyer, a leading player in the distribution of devices for veterinary medicine in Germany, has become official with a training held in Vicenza. «We are very glad to join forces with an avant-garde laser company that is able to provide us a product supported by clinical evidences» has commented Alexander Sprung, Eickemeyer Managing Director. Similar has been the satisfaction expressed by ASAlaser CEO Lucio Zaghetto: «We are confident that with Eickemeyer staff, well known for its professionalism, we will work better in order to give maximum emphasis to MLS® Laser Therapy also in Germany». The relationship between the two companies have been active from the beginning: Eickemeyer has dedicated to its House Organ "Plus" an article focused on MLS® and Mphi Vet product, while ASAlaser staff has organized two training days dedicated to Eickemeyer product specialist Nicola Hauser, veterinary technician with experience in laser therapy. Divided into a theoretical session (basic principles of MLS® Laser Therapy and Mphi Vet and Mphi Vet Orange devices) and in a practical one, the training has been very useful, having also allowed to verify the therapy effectiveness on case studies. At Azienda Agricola Corte Giorgiana, Dr. Hauser, led by Dr. Mila Speciani (ASAveterinary Product Specialist) has in fact performed therapy sessions with a Mphi Vet Equine directly on horses. «Great satisfaction has been expressed by the Eickemeyer referent at the end of the day - said Roberto Terruzzi, ASAlaser Area Manager - during which it has been also possible to verify the treatment on small animals, already deepened during two previous occasions. The goal of this course, strengthen the skills of our referent about MLS® Laser Therapy, has been fully achieved. We are confident that our partnership will be a success».
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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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