ASAlaser therapies land at university: the conference hall of the Academy of Sports Medicine and Rehabilitation of Bucharest, on February 22nd has hosted the course "Efficiency of MLS® Laser Therapy and Hilterapia® in the treatment of pain, inflammation and edema”, organized by the Romanian distributor S.C. Procardia in partnership with the "Societatea Fizioterapeutilor Dr. Nicolae Robanescu".
ASAlaser staff has entartained more than 50 members, including physicians and physiotherapists, in a double session of theoretical study with focus Hilterapia® and MLS® Laser Therapy, their basis, application protocols and devices. Attention has also been dedicated to practical tests carried out on patients, previously selected.
«I’ve had the honor to have by my side, at this stage, some leading figures of local health facilities - says Lucio Zaghetto, ASAlaser CEO and supervisor of the course - such as Dr. Gigi Theodoru, Head of the Department of Rehabilitation Central Military Hospital in Bucharest "Carol Davila", and Dr. Alina Momanu, Head of the Department of Rehabilitation Hospital Iaşi in Moldova. Their experiences, gained respectively in the use of HILT® and MLS® have been very useful, in particular during the second day of the course».
On February 23rd the two Romanian professionals, supported by Dr. Zoltan Csiki - user of Hilterapia® in his own private clinic (Optisport) and of MLS® in Jászberény Hospital (Hungary) – have continued the training with sessions dedicated to successful cases and further practical tests. «We are very pleased about the results of this course - says Roberto Terruzzi, ASAlaser Area Manager- first of all for the genuine interest among the participants, very active in both theoretical and practical sessions. They were very excited to understand new perspectives in their daily practice thanks to our two therapies».
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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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