With this belief, in collaboration with our partner Celtic SMR, the M-Hi & HIRO TT Tour was launched: a program of workshops and training that combined theory, practice, and clinical comparison to explore the potential of the ASA laser devices in rehabilitation protocols.
From 30 September to 3 October, the tour visited three cities in the United Kingdom, involving physiotherapists and specialists who have chosen the M-Hi and HIRO TT laser systems.
Each stage was designed to offer a comprehensive training experience, thanks to the guidance of Salvatore Germano, ASA Field Application Specialist, who alternated theoretical sessions with practical sessions on real cases.
The first workshop took place in an exclusive setting: a Corporate Box at the “Tetley Leeds Stadium”, where 12 professionals took part in an interactive session supported by chiropractor Mark Kingham.
The meeting focused on laser therapy principles, EU MDR-approved ASA protocols, and strategies for an effective clinical use of laser technology.
Training on HIRO TT, the first device installed in the UK, was held at Mark Kingham's Spine Care in Motion clinic.
This was an opportunity to learn more about the applications of the patented Hilterapia® technology for musculoskeletal conditions and to experience the laser system's performance firsthand.
The final stage took place at Mike Grice's Movement Therapy clinic, a sports specialist and ultrasound consultant for Celtic SMR.
Here, a group of professionals took part in an advanced practical session dedicated to the correct therapeutic approach and to customising the laser protocols, with a particular focus on the sports sector.
Investing in targeted and in-depth sessions means providing professionals not only with excellent technology, but also with the expertise needed to best exploit this, improving treatment outcomes and patient satisfaction.
The collaboration with Celtic SMR is part of this vision: to build, together with our international partners, a shared laser therapy culture based on knowledge, continuous training, and quality.
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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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