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ProductPhysiotherapy & Orthopaedic Technology

LUMIX Q Nd:YAG Q-Switched Laser for Physiotherapy

Verduno (CN), Italy

Q-switched Nd:YAG laser system for physiotherapy and orthopedic treatment. Delivers high-peak-power pulses for pain management, tissue stimulation, and therapeutic applications in musculoskeletal rehabilitation. Suitable for clinical and rehabilitation settings.

Manufactured by

Verduno (CN), Italy

Fisioline® is an italian manufacturer of electromedical equipment which was established in 1985 and has been operating internationally for several years. Fisioline® sectors of experience are: PHYSIOTHERAPY, REHABILITATION, SPORTS MEDICINE, DENTISTRY, SURGERY, AESTETHIC MEDICINE, DERMATOLOGY, BEAUTY, PODIATRY and VETERINARY. Within Fisioline®, the Research and Development department holds a prominent position. A team of electronic engineers with solid experience in the electromedical field are always on the lookout for innovative solutions for developing cutting-edge equipment. Fisioline® has an internal production department managed by electronic technicians, guaranteeing a technical support and a direct and full technical assistance. Fisioline® manufactures avanguard laser devices. The cooperation of its engineers to projects with internationally well known universities has allowed Fisioline® to become the first Italian company that manufactured high power pulsed lasers back in 1993, opening up a new horizon for this kind of devices. The quality of Fisioline® products is certified in accordance with the main international standards. Striving for constant improvement has enabled Fisioline® to obtain certification for its Company Quality System in accordance with the UNI EN ISO 9001 and UNI CEI EN 13485standards. These certifications allow Fisioline® to effectively and safely operate concerning the design, the production and the technical assistance of its products, under a quality system that regulates the development. Fisioline® has always invested in scientific research reaching important goals as the FDA approval of its therapeutic laser devices. The FDA is the American governmental agency responsible for public health protection in USA. All electromedical equipment manufactured by Fisioline® comes with CE Medical certification, as required by the Directive 93/42/EEC, modified by the Directive 2007/47/EC on medical devices. Since 2004 Fisioline® laser devices have been obtained the FDA (Food and Drug Administration) approval. Fisioline follows a quality politicy aimed at a constant improvement of its products/services. Primary goals of the quality politicy: Therapeutic result Customer s satisfaction Constant improvement of the qualitative level Personnel s involvement Fisioline is a reliable partner! Why choose Fisioline? Made in Italy technologies Experience of more than 30 years in the Medical Field There are Fisioline Centers in over 30 Countries in the world 7 Divisions: MEDICAL, DENTAL, AESTHETIC MEDICINE, BEAUTY, SURGERY, PODIATRY, VETERINARY Complete range of devices Experimentations and scientific Support Rapid and long-lasting results Training with our Company Consultants Exclusive and solid working methodologies Prompt and qualified technical assistance A factor of uniqueness which distinguishes Fisioline® is the constant research in close collaboration with universities and professionals to produce scientific material, publications and working methods, which are available for the clients, to ensure the best results on patients.

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