The company operates according to a quality system certified ISO 13485: 2012 and in compliance with the European Directive for Medical Devices 93/42 / EEC (and subsequent updates). The products destined to the American market are FDA (USA Food and Drug Administration) registered. The reliability of Magic Care products is also guaranteed both at the European level by the CE0051 marking and by the monitoring of the product and production system by the most prestigious international approval Authorities (IMQ, Intertek, SGS, TÜV Rheinland, etc.) which, with their quality brands, certify their absolute compliance with current regulations.

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