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The Sani System is an electromedical device for high-level sanitization in environments with a high risk of biological contamination (class IIA medical device for professional use). Fields of application: sanitisation public places - sanitisation doctors’ surgeries - sanitisation dentists’ surgeries - sanitisation hospitals - sanitisation transport


Clinical testing of tolerability

The sanitising solution HPMed to be used with Sani System as an adjuvant to the sanitising action of steam was subjected to laboratory tests in order to examine its safety of use.

The clinical tests conducted by important microbiology research centres have shown that the mixture of steam and HPMed can be released in the presence of people.

  • Evaluation of acute inhalation toxicity
    Chemservice Laboratory, Milan, Italy

    The results obtained by means of in vivo laboratory tests of acute inhalation toxicity on rats have shown that the sanitising solution HPMed does not result as classified according to the GHS (Globally Harmonised System) classification and labelling system, at the highest concentration that can be reached ("Unclassified, because no effects were observed at the maximum achievable concentration"). On the basis of this result, according to the current European Community regulations (European Community Classification and Labelling Requirements for Dangerous Substances and Preparations), HPMed does not require any symbol/code or risk phrase whatsoever.


  • Dermatological evaluation study
    Chelab Laboratory, Treviso, Italy

    The results obtained with patch tests used for examining the skin compatibility in healthy volunteers showed that the sanitising solution HPMed, applied in non-occlusive conditions to the healthy skin of 20 volunteers caused an average irritation index of nil and did not therefore result as classified according to the GHS (Globally Harmonised System).