

- Class Iª medical device pursuant to Regulation (EU) 2017/745. National Classification of Medical Devices (CND) pursuant to D.M. Min. Health of June 8, 2016: Cod. T010201. D.M. enrolled in the Repertoire of Medical Devices pursuant to D.M. Min. Health of 20.2.2007 as amended. Conforms to EN 455 standards 1,2,3,4. - Type B Personal Protective Equipment against chemicals and microorganisms, including viruses, to be used for activities falling under risk category III (Regulation (EU) 2016/425). Complies with the Technical Standards EN ISO 374-1:2016 +A1:2018 , EN ISO 374-5:2016 and EN 420:2003 + A1:2009 harmonized with Regulation (EU) 2016/425
- Class Iª medical device pursuant to Regulation (EU) 2017/745. National Classification of Medical Devices (CND) pursuant to D.M. Min. Health of June 8, 2016: Cod. T010201. D.M. enrolled in the Repertoire of Medical Devices pursuant to D.M. Min. Health of 20.2.2007 as amended. Conforms to EN 455 standards 1,2,3,4. - Type B Personal Protective Equipment against chemicals and microorganisms, including viruses, to be used for activities falling under risk category III (Regulation (EU) 2016/425). Complies with the Technical Standards EN ISO 374-1:2016 +A1:2018 , EN ISO 374-5:2016 and EN 420:2003 + A1:2009 harmonized with Regulation (EU) 2016/425
- Class Iª medical device pursuant to Regulation (EU) 2017/745. National Classification of Medical Devices (CND) pursuant to D.M. Min. Health of June 8, 2016: Cod. T010201. D.M. enrolled in the Repertoire of Medical Devices pursuant to D.M. Min. Health of 20.2.2007 as amended. Conforms to EN 455 standards 1,2,3,4. - Type B Personal Protective Equipment against chemicals and microorganisms, including viruses, to be used for activities falling under risk category III (Regulation (EU) 2016/425). Complies with the Technical Standards EN ISO 374-1:2016 +A1:2018 , EN ISO 374-5:2016 and EN 420:2003 + A1:2009 harmonized with Regulation (EU) 2016/425