Medical Devices Regulation - Hazardous Substances

EU. Hazardous Substances for Purposes of Medical Devices Regulation 2017/745/EU, 5 May 2017, as amended by Regulation 2020/561/EU, 24 April 2020

This list contains hazardous substances for purposes of the Medical Devices Regulation (MDR), based on the legislation's Annex I general safety and performance requirements, including for chemical, physical and biological properties. Specifically, the non-exhaustive database is derived from: Table 3 of Annex VI to CLP, REACH Candidate List of SVHCs, and Directive 2000/54/EC's Annex III (Biological Agents list).

oxiranemethanol, 4-methylbenzene-sulfonate, (S)-

DAISO CCS-1S-E; S-GLYTO EC / List no: 417-210-7 CAS no: 70987-78-9
EU CLP (1272/2008)
Carc. 1B; Muta. 2; Eye Dam. 1; Skin Sens. 1