In Vitro Diagnostic Medical Devices Directive - Hazardous Substances

EU. Hazardous Substances for Purposes of Article 3 & Annex I (Essential Requirements), Directive 98/79/EC on In Vitro Diagnostic Medical Devices, 7 December 1998

This list contains a non-exhaustive inventory of hazardous substances for purposes of essential requirements (Article 3 and Annex I) for general safety, design, manufacture and hazard communication of in vitro diagnostic medical devices. It 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). Note that Regulation 2017/746/EU on in vitro diagnostic medical devices was published in the EU Official Journal on 5 May 2017. With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.

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Last updated 14 lipnja 2024. Database contains 4821 unique substances/entries.
Substance Name EC No. CAS No. EU CLP (1272/2008) EU_BA Directive 2000/54/EC EU REACH: List of SVHC
Platinate(2-), tetrachloro-, dihydrogen, (SP-4-1) EC / List no: - | CAS no: 17083-70-4
Disodium tetrachloroplatinate EC / List no: 233-051-4 | CAS no: 10026-00-3
Diammonium tetrachloroplatinate EC / List no: 237-499-1 | CAS no: 13820-41-2
Dirubidium tetrachloroplatinate EC / List no: 237-503-1 | CAS no: 13820-56-9
Tetraammineplatinum tetrachloroplatinate EC / List no: 237-501-0 | CAS no: 13820-46-7
Dipotassium tetrachloroplatinate EC / List no: 233-050-9 | CAS no: 10025-99-7
Diamminetetrachloroplatinum EC / List no: 240-930-6 | CAS no: 16893-05-3
Acute Tox. 3; Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1

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