EU-IN_VITRO_MEDICAL_DEVICE_REG-ART_5_2_ANX_1

In Vitro Diagnostic Medical Devices Regulation - Hazardous Substances

EU. Hazardous Substances for Purposes of Art. 5(2) and Annex I of Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices, 5 May 2017, as corrected 27 December 2019

This list contains a non-exhaustive inventory of hazardous substances for purposes of Regulation (EU) 2017/746, including Chap. 2 (Placing on the market and putting into service) and Annex I (General Safety and Performance Requirements). 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).

EU CLP (1272/2008)
Acute Tox. 3; Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1

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Group members
This group of substance has the following member substances:
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Name EC / List no. CAS no. Association
Dipotassium tetrachloroplatinate 233-050-9 10025-99-7 Expert judgement
Tetraammineplatinum tetrachloroplatinate 237-501-0 13820-46-7 Expert judgement
Diammonium tetrachloroplatinate 237-499-1 13820-41-2 Expert judgement
Disodium tetrachloroplatinate 233-051-4 10026-00-3 Expert judgement
Dirubidium tetrachloroplatinate 237-503-1 13820-56-9 Expert judgement
Diamminetetrachloroplatinum 240-930-6 16893-05-3 Expert judgement
Platinate(2-), tetrachloro-, dihydrogen, (SP-4-1) - 17083-70-4 Expert judgement