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).

RELEVANT LEGISLATION
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lead alkyls

EC / List no: - CAS no: -
EU CLP (1272/2008)
Repr. 1A; Acute Tox. 2; Acute Tox. 1; STOT RE 2

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Group members
This group of substance has the following member substances:
Results list is empty
Name EC / List no. CAS no. Association
Ethyltrimethylplumbane 217-169-3 1762-26-1 Expert judgement
Tetramethyllead 200-897-0 75-74-1 Expert judgement
Lead, tetrapropyl- - 3440-75-3 Expert judgement
Plumbane, dibutyldiethyl- - 65121-94-0 Expert judgement
Plumbane, tetrakis(1-methylpropyl)- - 65151-08-8 Expert judgement
Plumbane, tetrakis(1-methylethyl)- - 14846-40-3 Expert judgement
Tetrabutylplumbane 217-649-2 1920-90-7 Expert judgement
Diethyldimethylplumbane 217-170-9 1762-27-2 Expert judgement
Triethylmethylplumbane 217-171-4 1762-28-3 Expert judgement
Tetraethyllead 201-075-4 78-00-2 Expert judgement