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
Back to the List

EU CLP (1272/2008)
Repr. 2; Acute Tox. 2; Acute Tox. 3; Skin Sens. 1

Help Help
Group members
This group of substance has the following member substances:
Results list is empty
Name EC / List no. CAS no. Association
2,6-dibromo-4-cyanophenyl butyrate 223-374-9 3861-41-4 Official source
2,6-dibromo-4-cyanophenyl octanoate 216-885-3 1689-99-2 Official source
2,6-dibromo-4-cyanophenyl heptanoate 260-300-4 56634-95-8 Official source
3,5-dibromo-4-hydroxybenzonitrile 216-882-7 1689-84-5 Official source