EU-MEDICAL_DEVICES_REGULATION-ANX_I_SEC_10

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).

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Asbestos fibres

EC / List no: - CAS no: -
EU CLP (1272/2008)
Carc. 1A; STOT RE 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
Asbestos, chrysotile 601-650-3 12001-29-5 Expert judgement (ECHA)
Asbestos, amosite 601-801-3 12172-73-5 Expert judgement (ECHA)
Asbestos, actinolite 616-471-6 77536-66-4 Expert judgement (ECHA)
Asbestos, tremolite 616-473-7 77536-68-6 Expert judgement (ECHA)
Asbestos, anthophyllite 616-472-1 77536-67-5 Expert judgement (ECHA)
Asbestos, crocidolite 601-649-8 12001-28-4 Expert judgement (ECHA)