EU-MEDICAL_DEVICES_REGULATION-ANX_I_SEC_10
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).
Last updated 13 rujna 2024. Database contains 4917 unique substances/entries.
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429-170-8
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134575-17-0
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Acute Tox. 4; STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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262-967-7
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61788-32-7
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VPVB very Persistent and very Bioaccumulative (article 57e) |
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262-967-7
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61788-32-7
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VPVB very Persistent and very Bioaccumulative (article 57e) |
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227-637-9
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5915-41-3
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Acute Tox. 4; STOT RE 2 |
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251-637-8
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33693-04-8
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Acute Tox. 4 |
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235-963-8
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13071-79-9
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Acute Tox. 1; Acute Tox. 2 |
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604-715-4
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149979-41-9
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Carc. 2; Repr. 2 |
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203-495-3
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107-49-3
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Acute Tox. 1; Acute Tox. 2 |
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608-879-8
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335104-84-2
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Repr. 2; STOT RE 2; Skin Sens. 1 |
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231-193-1
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7446-07-3
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Repr. 1B; Lact. |
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