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 26 srpnja 2024. Database contains 4917 unique substances/entries.
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701-162-1
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Repr. 1B |
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701-118-1
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2156592-54-8
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Repr. 1B; Eye Irrit. 2 |
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701-107-1
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1801269-77-1
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Repr. 1B; Skin Corr. 1C; Eye Dam. 1 |
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701-105-0
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1801269-80-6
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Repr. 1B; Skin Corr. 1C; Eye Dam. 1 |
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700-960-7
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VPVB very Persistent and very Bioaccumulative (article 57e) |
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700-242-3
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62037-80-3
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E Equivalent level of concern having probable serious effects to the environment (Article 57(f) - environment) HH Equivalent level of concern having probable serious effects to human health (Article 57(f) - human health) |
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695-989-4
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2527-66-4
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Acute Tox. 4; Acute Tox. 3; Skin Corr. 1C; Eye Dam. 1; Skin Sens. 1A |
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692-456-8
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688046-61-9
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Carc. 2 |
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691-719-4
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1072957-71-1
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Acute Tox. 3 |
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688-331-2
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874967-67-6
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Carc. 2 |
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