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 04 listopada 2024. Database contains 4917 unique substances/entries.
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Acute Tox. 4 |
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Acute Tox. 4 |
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Acute Tox. 3; STOT RE 2 |
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Acute Tox. 4 |
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Repr. 2; Acute Tox. 2; Acute Tox. 3; Skin Sens. 1 |
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Carc. 1A; Acute Tox. 4 |
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Carc. 1A; Acute Tox. 4 |
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Acute Tox. 2 |
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Benzenesulfonic acid, 2(or 4)-methyl-, compd. with benzenamine (1:1)
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70788-38-4
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Carc. 2; Muta. 2; Acute Tox. 3; STOT RE 1; Eye Dam. 1; Skin Sens. 1 |
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Acute Tox. 2 |
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