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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603-804-5
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134237-52-8
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PBT Persistent, Bioaccumulative and Toxic (article 57d) |
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603-802-4
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134237-51-7
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PBT Persistent, Bioaccumulative and Toxic (article 57d) |
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603-801-9
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134237-50-6
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PBT Persistent, Bioaccumulative and Toxic (article 57d) |
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603-792-1
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134098-61-6
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Acute Tox. 3; Acute Tox. 2; Skin Sens. 1B |
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603-524-3
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131860-33-8
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Acute Tox. 3 |
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603-520-1
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131807-57-3
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STOT RE 2 |
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603-411-9
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1303-96-4
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Repr. 1B |
R Toxic for reproduction (article 57c) |
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603-404-0
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130328-20-0
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Repr. 2; Skin Irrit. 2; Eye Dam. 1 |
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603-146-9
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126535-15-7
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Carc. 2 |
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603-038-1
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125225-28-7
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Repr. 1B; Acute Tox. 4; STOT RE 2 |
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