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 06 rujna 2024. Database contains 4917 unique substances/entries.
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V Viruses: Member States are to ensure that all viruses which have already been isolated in humains and which have not been assessed and allocated in this Annex are classified in group 2 as a minimum, except where Member States have proof that they are unlikely to cause disease in humans. |
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V Viruses: Member States are to ensure that all viruses which have already been isolated in humains and which have not been assessed and allocated in this Annex are classified in group 2 as a minimum, except where Member States have proof that they are unlikely to cause disease in humans. |
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213-801-7
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1014-70-6
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Acute Tox. 4 |
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204-535-2
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122-34-9
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Carc. 2 |
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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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231-853-9
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7761-88-8
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Ox. Sol. 2; Skin Corr. 1B |
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605-752-9
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175217-20-6
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STOT RE 2 |
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233-054-0
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10026-04-7
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Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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308076-74-6
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Carc. 1B |
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206-991-8
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409-21-2
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Carc. 1B |
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