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 19 rujna 2024. Database contains 4917 unique substances/entries.
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B Bacteria and similar species |
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B Bacteria and similar species |
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B Bacteria and similar species |
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BASIC YELLOW 105; C.I. BASIC YELLOW 105
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405-860-4
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121315-16-0
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Skin Sens. 1 |
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405-060-5
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118712-89-3
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Carc. 2; Acute Tox. 4; STOT SE 1 |
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443-150-6
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101226-85-1
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Flam. Liq. 3 |
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250-517-2
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31218-83-4
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Acute Tox. 3 |
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205-860-2
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156-60-5
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Flam. Liq. 2; Acute Tox. 4 |
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238-009-9
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14166-21-3
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
RSP Respiratory sensitising properties (Article 57(f)) - human health) |
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SQ 27,616
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416-020-1
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96314-26-0
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Repr. 2; Skin Sens. 1 |
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