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 11 listopada 2024. Database contains 4918 unique substances/entries.
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202-776-8
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99-65-0
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Acute Tox. 2; Acute Tox. 1; STOT RE 2 |
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211-463-5
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646-06-0
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Flam. Liq. 2 |
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203-002-1
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102-06-7
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Repr. 2; Acute Tox. 4; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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214-317-9
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1120-71-4
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Carc. 1B; Acute Tox. 4 |
C Carcinogenic (article 57a) |
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207-964-3
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503-30-0
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Flam. Liq. 2; Acute Tox. 4 |
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204-077-3
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115-27-5
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Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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219-603-7
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2475-45-8
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Carc. 1B; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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425-450-9
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294-90-6
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Skin Corr. 1B; Acute Tox. 4 |
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AZA-KRONE-DISULFAT; SQ 84,042F
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412-080-8
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112193-77-8
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Acute Tox. 4; STOT SE 3; Eye Dam. 1 |
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AZA-KRONE-TETRATOSYLAT
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414-030-0
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52667-88-6
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Skin Sens. 1 |
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