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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425-240-7
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-
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Eye Dam. 1 |
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KELCOR; LIPOKEL; SEQUOL
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425-230-2
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16610-63-2
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Skin Corr. 1B |
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425-210-3
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169939-84-8
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Skin Sens. 1 |
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425-190-6
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119916-05-1
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STOT RE 2 |
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425-160-2
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24085-06-1
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Acute Tox. 4; STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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425-150-8
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94723-86-1
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Repr. 1B; Acute Tox. 4; Skin Sens. 1 |
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425-080-8
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104860-26-6
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Acute Tox. 4; STOT RE 2; Eye Dam. 1 |
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425-050-4
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10217-34-2
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Skin Sens. 1 |
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425-030-5
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159939-85-2
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Repr. 2; Acute Tox. 4; Skin Corr. 1B; Skin Sens. 1 |
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424-980-8
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22288-41-1
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Flam. Liq. 2; Org. Perox. D; Skin Irrit. 2; Skin Sens. 1 |
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