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 04 listopada 2024. Database contains 4917 unique substances/entries.
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90568-23-3
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R Toxic for reproduction (article 57c) |
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ADK STAB AO 80; SUMILIZER GA-80
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410-730-5
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90498-90-1
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Acute Tox. 4 |
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291-844-0
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90481-04-2
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ENDE Endocrine disrupting properties (Article 57(f) - environment) |
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618-541-1
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9036-19-5
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ENDE Endocrine disrupting properties (Article 57(f) - environment) |
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427-880-2
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90357-53-2
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STOT RE 2 |
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PAYLEAN; RACTOPAMINE HYDROCHLORIDE
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415-170-5
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90274-24-1
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Acute Tox. 4; Skin Sens. 1 |
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620-365-5
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9016-72-2
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Acute Tox. 4; STOT RE 2; Skin Sens. 1 |
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500-024-6
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9016-45-9
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ENDE Endocrine disrupting properties (Article 57(f) - environment) |
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232-752-2
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9014-01-1
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STOT SE 3; Skin Irrit. 2; Eye Dam. 1; Resp. Sens. 1 |
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232-734-4
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9012-54-8
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Resp. Sens. 1 |
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