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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201-501-9
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83-79-4
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Acute Tox. 3; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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822-682-6
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1417782-03-6
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Skin Sens. 1 |
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-
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75166-30-2
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R Toxic for reproduction (article 57c) |
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443-560-5
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88784-33-2
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Eye Irrit. 2 |
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208-164-7
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513-49-5
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Flam. Liq. 2; Acute Tox. 4; Skin Corr. 1A |
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427-200-4
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76646-91-8
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Acute Tox. 4; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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CIN 10094329; SENSIBILISATOR KF 693 PINA; SENSITIZER KF 693 PINA
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422-240-9
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166596-68-5
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Eye Dam. 1; Skin Sens. 1 |
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265-294-7
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64969-36-4
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Carc. 1B; Acute Tox. 4 |
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428-230-0
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79568-06-2
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STOT RE 2 |
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222-048-3
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3327-22-8
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Carc. 2 |
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