EU-IN_VITRO_MEDICAL_DEVICES-ART_3_ANX_1
EU-IN_VITRO_MEDICAL_DEVICES-ART_3_ANX_1
In Vitro Diagnostic Medical Devices Directive - Hazardous Substances
EU. Hazardous Substances for Purposes of Article 3 & Annex I (Essential Requirements), Directive 98/79/EC on In Vitro Diagnostic Medical Devices, 7 December 1998
This list contains a non-exhaustive inventory of hazardous substances for purposes of essential requirements (Article 3 and Annex I) for general safety, design, manufacture and hazard communication of in vitro diagnostic medical devices. It 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). Note that Regulation 2017/746/EU on in vitro diagnostic medical devices was published in the EU Official Journal on 5 May 2017. With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.
Last updated 07 listopada 2024. Database contains 4821 unique substances/entries.
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CLETOPROPAMINHYDROCHLORID
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429-740-6
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40722-80-3
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Carc. 1B; Muta. 1B; STOT RE 2; Skin Sens. 1 |
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284-351-7
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84852-39-1
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Carc. 1A; Muta. 2; Repr. 1B; STOT RE 1; Resp. Sens. 1; Skin Sens. 1 |
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287-470-2
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85508-45-8
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Carc. 1A; Muta. 2; Repr. 1B; STOT RE 1; Resp. Sens. 1; Skin Sens. 1 |
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440-620-2
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920-36-5
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Water-react. 1; Pyr. Liq. 1; Skin Corr. 1A; STOT SE 3 |
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420-370-0
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6485-67-2
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Eye Irrit. 2; Skin Sens. 1 |
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-
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75166-31-3
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yes |
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UK-103,449-BV
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427-100-0
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-
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Acute Tox. 4; Eye Dam. 1; Skin Sens. 1 |
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433-820-6
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118058-74-5
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Eye Irrit. 2 |
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4-AA; AOSA; AZETIDONE-KANEKA; GR91990X
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408-050-9
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76855-69-1
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Eye Irrit. 2; Skin Sens. 1 |
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425-260-6
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244634-31-9
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STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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