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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 10 rujna 2024. Database contains 4821 unique substances/entries.
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U 9649
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401-380-4
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89066-61-5
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Eye Irrit. 2 |
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201-956-3
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89-98-5
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Skin Corr. 1B |
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201-944-8
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89-83-8
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Acute Tox. 4; Skin Corr. 1B |
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201-898-9
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89-32-7
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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SCH.19927 DIBENZOYLTARTRATE
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404-390-7
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88976-55-0
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Flam. Sol. 1; Skin Sens. 1 |
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SULPHONAMIDO-ANILINE
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406-010-5
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88918-84-7
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Eye Dam. 1; Skin Sens. 1 |
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CA 875 B
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414-450-4
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88805-65-6
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Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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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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SYSTHANE TECHNICAL
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410-400-0
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88671-89-0
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Repr. 2; Acute Tox. 4; Eye Irrit. 2 |
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SIS 46 305
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408-010-0
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88558-41-2
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Acute Tox. 4; Eye Dam. 1 |
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