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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 04 listopada 2024. Database contains 4821 unique substances/entries.
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201-969-4
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90-15-3
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Acute Tox. 4; STOT SE 3; Skin Irrit. 2; Eye Dam. 1 |
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203-544-9
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108-03-2
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Flam. Liq. 3; Acute Tox. 4 |
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200-752-1
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71-41-0
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Flam. Liq. 3; Acute Tox. 4; STOT SE 3; Skin Irrit. 2 |
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202-155-1
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92-43-3
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Acute Tox. 4 |
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202-706-6
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618-36-0;98-84-0
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Acute Tox. 4; Skin Corr. 1B |
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202-706-6
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618-36-0;98-84-0
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Acute Tox. 4; Skin Corr. 1B |
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201-800-4
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88-12-0
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Carc. 2; Acute Tox. 4; STOT RE 2; STOT SE 3; Eye Dam. 1 |
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214-012-0
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1072-63-5
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Repr. 1B |
yes |
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282-263-3
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84145-37-9
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Flam. Liq. 3 |
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203-872-2
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111-46-6
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Acute Tox. 4 |
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