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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 13 rujna 2024. Database contains 4821 unique substances/entries.
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229-977-3
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6876-12-6
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Flam. Liq. 3; Skin Irrit. 2; Skin Sens. 1 |
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DHP OPT
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445-770-2
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42031-28-7
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Eye Dam. 1 |
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231-186-3
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7443-52-9
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Acute Tox. 4 |
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SQ28,646
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419-160-1
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90657-55-9
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Repr. 2; Acute Tox. 4; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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SQ 27,616
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416-020-1
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96314-26-0
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Repr. 2; Skin Sens. 1 |
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238-009-9
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14166-21-3
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
yes |
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205-860-2
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156-60-5
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Flam. Liq. 2; Acute Tox. 4 |
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250-517-2
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31218-83-4
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Acute Tox. 3 |
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443-150-6
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101226-85-1
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Flam. Liq. 3 |
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405-060-5
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118712-89-3
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Skin Irrit. 2 |
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