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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 14 listopada 2024. Database contains 4821 unique substances/entries.
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434-120-3
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1380001-48-8
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Skin Sens. 1 |
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204-318-2
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119-38-0
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Acute Tox. 1; Acute Tox. 2 |
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203-539-1
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107-98-2
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Flam. Liq. 3; STOT SE 3 |
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424-160-1
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139481-22-4
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Acute Tox. 4 |
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423-960-6
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139756-01-7
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Acute Tox. 4; STOT RE 2 |
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243-105-9
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19485-03-1
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Acute Tox. 4; Skin Corr. 1B; Skin Sens. 1 |
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205-138-7
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134-32-7
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Acute Tox. 4 |
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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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TUPH
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424-620-1
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13909-63-2
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Acute Tox. 4; STOT RE 2 |
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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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