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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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M-TMI
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402-440-2
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2094-99-7
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Acute Tox. 2; Skin Corr. 1B; STOT RE 2; Resp. Sens. 1; Skin Sens. 1 |
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244-879-0
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22259-30-9
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Acute Tox. 2; Skin Sens. 1 |
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245-656-0
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23422-53-9
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Acute Tox. 2; Skin Sens. 1 |
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209-854-0
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594-72-9
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Acute Tox. 3 |
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200-629-2
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66-71-7
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Acute Tox. 3 |
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TRIAZAMATE
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411-650-3
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110895-43-7
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Acute Tox. 3 |
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200-733-8
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70-30-4
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Acute Tox. 3 |
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-
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7076-53-1
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Acute Tox. 3 |
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T 1049
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403-350-6
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17742-69-7
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Acute Tox. 3 |
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-
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2532-43-6
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Acute Tox. 3 |
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