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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 15 listopada 2024. Database contains 4821 unique substances/entries.
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4'-(4-PENTYLCYCLOHEXYL)ACETOPHENONE
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426-830-7
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78531-59-6
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Skin Sens. 1 |
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431-450-1
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41870-52-4
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Skin Irrit. 2 |
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420-240-3
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162515-68-6
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Skin Corr. 1B; Acute Tox. 4; Skin Sens. 1 |
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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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MIXOFAM
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411-510-1
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3353-51-3
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Skin Sens. 1 |
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430-920-1
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73096-98-7
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Acute Tox. 4; Eye Dam. 1 |
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FT-310; PF-310
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407-400-8
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59493-72-0
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Eye Dam. 1 |
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429-040-0
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272460-97-6
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Eye Dam. 1 |
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SANDUVOR 3058; SANDUVOR 3058 LIQ.
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411-930-5
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106917-31-1
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Skin Irrit. 2; Skin Sens. 1 |
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CFA; HOE 108219
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406-630-6
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121626-73-1
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Skin Irrit. 2 |
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