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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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430-910-7
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13335-71-2
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Acute Tox. 4; Eye Dam. 1 |
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420-380-5
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136465-81-1
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Acute Tox. 4; Eye Dam. 1 |
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424-740-2
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138271-16-6
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Acute Tox. 4; Eye Dam. 1 |
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BRL 44742
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415-550-0
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109887-53-8
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Acute Tox. 4; Eye Dam. 1 |
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CG 24-020; FERROCEN-SBF6
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407-840-0
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100011-37-8
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Acute Tox. 4; Eye Dam. 1 |
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420-930-4
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135756-61-5
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Acute Tox. 4; Eye Dam. 1 |
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431-010-7
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154486-26-7
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Acute Tox. 4; Eye Dam. 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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448-720-8
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363138-44-7
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Acute Tox. 4; Eye Dam. 1 |
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429-610-9
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1030366-98-3
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Acute Tox. 4; Eye Dam. 1 |
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