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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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215-209-4
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1313-60-6
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Ox. Sol. 1; Skin Corr. 1A |
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231-511-9
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7601-89-0
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Ox. Sol. 1; Acute Tox. 4 |
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231-555-9
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7632-00-0
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Ox. Sol. 3; Acute Tox. 3 |
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274-357-8
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70161-44-3
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Carc. 1B; Muta. 2; Acute Tox. 4; STOT SE 3; Skin Irrit. 2; Eye Irrit. 2; Skin Sens. 1 |
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218-953-8
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2302-17-2
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Skin Sens. 1 |
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204-699-5
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124-41-4
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Self-heat. 1; Skin Corr. 1B |
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231-673-0
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7681-57-4
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Acute Tox. 4; Eye Dam. 1 |
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231-668-3
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7681-52-9
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Skin Corr. 1B; Eye Dam. 1 |
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215-185-5
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1310-73-2
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Skin Corr. 1A |
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231-548-0
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7631-90-5
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Acute Tox. 4 |
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