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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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PARMANYL
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415-220-6
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142653-61-0
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Acute Tox. 3; Acute Tox. 4 |
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620-041-3
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907204-31-3
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Lact. |
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3-(DIMETHYLAMINO)PROPYL UREA; HST 2844
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401-950-2
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31506-43-1
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Eye Dam. 1 |
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FYROL 3-HPP; HIRETAR-205; PHOSGARD PF 100
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411-200-6
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14657-64-8
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Eye Dam. 1 |
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IMEXINE FAE
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403-440-5
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93633-79-5
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Acute Tox. 4 |
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421-310-6
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87691-88-1
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Repr. 2; Acute Tox. 4; Eye Irrit. 2; Skin Sens. 1 |
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425-370-4
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93957-50-7
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Skin Sens. 1 |
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ADDITIVE F6
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421-600-2
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719-86-8
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STOT RE 2 |
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208-293-9
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520-45-6
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Acute Tox. 4 |
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FAT 92.346 B
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411-520-6
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112195-27-4
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Eye Dam. 1; Skin Sens. 1 |
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