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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 26 srpnja 2024. Database contains 4821 unique substances/entries.
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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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CG 26-751
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407-880-9
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117549-13-0
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Acute Tox. 4 |
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204-528-4
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122-20-3
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Eye Irrit. 2 |
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COMPIMIDE™ 121
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405-840-5
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110866-35-8
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Skin Sens. 1 |
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219-306-2
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2407-94-5
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Org. Perox. A; Skin Corr. 1B; Acute Tox. 4 |
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219-306-2
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2407-94-5
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Org. Perox. C; Acute Tox. 4; Skin Corr. 1B |
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203-820-9
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110-97-4
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Eye Irrit. 2 |
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430-250-1
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406-58-6
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Flam. Liq. 2 |
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200-756-3
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71-55-6
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Acute Tox. 4 |
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201-191-5
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79-27-6
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Acute Tox. 2; Eye Irrit. 2 |
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