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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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200-340-1
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57-57-8
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Carc. 1B; Acute Tox. 2; Eye Irrit. 2; Skin Irrit. 2 |
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Z-29
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418-990-1
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778577-53-0
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STOT RE 2; Eye Irrit. 2; Skin Irrit. 2 |
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201-052-9
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77-73-6
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Flam. Liq. 2; Acute Tox. 4; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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LICHTSCHUTZMITTEL 2577
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407-600-5
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120187-29-3
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Muta. 2 |
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DMA
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407-500-1
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21983-80-2
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Skin Sens. 1 |
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428-970-4
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13595-25-0
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Repr. 2; Skin Sens. 1 |
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201-025-1
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77-40-7
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yes |
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209-321-2
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569-61-9
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Carc. 1B |
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DIGLYCERINDIFORMAL (DGDF)
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423-230-7
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56552-15-9
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Eye Dam. 1 |
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204-358-0
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119-93-7
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Carc. 1B; Acute Tox. 4 |
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