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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 06 rujna 2024. Database contains 4821 unique substances/entries.
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Acute Tox. 3; Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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TETRACONAZOLE
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407-760-6
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112281-77-3
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Acute Tox. 4 |
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215-582-3
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1333-22-8
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Acute Tox. 4 |
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682-362-5
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12527-76-3
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Acute Tox. 4 |
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215-910-5
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1449-55-4
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Acute Tox. 4 |
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KAYASET BLACK T-2
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405-110-6
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88377-66-6
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STOT RE 2 |
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429-270-1
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136210-30-5
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Skin Sens. 1 |
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201-083-8
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78-10-4
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Flam. Liq. 3; Acute Tox. 4; Eye Irrit. 2; STOT SE 3 |
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204-126-9
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116-14-3
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Carc. 1B |
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230-625-6
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7226-23-5
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Repr. 2; Acute Tox. 4; Eye Dam. 1 |
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