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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 11 listopada 2024. Database contains 4821 unique substances/entries.
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yes |
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621-341-7
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2315-61-9
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yes |
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205-426-2
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140-66-9
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Skin Irrit. 2; Eye Dam. 1 |
yes |
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423-860-2
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56309-94-5
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Skin Sens. 1 |
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257-907-1
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52427-13-1
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yes |
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ACRYLOYLMORPHOLIN
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418-140-1
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5117-12-4
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Acute Tox. 4; STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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635-388-6
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521947-27-3
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yes |
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WL 125892
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402-190-4
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113674-95-6
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STOT RE 1; Acute Tox. 4; STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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LICHTSCHUTZMITTEL 1071
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413-510-7
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147374-67-2
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STOT RE 2; Skin Sens. 1 |
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4-ALLYLOXYBENZOESÄURE-(4-METHACRYLOYL)PHENYLESTER
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429-000-2
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159235-16-2
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Skin Sens. 1 |
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