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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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200-629-2
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66-71-7
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Acute Tox. 3 |
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210-168-9
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608-73-1
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Carc. 2; Acute Tox. 3; Acute Tox. 4 |
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212-230-0
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771-29-9
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Org. Perox. D; Acute Tox. 4; Skin Corr. 1B |
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RO 1173
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414-270-6
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41959-35-7
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Acute Tox. 4 |
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204-340-2
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119-64-2
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Eye Irrit. 2; Skin Irrit. 2 |
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6202-15-9
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Expl. 1.1; Acute Tox. 4 |
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212-557-9
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826-62-0
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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226-247-6
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5333-84-6
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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222-323-8
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3425-89-6
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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247-830-1
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26590-20-5
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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