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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 07 listopada 2024. Database contains 4821 unique substances/entries.
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427-880-2
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90357-53-2
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STOT RE 2 |
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424-550-1
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84245-12-5
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Carc. 1B; Muta. 1B; Repr. 1B |
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429-120-5
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208535-04-0
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Eye Dam. 1 |
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425-300-2
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186450-73-7
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Skin Sens. 1 |
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EP 389
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407-730-2
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104958-67-0
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Eye Irrit. 2; Skin Sens. 1 |
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DISPERSOL YELLOW XF
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407-970-8
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75511-91-0
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Skin Sens. 1 |
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PREVENTOL VP OC 3061
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423-990-1
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149118-66-1
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Acute Tox. 4; Eye Dam. 1 |
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DIMETHYLPAPAMIDOLAURDIMONIUM TOSYLATE
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421-130-8
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156679-41-3
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Eye Dam. 1; Skin Sens. 1 |
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437-720-3
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227085-51-0
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Eye Dam. 1 |
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CATALYST 4017
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407-780-5
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4186-71-4
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Acute Tox. 4 |
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