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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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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GUAIACOL-O-ETHYLBROMIDE
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402-010-4
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4463-59-6
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Acute Tox. 4 |
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BRL 47539
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411-780-0
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127047-77-2
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Acute Tox. 4 |
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CHLORGELB; HC YELLOW 12
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413-280-8
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59320-13-7
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Acute Tox. 4 |
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202-544-6
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96-91-3
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Acute Tox. 4 |
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DPX N6186; N 6186
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410-050-9
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5734-64-5
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Acute Tox. 4 |
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DPX-D-7556
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403-580-7
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62096-63-3
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Acute Tox. 4 |
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CITROWANIL B
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407-870-4
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97384-48-0
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Acute Tox. 4 |
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429-430-0
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444-14-4
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Acute Tox. 4 |
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203-933-3
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112-07-2
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Acute Tox. 4 |
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204-502-2
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121-87-9
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Acute Tox. 4 |
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