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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 02 listopada 2024. Database contains 4821 unique substances/entries.
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200-087-7
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51-28-5
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Acute Tox. 3; Acute Tox. 2; STOT RE 1 |
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204-450-0
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121-14-2
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Carc. 1B; Muta. 2; Repr. 2; Acute Tox. 3; STOT RE 2 |
yes |
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203-321-6
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105-67-9
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Acute Tox. 3; Skin Corr. 1B |
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209-745-8
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592-13-2
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Flam. Liq. 2; Asp. Tox. 1; Skin Irrit. 2; STOT SE 3 |
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206-348-1
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329-71-5
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Acute Tox. 3; STOT RE 2 |
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210-581-4
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619-15-8
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Carc. 1B; Muta. 2; Repr. 2; Acute Tox. 3; STOT RE 2 |
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202-461-5
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95-87-4
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Acute Tox. 3; Skin Corr. 1B |
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218-255-3
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2095-01-4
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Acute Tox. 4; STOT RE 2; Eye Irrit. 2 |
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209-445-7
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579-66-8
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Acute Tox. 4 |
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203-620-1
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108-83-8
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Flam. Liq. 3; STOT SE 3 |
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