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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 26 srpnja 2024. Database contains 4821 unique substances/entries.
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213-666-4
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999-81-5
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Acute Tox. 4 |
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213-663-8
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999-61-1
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Acute Tox. 3; Skin Corr. 1B; Skin Sens. 1 |
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2,4-DICHLORO-3-ETHYL-6-NITROPHENOL
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420-740-1
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99817-36-4
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Acute Tox. 3; Eye Dam. 1; Skin Sens. 1 |
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DBBT
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402-210-1
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99688-47-8
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STOT RE 2; Skin Sens. 1 |
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PIKRAMINROT
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412-520-9
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99610-72-7
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Flam. Sol. 2; Repr. 2; Acute Tox. 4 |
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ECPA
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427-630-2
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99469-99-5
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Eye Dam. 1 |
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444-950-8
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99464-83-2
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Muta. 2; Skin Sens. 1 |
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213-611-4
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994-05-8
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Flam. Liq. 2; Acute Tox. 4; STOT SE 3 |
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213-608-8
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993-16-8
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Repr. 2 |
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T001446
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419-600-2
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99199-90-3
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Skin Sens. 1 |
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