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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 14 listopada 2024. Database contains 4821 unique substances/entries.
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200-541-4
62-55-5
Carc. 1B; Acute Tox. 4; Eye Irrit. 2; Skin Irrit. 2
248-924-5
28249-77-6
Acute Tox. 4
207-341-6
463-71-8
Acute Tox. 3; Acute Tox. 4; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2
207-337-4
463-56-9
Acute Tox. 4
254-346-4
39196-18-4
Acute Tox. 1; Acute Tox. 2
200-677-4
68-11-1
Acute Tox. 3; Skin Corr. 1B
211-362-6
640-15-3
Acute Tox. 3; Acute Tox. 4
206-049-6
297-97-2
Acute Tox. 1; Acute Tox. 2
RT 1766A
404-820-3
164637-97-2
Skin Irrit. 2; Skin Sens. 1
231-748-8
7719-09-7
Acute Tox. 4; Skin Corr. 1A

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