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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 24 svibnja 2024. Database contains 4821 unique substances/entries.
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CG 24-020; FERROCEN-SBF6
407-840-0
100011-37-8
Acute Tox. 4; Eye Dam. 1
CG 26-751
407-880-9
117549-13-0
Acute Tox. 4
204-528-4
122-20-3
Eye Irrit. 2
COMPIMIDE™ 121
405-840-5
110866-35-8
Skin Sens. 1
219-306-2
2407-94-5
Org. Perox. A; Skin Corr. 1B; Acute Tox. 4
219-306-2
2407-94-5
Org. Perox. C; Acute Tox. 4; Skin Corr. 1B
203-820-9
110-97-4
Eye Irrit. 2
430-250-1
406-58-6
Flam. Liq. 2
200-756-3
71-55-6
Acute Tox. 4
201-191-5
79-27-6
Acute Tox. 2; Eye Irrit. 2

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