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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 12 srpnja 2024. Database contains 4821 unique substances/entries.
Filter the list

-
15271-41-7
Acute Tox. 2; Acute Tox. 3
-
72319-19-8
Carc. 1A; Muta. 2; Repr. 1B; STOT RE 1; Resp. Sens. 1; Skin Sens. 1
-
21436-97-5
Carc. 1B; Acute Tox. 3
-
130014-35-6
Eye Irrit. 2; Skin Irrit. 2; Skin Sens. 1
-
1065124-65-3
Acute Tox. 4; STOT SE 2
-
7076-53-1
Acute Tox. 3
-
5836-73-7
Acute Tox. 2
-
-
yes
-
540-73-8
Carc. 1B; Acute Tox. 3
-
6202-15-9
Expl. 1.1; Acute Tox. 4
-
4482-55-7
Skin Irrit. 2
-
178961-20-1
Skin Sens. 1
-
75166-30-2
yes
-
75166-31-3
yes
-
852541-25-4
yes
-
852541-30-1
yes
-
135821-74-8
yes
-
135821-03-3
yes
-
741687-98-9
yes
-
852541-21-0
yes
-
95342-41-9
yes

Export search results to: