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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 11 listopada 2024. Database contains 4821 unique substances/entries.
Filter the list
|
show/hide
|
233-296-7
|
10108-64-2
|
Carc. 1B; Muta. 1B; Repr. 1B; Acute Tox. 2; Acute Tox. 3; STOT RE 1 |
yes |
|
|
640-998-0
|
7790-78-5
|
yes |
|||
|
232-222-0
|
7790-79-6
|
Carc. 1B; Muta. 1B; Repr. 1B; Acute Tox. 2; Acute Tox. 3; STOT RE 1 |
yes |
||
|
244-168-5
|
21041-95-2
|
Carc. 1B; Muta. 1B; Acute Tox. 4; STOT RE 1 |
yes |
||
|
-
|
-
|
yes |
|||
|
show/hide
|
215-146-2
|
1306-19-0
|
Carc. 1B; Muta. 2; Repr. 2; Acute Tox. 2; STOT RE 1 |
yes |
|
|
show/hide
|
233-331-6
|
10124-36-4;31119-53-6
|
yes |
||
|
show/hide
|
233-331-6
|
10124-36-4;31119-53-6
|
Carc. 1B; Muta. 1B; Repr. 1B; Acute Tox. 2; Acute Tox. 3; STOT RE 1 |
yes |
|
|
215-147-8
|
1306-23-6
|
Carc. 1B; Muta. 2; Repr. 2; STOT RE 1; Acute Tox. 4 |
yes |
||
|
231-152-8
|
7440-43-9
|
yes |
|||