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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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.
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440-030-5
338735-71-0
Skin Irrit. 2; Eye Dam. 1
429-460-4
7078-98-0
Skin Sens. 1
444-250-2
144111-81-9
Self-react. C
VIOLETT MIP 3250
424-120-1
174514-06-8
Eye Dam. 1
218-255-3
2095-01-4
Acute Tox. 4; STOT RE 2; Eye Irrit. 2
AZOGELB
421-430-9
28365-08-4
Acute Tox. 4; STOT RE 2
FPB 800
427-400-1
140623-89-8
Skin Corr. 1B; Acute Tox. 4; Skin Sens. 1
T 1049
403-350-6
17742-69-7
Acute Tox. 3
DICHLORO-2,6 P.T.F.M.A.
416-430-0
24279-39-8
Acute Tox. 4; Skin Irrit. 2; Skin Sens. 1
209-445-7
579-66-8
Acute Tox. 4

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