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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 09 rujna 2024. Database contains 4821 unique substances/entries.
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432-190-1
182176-52-9
Acute Tox. 4; STOT RE 2; Eye Dam. 1
425-910-9
32480-08-3
Skin Irrit. 2
ACRYLSKUM; T-2816 FOAMER
407-810-7
-
STOT RE 2
ROT Y; RUBINOT Y; RUBINROT Y
408-240-1
-
Acute Tox. 4
440-510-4
-
Eye Dam. 1; Skin Sens. 1
442-290-5
457624-86-1
Eye Dam. 1
435-440-6
-
Eye Dam. 1
DISPERSIONSROT 2754
411-880-4
-
Skin Sens. 1
431-440-5
-
Eye Dam. 1
FORMYLTRICYCLODECEN, EXO
410-480-7
-
Skin Sens. 1

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