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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 04 listopada 2024. Database contains 4821 unique substances/entries.
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445-280-9
371921-40-3
Eye Dam. 1; Skin Sens. 1
MARINE REN 600
424-320-9
180778-23-8
Eye Dam. 1
COLUMBIADUNKELBLAU R
415-350-3
-
Eye Dam. 1
422-500-1
-
STOT RE 2
433-860-4
-
Eye Irrit. 2; Skin Sens. 1
T-271
417-980-4
157321-59-0
Self-react. C; Carc. 2
EVAPORATED ELEMINOL JS-2 MATERIAL
410-230-7
-
Skin Corr. 1B; Skin Sens. 1
TASP
411-250-9
-
Skin Sens. 1
426-470-0
214897-29-7
Skin Sens. 1
427-740-0
-
Eye Dam. 1; Skin Sens. 1

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