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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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.
Filter the list

MDI
406-550-1
-
Skin Sens. 1
422-920-5
-
STOT RE 2
SP 7053
415-930-6
-
Repr. 2; Skin Sens. 1
SP 7077
430-180-1
-
Skin Irrit. 2
429-990-6
-
Eye Dam. 1; Skin Sens. 1
NEWLON AM-92I
407-490-9
-
Acute Tox. 4; Skin Corr. 1B
OLOA 224 (OIL FREE)
420-470-4
-
Eye Irrit. 2; Skin Irrit. 2; Skin Sens. 1
427-140-9
-
Carc. 2
435-960-3
-
Carc. 1B; Muta. 1B; Skin Sens. 1
DYE K
402-660-9
-
Repr. 1B

Export search results to: