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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 16 rujna 2024. Database contains 4821 unique substances/entries.
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METHYLGELB
408-090-7
100418-33-5
Acute Tox. 4; Skin Sens. 1
2S4TBP
421-740-4
51390-14-8
Skin Corr. 1B
426-480-5
63562-33-4
Skin Sens. 1
TAA
407-850-5
89544-40-1
Acute Tox. 4; Eye Dam. 1
EPO
411-210-0
89544-48-9
Skin Irrit. 2; Skin Sens. 1
THANCAT AN 20
407-360-1
116230-20-7
Acute Tox. 4; STOT RE 2; Skin Irrit. 2; Eye Dam. 1
31 AC-HCL
410-620-7
119154-86-8
Acute Tox. 4; Skin Corr. 1B; Skin Sens. 1
203-867-5
111-41-1
Repr. 1B; Skin Corr. 1B; Skin Sens. 1
GUAIACOL-O-ETHYLBROMIDE
402-010-4
4463-59-6
Acute Tox. 4
203-961-6
112-34-5
Eye Irrit. 2

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