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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 24 srpnja 2024. Database contains 4821 unique substances/entries.
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204-539-4
122-39-4
Acute Tox. 3; STOT RE 2
202-729-1
99-09-2
Acute Tox. 3; STOT RE 2
203-583-1
108-44-1
Acute Tox. 3; STOT RE 2
202-088-8
91-66-7
Acute Tox. 3; STOT RE 2
204-495-6
121-72-2
Acute Tox. 3; STOT RE 2
210-199-8
609-72-3
Acute Tox. 3; STOT RE 2
202-805-4
99-97-8
Acute Tox. 3; STOT RE 2
203-135-5
103-69-5
Acute Tox. 3; STOT RE 2
211-795-0
696-44-6
Acute Tox. 3; STOT RE 2
210-260-9
611-21-2
Acute Tox. 3; STOT RE 2

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