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 With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.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 15 listopada 2024. Database contains 4821 unique substances/entries.
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204-318-2
119-38-0
Acute Tox. 1; Acute Tox. 2
246-538-1
24934-91-6
Acute Tox. 1; Acute Tox. 2
620-378-6
8065-48-3
Acute Tox. 1; Acute Tox. 2
206-053-8
298-03-3
Acute Tox. 1; Acute Tox. 2
204-801-8
126-75-0
Acute Tox. 1; Acute Tox. 2
204-076-8
115-26-4
Acute Tox. 1; Acute Tox. 2
620-379-1
3254-63-5
Acute Tox. 1; Acute Tox. 2
206-054-3
298-04-4
Acute Tox. 1; Acute Tox. 2
204-114-3
115-90-2
Acute Tox. 1; Acute Tox. 2
-
4301-50-2
Acute Tox. 1; Acute Tox. 2

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