EU-MEDICAL_DEVICES_REGULATION-ANX_I_SEC_10

Medical Devices Regulation - Hazardous Substances

EU. Hazardous Substances for Purposes of Medical Devices Regulation 2017/745/EU, 5 May 2017, as amended by Regulation 2020/561/EU, 24 April 2020

This list contains hazardous substances for purposes of the Medical Devices Regulation (MDR), based on the legislation's Annex I general safety and performance requirements, including for chemical, physical and biological properties. Specifically, the non-exhaustive database 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).

Last updated 20 rujna 2024. Database contains 4917 unique substances/entries.
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605-752-9
175217-20-6
STOT RE 2
Details
605-747-1
175013-18-0
Acute Tox. 3; Skin Irrit. 2
Details
605-683-4
173584-44-6
Acute Tox. 3; Acute Tox. 4; STOT RE 1; Skin Sens. 1B
Details
605-666-1
173159-57-4
Carc. 2
Details
605-329-9
163515-14-8
Acute Tox. 4; Skin Sens. 1
Details
605-127-0
158062-67-0
Acute Tox. 4
Details
605-037-1
156052-68-5
Skin Sens. 1
Details
605-015-1
155569-91-8
Acute Tox. 3; STOT SE 1; STOT RE 1; Eye Dam. 1
Details
604-715-4
149979-41-9
Carc. 2; Repr. 2
Details
604-712-8
149961-52-4
Carc. 2; Repr. 2; Acute Tox. 4
Details

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