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 19 rujna 2024. Database contains 4917 unique substances/entries.
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219-007-7
2312-76-7
Acute Tox. 3; STOT RE 2
Details
223-498-3
3926-62-3
Acute Tox. 3; Skin Irrit. 2
Details
435-350-7
141250-43-3
Eye Dam. 1
Details
215-686-9
1344-08-7
Acute Tox. 3; Skin Corr. 1B
Details
231-556-4
7632-04-4
R Toxic for reproduction (article 57c)
Details
231-556-4
7632-04-4
Ox. Sol. 2; Repr. 1B; Acute Tox. 3; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
231-556-4
7632-04-4
Ox. Sol. 2; Repr. 1B; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
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Repr. 1B; STOT SE 3; Eye Dam. 1
Details
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Repr. 1B; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
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Ox. Sol. 2; Repr. 1B; Acute Tox. 3; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details

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