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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236-813-4
13494-80-9
Repr. 1B; Lact.
Details
616-699-6
79538-32-2
Acute Tox. 1; Acute Tox. 2
Details
204-178-2
117-18-0
Acute Tox. 4; Skin Sens. 1
Details
251-793-7
34014-18-1
Acute Tox. 4
Details
601-585-0
119168-77-3
Acute Tox. 3; Acute Tox. 4; STOT RE 2; Skin Sens. 1B
Details
TEBUCONAZOLE RESP. HWG 1608
403-640-2
107534-96-3
Repr. 2; Acute Tox. 4
Details
211-479-2
650-51-1
STOT SE 3
Details
200-927-2
76-03-9
Skin Corr. 1A
Details
600-363-0
102851-06-9
Acute Tox. 4; Skin Irrit. 2
Details
The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydrocarbons, phenolic compounds, nitrogen bases and thiophene.
232-361-7
8007-45-2
Carc. 1A
Details

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