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 13 rujna 2024. Database contains 4917 unique substances/entries.
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428-700-5
1873-90-1
Acute Tox. 4
Details
428-690-2
1668-86-6
Acute Tox. 4; Eye Irrit. 2
Details
428-650-4
153719-23-4
Repr. 2; Acute Tox. 4
Details
428-630-5
-
Skin Sens. 1
Details
428-410-9
67014-36-2
Acute Tox. 4; Skin Sens. 1
Details
428-400-4
-
Eye Dam. 1
Details
428-390-1
86393-34-2
STOT SE 3; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1
Details
H-604
428-350-3
93629-90-4
Muta. 2; Eye Dam. 1; Skin Sens. 1
Details
428-340-9
238088-70-5
Skin Irrit. 2
Details
428-330-4
2833-30-9
Skin Corr. 1B; Acute Tox. 4; STOT RE 2; Skin Sens. 1
Details

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