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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424-530-0
93076-03-0
Acute Tox. 3; STOT SE 2; STOT RE 2; Eye Dam. 1; Skin Sens. 1
Details
424-520-6
65753-47-1
Acute Tox. 3; STOT RE 1; Skin Corr. 1B
Details
424-510-1
-
Eye Dam. 1
Details
424-460-0
283167-56-6
Acute Tox. 4; Skin Sens. 1
Details
424-390-0
93280-40-1
Acute Tox. 4; STOT RE 2; Eye Dam. 1
Details
424-380-6
43057-68-7
Acute Tox. 4; STOT RE 2
Details
424-370-1
125496-22-2
Skin Irrit. 2; Skin Sens. 1
Details
MARINE REN 600
424-320-9
180778-23-8
Eye Dam. 1
Details
BLUE PE 3811
424-310-4
178452-66-9
Eye Dam. 1
Details
424-290-7
188070-47-5
Skin Sens. 1
Details

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