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 12 lipnja 2024. Database contains 4917 unique substances/entries.
Filter the list

 
603-804-5
134237-52-8
PBT Persistent, Bioaccumulative and Toxic (article 57d)
Details
603-802-4
134237-51-7
PBT Persistent, Bioaccumulative and Toxic (article 57d)
Details
603-801-9
134237-50-6
PBT Persistent, Bioaccumulative and Toxic (article 57d)
Details
603-792-1
134098-61-6
Acute Tox. 3; Acute Tox. 2; Skin Sens. 1B
Details
603-524-3
131860-33-8
Acute Tox. 3
Details
603-520-1
131807-57-3
STOT RE 2
Details
603-411-9
1303-96-4
Repr. 1B
R Toxic for reproduction (article 57c)
Details
603-404-0
130328-20-0
Repr. 2; Skin Irrit. 2; Eye Dam. 1
Details
603-146-9
126535-15-7
Carc. 2
Details
603-038-1
125225-28-7
Repr. 1B; Acute Tox. 4; STOT RE 2
Details

Export search results to: