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 14 lipnja 2024. Database contains 4917 unique substances/entries.
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604-237-6
141517-21-7
Lact.; Skin Sens. 1
Details
604-222-4
141112-29-0
Repr. 2
Details
604-209-3
140923-17-7
Carc. 2
Details
604-167-6
139968-49-3
Repr. 2; Lact.; STOT RE 2
Details
604-105-8
139001-49-3
Carc. 2; Repr. 2; Skin Sens. 1
Details
604-030-0
137641-05-5
STOT RE 2
Details
603-921-1
135410-20-7
Repr. 2; Acute Tox. 3
Details
603-902-8
13517-20-9
Repr. 1B; STOT SE 3; Eye Dam. 1
Details
603-902-8
13517-20-9
R Toxic for reproduction (article 57c)
Details
603-902-8
13517-20-9
Repr. 1B; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details

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