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 04 listopada 2024. Database contains 4917 unique substances/entries.
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RO 1082
411-260-3
117907-43-4
Eye Dam. 1; Skin Sens. 1
Details
METHYLGELB
408-090-7
100418-33-5
Acute Tox. 4; Skin Sens. 1
Details
2S4TBP
421-740-4
51390-14-8
Skin Corr. 1B
Details
426-480-5
63562-33-4
Skin Sens. 1
Details
TAA
407-850-5
89544-40-1
Acute Tox. 4; Eye Dam. 1
Details
EPO
411-210-0
89544-48-9
Skin Irrit. 2; Skin Sens. 1
Details
413-720-9
117933-89-8
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
413-720-9
117933-89-8
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
413-720-9
117933-89-8
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
THANCAT AN 20
407-360-1
116230-20-7
Acute Tox. 4; STOT RE 2; Skin Irrit. 2; Eye Dam. 1
Details

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