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 srpnja 2024. Database contains 4917 unique substances/entries.
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GUANIDINIUMBENZOAT
429-820-0
26739-54-8
Acute Tox. 4
Details
CLETOPROPAMINHYDROCHLORID
429-740-6
40722-80-3
Carc. 1B; Muta. 1B; STOT RE 2; Skin Sens. 1
Details
429-730-1
193562-37-7
Eye Dam. 1; Skin Sens. 1
Details
429-710-2
-
Self-react. D; Acute Tox. 4
Details
429-680-0
122665-86-5
Skin Sens. 1
Details
BMS 208143-01; BTHC
429-670-6
105996-54-1
Eye Dam. 1; Skin Sens. 1
Details
DOWFAX (R) DRY HYDROTROPE POWDER
429-650-7
147732-60-3
Eye Irrit. 2
Details
429-640-2
52870-46-9
Eye Irrit. 2
Details
429-620-3
110028-14-3
Skin Irrit. 2; Skin Sens. 1
Details
429-610-9
1030366-98-3
Acute Tox. 4; Eye Dam. 1
Details

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