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 11 rujna 2024. Database contains 4917 unique substances/entries.
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427-710-7
215612-56-9
Eye Dam. 1; Skin Sens. 1
Details
TRIETHYLARSENAT; TRIETHYLARSENATE; TRIETHYLARSENATE (TEASAT)
427-700-2
15606-95-8
Carc. 1A; Acute Tox. 3
C Carcinogenic (article 57a)
Details
427-680-5
188907-52-0
Eye Dam. 1; Skin Sens. 1
Details
ECPA
427-630-2
99469-99-5
Eye Dam. 1
Details
427-580-1
211299-54-6
Skin Irrit. 2
Details
427-480-8
176429-22-4
STOT SE 3; Skin Irrit. 2; Eye Dam. 1
Details
427-470-3
137864-22-3
Acute Tox. 4; Skin Sens. 1
Details
427-450-4
152630-47-2
Acute Tox. 4; STOT RE 2; Skin Sens. 1
Details
FPB 800
427-400-1
140623-89-8
Skin Corr. 1B; Acute Tox. 4; Skin Sens. 1
Details
SUBSTANCE S171393
427-390-9
-
Skin Sens. 1
Details

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