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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434-240-6
-
Skin Sens. 1
Details
424-290-7
188070-47-5
Skin Sens. 1
Details
435-450-0
5460-63-9
Skin Sens. 1
Details
MCP 938
410-720-0
141847-13-4
Eye Dam. 1
Details
BONTRON E-88
406-890-0
130296-87-6
Acute Tox. 4
Details
CYANEX (R) EXTRACTANT; CYANEX 923 EXTRACTANT
403-470-9
-
Skin Corr. 1B
Details
FRUITATE
407-520-0
80657-64-3
Skin Irrit. 2
Details
427-090-8
116044-44-1
Skin Sens. 1
Details
434-420-4
-
Skin Irrit. 2; Eye Dam. 1
Details
VP SANDUVOR 3052 LIQUIDE
405-670-1
119530-69-7
Acute Tox. 4; STOT RE 2; Skin Corr. 1B
Details

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