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 08 listopada 2024. Database contains 4918 unique substances/entries.
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BLAU MUB 557
419-520-8
172890-93-6
Skin Sens. 1
Details
RED REN 363
419-500-9
171599-85-2
Eye Dam. 1; Skin Sens. 1
Details
REACTIVE YELLOW FC 75560
419-450-8
-
Skin Sens. 1
Details
D 28-283
419-430-9
56533-00-7
Acute Tox. 4; STOT RE 2; Skin Corr. 1B
Details
DIETHYLDIMETHYLAMMONIUMHYDROXIDE
419-400-5
95500-19-9
Acute Tox. 4; Skin Corr. 1A
Details
T001769
419-290-9
780757-44-0
Skin Sens. 1
Details
419-270-1
123599-82-6
Eye Irrit. 2
Details
BROWN JR 547
419-260-5
-
Eye Dam. 1
Details
419-240-6
171054-89-0
Eye Dam. 1
Details
BLACK JR 578
419-230-1
-
Skin Sens. 1
Details

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