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 10 rujna 2024. Database contains 4917 unique substances/entries.
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TURQUOISE 10 40 518
411-430-7
-
Eye Dam. 1; Skin Sens. 1
Details
423-100-1
-
Eye Dam. 1
Details
C.I. REACTIVE YELLOW 174; GIALLO REATTIVO 174; JAUNE REACTIF 174; REAKTIV GELB 174
402-170-5
106359-91-5
Skin Sens. 1
Details
440-480-2
341026-59-3
Eye Dam. 1; Skin Sens. 1
Details
430-280-3
844491-96-9
Skin Sens. 1
Details
BLEU REACTIF CAC 10; DIOXAZINE MONCHLORTRIAZINE; FAT NO. 40 407; REACTIVE BLUE CAC 10
410-130-3
136248-03-8
Skin Sens. 1
Details
429-240-8
212652-59-0
Eye Dam. 1
Details
427-710-7
215612-56-9
Eye Dam. 1; Skin Sens. 1
Details
BLUE TZ 4312
423-770-3
-
Eye Dam. 1
Details
SCARLET 12 04 262
406-820-9
159317-41-6
Eye Irrit. 2
Details

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