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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HFR-990
423-180-6
-
STOT RE 2
Details
GR101655A
423-170-1
618-26-8
Flam. Liq. 2; STOT RE 1; Acute Tox. 4; Eye Dam. 1; Skin Sens. 1
Details
YELLOW JB 1238
423-110-4
-
Eye Dam. 1
Details
423-100-1
-
Eye Dam. 1
Details
423-010-0
-
Eye Dam. 1
Details
ORANGE DER 8068
422-980-2
187026-95-5
Eye Dam. 1
Details
PHOTOAMORCEUR 22074; RHODORSIL PHOTOINITIATOR 2074; TEPBI
422-960-3
178233-72-2
Acute Tox. 4; STOT RE 2
Details
422-950-9
17193-28-1
STOT RE 1; Acute Tox. 4; Eye Dam. 1
Details
422-920-5
-
STOT RE 2
Details
422-900-6
158894-67-8
Flam. Liq. 3; Carc. 2; Skin Corr. 1B; Skin Sens. 1
Details

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