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 12 rujna 2024. Database contains 4917 unique substances/entries.
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427-200-4
76646-91-8
Acute Tox. 4; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1
Details
CIN 10094329; SENSIBILISATOR KF 693 PINA; SENSITIZER KF 693 PINA
422-240-9
166596-68-5
Eye Dam. 1; Skin Sens. 1
Details
265-294-7
64969-36-4
Carc. 1B; Acute Tox. 4
Details
428-230-0
79568-06-2
STOT RE 2
Details
222-048-3
3327-22-8
Carc. 2
Details
T 1569; T001569
423-290-4
66938-41-8
Muta. 2
Details
701-394-3
1782069-81-1
END Endocrine disrupting properties (Article 57(f) - human health)
Details
420-380-5
136465-81-1
Acute Tox. 4; Eye Dam. 1
Details
444-350-6
133413-70-4
Eye Irrit. 2
Details
PTH-AA
430-230-0
136522-17-3
Acute Tox. 4
Details

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