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 13 mai 2024. Database contains 4917 unique substances/entries.
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852541-30-1
END Endocrine disrupting properties (Article 57(f) - human health)
Details
P-NITROBENZYLESTER PGSO
412-670-5
54275-93-3
Resp. Sens. 1
Details
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852541-25-4
END Endocrine disrupting properties (Article 57(f) - human health)
Details
G-EXOMETHYLENE SULFOXIDE ESTER
412-800-0
76109-32-5
Resp. Sens. 1
Details
426-200-1
172015-79-1
STOT RE 1; Acute Tox. 4; Eye Dam. 1; Skin Sens. 1
Details
SERTRALINE STEP 2
420-560-3
79617-97-3
Eye Dam. 1
Details
220-384-5
2746-19-2
Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1
Details
CP-141,845-27
426-740-8
256369-40-1
Acute Tox. 4; Eye Dam. 1
Details
BLUE 10 25 964
407-240-9
159604-94-1
Skin Sens. 1
Details
443-840-7
4084-38-2
Acute Tox. 4; Eye Irrit. 2; Skin Sens. 1
Details

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