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 18 rujna 2024. Database contains 4917 unique substances/entries.
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445-890-5
201290-01-9
Acute Tox. 4; Skin Sens. 1
Details
DHP OPT
445-770-2
42031-28-7
Eye Dam. 1
Details
445-750-3
839705-03-2
Acute Tox. 4; Eye Dam. 1; Skin Sens. 1
Details
445-590-4
202197-26-0
Muta. 2; Acute Tox. 4; STOT RE 2
Details
445-280-9
371921-40-3
Eye Dam. 1; Skin Sens. 1
Details
444-950-8
99464-83-2
Muta. 2; Skin Sens. 1
Details
444-860-9
474510-57-1
STOT RE 2
Details
BUTAMINONITRODARONE; SR33581
444-800-1
141645-23-0
Flam. Liq. 3; Acute Tox. 4; STOT RE 2; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1
Details
444-480-3
676125-00-1
Skin Irrit. 2
Details
444-440-5
220689-12-3
Acute Tox. 4
Details

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