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 17 srpnja 2024. Database contains 4917 unique substances/entries.
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201-944-8
89-83-8
Acute Tox. 4; Skin Corr. 1B
Details
205-286-2
137-26-8
Acute Tox. 4; STOT RE 2; Eye Irrit. 2; Skin Irrit. 2; Skin Sens. 1
Details
200-543-5
62-56-6
Carc. 2; Repr. 2; Acute Tox. 4
Details
202-272-8
93-75-4
Acute Tox. 4
Details
245-740-7
23564-05-8
Carc. 2; Muta. 2; Acute Tox. 4; Skin Sens. 1
Details
231-748-8
7719-09-7
Acute Tox. 4; Skin Corr. 1A
Details
RT 1766A
404-820-3
164637-97-2
Skin Irrit. 2; Skin Sens. 1
Details
206-049-6
297-97-2
Acute Tox. 1; Acute Tox. 2
Details
211-362-6
640-15-3
Acute Tox. 3; Acute Tox. 4
Details
200-677-4
68-11-1
Acute Tox. 3; Skin Corr. 1B
Details

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