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 24 lipnja 2024. Database contains 4917 unique substances/entries.
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600-611-8
10486-00-7
R Toxic for reproduction (article 57c)
Details
600-611-8
10486-00-7
Repr. 1B; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
600-594-7
104653-34-1
Repr. 1B; Acute Tox. 1; STOT RE 1
Details
600-533-4
104206-82-8
Repr. 2; STOT RE 2
Details
600-425-7
103361-09-7
Repr. 2
Details
600-419-4
10332-33-9
Ox. Sol. 3; Repr. 1B; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
600-419-4
10332-33-9
Ox. Sol. 3; Repr. 1B; Acute Tox. 3; Acute Tox. 4; STOT SE 3; Eye Dam. 1
Details
600-419-4
10332-33-9
R Toxic for reproduction (article 57c)
Details
600-363-0
102851-06-9
Acute Tox. 4; Skin Irrit. 2
Details
600-130-3
100784-20-1
Repr. 1B
Details

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