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 14 lipnja 2024. Database contains 4917 unique substances/entries.
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115850-69-6
Repr. 1B; Acute Tox. 4; STOT RE 2
Details
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115937-89-8
Repr. 1B; Acute Tox. 4; STOT RE 2
Details
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95342-41-9
END Endocrine disrupting properties (Article 57(f) - human health)
Details
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852541-21-0
END Endocrine disrupting properties (Article 57(f) - human health)
Details
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741687-98-9
END Endocrine disrupting properties (Article 57(f) - human health)
Details
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135821-03-3
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
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135821-74-8
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
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852541-30-1
END Endocrine disrupting properties (Article 57(f) - human health)
Details
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852541-25-4
END Endocrine disrupting properties (Article 57(f) - human health)
Details
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166900-80-7
Repr. 2; Acute Tox. 4; STOT RE 2; Skin Sens. 1
Details

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