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 19 lipnja 2024. Database contains 4917 unique substances/entries.
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1 - 2.5 moles ethoxylated
500-315-8
127087-87-0
ENDE Endocrine disrupting properties (Article 57(f) - environment)
Details
1 - 2.5 moles ethoxylated
500-209-1
68412-54-4
ENDE Endocrine disrupting properties (Article 57(f) - environment)
Details
1 - 2.5 moles ethoxylated
500-045-0
26027-38-3
ENDE Endocrine disrupting properties (Article 57(f) - environment)
Details
500-036-1
25214-70-4
C Carcinogenic (article 57a)
Details
500-033-5
25068-38-6
Eye Irrit. 2; Skin Irrit. 2; Skin Sens. 1
Details
500-024-6
9016-45-9
ENDE Endocrine disrupting properties (Article 57(f) - environment)
Details
479-100-5
577705-90-9
Repr. 1B
Details
477-690-9
874819-71-3
Repr. 1B; STOT RE 2
Details
473-390-7
-
VPVB very Persistent and very Bioaccumulative (article 57e)
Details
451-440-9
586372-44-3
Eye Dam. 1
Details

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