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 lipnja 2024. Database contains 4917 unique substances/entries.
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701-162-1
-
Repr. 1B
Details
701-118-1
2156592-54-8
Repr. 1B; Eye Irrit. 2
Details
701-107-1
1801269-77-1
Repr. 1B; Skin Corr. 1C; Eye Dam. 1
Details
701-105-0
1801269-80-6
Repr. 1B; Skin Corr. 1C; Eye Dam. 1
Details
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Phenol, methylstyrenated EC / List no: 270-966-8 | CAS no: 68512-30-1
700-960-7
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VPVB very Persistent and very Bioaccumulative (article 57e)
Details
700-242-3
62037-80-3
E Equivalent level of concern having probable serious effects to the environment (Article 57(f) - environment)
HH Equivalent level of concern having probable serious effects to human health (Article 57(f) - human health)
Details
695-989-4
2527-66-4
Acute Tox. 4; Acute Tox. 3; Skin Corr. 1C; Eye Dam. 1; Skin Sens. 1A
Details
692-456-8
688046-61-9
Carc. 2
Details
691-719-4
1072957-71-1
Acute Tox. 3
Details
688-331-2
874967-67-6
Carc. 2
Details

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