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 11 rujna 2024. Database contains 4917 unique substances/entries.
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202-851-5
100-42-5
Flam. Liq. 3; Repr. 2; Acute Tox. 4; STOT RE 1; Skin Irrit. 2; Eye Irrit. 2
Details
200-319-7
57-24-9
Acute Tox. 1; Acute Tox. 2
Details
269-439-5
68239-26-9
Acute Tox. 2
Details
269-710-8
68310-42-9
Acute Tox. 2
Details
234-239-9
11005-63-3
Acute Tox. 3; STOT RE 2
Details
232-142-6
7789-06-2
Carc. 1B; Acute Tox. 4
C Carcinogenic (article 57a)
Details
427-930-3
250639-69-1
Skin Sens. 1
Details
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P Parasites
Details
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P Parasites
Details
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B Bacteria and similar species
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