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 06 rujna 2024. Database contains 4917 unique substances/entries.
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231-205-5
7446-27-7
Repr. 1A; STOT RE 2
Details
235-688-3
12519-85-6
Carc. 1A; STOT RE 1; Skin Sens. 1
Details
603-146-9
126535-15-7
Carc. 2
Details
216-428-8
1582-09-8
Carc. 2; Skin Sens. 1
Details
219-014-5
2314-97-8
Muta. 2
Details
200-929-3
76-05-1
Acute Tox. 4; Skin Corr. 1A
Details
614-708-8
68694-11-1
Repr. 1B; Acute Tox. 4; STOT RE 2; Skin Sens. 1
Details
604-237-6
141517-21-7
Lact.; Skin Sens. 1
Details
215-812-2
1420-06-0
Acute Tox. 4
Details
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Acute Tox. 2; Acute Tox. 1
Details

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