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 04 listopada 2024. Database contains 4917 unique substances/entries.
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202-752-7
99-35-4
Expl. 1.1; Acute Tox. 2; Acute Tox. 1; STOT RE 2
Details
203-812-5
110-88-3
Flam. Sol. 1; Repr. 2; STOT SE 3
Details
219-514-3
2451-62-9
Muta. 1B; Acute Tox. 3; STOT RE 2; Eye Dam. 1; Skin Sens. 1
M Mutagen (article 57b)
Details
220-474-4
2778-42-9
Resp. Sens. 1; Skin Sens. 1A
Details
241-536-7
17557-23-2
Skin Irrit. 2; Skin Sens. 1
Details
222-852-4
3634-83-1
Resp. Sens. 1; Skin Sens. 1A
Details
203-450-8
106-99-0
Flam. Gas 1; Press. Gas; Carc. 1A; Muta. 1B
Details
208-792-1
541-73-1
Acute Tox. 4
Details
202-491-9
96-23-1
Carc. 1B; Acute Tox. 3; Acute Tox. 4
Details
208-826-5
542-75-6
Flam. Liq. 3; Acute Tox. 3; Acute Tox. 4; Asp. Tox. 1; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2; Skin Sens. 1
Details

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