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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CIN 10096132; MTI
407-630-9
82633-79-2
Acute Tox. 3; Eye Dam. 1; Skin Sens. 1
Details
212-557-9
826-62-0
Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1
Details
617-356-3
82560-54-1
Repr. 2; Acute Tox. 3; Acute Tox. 4
Details
128719
401-460-9
82560-06-3
Acute Tox. 3; Eye Dam. 1
Details
CP-166,221
428-010-4
82413-20-5
Carc. 2; Repr. 1B; Skin Sens. 1
Details
2-FLUOR-4-HYDROXYBENZONITRIL
422-810-7
82380-18-5
Acute Tox. 4; Eye Dam. 1
Details
212-513-9
823-40-5
Muta. 2; Acute Tox. 4; Skin Sens. 1
Details
212-497-3
822-36-6
Carc. 1B; Repr. 1B
Details
212-485-8
822-06-0
Acute Tox. 3; Eye Irrit. 2; STOT SE 3; Skin Irrit. 2; Resp. Sens. 1; Skin Sens. 1
Details
201-436-6
82-71-3
Expl. 1.1; Acute Tox. 4
Details

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