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 19 rujna 2024. Database contains 4917 unique substances/entries.
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422-500-1
-
STOT RE 2
Details
UK-103,442
422-460-5
137234-87-8
Acute Tox. 4
Details
UK-111,975
422-390-5
143322-57-0
Repr. 2; STOT RE 1; Acute Tox. 4; Skin Sens. 1
Details
422-360-1
100491-29-0
Skin Sens. 1
Details
422-260-8
20701-68-2
Eye Dam. 1
Details
CIN 10094329; SENSIBILISATOR KF 693 PINA; SENSITIZER KF 693 PINA
422-240-9
166596-68-5
Eye Dam. 1; Skin Sens. 1
Details
T3P
422-210-5
68957-94-8
Skin Corr. 1B
Details
TICA 118
422-200-0
178277-55-9
Skin Corr. 1B; Acute Tox. 4
Details
422-100-7
102061-82-5
Eye Dam. 1; Skin Sens. 1
Details
422-090-4
172737-80-3
Eye Dam. 1
Details

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