EU-MEDICAL_DEVICES_REGULATION-ANX_I_SEC_10
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 08 listopada 2024. Database contains 4918 unique substances/entries.
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2,4-DICHLORO-3-ETHYL-6-NITROPHENOL
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420-740-1
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99817-36-4
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Acute Tox. 3; Eye Dam. 1; Skin Sens. 1 |
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B2,4DBB
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420-710-8
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23085-60-1
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Repr. 2; Skin Irrit. 2; Skin Sens. 1 |
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METHFAT
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420-670-1
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37443-42-8
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Eye Dam. 1 |
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CORANOL
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420-630-3
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83926-73-2
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Eye Dam. 1 |
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420-610-4
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36394-75-9
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Acute Tox. 4; Skin Corr. 1B; Skin Sens. 1 |
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PERGASCRIPT BLACK 20223 AMIDE INTERMEDIATE
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420-600-1
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-
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STOT RE 2 |
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SUBSTANCE S123386; VANQUISH 100
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420-590-7
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4299-07-4
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Skin Corr. 1B; Skin Sens. 1 |
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P-964
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420-580-2
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151798-26-4
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Repr. 1B |
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SERTRALINE STEP 2
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420-560-3
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79617-97-3
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Eye Dam. 1 |
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420-530-1
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177027-34-8
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Resp. Sens. 1; Skin Sens. 1 |
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