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 04 listopada 2024. Database contains 4917 unique substances/entries.
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C25-ALDEHYD
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415-770-7
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1638-05-7
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STOT RE 2; Skin Sens. 1 |
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7-PACA
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415-750-8
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106447-44-3
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Skin Sens. 1 |
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POTASSIUM N-(4-FLUOROPHENYL)GLYCINATE
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415-710-1
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184637-63-6
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STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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POTASSIUM 2,5-DICHLOROBENZOATE
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415-700-5
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184637-62-5
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Acute Tox. 4; Eye Dam. 1 |
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SB-201999
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415-680-8
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143468-96-6
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Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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GR138766X
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415-670-3
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78850-37-0
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Eye Dam. 1 |
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DOXAZOSIN 4; DOXAZOSIN STEP 4
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415-660-9
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70918-74-0
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Acute Tox. 3; STOT RE 2 |
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ROMILAT
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415-610-6
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104468-21-5
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Skin Irrit. 2 |
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CA 946 A
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415-580-4
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130841-23-5
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Acute Tox. 4; Skin Sens. 1 |
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BRL 44742
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415-550-0
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109887-53-8
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Acute Tox. 4; Eye Dam. 1 |
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