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 11 rujna 2024. Database contains 4917 unique substances/entries.
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247-570-9
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26266-63-7
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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234-290-7
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11070-44-3
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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203-239-0
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104-80-3
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Eye Irrit. 2; STOT SE 3; Skin Irrit. 2 |
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203-726-8
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109-99-9
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Flam. Liq. 2; Carc. 2; Eye Irrit. 2; STOT SE 3 |
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251-823-9
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34090-76-1
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Eye Dam. 1; Resp. Sens. 1; Skin Sens. 1 |
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CIS/TRANS-TIMO; FLOROL; FLOROSA
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405-040-6
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63500-71-0
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Eye Irrit. 2 |
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202-625-6
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97-99-4
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Repr. 1B; Eye Irrit. 2 |
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230-625-6
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7226-23-5
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Repr. 2; Acute Tox. 4; Eye Dam. 1 |
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204-126-9
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116-14-3
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Carc. 1B |
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201-083-8
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78-10-4
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Flam. Liq. 3; Acute Tox. 4; Eye Irrit. 2; STOT SE 3 |
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