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 listopada 2024. Database contains 4918 unique substances/entries.
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Acute Tox. 3; STOT RE 2 |
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247-109-1
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25567-67-3
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Acute Tox. 3; STOT RE 2 |
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200-760-5
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71-63-6
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Acute Tox. 3; STOT RE 2 |
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247-096-2
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25550-58-7
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Acute Tox. 3; STOT RE 2 |
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204-539-4
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122-39-4
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Acute Tox. 3; STOT RE 2 |
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202-729-1
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99-09-2
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Acute Tox. 3; STOT RE 2 |
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203-583-1
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108-44-1
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Acute Tox. 3; STOT RE 2 |
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202-088-8
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91-66-7
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Acute Tox. 3; STOT RE 2 |
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204-495-6
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121-72-2
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Acute Tox. 3; STOT RE 2 |
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210-199-8
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609-72-3
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Acute Tox. 3; STOT RE 2 |
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