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 10 rujna 2024. Database contains 4917 unique substances/entries.
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234-829-6
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12035-72-2
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Carc. 1A; Muta. 2; Acute Tox. 3; STOT RE 1; Skin Sens. 1 |
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234-495-1
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12007-02-2
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Carc. 1A; STOT RE 1; Skin Sens. 1 |
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233-844-5
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10381-36-9
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Carc. 1A; STOT RE 1; Resp. Sens. 1; Skin Sens. 1 |
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-
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74646-29-0
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Carc. 1A; STOT RE 1; Skin Sens. 1 |
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236-771-7
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13477-70-8
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Carc. 1A; STOT RE 1; Skin Sens. 1 |
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680-302-2
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95266-40-3
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STOT RE 2; Skin Sens. 1B |
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-
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-
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Acute Tox. 2; Acute Tox. 1 |
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257-765-0
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52234-82-9
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Muta. 2; Eye Dam. 1; Skin Sens. 1 |
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1,3-PDTA; AGENT CHELATANT KODAK NO.1; DISSOLVINE PDZ; HAMPSHIRE PDTA; KODAK CHELATING AGENT NO.1; TRILON R FS
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400-400-9
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1939-36-2
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Acute Tox. 4; Eye Dam. 1 |
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204-468-9
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121-43-7
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Flam. Liq. 3; Acute Tox. 4 |
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