EU-IN_VITRO_MEDICAL_DEVICES-ART_3_ANX_1
EU-IN_VITRO_MEDICAL_DEVICES-ART_3_ANX_1
In Vitro Diagnostic Medical Devices Directive - Hazardous Substances
EU. Hazardous Substances for Purposes of Article 3 & Annex I (Essential Requirements), Directive 98/79/EC on In Vitro Diagnostic Medical Devices, 7 December 1998
This list contains a non-exhaustive inventory of hazardous substances for purposes of essential requirements (Article 3 and Annex I) for general safety, design, manufacture and hazard communication of in vitro diagnostic medical devices. It 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). Note that Regulation 2017/746/EU on in vitro diagnostic medical devices was published in the EU Official Journal on 5 May 2017. With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.
Last updated 07 listopada 2024. Database contains 4821 unique substances/entries.
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C.I. DIRECT BLUE 301; DIRECT BLUE 301
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408-210-8
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124605-82-9
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Skin Sens. 1 |
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425-270-0
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134620-00-1
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Acute Tox. 4; STOT RE 2; Eye Dam. 1; Skin Sens. 1 |
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426-730-3
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123439-82-7
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Acute Tox. 4; Eye Dam. 1 |
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PRO-JET BLACK 286 COLOUR; SUBSTANZ H112286
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405-130-5
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128351-36-0
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Skin Sens. 1 |
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444-440-5
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220689-12-3
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Acute Tox. 4 |
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424-710-9
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156126-48-6
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Acute Tox. 4; STOT RE 2; Skin Irrit. 2; Eye Dam. 1; Skin Sens. 1 |
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P3B
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418-080-4
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120307-06-4
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Skin Sens. 1 |
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TETRACONAZOLE
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407-760-6
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112281-77-3
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Acute Tox. 4 |
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KAYASET BLACK T-2
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405-110-6
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88377-66-6
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STOT RE 2 |
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429-270-1
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136210-30-5
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Skin Sens. 1 |
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