+ANNESS V Atti legali tal-unjoni msemmija fl-Artikoli 11 u 27

ANNESS V Atti legali tal-unjoni msemmija fl-Artikoli 11 u 27

ANNESS V

Atti legali tal-unjoni msemmija fl-Artikoli 11 u 27

Kull referenza għall-atti legali tal-Unjoni elenkati f’dan l-Anness għandha tinftiehem bħala referenza għad-data dwar is-sustanzi kimiċi f’oġġetti jew fi prodotti ġġenerati jew sottomessi bħala parti mill-implimentazzjoni tal-att legali tal-Unjoni kkonċernat.

1.   

Ir-Regolament (UE) 2017/745 tal-Parlament Ewropew u tal-Kunsill tal-5 ta’ April 2017 dwar apparati mediċi, li jemenda d-Direttiva 2001/83/KE, ir-Regolament (KE) Nru 178/2002 u r-Regolament (KE) Nru 1223/2009 u li jħassar id-Direttivi tal-Kunsill 90/385/KEE u 93/42/KEE (ĠU L 117, 5.5.2017, p. 1)

2.   

Id-Direttiva 2008/98/KE tal-Parlament Ewropew u tal-Kunsill tad-19 ta’ Novembru 2008 dwar l-iskart u li tħassar ċerti Direttivi (ĠU L 312, 22.11.2008, p. 3)

3.   

Ir-Regolament (UE) 2024/1781 tal-Parlament Ewropew u tal-Kunsill tat-13 ta’ Ġunju 2024 li jistabbilixxi qafas għall-istabbiliment ta’ rekwiżiti tal-ekodisinn għal prodotti sostenibbli, li jemenda d-Direttiva (UE) 2020/1828 u r-Regolament (UE) 2023/1542 u li jħassar id-Direttiva 2009/125/KE (ĠU L, 2024/1781, 28.6.2024)

1. Ħarsa ġenerali

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1.1 Referenzi

1.2 Rekwiżiti identifikati

1.3 Standards relatati

2. Rekwiżiti identifikati

Rekwiżiti

3. Standards relatati

Standards
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