Gaois

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2 results

  1. ENVIRONMENT|environmental policy|waste management · ENVIRONMENT|deterioration of the environment|waste

    #682217

    IATE #3510062
    freagracht leathnaithe táirgeora Reference "Rialachán (AE) 2025/40 maidir le pacáistíocht agus dramhaíl ó phacáistíocht, lena leasaítear Rialachán (AE) 2019/1020 agus Treoir (AE) 2019/904, agus lena n-aisghairtear Treoir 94/62/CE"
    ga
    Context Bunaítear leis an Rialachán seo ceanglais le haghaidh shaolré iomlán na pacáistíochta a mhéid a bhaineann le hinbhuanaitheacht comhshaoil agus lipéadú ionas gur féidir í a chur ar an margadh. Bunaítear leis freisin ceanglais maidir le freagracht leathnaithe táirgeora, dramhaíl ó phacáistíocht a chosc, amhail pacáistíocht neamhriachtanach a laghdú agus pacáistíocht a athúsáid nó a athlíonadh, chomh maith le dramhaíl ó phacáistíocht a bhailiú agus a chóireáil, lena n-áirítear athchúrsáil. Reference "Rialachán (AE) 2025/40 maidir le pacáistíocht agus dramhaíl ó phacáistíocht, lena leasaítear Rialachán (AE) 2019/1020 agus Treoir (AE) 2019/904, agus lena n-aisghairtear Treoir 94/62/CE"
    FLT Reference Téarmeolaithe COM-GA
    ga
    Language usage Cinneadh gur chuí an giorrúchán a bhunú ar an téarma Gaeilge, arae níor léir aon chúis sháraitheach le gan sin a dhéanamh
    erweiterte Herstellerverantwortung
    de
    extended producer responsibility | EPR
    en
    Definition concept where manufacturers and importers of products should bear a significant degree of responsibility for the environmental impacts of their products throughout the product life-cycle, including upstream impacts inherent in the selection of materials for the products, impacts from manufacturers’ production process itself, and downstream impacts from the use and disposal of the products Reference "OECD > Environment Directorate > Waste > 'Fact Sheet : Extended Producer Responsibility' (29.11.2022)."
    Comment Producers accept their responsibility when designing their products to minimise life-cycle environmental impacts, and when accepting legal, physical or socio-economic responsibility for environmental impacts that cannot be eliminated by design.
    responsabilité élargie du producteur | responsabilité élargie des producteurs | REP
    fr
  2. SOCIAL QUESTIONS|health|health policy|organisation of health care|medical device

    #690679

    IATE #3648609
    Meitheal um Aicmiú Feistí Leighis agus Feistí Leighis Teorannacha Reference Téarmeolaithe COM-GA
    ga
    Aicmiú Feistí Leighis agus Feistí Leighis Teorannacha Reference Téarmeolaithe COM-GA
    ga
    AFL&FLT Reference Téarmeolaithe COM-GA
    ga
    meitheal um Aicmiú Feistí Leighis agus Feistí Leighis Teorannacha Reference Téarmeolaithe COM-GA
    ga
    Definition "meitheal a thugann cúnamh don Ghrúpa Comhordaithe maidir le Feistí Leighis i dtaca le saincheisteanna a bhaineann leis an méid seo a leanas: (i) táirge a cháiliú mar fheiste leighis/mar ghabhálas feiste leighis faoi Rialachán (AE) 2017/745 (RFL), agus faoi fheiste leighis dhiagnóiseach in vitro/mar ghabhálas le haghaidh feiste leighis diagnóiseach in vitro faoi Rialachán (AE) 2017/746 (RDIV); (ii) cáilíocht táirgí nár beartaíodh críoch leighis dóibh i gcomhréir le hIarscríbhinn XVI den RFL; (iii) feistí leighis a aicmiú i gcomhréir le hIarscríbhinn VIII RFL agus feistí leighis diagnóiseacha in vitro a aicmiú i gcomhréir le hIarscríbhinn VIII RDIV" Reference "Téarmeolaithe COM-GA, arna bhunú ar dhoiciméad inmheanach de chuid an Choimisiúin, 'TERMS OF REFERENCE OF THE MDCG WORKING GROUP. WORKING GROUP ON BORDERLINE & CLASSIFICATION'"
    Arbeitsgruppe Borderline-Produkte und Klassifizierung | Borderline-Produkte und Klassifizierung | B&C
    de
    Definition Arbeitsgruppe zur Unterstützung der Koordinierungsgruppe Medizinprodukte bei Fragen zur Einstufung eines Produkts als Medizinprodukt oder Zubehör eines Medizinprodukts (und eines In-vitro-Diagnostikums) und zur Einstufung von Produkten ohne medizinische Zweckbestimmung Reference "Europäische Kommission > Arbeitsgruppen der Koordinierungsgruppe Medizinprodukte (29.1.2025)"
    Working Group on Borderline & Classification | Borderline & Classification | B&C | Borderline and Classification working group
    en
    Definition "working group that assists the Medical Device Coordination Group (MDCG) on issues related to: (i) qualification of a product as a medical device / an accessory for a medical device under Regulation (EU) 2017/745 (MDR), and in-vitro diagnostic medical device / an accessory for an in-vitro diagnostic medical device under Regulation (EU) 2017/746 (IVDR); (ii) qualification of products without an intended medical purpose in accordance with Annex XVI MDR; (iii) classification of medical devices in accordance with Annex VIII MDR and classification of in-vitro diagnostic medical devices in accordance with Annex VIII IVDR" Reference "COM-Terminology Coordination, based on: European Commission. 'TERMS OF REFERENCE OF THE MDCG WORKING GROUP. WORKING GROUP ON BORDERLINE & CLASSIFICATION' (2.12.2024)"
    groupe de travail dispositifs limites et classification | Dispositifs limites et classification
    fr
    Definition "un des treize sous-groupes du groupe de coordination en matière de dispositifs médicaux (GCDM) (8.1.2025) présidé par la Commission européenne, qui assiste ce dernier en ce qui concerne la qualification d’un produit en tant que dispositif médical ou accessoire de dispositif médical (et de dispositif médical de diagnostic in vitro), ainsi que la qualification de produits n’ayant pas une destination médicale" Reference "COM-FR, d’après Commission européenne, Santé publique, Groupes de travail du groupe de coordination en matière de dispositifs médicaux (8.1.2025)"