Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998
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Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998
Summary
Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 is a directive of the European Union[1].
Key Facts
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's instance of is recorded as directive of the European Union[2].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 was published on 1998[3].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's work available at URL is recorded as https://www.legislation.gov.uk/id/eudr/1998/79[4].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's work available at URL is recorded as https://eur-lex.europa.eu/legal-content/EN/ALL/?uri=CELEX:31998L0079[5].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's applies to jurisdiction is recorded as European Union[6].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's title is recorded as Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices[7].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's title is recorded as Euroopan parlamentin ja neuvoston direktiivi 98/79/EY, annettu 27 päivänä lokakuuta 1998, in vitro-diagnostiikkaan tarkoitetuista lääkinnällisistä laitteista[8].
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998's repealed by is recorded as Regulation on in vitro diagnostic medical devices[9].