Regulation on in vitro diagnostic medical devices

Summary

Regulation on in vitro diagnostic medical devices is a regulation of the European Union^[1]. It draws 9 Wikipedia views per month (regulation_of_the_european_union category, ranking #31 of 49).^[2]

Key Facts

• Regulation on in vitro diagnostic medical devices authored European Parliament^[3].
• Regulation on in vitro diagnostic medical devices authored Council of the European Union^[4].
• Regulation on in vitro diagnostic medical devices's instance of is recorded as regulation of the European Union^[5].
• Regulation on in vitro diagnostic medical devices's CELEX number is recorded as 32017R0746^[6].
• +2017-04-05T00:00:00Z marks the founding of Regulation on in vitro diagnostic medical devices^[7].
• Regulation on in vitro diagnostic medical devices's publication date is recorded as +2017-05-05T00:00:00Z^[8].
• Regulation on in vitro diagnostic medical devices's start time is recorded as +2017-05-25T00:00:00Z^[9].
• Regulation on in vitro diagnostic medical devices's main subject is recorded as in vitro diagnostics^[10].
• Regulation on in vitro diagnostic medical devices's applies to jurisdiction is recorded as European Union^[11].
• Regulation on in vitro diagnostic medical devices's replaces is recorded as Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998^[12].
• Regulation on in vitro diagnostic medical devices's published in is recorded as Official Journal of the European Union^[13].
• Regulation on in vitro diagnostic medical devices's title is recorded as Europa-Parlamentets og Rådets forordning (EU) 2017/746 af 5. april 2017 om medicinsk udstyr til in vitro-diagnostik og om ophævelse af direktiv 98/79/EF og Kommissionens afgørelse 2010/227/EU (EØS-relevant tekst. )^[14].
• Regulation on in vitro diagnostic medical devices's title is recorded as 2017 m. balandžio 5 d. Europos Parlamento ir Tarybos reglamentas (ES) 2017/746 dėl in vitro diagnostikos medicinos priemonių, kuriuo panaikinama Direktyva 98/79/EB ir Komisijos sprendimas 2010/227/ES (Tekstas svarbus EEE. )^[15].
• Regulation on in vitro diagnostic medical devices's title is recorded as Reglamento (UE) 2017/746 del Parlamento Europeo y del Consejo, de 5 de abril de 2017, sobre los productos sanitarios para diagnóstico in vitro y por el que se derogan la Directiva 98/79/CE y la Decisión 2010/227/UE de la Comisión (Texto pertinente an efectos del EEE. )^[16].
• Regulation on in vitro diagnostic medical devices's title is recorded as Verordnung (EU) 2017/746 des Europäischen Parlaments und des Rates vom 5. April 2017 über In-vitro-Diagnostika und zur Aufhebung der Richtlinie 98/79/EG und des Beschlusses 2010/227/EU der Kommission (Text von Bedeutung für den EWR. )^[17].
• Regulation on in vitro diagnostic medical devices's title is recorded as Az Európai Parlament és a Tanács (EU) 2017/746 rendelete (2017. április 5.) az in vitro diagnosztikai orvostechnikai eszközökről, valamint a 98/79/EK irányelv és a 2010/227/EU bizottsági határozat hatályon kívül helyezéséről (EGT-vonatkozású szöveg. )^[18].
• Regulation on in vitro diagnostic medical devices's title is recorded as Κανονισμός (EE) 2017/746 του Ευρωπαϊκού Κοινοβουλίου και του Συμβουλίου, της 5ης Απριλίου 2017, για τα in vitro διαγνωστικά ιατροτεχνολογικά προϊόντα και για την κατάργηση της οδηγίας 98/79/ΕΚ και της απόφασης 2010/227/ΕΕ της Επιτροπής (Κείμενο που παρουσιάζει ενδιαφέρον για τον ΕΟΧ )^[19].
• Regulation on in vitro diagnostic medical devices's title is recorded as Nařízení Evropského parlamentu a Rady (EU) 2017/746 ze dne 5. dubna 2017 o diagnostických zdravotnických prostředcích in vitro an o zrušení směrnice 98/79/ES a rozhodnutí Komise 2010/227/EU (Text s významem pro EHP. )^[20].
• Regulation on in vitro diagnostic medical devices's title is recorded as Regulamentul (UE) 2017/746 al Parlamentului European și al Consiliului din 5 aprilie 2017 privind dispozitivele medicale pentru diagnostic in vitro și de abrogare a Directivei 98/79/CE și a Deciziei 2010/227/UE a Comisiei (Text cu relevanță pentru SEE. )^[21].
• Regulation on in vitro diagnostic medical devices's title is recorded as Rozporządzenie Parlamentu Europejskiego i Rady (UE) 2017/746 z dnia 5 kwietnia 2017 r. w sprawie wyrobów medycznych do diagnostyki in vitro oraz uchylenia dyrektywy 98/79/WE i decyzji Komisji 2010/227/UE (Tekst mający znaczenie dla EOG. )^[22].
• Regulation on in vitro diagnostic medical devices's title is recorded as Nariadenie Európskeho parlamentu a Rady (EÚ) 2017/746 z 5. apríla 2017 o diagnostických zdravotníckych pomôckach in vitro an o zrušení smernice 98/79/ES a rozhodnutia Komisie 2010/227/EÚ (Text s významom pre EHP )^[23].
• Regulation on in vitro diagnostic medical devices's title is recorded as Verordening (EU) 2017/746 van het Europees Parlement en de Raad van 5 april 2017 betreffende medische hulpmiddelen voor in-vitrodiagnostiek en tot intrekking van Richtlijn 98/79/EG en Besluit 2010/227/EU van de Commissie (Voor de EER relevante tekst. )^[24].
• Regulation on in vitro diagnostic medical devices's title is recorded as Regolament (UE) 2017/746 tal-Parlament Ewropew u tal-Kunsill tal-5 ta' April 2017 dwar apparati mediċi dijanjostiċi in vitro u li jħassar id-Direttiva 98/79/KE u d-Deċiżjoni tal-Kummissjoni 2010/227/UE (Test b'rilevanza għaż-ŻEE. )^[25].
• Regulation on in vitro diagnostic medical devices's title is recorded as Eiropas Parlamenta un Padomes Regula (ES) 2017/746 (2017. gada 5. aprīlis) par in vitro diagnostikas medicīniskām ierīcēm un ar ko atceļ Direktīvu 98/79/EK un Komisijas Lēmumu 2010/227/ES (Dokuments attiecas uz EEZ. )^[26].
• Regulation on in vitro diagnostic medical devices's title is recorded as Rialachán (AE) 2017/746 ó pharlaimint na hEorpa agus ón gComhairle an 5 Aibreán 2017 maidir le feistí leighis diagnóiseacha in vitro agus lena n-aisghairtear Treoir 98/79/CE agus Cinneadh 2010/227/AE ón gCoimisiún (Téacs atá ábhartha maidir leis an LEE )^[27].

Body

Works and Contributions

Authored works include European Parliament^[3], an institutions of the European Union^[28], in European Union^[29], founded in 1957^[30], headquartered in Seat of the European Parliament in Strasbourg^[31] and Council of the European Union^[4], an institutions of the European Union^[32], in Belgium^[33], founded in 1957^[34], headquartered in Europa building^[35].

Why It Matters

Regulation on in vitro diagnostic medical devices draws 9 Wikipedia views per month (regulation_of_the_european_union category, ranking #31 of 49).^[2]