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Naujausia informacija
26 Vasaris 2021
Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional
24 Vasaris 2021
COVID-19 tests: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19
18 Sausis 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
11 Sausis 2021
Covid-19: Commission Notice on audits to be performed by notified bodies
18 Gruodis 2020
Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
18 Gruodis 2020
Updated - Ongoing guidance development within MDCG Subgroups
15 Gruodis 2020
MDCG 2020-18 - MDCG Position Paper on UDI assignment for Spectacle lenses & Ready readers
02 Gruodis 2020
MDCG 2020-17 - Questions and Answers related to MDCG 2020-4: “Guidance on temporary extraordinary measures related to medical device notified body audits during COVID-19 quarantine orders and travel restrictions”
01 Gruodis 2020
The EUDAMED Actor module is in production. On 1st December 2020 the European Commission has made available the Actor registration module to Member States and economic operators
13 Lapkritis 2020
Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746
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E. informacinis biuletenis
E. informacinis biuletenis
E. informacinis biuletenis
Mon, 03/01/2021
„Nuo ūkio iki stalo“ – atspari maisto sistemų tobulinimo strategija
Naujausia informacija
Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional
Paskelbta
26 Vasaris 2021
COVID-19 tests: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19
Paskelbta
24 Vasaris 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
Paskelbta
18 Sausis 2021
Mūsų žinutės tinkle „Twitter“
Daugiau
Svarbiausia informacija
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
Commission Notice on notified bodies’ audits performed during Covid-19 exceptional circumstances
Commission Implementing Regulation (EU) 2020/1207 laying down rules as regards common specifications for the reprocessing of single-use devices
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