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Elamine, töötamine ja reisimine ELis
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Medical Devices - Sector
Medical Devices - Sector
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Medical devices
Medical Devices - Sector
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Medical Devices - Expert Panels
Medical Devices - EUDAMED
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Endocrine disruptors
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Viimased uuendused
13 Aprill 2021
Registration open: Webinar for Patients – Safe and performant Medical Devices for all (26 May 2021)
09 Aprill 2021
Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746
09 Aprill 2021
Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
01 Aprill 2021
The expert panels in the field of medical devices now accept submissions from notified bodies for the Clinical Evaluation Consultation Procedure
23 Märts 2021
Infographic - Is your software a Medical Device?
15 Märts 2021
Guidance on state of the art of COVID-19 rapid antibody tests
15 Märts 2021
Questions and Answers on Custom-Made Devices
26 Veebruar 2021
Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional
24 Veebruar 2021
COVID-19 tests: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19
18 Jaanuar 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
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E-uudiskiri
E-uudiskiri
E-uudiskiri
Wed, 03/31/2021
Komisjon toetab läbipaistvust uue toidualase määrusega
Viimased uuendused
Registration open: Webinar for Patients – Safe and performant Medical Devices for all (26 May 2021)
Avaldamise kuupäev
13 Aprill 2021
Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746
Avaldamise kuupäev
09 Aprill 2021
Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
Avaldamise kuupäev
09 Aprill 2021
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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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