Questions & Answers
Dokumento data: Mon Jul 24 00:00:00 CEST 2023
- Sukūrė GROW.F.2
- Paskelbimo data: n/a
- Paskutinį kartą atnaujinta: Mon Jul 24 16:34:30 CEST 2023
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Manual on borderline and classification in the community regulatory framework for medical devices
Dokumento data: Thu Jul 17 00:00:00 CEST 2014
- Sukūrė GROW.R.4
- Paskelbimo data: Tue May 19 06:45:10 CEST 2015
- Paskutinį kartą atnaujinta: Fri Oct 02 13:53:19 CEST 2015
Nukreipti: http://ec.europa.eu/DocsRoom/documents/12867
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Guidance document - Market surveillance - Guidelines on a Medical Devices Vigilance System - MEDDEV 2.12/1 rev.8
Dokumento data: Sat Jan 19 00:00:00 CET 2013
- Sukūrė GROW.DDG1.D.4
- Paskelbimo data: Tue Nov 06 15:11:17 CET 2018
- Paskutinį kartą atnaujinta: Tue Nov 06 15:12:32 CET 2018
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Guidance document - Market surveillance - Guidelines on a Medical Devices Vigilance System - MEDDEV 2.12/1 rev.8
Dokumento data: Sat Jan 19 00:00:00 CET 2013
- Sukūrė GROW.DDG1.D.4
- Paskelbimo data: Tue Nov 06 18:01:52 CET 2018
- Paskutinį kartą atnaujinta: Wed Nov 28 13:16:04 CET 2018
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Guidance document - In vitro diagnostic medical devices - CE marking of blood based in vitro diagnostic medical devices for variant Creutzfeldt-Jakob Disease (vCJD) based on detection of abnormal PrP (host protein) - MEDDEV 2.14/4
Dokumento data: Mon Jan 30 00:00:00 CET 2012
- Sukūrė GROW.R.4
- Paskelbimo data: Mon May 18 13:54:40 CEST 2015
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