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Questions & Answers
Document date: Mon Jul 24 00:00:00 CEST 2023
- Created by GROW.F.2
- Publication date: n/a
- Last update: 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
Document date: Thu Jul 17 00:00:00 CEST 2014
- Created by GROW.R.4
- Publication date: Tue May 19 06:45:10 CEST 2015
- Last update: Fri Oct 02 13:53:19 CEST 2015
Redirected to: 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
Document date: Sat Jan 19 00:00:00 CET 2013
- Created by GROW.DDG1.D.4
- Publication date: Tue Nov 06 15:11:17 CET 2018
- Last update: 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
Document date: Sat Jan 19 00:00:00 CET 2013
- Created by GROW.DDG1.D.4
- Publication date: Tue Nov 06 18:01:52 CET 2018
- Last update: 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
Document date: Mon Jan 30 00:00:00 CET 2012
- Created by GROW.R.4
- Publication date: Mon May 18 13:54:40 CEST 2015
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