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Guidance document Medical Devices - Conformity assessment procedure - Guideline for Authorised Representatives - MEDDEV 2.5/10
Document date: Mon Jan 30 00:00:00 CET 2012 - Created by GROW.R.4 - Publication date: Mon May 18 14:03:25 CEST 2015
Guidance document - In vitro diagnostic medical devices - Borderline and Classification issues. A guide for manufacturers and notified bodies - MEDDEV 2.14/1 rev.2
Document date: Mon Jan 23 00:00:00 CET 2012 - Created by GROW.R.4 - Publication date: Mon May 18 07:33:34 CEST 2015
Guidance document Medical Devices - Essential requirements - Conformity assessment of In Vitro Fertilisation (IVF) and Assisted Reproduction Technologies (ART) products - MEDDEV 2.2/4
Document date: Wed Jan 18 00:00:00 CET 2012 - Created by GROW.R.4 - Publication date: Mon May 18 14:08:22 CEST 2015
Guidance document Medical Devices - Scope, field of application, definition - Qualification and Classification of stand alone software - MEDDEV 2.1/6
Document date: Wed Jan 18 00:00:00 CET 2012 - Created by GROW.DDG1.D.4 - Publication date: Fri Jul 15 08:03:00 CEST 2016 - Last update: Fri Jul 15 08:04:00 CEST 2016
Guidance document Medical devices - Market surveillance - Post Market Clinical Follow-up studies - MEDDEV 2.12/2 rev.2
Document date: Wed Jan 11 00:00:00 CET 2012 - Created by GROW.R.4 - Publication date: Mon May 18 12:39:38 CEST 2015
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