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Date	Title
06/12/2012	Field Safety Notice Monthly Summary Sheet - November 2012
05/10/2012	Manufacturer application for compassionate use of a non-CE marked medical device
12/09/2012	Guide to Applications for Certificates of Free Sale for Medical Devices
04/09/2012	Field Safety Notice Monthly Summary Sheet - August 2012
22/08/2012	Field Safety Corrective Action Report Form
22/08/2012	Manufacturer's Incident Report Form
02/08/2012	Medical device registration system user name and password conditions of use
02/08/2012	Clinical investigations on medical devices
02/08/2012	Guide to the on-line registration system for medical devices
01/08/2012	Guide to Field Safety Corrective Actions for Medical Devices and In-vitro Diagnostic Medical Devices
01/08/2012	Guide to Incident Reporting for In-vitro Diagnostic Medical Devices
19/07/2012	Registration of persons responsible for placing Medical Devices on the market
19/07/2012	Registration of persons responsible for placing In-vitro Diagnostic Medical Devices on the market
16/07/2012	Medical Devices Newsletter No. 34 - June 2012
06/07/2012	Guide to Incident Reporting for General Medical Devices and Active Implantable Medical Devices
02/07/2012	Application for certificates of free sale for medical devices
18/06/2012	Guide to the In-vitro Diagnostic Medical Devices Legislation
18/06/2012	Guide for Custom-made Medical Device Manufacturers on Compliance with European Communities (Medical Devices) Regulations, 1994
04/04/2012	Field Safety Notice Monthly Summary Sheet - March 2012
01/03/2012	Field Safety Notice Monthly Summary Sheet - February 2012