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Date	Title
12/09/2012	Guide to Applications for Certificates of Free Sale for 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
06/07/2012	Guide to Incident Reporting for General Medical Devices and Active Implantable 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
27/08/2010	Guide for Class I Manufacturers on Compliance with European Communities (Medical Devices) Regulations, 1994
23/08/2010	Guide for Medical Device Manufacturers on Auditing by the Irish Medicines Board to the Medical Device Regulations
09/08/2010	Guide for Manufacturers of System and Procedure Packs regarding Legislative Requirements
04/06/2010	Guide for Ethics Committees on Clinical Investigation of Medical Devices
11/05/2009	Guide for Manufacturers of General Class In-vitro Diagnostic Medical Devices
27/04/2009	Guide to the Classification of a Medical Device
14/01/2009	Guide for Industry users to the on-line Vigilance Reporting System for Medical Devices
01/01/2009	Medical Devices EToken User Guide
01/05/2007	IMB Position Paper: Manufacturing / Adaption of Splints and Splinting Material by Professional Users
05/09/2005	Guide: Manufacture of Medical Devices within Healthcare Institutions
26/03/2004	Guidance Note 6: Glossary of Terms for Medical Devices