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Date Title
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
18/06/2012 Guide for Custom-made Medical Device Manufacturers on Compliance with European Communities (Medical Devices) Regulations, 1994
18/06/2012 Guide to the In-vitro Diagnostic Medical Devices Legislation
12/03/2012 Guide for suppliers of first aid kits, containing medicinal products, supplying solely to the end-user
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
11/05/2009 Guide for Manufacturers of General Class In-vitro Diagnostic Medical Devices
05/09/2005 Guide: Manufacture of Medical Devices within Healthcare Institutions
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Date Printed: 21 May 2013

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