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121	I am responding to the Public Consultation on the Recast of the Medical Devices Directives as an individual, not on behalf of any organization, but from my position and experience as a CEN Consultant for the medical devi Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:15 European Union directives Medical device Medical Devices Directive Notified Body ISO 13485 CE mark Technology Medical technology Medical equipment
122	RECAST OF THE MEDICAL DEVICES DIRECTIVES PUBLIC CONSULTATION 1. THE SIMPLIFICATION PROGRAMME Based on the New Approach, rules relating to the safety and performance of medical devices were harmonised in the EU in the nin Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:38:58 Medical technology European Union directives Medical device Medical Devices Directive CE mark Notified Body Global Harmonization Task Force European Medicines Agency Unique Device Identification Medicine Technology Medical equipment
123	Guidance document Construction Products Regulation (EU) Euralarm/GL[removed]Table of Contents 1. Common Abbreviations .............................................................................................. Add to Reading List Source URL: www.euralarm.org Language: English - Date: 2013-05-15 02:47:07 Quality Construction Products Directive CE mark Type approval Notified Body Cardiopulmonary resuscitation Dangerous goods Specification Regulation (EU) No 305/2011 Product certification Evaluation European Union directives
124	Recast of the European Medical Devices Directives: an opportunity to reinforce patient safety ● Response to the public consultation on the recast of the Medical Devices Directives (1); deadline 2 July 2008 The Medicine Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:38:37 Medical technology Medical device Global Harmonization Task Force CE mark Notified Body Patient safety Medical Devices Directive European Medical Devices Industry Group Medicines and Healthcare products Regulatory Agency Medicine Health Medical equipment
125	CECE guidance on the ‘Declaration of Conformity’ for the machinery directive[removed]EC EC Declaration of Conformity Add to Reading List Source URL: www.cece.eu Language: English - Date: 2014-01-07 05:06:06 Notified Body Reference Standards CE mark Pressure Equipment Directive European Union directives Evaluation Product certification
126	NLF interpretative Fiche Orgalime Position Paper Fiche Nr: Title Short: Add to Reading List Source URL: www.orgalime.org Language: English - Date: 2014-09-15 07:22:27 Type approval ATEX directive Orgalime Public key certificate Sociology Ethics Science CE mark European Union directives Product certification Notified Body
127	NBOG_Answers_Public_Consultation_Recast Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:27 Notified Body Product certification
128	Recast of Medical Devices Directives Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:35:13 Medical equipment European Union directives Medical device Medical Devices Directive Notified Body ISO 13485 CE mark Medicine Technology Medical technology
129	VM Direktivas groz[removed]doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:41 Medical technology Medical device Global Harmonization Task Force CE mark Medical Devices Directive Notified Body Health care Medicine Medical equipment Technology
130	Today the legislative framework for medical devices in Europe comprises three main Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:14 Medical technology Medical device European Union directives Pharmaceutical industry Medical Devices Directive CE mark Notified Body Unique Device Identification Breast implant Medicine Technology Medical equipment

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