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ISO 14708-1:2014
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Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
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ISO 14117:2012
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Active implantable medical devices Electromagnetic compatibility EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
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AAMI ISO 14117 : 2012
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ACTIVE IMPLANTABLE MEDICAL DEVICES - ELECTROMAGNETIC COMPATIBILITY - EMC TEST PROTOCOLS FOR IMPLANTABLE CARDIAC PACEMAKERS, IMPLANTABLE CARDIOVERTER DEFIBRILLATORS AND CARDIAC RESYNCHRONIZATION DEVICES
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CSA ISO/IEC TR 20017:14 (R2019)
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Information technology - Radio frequency identification for item management - Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators (Adopted ISO/IEC TR 20017:2011, first edition, 2011-12-15)
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BS ISO 14117:2012
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Active implantable medical devices. Electromagnetic compatibility. EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
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EN 50077 : 93 AC 93
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LOW-PROFILE CONNECTOR FOR IMPLANTABLE PACEMAKERS
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BS 5724-2.31(1995) : 1995
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MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY - SPECIFICATION FOR EXTERNAL CARDIAC PACEMAKERS WITH INTERNAL POWER SOURCE
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BS EN 45502-2-3:2010
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Active implantable medical devices Particular requirements for cochlear and auditory brainstem implant systems
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ISO 14708-2:2012
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Implants for surgery Active implantable medical devices Part 2: Cardiac pacemakers
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BS EN 45502-1:2015
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Implants for surgery. Active implantable medical devices General requirements for safety, marking and for information to be provided by the manufacturer
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I.S. EN 45502-1:2015
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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EN 45502-1:2015
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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UNI CEI EN 45502-2-3 : 2010
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ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-3: PARTICULAR REQUIREMENTS FOR COCHLEAR AND AUDITORY BRAINSTEM IMPLANT SYSTEMS
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13/30233325 DC : 0
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BS EN 45502-1 - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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ISO/IEC TR 20017:2011
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Information technology Radio frequency identification for item management Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators
|
|
ANSI/AAMI/ISO 14708-1:2014
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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UNE-EN 45502-2-3:2010
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Active implantable medical devices -- Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems
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EN 45502-2-3:2010
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Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems
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PREN 45502-1 : DRAFT 2013
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ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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|
CEI EN 50077 : 1998
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LOW-PROFILE CONNECTOR FOR IMPLANTABLE CARDIAC PACEMAKERS
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|
I.S. EN 45502-2-3:2010
|
ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-3: PARTICULAR REQUIREMENTS FOR COCHLEAR AND AUDITORY BRAINSTEM IMPLANT SYSTEMS
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EN 45502-1 : 2015
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER
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