DIN EN ISO 12417-1 E : 2016
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 12417-1:2015) |
DD ISO/TS 12417:2011
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
04/300654 DC : DRAFT JAN 2004
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BS EN ISO 14630 - NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
I.S. EN ISO 14607:2009
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NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS (ISO 14607:2018) |
ISO 14607:2007
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Non-active surgical implants Mammary implants Particular requirements |
ISO/TS 12417:2011
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Cardiovascular implants and extracorporeal systems Vascular device-drug combination products |
PD ISO/TS 17137:2014
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - CARDIOVASCULAR ABSORBABLE IMPLANTS |
UNE-EN ISO 14602:2012
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Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010) |
BS EN ISO 22803:2005
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Dentistry. Membrane materials for guided tissue regeneration in oral and maxillofacial surgery. Contents of a technical file |
BS EN ISO 14630:2012
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Non-active surgical implants. General requirements |
14/30251609 DC : 0
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BS EN ISO 12417-1 - CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS |
ISO 14708-2:2012
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Implants for surgery Active implantable medical devices Part 2: Cardiac pacemakers |
AAMI ISO TIR 17137 : 2014
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - CARDIOVASCULAR ABSORBABLE IMPLANTS |
UNI EN ISO 14607 : 2009
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NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS |
BS EN ISO 14607:2009
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NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS |
DIN EN ISO 22803:2006-01
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Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
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 |
I.S. EN ISO 14602:2011
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NON-ACTIVE SURGICAL IMPLANTS - IMPLANTS FOR OSTEOSYNTHESIS - PARTICULAR REQUIREMENTS (ISO 14602:2010) |
I.S. EN ISO 22794:2009
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DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
I.S. EN ISO 14630:2012
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NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 14630:2012) |
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 |
BIS IS/ISO 14708-3 : 2008
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 3: IMPLANTABLE NEUROSTIMULATORS |
BS EN ISO 12417-1:2015
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Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products General requirements |
17/30250386 DC : 0
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BS ISO 17327-1 - NON-ACTIVE SURGICAL IMPLANTS - IMPLANT COATING - PART 1: GENERAL REQUIREMENTS |
03/101659 DC : DRAFT JAN 2003
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ISO 22803 - DENTISTRY - MEMBRANE MATERIALS FOR GUIDED TISSUE REGENERATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
AAMI ISO 14708-5 : 2010
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 5: CIRCULATORY SUPPORT DEVICES |
ISO 14708-6:2010
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Implants for surgery Active implantable medical devices Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators) |
DIN EN ISO 22794:2009-11
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Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file (ISO 22794:2007, corrected version 2009-01-15) |
ISO 22794:2007
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Dentistry Implantable materials for bone filling and augmentation in oral and maxillofacial surgery Contents of a technical file |
ISO 14602:2010
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Non-active surgical implants — Implants for osteosynthesis — Particular requirements |
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 |
UNI EN ISO 14602 : 2012
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NON-ACTIVE SURGICAL IMPLANTS - IMPLANTS FOR OSTEOSYNTHESIS - PARTICULAR REQUIREMENTS |
UNI EN ISO 14630 : 2013
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NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
I.S. EN ISO 12417-1:2015
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 12417-1:2015) |
AAMI ISO 14708-4 : 2008
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 4: IMPLANTABLE INFUSION PUMPS |
ISO/TR 12417-2:2017
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Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information |
UNE-EN ISO 12417-1:2016
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Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
AAMI ISO 12417-1 : 2015
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS |
ANSI/AAMI/ISO 14708-3:2017
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 3: IMPLANTABLE NEUROSTIMULATORS |
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 |
ISO 14708-4:2008
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Implants for surgery Active implantable medical devices Part 4: Implantable infusion pumps |
EN ISO 14607:2018
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Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2018, Corrected version 2018-08) |
DIN EN ISO 14630:2013-03
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Non-active surgical implants - General requirements (ISO 14630:2012) |
DIN EN ISO 14602:2012-06
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Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010) |
BS EN ISO 14602:2011
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Non-active surgical implants. Implants for osteosynthesis. Particular requirements |
UNE-EN ISO 14630:2013
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Non-active surgical implants - General requirements (ISO 14630:2012) |
ISO 12417-1:2015
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Cardiovascular implants and extracorporeal systems Vascular device-drug combination products Part 1: General requirements |
BS EN ISO 22794:2009
|
DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
EN ISO 22803:2005
|
Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
EN ISO 14602:2011
|
Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010) |
EN ISO 22794:2009
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Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file (ISO 22794:2007, corrected version 2009-01-15) |
EN ISO 14630:2012
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Non-active surgical implants - General requirements (ISO 14630:2012) |
EN ISO 12417-1:2015
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Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
AAMI ISO TIR 12417 : 2011
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
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 |
DIN EN ISO 12417-1:2016-02
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 12417-1:2015) |
ISO 14708-3:2017
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Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators |
ISO/TS 17137:2014
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Cardiovascular implants and extracorporeal systems Cardiovascular absorbable implants |
AAMI ISO 14708-4:2008(R2011)
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IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 4: IMPLANTABLE INFUSION PUMPS |
ISO 17327-1:2018
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Non-active surgical implants — Implant coating — Part 1: General requirements |
DIN EN ISO 14607:2009-08
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NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS |
ISO 14708-5:2010
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Implants for surgery Active implantable medical devices Part 5: Circulatory support devices |
UNI EN ISO 22794 : 2009
|
DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
ISO 22803:2004
|
Dentistry — Membrane materials for guided tissue regeneration in oral and maxillofacial surgery — Contents of a technical file |
ISO 14630:2012
|
Non-active surgical implants General requirements |
EN 45502-1 : 2015
|
IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND FOR INFORMATION TO BE PROVIDED BY THE MANUFACTURER |