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) |
ISO 20697:2018
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Sterile drainage catheters and accessory devices for single use |
13/30261812 DC : 0
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BS ISO 10555-6 - INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS |
14/30270462 DC : 0
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BS EN ISO 5840-1 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS |
BS EN ISO 5840-2:2015
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES |
ANSI/AAMI CI86:2017
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COCHLEAR IMPLANT SYSTEMS: REQUIREMENTS FOR SAFETY, FUNCTIONAL VERIFICATION, LABELING AND RELIABILITY REPORTING |
09/30177654 DC : 0
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BS EN 62570 - MAGNETIC RESONANCE EQUIPMENT FOR MEDICAL IMAGING - INSTRUCTIONS FOR MARKING ITEMS WITHIN THE CONTROLLED ACCESS AREA |
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) |
UNE-EN ISO 25539-3:2012
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Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011) |
17/30336577 DC : 0
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BS EN ISO 20697 - STERILE DRAINAGE CATHETERS AND ACCESSORY DEVICES FOR SINGLE USE |
17/30336573 DC : 0
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BS EN ISO 20696 - STERILE URETHAL CATHETERS FOR SINGLE USE |
I.S. EN ISO 10555-6:2017
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INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
DIN EN ISO 5840-3:2013-06
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Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2013) |
ANSI/AAMI/ISO 25539-1:2017
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES |
ISO/TR 12417-2:2017
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Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information |
ANSI/AAMI/ISO 5840-3:2013
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY TRANSCATHETER TECHNIQUES |
ISO/TS 17137:2014
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Cardiovascular implants and extracorporeal systems Cardiovascular absorbable implants |
AAMI ISO TIR 10974 : 2012
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ASSESSMENT OF THE SAFETY OF MAGNETIC RESONANCE IMAGING FOR PATIENTS WITH AN ACTIVE IMPLANTABLE MEDICAL DEVICE |
DIN EN ISO 10555-6:2017-11
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INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
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 |
ISO 25539-3:2011
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Cardiovascular implants Endovascular devices Part 3: Vena cava filters |
BS EN ISO 14630:2012
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Non-active surgical implants. General requirements |
EN ISO 25539-3:2011
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Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011) |
EN 62570:2015
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Standard practice for marking medical devices and other items for safety in the magnetic resonance environment |
UNE-EN ISO 25539-2:2013
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Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012) |
17/30345938 DC : 0
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BS ISO 20698 - CATHETER SYSTEMS FOR NEURAXIAL APPLICATION - STERILE AND SINGLE-USE CATHETERS AND ACCESSORIES |
11/30243761 DC : 0
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BS ISO 14708-7 - IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 7: PARTICULAR REQUIREMENTS FOR COCHLEAR IMPLANT SYSTEMS |
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 20696:2018
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Sterile urethral catheters for single use |
I.S. EN ISO 5840-3:2013
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY TRANSCATHETER TECHNIQUES (ISO 5840-3:2013) |
14/30281560 DC : 0
|
BS EN ISO 5840-2 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES |
DIN EN ISO 25539-3:2012-03
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Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011) |
BS 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 |
UNI EN ISO 5840-3 : 2013
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY TRANSCATHETER TECHNIQUES |
AAMI ISO TIR 17137 : 2014
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CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - CARDIOVASCULAR ABSORBABLE IMPLANTS |
I.S. EN ISO 5840-1:2015
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS (ISO 5840-1:2015) |
ISO 14708-7:2013
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Implants for surgery Active implantable medical devices Part 7: Particular requirements for cochlear implant systems |
DIN EN ISO 5840-2 E : 2016
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES (ISO 5840-2:2015) |
EN ISO 5840-2:2015
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Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2015) |
EN ISO 5840-1:2015
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Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements (ISO 5840-1:2015) |
EN ISO 5840-3:2013
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Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2013) |
I.S. EN ISO 14630:2012
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NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 14630:2012) |
UNE-EN ISO 5840-2:2016
|
Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2015) |
DIN EN ISO 10555-6 E : 2017
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INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS (ISO 10555-6:2015) |
BS ISO 18190:2016
|
Anaesthetic and respiratory equipment. General requirements for airways and related equipment |
BS EN ISO 12417-1:2015
|
Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products General requirements |
BS EN 62570:2015
|
STANDARD PRACTICE FOR MARKING MEDICAL DEVICES AND OTHER ITEMS FOR SAFETY IN THE MAGNETIC RESONANCE ENVIRONMENT |
BS EN ISO 5840-1:2015
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS |
ASTM F 2052 : 2015 : REDLINE
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Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment |
ANSI/AAMI/ISO 25539-2:2012
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS |
BS EN ISO 5840-3:2013
|
Cardiovascular implants. Cardiac valve prostheses Heart valve substitutes implanted by transcatheter techniques |
UNE-EN ISO 5840-1:2016
|
Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements (ISO 5840-1:2015) |
DIN EN ISO 5840-2:2016-05
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Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2015) |
DIN EN ISO 5840-1:2015-12
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Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements (ISO 5840-1:2015) |
AAMI ISO 25539-3 : 2011
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 3: VENA CAVA FILTERS |
I.S. EN ISO 5840-2:2015
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES (ISO 5840-2:2015) |
I.S. EN ISO 25539-2:2012
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS (ISO 25539-2:2012) |
AAMI ISO 5840-1 : 2016
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS |
I.S. EN ISO 25539-3:2011
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 3: VENA CAVA FILTERS (ISO 25539-3:2011) |
ASTM F 2119 : 2007
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Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants |
UNI EN ISO 25539-3 : 2012
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 3: VENA CAVA FILTERS |
BS EN ISO 10555-6:2017
|
Intravascular catheters. Sterile and single-use catheters Subcutaneous implanted ports |
ASTM F 2119 : 2007 : R2013
|
Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants (Withdrawn 2022) |
ASTM F 2503 : 2013 : REDLINE
|
Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment |
ISO 10555-6:2015
|
Intravascular catheters Sterile and single-use catheters Part 6: Subcutaneous implanted ports |
EN ISO 25539-2:2012
|
Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012) |
UNI CEI EN 45502-2-3 : 2010
|
ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-3: PARTICULAR REQUIREMENTS FOR COCHLEAR AND AUDITORY BRAINSTEM IMPLANT SYSTEMS |
UNI EN ISO 14630 : 2013
|
NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
10/30196945 DC : 0
|
BS ISO 25539-3 - CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 3: VENA CAVA FILTERS |
BS EN ISO 25539-1:2017
|
Cardiovascular implants. Endovascular devices Endovascular prostheses |
BS EN ISO 25539-3:2011
|
Cardiovascular implants. Endovascular devices Vena cava filters |
11/30219211 DC : 0
|
BS EN ISO 5840-3 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY MINIMALLY INVASIVE TECHNIQUES |
UNE-EN ISO 12417-1:2016
|
Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
UNI EN ISO 25539-2 : 2013
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS |
DIN EN ISO 25539-2:2013-05
|
Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012) |
AAMI ISO 12417-1 : 2015
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS |
I.S. EN 62570:2015
|
STANDARD PRACTICE FOR MARKING MEDICAL DEVICES AND OTHER ITEMS FOR SAFETY IN THE MAGNETIC RESONANCE ENVIRONMENT |
I.S. EN ISO 25539-1:2017
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |
ASTM F 1831 : 2017 : REDLINE
|
Standard Specification for Cranial Traction Tongs and Halo External Spinal Immobilization Devices |
ASTM F 3160 : 2016
|
Standard Guide for Metallurgical Characterization of Absorbable Metallic Materials for Medical Implants |
ISO/TS 10974:2012
|
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device |
DIN EN ISO 14630:2013-03
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
ISO 5840-3:2013
|
Cardiovascular implants Cardiac valve prostheses Part 3: Heart valve substitutes implanted by transcatheter techniques |
ISO 25539-2:2012
|
Cardiovascular implants Endovascular devices Part 2: Vascular stents |
IEC 62570:2014
|
Standard practice for marking medical devices and other items for safety in the magnetic resonance environment |
ISO 5840-2:2015
|
Cardiovascular implants Cardiac valve prostheses Part 2: Surgically implanted heart valve substitutes |
UNE-EN ISO 14630:2013
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
UNE-EN 45502-2-3:2010
|
Active implantable medical devices -- Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems |
ISO 12417-1:2015
|
Cardiovascular implants and extracorporeal systems Vascular device-drug combination products Part 1: General requirements |
EN 45502-2-3:2010
|
Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems |
EN ISO 12417-1:2015
|
Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
EN ISO 14630:2012
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
AAMI ISO TIR 12417 : 2011
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
DIN EN ISO 5840-1 E : 2015
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS (ISO 58401:2015) |
BS ISO 10555-6 : 2015
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 6: SUBCUTANEOUS IMPLANTED PORTS |
DD ISO/TS 12417:2011
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
UNE-EN ISO 5840-3:2013
|
Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2013) |
DIN EN ISO 25539-1:2015-07 (Draft)
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |
BS EN ISO 25539-2:2012
|
Cardiovascular implants. Endovascular devices Vascular stents |
BS PD ISO/TS 10974 : 2012
|
ASSESSMENT OF THE SAFETY OF MAGNETIC RESONANCE IMAGING FOR PATIENTS WITH AN ACTIVE IMPLANTABLE MEDICAL DEVICE |
EN ISO 10555-6:2017
|
Intravascular catheters - Sterile and single-use catheters - Part 6: Subcutaneous implanted ports (ISO 10555-6:2015) |
CEI EN 62570 : 2016
|
STANDARD PRACTICE FOR MARKING MEDICAL DEVICES AND OTHER ITEMS FOR SAFETY IN THE MAGNETIC RESONANCE ENVIRONMENT |
I.S. EN 45502-2-3:2010
|
ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-3: PARTICULAR REQUIREMENTS FOR COCHLEAR AND AUDITORY BRAINSTEM IMPLANT SYSTEMS |
ISO 18190:2016
|
Anaesthetic and respiratory equipment — General requirements for airways and related equipment |
I.S. EN ISO 12417-1:2015
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 12417-1:2015) |
ISO 25539-1:2017
|
Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses |
ISO 5840-1:2015
|
Cardiovascular implants Cardiac valve prostheses Part 1: General requirements |
ISO 14630:2012
|
Non-active surgical implants General requirements |
DIN EN ISO 25539-1:2017-09
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |