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) |
BS EN ISO 5840-2:2015
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Cardiovascular implants. Cardiac valve prostheses 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 |
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) |
DIN EN ISO 7197:2009-08
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NEUROSURGICAL IMPLANTS - STERILE, SINGLE-USE HYDROCEPHALUS SHUNTS AND COMPONENTS |
NF EN ISO 5366 : 2016
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ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES AND CONNECTORS |
BS EN ISO 25539-2:2012
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Cardiovascular implants. Endovascular devices Vascular stents |
ASTM F 564 : 2017 : REDLINE
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Standard Specification and Test Methods for Metallic Bone Staples |
ANSI/AAMI/ISO 25539-1:2017
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES |
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 5840-3:2013
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 3: HEART VALVE SUBSTITUTES IMPLANTED BY TRANSCATHETER TECHNIQUES |
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 |
ASTM F 366 : 2017 : REDLINE
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Standard Specification for Fixation Pins and Wires |
ASTM F 382 : 2017 : REDLINE
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Standard Specification and Test Method for Metallic Bone Plates |
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 ISO 5366:2016
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Anaesthetic and respiratory equipment - Tracheostomy tubes and connectors (ISO 5366:2016) |
ASTM F 2978 : 2013
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Guide to Optimize Scan Sequences for Clinical Diagnostic Evaluation of Metal-on-Metal Hip Arthroplasty Devices using Magnetic Resonance Imaging |
UNE-EN ISO 25539-2:2013
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Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012) |
DIN EN ISO 5366:2015-10 (Draft)
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ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES AND CONNECTORS (ISO 5366:2016) |
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 |
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) |
14/30303965 DC : 0
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BS EN 60601-2-33/A2 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-33: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF MAGNETIC RESONANCE EQUIPMENT FOR MEDICAL DIAGNOSIS |
DIN EN ISO 25539-3:2012-03
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Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011) |
ANSI/AAMI/ISO 25539-2:2012
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS |
ISO/TR 12417-2:2017
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Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information |
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
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS (ISO 5840-1:2015) |
ISO/TS 17137:2014
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Cardiovascular implants and extracorporeal systems Cardiovascular absorbable implants |
ASTM F 2502 : 2017 : REDLINE
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Standard Specification and Test Methods for Absorbable Plates and Screws for Internal Fixation Implants |
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) |
DIN EN ISO 5366:2017-04
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Anaesthetic and respiratory equipment - Tracheostomy tubes and connectors (ISO 5366:2016); German version EN ISO 5366:2016 |
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
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Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2015) |
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 7197:2009
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Neurosurgical implants. Sterile, single-use hydrocephalus shunts and components |
11/30219124 DC : 0
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BS EN ISO 14630 AMD 1 - NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
BS ISO 18190:2016
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Anaesthetic and respiratory equipment. General requirements for airways and related equipment |
BS EN ISO 12417-1:2015
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Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products General requirements |
DIN EN ISO 5366 E : 2017
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ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES AND CONNECTORS (ISO 5366:2016) |
BS EN ISO 5840-3:2013
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Cardiovascular implants. Cardiac valve prostheses Heart valve substitutes implanted by transcatheter techniques |
UNE-EN ISO 5840-1:2016
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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
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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
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CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS |
NF EN ISO 7197 : 2009
|
NEUROSURGICAL IMPLANTS - STERILE, SINGLE-USE HYDROCEPHALUS SHUNTS AND COMPONENTS |
I.S. EN ISO 25539-3:2011
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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 |
ASTM F 384 : 2017 : REDLINE
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Standard Specifications and Test Methods for Metallic Angled Orthopedic Fracture Fixation Devices |
ASTM F 543 : 2017 : REDLINE
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Standard Specification and Test Methods for Metallic Medical Bone Screws |
ASTM F 2119 : 2007 : R2013
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Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants (Withdrawn 2022) |
I.S. EN ISO 7197:2009
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NEUROSURGICAL IMPLANTS - STERILE, SINGLE-USE HYDROCEPHALUS SHUNTS AND COMPONENTS |
ISO 7197:2006
|
Neurosurgical implants Sterile, single-use hydrocephalus shunts and components |
EN ISO 25539-2:2012
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Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012) |
UNI EN ISO 14630 : 2013
|
NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
10/30196945 DC : 0
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BS ISO 25539-3 - CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 3: VENA CAVA FILTERS |
BS EN ISO 25539-3:2011
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Cardiovascular implants. Endovascular devices Vena cava filters |
15/30273269 DC : 0
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BS EN ISO 5366 - ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES - PART: TUBES AND CONNECTORS FOR USE IN ADULTS |
CGA SA 21 : 2008(R2009)
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SAFETY ALERT, HAZARDS OF COMPRESSED GAS CYLINDERS IN THE MAGNETIC RESONANCE IMAGING (MRI) ENVIRONMENT |
UNI EN ISO 7197 : 2009
|
NEUROSURGICAL IMPLANTS - STERILE, SINGLE-USE HYDROCEPHALUS SHUNTS AND COMPONENTS |
BS EN ISO 5840-1:2015
|
Cardiovascular implants. Cardiac valve prostheses General requirements |
BS EN ISO 5366:2016
|
Anaesthetic and respiratory equipment. Tracheostomy tubes and connectors |
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
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CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS |
ASTM F 1541 : 2017 : REDLINE
|
Standard Specification and Test Methods for External Skeletal Fixation Devices |
DIN EN ISO 25539-2:2013-05
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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 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 |
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 5366:2016
|
Anaesthetic and respiratory equipment — Tracheostomy tubes and connectors |
IEC 60601-2-33:2010+AMD1:2013+AMD2:2015 CSV
|
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
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 |
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) |
ISO 12417-1:2015
|
Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements |
EN ISO 7197:2009
|
Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007) |
EN ISO 14630:2012
|
Non-active surgical implants - General requirements (ISO 14630:2012) |
EN ISO 12417-1:2015
|
Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
AAMI ISO TIR 12417 : 2011
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
BS EN ISO 25539-1:2017
|
Cardiovascular implants. Endovascular devices Endovascular prostheses |
DIN EN ISO 5840-1 E : 2015
|
CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 1: GENERAL REQUIREMENTS (ISO 58401:2015) |
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) |
14/30281560 DC : 0
|
BS EN ISO 5840-2 - CARDIOVASCULAR IMPLANTS - CARDIAC VALVE PROSTHESES - PART 2: SURGICALLY IMPLANTED HEART VALVE SUBSTITUTES |
PD ISO/TS 10974:2012
|
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device |
ASTM F 2180 : 2017 : REDLINE
|
Standard Specification for Metallic Implantable Strands and Cables |
DIN EN ISO 25539-1:2015-07 (Draft)
|
CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |
ISO 18190:2016
|
Anaesthetic and respiratory equipment — General requirements for airways and related equipment |
UNE-EN ISO 5366:2017
|
Anaesthetic and respiratory equipment - Tracheostomy tubes and connectors (ISO 5366:2016) |
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) |
ASTM F 2052 : 2015 : REDLINE
|
Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment |
ASTM F 2213 : 2017 : REDLINE
|
Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment |
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) |