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ASTM F 1714 : 1996 : R2013
|
Standard Guide for Gravimetric Wear Assessment of Prosthetic Hip Designs in Simulator Devices |
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ASTM F 1715 : 2000
|
Standard Guide for Wear Assessment of Prosthetic Knee Designs in Simulator Devices |
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ASTM F 603 : 2012
|
Standard Specification for High-Purity Dense Aluminum Oxide for Medical Application |
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ASTM F 2665 : 2009 : R2014
|
Standard Specification for Total Ankle Replacement Prosthesis |
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ASTM F 1714 : 1996 : R2008
|
Standard Guide for Gravimetric Wear Assessment of Prosthetic Hip Designs in Simulator Devices |
|
BS 6444-1:1990
|
Cardiovascular implants Methods of test for heart valve substitutes and requirements for their packaging and labelling |
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09/30180393 DC : 0
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BS EN ISO 10451 - DENTISTRY - CONTENTS OF TECHNICAL FILE FOR DENTAL IMPLANT SYSTEMS |
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ASTM F 2665 : 2009
|
Standard Specification for Total Ankle Replacement Prosthesis |
|
ASTM F 2027 : 2016 : REDLINE
|
Standard Guide for Characterization and Testing of Raw or Starting Materials for Tissue-Engineered Medical Products |
|
ASTM F 1714 : 1996 : R2002
|
Standard Guide for Gravimetric Wear Assessment of Prosthetic Hip-Designs in Simulator Devices |
|
BS EN 12010:1998
|
Non-active surgical implants. Joint replacement implants. Particular requirements |
|
I.S. EN ISO 14727:1999
|
DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE |
|
I.S. EN ISO 10993-14:2009
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 14: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM CERAMICS (ISO 10993-14:2001) |
|
14/30290166 DC : 0
|
BS ISO 16142-1 - MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 1: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL NON-IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
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AAMI ISO 10993-14 : 2001
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 14: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM CERAMICS |
|
ASTM F 603 : 2012 : R2016
|
Standard Specification for High-Purity Dense Aluminum Oxide for Medical Application |
|
UNI EN ISO 10993-14 : 2009
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 14: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM CERAMICS |
|
ASTM F 1714 : 1996
|
Standard Guide for Gravimetric Wear Assessment of Prosthetic Hip-Designs in Simulator Devices |
|
ANSI/AAMI/ISO 10993-14:2001(R2011)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 14: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM CERAMICS |
|
CSA ISO 10993-6 : 1997(R2009)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
|
BS EN ISO 10993-14:2009
|
Biological evaluation of medical devices Identification and quantification of degradation products from ceramics |
|
ISO 14727:1998
|
Dental implants Prefabricated parts connecting suprastructures to dental implants Contents of technical file |
|
BS EN ISO 14727:1999
|
Dental implants. Prefabricated parts connecting suprastructures to dental implants. Contents of technical file |
|
BS EN 30993-6:1995
|
Biological evaluation of medical devices Tests for local effects after implantation |
|
ISO 10993-14:2001
|
Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics |
|
EN ISO 14727:1998/AC:1998
|
DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE |
|
EN ISO 10993-14:2009
|
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) |
|
DIN EN ISO 10993-14 E : 2009
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 14: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM CERAMICS |
|
DIN EN ISO 10993-14:2009-08
|
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) |