ISO 6474:1994
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Implants for surgery Ceramic materials based on high purity alumina
Available format(s)
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
Withdrawn date
21-02-2019
Superseded by
Language(s)
English, French
Published date
03-02-1994
Important note : Users cannot be edited or removed once added to your Multi user PDF.
Specification of characteristics and corresponding test methods for biocompatible and bio-stable ceramic bone substitutes based on high purity alumina.
| DevelopmentNote |
DRAFT ISO/DIS 6474 is also available for this standard. (03/2003) Also numbered as BS 7253-2(1997) (09/2005)
|
| DocumentType |
Standard
|
| Pages |
6
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| NFS 90 408 : 1981 | Similar to |
| DIN ISO 6474 E : 2001 | Identical |
| BIS IS 5347-9 : 1998(R2003) | Identical |
| DIN ISO 6474:2001-06 | Identical |
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| ASTM F 1715 : 2000 | Standard Guide for Wear Assessment of Prosthetic Knee Designs in Simulator Devices |
| ASTM F 603 : 2012 | Standard Specification for High-Purity Dense Aluminum Oxide for Medical Application |
| ASTM F 2665 : 2009 : R2014 | Standard Specification for Total Ankle Replacement Prosthesis |
| 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 |
| 09/30180393 DC : 0 | BS EN ISO 10451 - DENTISTRY - CONTENTS OF TECHNICAL FILE FOR DENTAL IMPLANT SYSTEMS |
| 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 | 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 |
| 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 10993-14:2009-08 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) |
| ISO 5017:2013 | Dense shaped refractory products — Determination of bulk density, apparent porosity and true porosity |
| ISO 5436:1985 | Calibration specimens Stylus instruments Types, calibration and use of specimens |
| ISO 468:1982 | Surface roughness — Parameters, their values and general rules for specifying requirements |
| ISO 3611:2010 | Geometrical product specifications (GPS) — Dimensional measuring equipment: Micrometers for external measurements — Design and metrological characteristics |
| ASTM C 573 : 1981 : R1990 | Methods for Chemical Analysis of Fireclay and High-Alumina Refractories |
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