ISO 13779-1:2008
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Implants for surgery Hydroxyapatite Part 1: Ceramic hydroxyapatite
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
03-18-2019
English, French
09-17-2008
ISO 13779-1:2008 specifies requirements for ceramic hydroxyapatite intended for use as surgical implants.
It applies to hydroxyapatite blocks.
ISO 13779-1:2008 does not apply to hydroxyapatite coatings, hydroxyapatite powder or nanoparticle-type and calcium phosphate ceramics which are not mainly composed of crystalline hydroxyapatite.
DevelopmentNote |
Supersedes ISO/DIS 13779-1. (09/2008)
|
DocumentType |
Standard
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Pages |
3
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PublisherName |
International Organization for Standardization
|
Status |
Withdrawn
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Supersedes |
Standards | Relationship |
NF ISO 13779-1 : 2008 | Identical |
BS ISO 13779-1:2008 | Identical |
BS ISO 13779-2:2008 | Implants for surgery. Hydroxyapatite Coatings of hydroxyapatite |
BS ISO 13779-4:2002 | Implants for surgery. Hydroxyapatite Determination of coating adhesion strength |
ISO 13779-2:2008 | Implants for surgery Hydroxyapatite Part 2: Coatings of hydroxyapatite |
06/19977151 DC : DRAFT JUN 2006 | BS ISO 13779-3 - IMPLANTS FOR SURGERY - HYDROXYAPATITE - PART 3: CHEMICAL ANALYSIS AND CHARACTERIZATION OF CRYSTALLINITY AND PHASE PURITY |
14/30267655 DC : 0 | BS ISO 13779-6 - IMPLANTS FOR SURGERY - HYDROXYAPATITE - PART 6: POWDERS |
BS ISO 12891-2:2014 | Retrieval and analysis of surgical implants Analysis of retrieved surgical implants |
BS ISO 13779-3:2008 | Implants for surgery. Hydroxyapatite Chemical analysis and characterization of crystallinity and phase purity |
I.S. EN ISO 22794:2009 | DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
ISO 13779-4:2002 | Implants for surgery Hydroxyapatite Part 4: Determination of coating adhesion strength |
DIN EN ISO 22794:2009-11 | 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 | Dentistry Implantable materials for bone filling and augmentation in oral and maxillofacial surgery Contents of a technical file |
ISO 13779-3:2008 | Implants for surgery Hydroxyapatite Part 3: Chemical analysis and characterization of crystallinity and phase purity |
17/30302770 DC : 0 | BS ISO 13779-3 - IMPLANTS FOR SURGERY - HYDROXYAPATITE - PART 3: CHEMICAL ANALYSIS AND CHARACTERIZATION OF CRYSTALLINITY RATIO AND PHASE PURITY |
ISO 13779-6:2015 | Implants for surgery Hydroxyapatite Part 6: Powders |
ISO 12891-2:2014 | Retrieval and analysis of surgical implants Part 2: Analysis of retrieved surgical implants |
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 22794:2009 | 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) |
BS ISO 13779-6:2015 | Implants for surgery. Hydroxyapatite Powders |
UNI EN ISO 22794 : 2009 | DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE |
ISO 5961:1994 | Water quality Determination of cadmium by atomic absorption spectrometry |
ISO 13779-3:2008 | Implants for surgery Hydroxyapatite Part 3: Chemical analysis and characterization of crystallinity and phase purity |
NFS 94 067 : 1993 XP | MATERIALS FOR SURGICAL IMPLANTS - QUALITATIVE AND QUANTITATIVE - DETERMINATION OF THE FOREIGN PHASES PRESENT IN CALCIUM PHOSPHATE BASED POWDERS, DEPOSITS AND CERAMICS |
ISO 8288:1986 | Water quality — Determination of cobalt, nickel, copper, zinc, cadmium and lead — Flame atomic absorption spectrometric methods |
ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances |
NFS 94 068 : 1993 XP | MATERIALS FOR SURGICAL IMPLANTS - DETERMINATION OF THE CRYSTALLINITY AND OF THE APPARENT SIZE OF THE APATITE CRYSTALLITES OF HYDROXYAPATITE BASED POWDERS, DEPOSITS AND CERAMICS |
NFS 94 066 : 1998 | MATERIALS FOR SURGICAL IMPLANTS - QUANTITATIVE DETERMINATION OF THE CA/P RATIO OF CALCIUM PHOSPHATES |
NFS 94 065 : 1998 | MATERIALS FOR SURGICAL IMPLANTS - DETERMINATION OF ARSENIC, MERCURY, CADMIUM AND LEAD ON COATINGS BASED ON PHOSPHATE OF CALCIUM |
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