I.S. EN ISO 14727:1999
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE
Hardcopy , PDF
08-06-2005
English
28-05-1999
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Dates of withdrawal of national standards are available from NSAI.
Important note : Users cannot be edited or removed once added to your Multi user PDF.
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
Bibliography
Annex ZA (normative) Normative references to international
publications with their relevant European
publications
Defines requirements for the contents of a technical file for prefabricated parts connecting a dental suprastructure to a transgingival dental implant.
| DocumentType |
Standard
|
| Pages |
28
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Withdrawn
|
| Standards | Relationship |
| UNE-EN ISO 14727:1999 | Identical |
| DIN EN ISO 14727:1999-03 | Identical |
| BS EN ISO 14727:1999 | Identical |
| ISO 14727:1998 | Identical |
| NEN EN ISO 14727 : 1998 | Identical |
| SN EN ISO 14727 : 1999 | Identical |
| NS EN ISO 14727 : 99 AC 1999 | Identical |
| UNI EN ISO 14727 : 1999 | Identical |
| EN ISO 14727:1998/AC:1998 | Identical |
| NF EN ISO 14727 : 1999 | Identical |
| NBN EN ISO 14727 : 1998 | Identical |
| ISO 6507-1:2005 | Metallic materials Vickers hardness test Part 1: Test method |
| EN 21942-1 : 1991 | DENTAL VOCABULARY - GENERAL AND CLINICAL TERMS |
| ISO 6892:1998 | Metallic materials Tensile testing at ambient temperature |
| ISO 1942-1:1989 | Dental vocabulary Part 1: General and clinical terms |
| EN 540 : 1993 | CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS |
| ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
| ISO 7405:2008 | Dentistry Evaluation of biocompatibility of medical devices used in dentistry |
| ISO 406:1987 | Technical drawings Tolerancing of linear and angular dimensions |
| ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 5832-2:1999 | Implants for surgery Metallic materials Part 2: Unalloyed titanium |
| ISO 6474:1994 | Implants for surgery Ceramic materials based on high purity alumina |
| ISO 9001:2015 | Quality management systems — Requirements |
| ISO 14155:2011 | Clinical investigation of medical devices for human subjects Good clinical practice |
| EN 28601 : 1992 | DATA ELEMENTS AND INTERCHANGE FORMATS - INFORMATION INTERCHANGE - REPRESENTATION OF DATES AND TIMES |
| ISO 178:2010 | Plastics Determination of flexural properties |
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