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I.S. EN ISO 14727:1999

Withdrawn
Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE
Available format(s)

Hardcopy , PDF

Withdrawn date

08-06-2005

Language(s)

English

Published date

28-05-1999

Publisher

National Standards Authority of Ireland

Preview

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.

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Withdrawn

ISO 6507-1:2005 Metallic materials Vickers hardness test Part 1: Test method
EN 21942-1 : 1991 DENTAL VOCABULARY - GENERAL AND CLINICAL TERMS
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
EN ISO 10993-1:2009/AC:2010 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)

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Hardcopy - English
PDF - English
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