Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-01-2006

Publisher

German Institute for Standardisation (Deutsches Institut für Normung)

DocumentType	Standard
Pages	12
PublisherName	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Current

Standards	Relationship
NBN EN ISO 22803 : 2006	Identical
NS EN ISO 22803 : 1ED 2006	Identical
BS EN ISO 22803:2005	Identical
NF EN ISO 22803 : 2006	Identical
UNE-EN ISO 22803:2006	Identical
I.S. EN ISO 22803:2005	Identical
NEN EN ISO 22803 : 2005	Identical
EN ISO 22803:2005	Identical
ISO 22803:2004	Identical
SN EN ISO 22803 : 2005	Identical
UNI EN ISO 22803 : 2006	Identical

DIN HDBK 267/2 : 2ED 2014

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ISO 14160:2011	Sterilization of health care products Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
ISO 11135:2014	Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices
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ISO 10993-13:2010	Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
ISO 1942-1:1989	Dental vocabulary Part 1: General and clinical terms
ISO 14937:2009	Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
ISO 14155-1:2003	Clinical investigation of medical devices for human subjects Part 1: General requirements
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ISO 10993-2:2006	Biological evaluation of medical devices — Part 2: Animal welfare requirements
ISO 10993-14:2001	Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
ISO 14630:2012	Non-active surgical implants General requirements
ISO/TR 14283:2004	Implants for surgery Fundamental principles
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 10993-18:2005	Biological evaluation of medical devices Part 18: Chemical characterization of materials
DIN EN ISO 14155-1:2009-11	CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS - PART 1: GENERAL REQUIREMENTS
ISO 10993-10:2010	Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
DIN EN 980:2008-08	SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES
ISO 13408-1:2008	Aseptic processing of health care products — Part 1: General requirements
ISO 1942:2009	Dentistry Vocabulary
ISO 10993-11:2017	Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
ISO 10993-12:2012	Biological evaluation of medical devices Part 12: Sample preparation and reference materials
DIN EN ISO 11135-1:2007-08	STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
ISO 10993-7:2008	Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 11607:2003	Packaging for terminally sterilized medical devices
ISO 10993-9:2009	Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
ISO 11134:1994	Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization
DIN EN ISO 1942:2011-03	Dentistry - Vocabulary (ISO 1942:2009, Corrected version 2010-03-01)
ISO 14971:2007	Medical devices Application of risk management to medical devices
ISO 11137:1995	Sterilization of health care products Requirements for validation and routine control Radiation sterilization
EN 980:2008	Symbols for use in the labelling of medical devices
ISO 10993-6:2016	Biological evaluation of medical devices Part 6: Tests for local effects after implantation
ISO 15223:2000	Medical devices Symbols to be used with medical device labels, labelling and information to be supplied