DIN EN ISO 7405:2013-12
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
DENTISTRY - EVALUATION OF BIOCOMPATIBILITY OF MEDICAL DEVICES USED IN DENTISTRY (ISO 7405:2008 + AMD. 1:2013)
Hardcopy , PDF
03-02-2019
German, English
01-01-2013
This standard is included in DIN Handbook 267.
DevelopmentNote |
Supersedes DIN V 13930. (08/2002) Applies in conjunction with DIN EN ISO 10993 Reihe. (12/2013) DRAFT 2017 issued in April 2017. (04/2017)
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DocumentType |
Standard
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Pages |
42
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PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
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Status |
Superseded
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Supersedes |
Standards | Relationship |
SN EN ISO 7405 : 2009 AMD 1 2013 | Identical |
NF EN ISO 7405 : 2009 AMD 1 2013 | Identical |
ONORM EN ISO 7405 : 2013 | Identical |
UNI EN ISO 7405 : 2013 | Identical |
ISO 7405:2008 | Identical |
I.S. EN ISO 7405:2009 | Identical |
BS EN ISO 7405 : 2008 | Identical |
UNE-EN ISO 7405:2009 | Identical |
NBN EN ISO 7405 : 2009 AMD 1 2013 | Identical |
NEN EN ISO 7405 : 2009 AMD 1 2013 | Identical |
NS EN ISO 7405 : 2008 AMD 1 2013 | Identical |
EN ISO 7405:2008/A1:2013 | Identical |
DIN EN ISO 13017:2016-05 | DENTISTRY - MAGNETIC ATTACHMENTS (ISO 13017:2012 + AMD.1:2015) |
DIN EN ISO 11609:2016-07 (Draft) | DENTISTRY - DENTIFRICES - REQUIREMENTS, TEST METHODS AND MARKING (ISO 11609:2017) |
DIN EN ISO 6876:2012-10 | Dentistry - Root canal sealing materials (ISO 6876:2012) |
DIN EN ISO 22112:2016-04 (Draft) | DENTISTRY - ARTIFICIAL TEETH FOR DENTAL PROSTHESES (ISO 22112:2017) |
DIN EN ISO 9917-1:2008-01 | DENTISTRY - WATER-BASED CEMENTS - PART 1: POWDER/LIQUID ACID-BASE CEMENTS |
DIN EN ISO 9693-2:2016-07 | DENTISTRY - COMPATIBILITY TESTING - PART 2: CERAMIC-CERAMIC SYSTEMS (ISO 9693-2:2016) |
DIN EN ISO 13504:2012-10 | DENTISTRY - GENERAL REQUIREMENTS FOR INSTRUMENTS AND RELATED ACCESSORIES USED IN DENTAL IMPLANT PLACEMENT AND TREATMENT (ISO 13504:2012) |
DIN HDBK 267 : 2ED 2010 | |
DIN EN ISO 27020:2011-04 | DENTISTRY - BRACKETS AND TUBES FOR USE IN ORTHODONTICS |
DIN EN ISO 10451:2010-11 | Dentistry - Contents of technical file for dental implant systems (ISO 10451:2010) |
DIN EN ISO 1564:1999-03 | DENTAL AQUEOUS IMPRESSION MATERIALS BASED ON AGAR |
DIN EN ISO 10993-6:2009-08 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables |
DIN EN ISO 10993-2:2006-10 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
ISO 10993-13:2010 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices |
DIN ISO 6344-1:2000-04 | Coated abrasives - Grain size analysis - Part 1: Grain size distribution test (ISO 6344-1:1999) |
DIN EN ISO 10993-11:2015-12 (Draft) | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 11: TESTS FOR SYSTEMIC TOXICITY |
DIN EN ISO 14971:2013-04 | MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
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 10993-18:2005 | Biological evaluation of medical devices Part 18: Chemical characterization of materials |
DIN EN ISO 10993-5:2009-10 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY |
ISO 10993-10:2010 | Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
ISO 1942:2009 | Dentistry Vocabulary |
ISO 10993-11:2017 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
DIN EN ISO 10993-12:2012-10 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
ISO 10993-12:2012 | Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
ISO 10993-7:2008 | Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals |
ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances |
ADA 41 : 2015 | EVALUATION OF BIOCOMPATIBILITY OF MEDICAL DEVICES USED IN DENTISTRY |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
DIN EN ISO 10993-10:2014-10 | Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
ISO 10993-9:2009 | Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
ISO 6344-1:1998 | Coated abrasives Grain size analysis Part 1: Grain size distribution test |
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 10993-6:2016 | Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
DIN EN ISO 10993-9:2010-04 | Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) |
DIN EN ISO 10993-3:2015-02 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY AND REPRODUCTIVE TOXICITY (ISO 10993-3:2014) |
ISO/TS 22911:2016 | Dentistry Preclinical evaluation of dental implant systems Animal test methods |
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