Committee
|
TC 194 |
Development Note
|
Supersedes DIN EN 30993-3. (05/2004) |
Document Type
|
Standard |
ISBN
|
|
Pages
|
|
Published
|
|
Publisher
|
German Institute for Standardisation (Deutsches Institut für Normung)
|
Status
|
Current |
Supersedes
|
|
DIN EN ISO 11979-5:2010-11
|
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006) |
DIN EN ISO 10993-7:2009-02
|
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008) |
DIN EN ISO 10993-1:2010-04
|
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009) |
DIN EN ISO 7405:2013-12
|
DENTISTRY - EVALUATION OF BIOCOMPATIBILITY OF MEDICAL DEVICES USED IN DENTISTRY (ISO 7405:2008 + AMD. 1:2013) |
DIN EN ISO 14534:2015-08
|
Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011) |
DIN EN ISO 10993-6:2009-08
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
DIN EN ISO 10993-2:2006-10
|
Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
ISO/TR 10993-33:2015
|
Biological evaluation of medical devices Part 33: Guidance on tests to evaluate genotoxicity Supplement to ISO 10993-3 |
ISO 10993-2:2006
|
Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 10993-18:2005
|
Biological evaluation of medical devices Part 18: Chemical characterization of materials |
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 |
CFR 40(PTS700-789) : JUL 2016
|
PROTECTION OF ENVIRONMENT - ENVIRONMENTAL PROTECTION AGENCY |
DIN EN ISO 10993-18:2009-08
|
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005); German version EN ISO 10993-18:2009 |
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 10993-6:2016
|
Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
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