Document Type
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Standard |
ISBN
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|
Pages
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|
Published
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|
Publisher
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German Institute for Standardisation (Deutsches Institut für Normung)
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Status
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Current |
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 10993-10:2014-10
|
Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
DIN EN ISO 10993-15:2009-10
|
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) |
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) |
ISO 5017:2013
|
Dense shaped refractory products — Determination of bulk density, apparent porosity and true porosity |
ISO 3310-1:2016
|
Test sieves Technical requirements and testing Part 1: Test sieves of metal wire cloth |
ISO 6872:2015
|
Dentistry Ceramic materials |
EN ISO 10993-9:2009
|
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) |
DIN EN ISO 6872:2015-11
|
DENTISTRY - CERAMIC MATERIALS (ISO 6872:2015) |
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 6474:1994
|
Implants for surgery Ceramic materials based on high purity alumina |
ISO 10993-9:2009
|
Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
ISO 3696:1987
|
Water for analytical laboratory use — Specification and test methods |
EN ISO 3696:1995
|
Water for analytical laboratory use - Specification and test methods (ISO 3696:1987) |
DIN ISO 3696:1991-06
|
WATER FOR ANALYTICAL LABORATORY USE - SPECIFICATION AND TEST METHODS |
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) |
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) |
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