EN ISO 22523 : 2006
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EXTERNAL LIMB PROSTHESES AND EXTERNAL ORTHOSES - REQUIREMENTS AND TEST METHODS (ISO 22523:2006) |
VDI 2221:1993-05
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Systematic approach to the development and design of technical systems and products |
EN ISO 10993-5:2009
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Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) |
EN ISO 22675:2016
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Prosthetics - Testing of ankle-foot devices and foot units - Requirements and test methods (ISO 22675:2016) |
ISO 22523:2006
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External limb prostheses and external orthoses — Requirements and test methods |
EN ISO 14155:2011/AC:2011
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CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS - GOOD CLINICAL PRACTICE (ISO 14155:2011) |
VDI 3880:2011-10
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Olfactometry - Static sampling |
DIN EN ISO 14971:2013-04
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MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
DIN EN ISO 22675:2016-12
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PROSTHETICS - TESTING OF ANKLE-FOOT DEVICES AND FOOT UNITS - REQUIREMENTS AND TEST METHODS (ISO 22675:2016) |
EN ISO 10993-10:2013
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Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
DIN EN ISO 22523:2007-04
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External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006) |
EN 15259:2007
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Air quality - Measurement of stationary source emissions - Requirements for measurement sections and sites and for the measurement objective, plan and report |
ISO 10993-18:2005
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Biological evaluation of medical devices Part 18: Chemical characterization of materials |
VDI 1000:2017-02
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VDI Standardisation Work - Principles and procedures |
DIN EN ISO 10993-5:2009-10
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY |
ISO 10993-10:2010
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Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
DIN EN ISO 10993-12:2012-10
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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
ISO 10993-12:2012
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Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
DIN EN ISO 10993-18:2009-08
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Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005); German version EN ISO 10993-18:2009 |
ISO 10110-1:2006
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Optics and photonics Preparation of drawings for optical elements and systems Part 1: General |
DIN EN ISO 14155:2012-01
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CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS - GOOD CLINICAL PRACTICE (ISO 14155:2011 + COR. 1:2011) |
EN ISO 10993-18:2009
|
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) |
EN ISO 14971:2012
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Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
DIN EN ISO 10993-10:2014-10
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Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
EN ISO 10993-12:2012
|
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
ISO 14155:2011
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Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
VDI 2066 Blatt 1:1975-10
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Particulate matter measurement; measuring of particulate matter in flowing gases; gravimetric determination of dust load; fundamentals |
ISO 22675:2016
|
Prosthetics Testing of ankle-foot devices and foot units Requirements and test methods |
DIN EN 15259:2008-01
|
Air quality - Measurement of stationary source emissions - Requirements for measurement sections and sites and for the measurement objective, plan and report |
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) |