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Norm
ÖNORM EN ISO 10993-10
Issue date: 2010 01 01
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006)
This part of ISO 10993 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation ...
Withdrawn: 2010 10 15
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 64 Pages
Language:
German
| English
Currently valid:
Optionally co-design standards:
ICS
This part of ISO 10993 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and delayed-type hypersensitivity.
This part of ISO 10993 includes pretest considerations, details of the test procedures, and key factors for the interpretation of the results.
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ÖNORM EN ISO 10993-10
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ÖNORM EN ISO 10993-10
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Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensi...
Norm
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ÖNORM EN ISO 10993-10
2006 12 01
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensi...
Norm
ÖNORM EN ISO 10993-10
2003 03 01
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensi...
Norm
ÖNORM EN ISO 10993-10
1996 07 01
Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 1099...
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2006 07 06
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2009 11 30
Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products
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2007 10 31
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials (Corrected version 2008-02)
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2010 05 06
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
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2001 11 22
Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
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2000 11 30
Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys (Corrected version 2001-03)
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2005 06 30
Biological evaluation of medical devices — Part 18: Chemical characterization of materials
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2003 02 26
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2003 05 16
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1997 12 11
Biological evaluation of medical devices — Part 1: Evaluation and testing
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2006 07 06
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2019 11 26
Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products
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2010 06 04
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
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Issue date :
2001 11 22
Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
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Issue date :
2019 11 26
Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys
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2020 01 13
Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
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2003 02 26
Clinical investigation of medical devices for human subjects — Part 1: General requirements
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Issue date :
2003 05 16
Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans
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Issue date :
2010 10 15
Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
Norm
Issue date :
2002 09 26
Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity
