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STN EN ISO 10993-11 (856520)
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Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
WITHDRAWN published on 1.12.2006
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STN EN ISO 10993-12 (856521)
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Biological evaluation of medical devices. Part 12: Sample preparation and reference materials
WITHDRAWN published on 1.12.2000
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STN EN ISO 10993-12 (856521)
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Biological evaluation of medical devices. Part 12: Sample preparation and reference materials
WITHDRAWN published on 1.4.2005
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STN EN ISO 10993-12 (856521)
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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)
WITHDRAWN published on 1.5.2008
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STN EN ISO 10993-13 (856522)
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Biological evaluation of medical devices. Part 13: Identification and quantification of degradation products from polymeric medical devices
WITHDRAWN published on 1.7.2001
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STN EN ISO 10993-14 (856523)
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Biological evaluation of medical devices. Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
WITHDRAWN published on 1.4.2003
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STN EN ISO 10993-15 (856524)
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Biological evaluation of medical devices. Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)
WITHDRAWN published on 1.5.2003
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STN EN ISO 10993-16 (856525)
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Biological evaluation of medical devices. Part 16: Toxicokinetic study design for degradation products and leachables
WITHDRAWN published on 1.6.2001
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STN EN ISO 10993-17 (856526)
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Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
WITHDRAWN published on 1.1.2004
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STN EN ISO 10993-17 (856526)
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Biological evaluation of medical devices. Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
WITHDRAWN published on 1.4.2004
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