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About This Item
Full Description
- test sample selection;
- selection of representative portions from a device;
- test sample preparation;
- experimental controls;
- selection of and requirements for reference materials;
- preparation of extracts.
BS EN ISO 10993-12:2009 is not applicable to materials or devices containing live cells.
Cross References:
ISO 10993-1:2003
ISO 14971
ISO Guide 30
ISO Guide 31
ISO Guide 33
ISO Guide 34
ISO Guide 35
NF S 90-701
93/42/EEC
90/385/EEC
All current amendments available at time of purchase are included with the purchase of this document.
Document History
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BS EN ISO 10993-12:2021
Biological evaluation of medical devices-Sample preparation and reference materials- Most Recent
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BS EN ISO 10993-12:2012
Biological evaluation of medical devices-Sample preparation and reference materials- Historical Version
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BS EN ISO 10993-12:2009
viewing
Biological evaluation of medical devices-Sample preparation and reference materials- Historical Version
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BS EN ISO 10993-12:2007
Biological evaluation of medical devices-Sample preparation and reference materials- Historical Version
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BS 06/30145887 DC
EN ISO 10993-12. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials- Historical Version
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BS EN ISO 10993-12:2004
Biological evaluation of medical devices-Sample preparation and reference materials- Historical Version
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BS EN ISO 10993-12:1997
Biological evaluation of medical devices-Sample preparation and reference materials- Historical Version