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About This Item
Full Description
Cross References:
EN 980
ISO 8601
ISO 14971
ISO 15198
ISO 15223
ISO 18113-1
ISO 17511:2003
ISO 18113-5
ISO 18153
ISO/IEC Directives
EN 376:2001
CLSI C28-A2:2000
CLSI GP10-A.:1995
98/79/EC:1998
GHTF/SG1/N43:2005
Document History
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BS EN ISO 18113-4:2024
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing- Most Recent
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BS EN ISO 18113-4:2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing- Historical Version
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BS EN ISO 18113-4:2009
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing- Historical Version
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BS 06/30146522 DC
viewing
BS ISO 18113-4. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing- Historical Version
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BS EN 376:2002
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing- Historical Version
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BS EN 376:1992
Specification for labelling of in vitro diagnostic reagents for self-testing- Historical Version