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About This Item
Full Description
Cross References:
ISO 14971
ISO 15223-1
ISO 18113-1
EN 980
ISO 15197
ISO 17593
ISO 18113-5
ISO/IEC Directives Part 2
EN 376:2002
CLSI C28-A2:2000
CLSI GP10-A:1995
98/79/EC
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 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
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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
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