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About This Item
Full Description
Cross References:
ISO 8601
ISO 14971
ISO 15223-1
ISO 18113-1
EN 980
ISO 17511
ISO 18113-3
ISO 18153
ISO/IEC Directives Part 2
EN 375:2001
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 18113-2:2024
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for professional use- Most Recent
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BS EN ISO 18113-2:2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for professional use- Historical Version
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BS EN ISO 18113-2:2009
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In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for professional use- Historical Version
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BS 06/30146515 DC
BS ISO 18113-2. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use- Historical Version
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BS EN 375:2001
Information supplied by the manufacturer with in vitro diagnostic reagents for professional use- Historical Version
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BS EN 375:1992
Specification for labelling of in vitro diagnostic reagents for professional use- Historical Version