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About This Item
Full Description
Cross References:
EN 375:2001
EN 592:2002
EN 980
EN 28601
ISO 8601:1988
ISO 8601:1988/Technical Corrigendum:1991
ISO 3864
ISO 7000
67/548/EEC
88/379/EEC
91/325/EEC
98/79/EC
99/45/EC
ISO 1000
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
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
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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