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About This Item
Full Description
Cross References:
EN 980
IEC 61010-1
IEC 61010-2-101
IEC 61326
IEC 62366
ISO 14971
ISO 15198
ISO 15223
ISO 18113-1
ISO 18113-2
ISO/IEC Directives
EN 591:2001
98/79/EC:1998
GHTF/SG1/N43:2005
Document History
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BS EN ISO 18113-3:2024
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic instruments for professional use- Most Recent
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BS EN ISO 18113-3:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic instruments for professional use- Historical Version
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BS EN ISO 18113-3:2009
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic instruments for professional use- Historical Version
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BS 06/30146518 DC
viewing
BS ISO 18113-3. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use- Historical Version
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BS EN 591:2001
Instructions for use for in vitro diagnostic instruments for professional use- Historical Version
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BS EN 591:1995
Specification for user manuals for in vitro diagnostic instruments for professional use- Historical Version